JP2014058512A

JP2014058512A - Thiazole derivative and pest control agent

Info

Publication number: JP2014058512A
Application number: JP2013172466A
Authority: JP
Inventors: Hirotaka Furukawa; 裕貴古川; Akira Numata; 昭沼田; Kiminori Ando; 公則安藤
Original assignee: Nissan Chemical Corp
Current assignee: Nissan Chemical Corp
Priority date: 2012-08-22
Filing date: 2013-08-22
Publication date: 2014-04-03

Abstract

PROBLEM TO BE SOLVED: To provide a novel pest control agent, in particular, an insecticide or an acaricide.SOLUTION: This invention provides: a thiazole derivative expressed by Formula (1), where Arepresents N(O)or CR, Arepresents a pyrazole group which may be substituted, R, R, Reach independently represent a hydrogen atom, a halogen atom, C-Calkyl or the like, n represents an integer of 0-3, and m1 and m2 each independently represent an integer of 0 or 1; and a pest control agent containing the thiazole derivative.

Description

本発明は、新規なチアゾ−ル誘導体及びそれらの塩、並びに該化合物を有効成分として含有することを特徴とする有害生物防除剤に関するものである。本発明における有害生物防除剤とは、農園芸分野又は畜産・衛生分野（家畜や愛玩動物としての哺乳動物又は鳥類に対する内部寄生虫・外部寄生虫や家庭用及び業務用の衛生害虫・不快害虫）等における有害な節足動物を対象とした害虫防除剤を意味する。また、本発明における農薬とは、農園芸分野における殺虫・殺ダニ剤、殺線虫剤、除草剤及び殺菌剤等を意味する。 The present invention relates to a novel thiazol derivative and a salt thereof, and a pest control agent comprising the compound as an active ingredient. The pest control agent in the present invention is the field of agriculture and horticulture or the field of livestock and hygiene (internal parasites / external parasites for domestic animals and pets, hygiene pests and unpleasant pests for domestic and commercial use) It means a pest control agent for harmful arthropods such as The agrochemical in the present invention means an insecticide / acaricide, nematicide, herbicide, fungicide, etc. in the field of agriculture and horticulture.

例えば、特許文献５〜特許文献８及び非特許文献１には、チアゾ−ル誘導体が開示されているが、本発明に係るチアゾ−ル誘導体に関しては何ら開示されていない。さらに、その有害生物防除剤、特に殺虫・殺ダニ剤及び哺乳動物又は鳥類の内部もしくは外部寄生虫防除剤としての有用性も全く知られていない。 For example, Patent Documents 5 to 8 and Non-Patent Document 1 disclose thiazol derivatives, but none of the thiazole derivatives according to the present invention is disclosed. Furthermore, its usefulness as a pest control agent, particularly an insecticide / acaricide, and an internal or ectoparasite control agent for mammals or birds is not known at all.

また、特許文献１〜特許文献４には、チアゾール誘導体が殺虫剤として有用であることが開示されているが、本発明に係るチアゾール化合物については何ら開示されていない。 Patent Documents 1 to 4 disclose that thiazole derivatives are useful as insecticides, but do not disclose any thiazole compounds according to the present invention.

国際公開第２０１１／１５７７７８号International Publication No. 2011/157778 国際公開第２０１１／１３８２８５号International Publication No. 2011/138285 国際公開第２０１１／１３４９６４号International Publication No. 2011/134964 国際公開第２０１０／００６７１３号International Publication No. 2010/006713 国際公開第２０１０／０７１７４１号International Publication No. 2010/071741 国際公開第２００７／０３３７８０号International Publication No. 2007/033780 国際公開第２００３／０１５７７６号International Publication No. 2003/015776 米国特許出願公開第３９６４８９６号US Patent Application No. 3964896

バイオオーガニックアンドメディシナルケミストリ− レタース２０１０年，２０巻，２８２８頁Bioorganic and Medicinal Chemistry Letters 2010, 20, 2828

農園芸病害虫、森林病害虫、或いは衛生病害虫等、各種病害虫の防除を目的とする有害生物防除剤の開発が進み、多種多様な薬剤が今日まで実用に供されてきた。 The development of pest control agents for the purpose of controlling various pests such as agricultural and horticultural pests, forest pests, and hygiene pests has progressed, and a wide variety of drugs have been put to practical use to date.

しかしながら、こうした薬剤の長年にわたる使用により、近年、病害虫が薬剤抵抗性を獲得し、従来用いられてきた既存の殺虫剤や殺菌剤による防除が困難となる場面が増えてきている。また、既存の有害生物防除剤の一部のものは毒性が高く、或いはあるものは環境中に長期間残留することにより、生態系を攪乱するという問題も顕在化しつつある。このような状況下、高度な有害生物防除活性を有するのみならず、低毒性且つ低残留性の新規な有害生物防除剤の開発が常に期待されている。 However, due to the long-term use of such drugs, in recent years, pests have acquired drug resistance, making it difficult to control with existing insecticides and fungicides that have been used. In addition, some existing pest control agents are highly toxic, or some of them remain in the environment for a long time, and the problem of disturbing the ecosystem is becoming apparent. Under such circumstances, development of a novel pest control agent having not only high pest control activity but also low toxicity and low persistence is always expected.

本発明者らは、上記の課題解決を目標に鋭意研究を重ねた結果、本発明に係る下記式（１）で表される新規なチアゾ−ル誘導体が優れた有害生物防除活性、特に殺虫・殺ダニ活性を示し、且つ、ホ乳動物、魚類及び益虫等の非標的生物に対してほとんど悪影響の無い、極めて有用な化合物であることを見い出し、本発明を完成した。 As a result of intensive studies aimed at solving the above problems, the present inventors have found that the novel thiazol derivative represented by the following formula (1) according to the present invention has excellent pest control activity, particularly insecticide The present invention was completed by discovering that it is a very useful compound that exhibits acaricidal activity and has almost no adverse effect on non-target organisms such as mammals, fish and beneficial insects.

すなわち、本発明は下記〔１〕〜〔９〕に関するものである。 That is, the present invention relates to the following [1] to [9].

〔１〕
式（１）： [1]
Formula (1):

［式中、Ａ^１は、Ｎ（Ｏ）_ｍ２又はＣＲ^１を表し、
Ａ^２は、Ｄ１−１５、Ｄ１−１６又はＤ１−１７を表し、
Ｒ^１は、水素原子、ハロゲン原子、シアノ、ニトロ、−ＯＨ、−ＳＨ、−ＮＨ_２、-ＣＨＯ、−Ｃ（Ｏ）ＯＨ、−Ｃ（Ｏ）ＮＨ_２、−Ｃ（Ｓ）ＮＨ_２、−Ｓ（Ｏ）_２ＮＨ_２、Ｃ_１〜Ｃ_６アルキル、Ｃ_１〜Ｃ_６ハロアルキル、Ｃ_１〜Ｃ_６アルコキシ、Ｃ_１〜Ｃ_６ハロアルコキシ、Ｃ_１〜Ｃ_６アルキルチオ、Ｃ_１〜Ｃ_６アルキルスルフィニル、Ｃ_１〜Ｃ_６アルキルスルホニル、Ｃ_１〜Ｃ_６ハロアルキルチオ、Ｃ_１〜Ｃ_６ハロアルキルスルフィニル又はＣ_１〜Ｃ_６ハロアルキルスルホニルを表し、
Ｒ^２は、ハロゲン原子、シアノ、ニトロ、−ＯＨ、−ＳＨ、−ＮＨ_２、-ＣＨＯ、−Ｃ（Ｏ）ＯＨ、−Ｃ（Ｏ）ＮＨ_２、−Ｃ（Ｓ）ＮＨ_２、−Ｓ（Ｏ）_２ＮＨ_２、Ｃ_１〜Ｃ_６アルキル、Ｃ_１〜Ｃ_６ハロアルキル、Ｃ_１〜Ｃ_６アルコキシ、Ｃ_１〜Ｃ_６ハロアルコキシ、Ｃ_１〜Ｃ_６アルキルチオ、Ｃ_１〜Ｃ_６アルキルスルフィニル、Ｃ_１〜Ｃ_６アルキルスルホニル、Ｃ_１〜Ｃ_６ハロアルキルチオ、Ｃ_１〜Ｃ_６ハロアルキルスルフィニル又はＣ_１〜Ｃ_６ハロアルキルスルホニルを表し、ｎが２以上の整数を表すとき、各々のＲ^２は互いに同一であっても又は互いに相異なってもよく、
Ｒ^３は、水素原子、ハロゲン原子、シアノ、ニトロ、−ＯＨ、−ＳＨ、−ＮＨ_２、-ＣＨＯ、−Ｃ（Ｏ）ＯＨ、−Ｃ（Ｏ）ＮＨ_２、−Ｃ（Ｓ）ＮＨ_２、−Ｓ（Ｏ）_２ＮＨ_２、Ｃ_１〜Ｃ_６アルキル、Ｃ_３〜Ｃ_６シクロアルキル、Ｃ_２〜Ｃ_６アルケニル、Ｃ_２〜Ｃ_６アルキニル、Ｃ_１〜Ｃ_６ハロアルキル、Ｃ_１〜Ｃ_６アルコキシ、Ｃ_１〜Ｃ_６ハロアルコキシ、Ｃ_１〜Ｃ_６アルキルチオ、Ｃ_１〜Ｃ_６アルキルスルフィニル、Ｃ_１〜Ｃ_６アルキルスルホニル、Ｃ_１〜Ｃ_６ハロアルキルチオ、Ｃ_１〜Ｃ_６ハロアルキルスルフィニル、Ｃ_１〜Ｃ_６ハロアルキルスルホニル、シアノ、Ｃ_１〜Ｃ_６アルコキシカルボニル、Ｃ_１〜Ｃ_６アルキルカルボニル、Ｃ_１〜Ｃ_６アルキルアミノカルボニル又はジ（Ｃ_１〜Ｃ_６アルキル）アミノカルボニルを表し、
Ｄ１−１５、Ｄ１−１６及びＤ１−１７は、それぞれ下記の構造式で表される環を表し、 [Wherein A ¹ represents N (O) _{m 2} or CR ¹ ;
A ² represents D1-15, D1-16 or D1-17,
R ¹ is a hydrogen atom, a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , —CHO, —C (O) OH, —C (O) NH ₂ , —C (S) NH ₂ , _{_{_{-S (O) 2 NH 2,}}} C 1 ~C 6 _alkyl, C 1 -C ₆ _haloalkyl, C 1 -C ₆ _alkoxy, C 1 -C ₆ _haloalkoxy, C 1 -C ₆ _alkylthio, C 1 -C ₆ represents _{alkylsulfinyl,} C 1 -C ₆ _{alkylsulfonyl,} C 1 -C ₆ _{haloalkylthio,} a C 1 -C ₆ haloalkylsulfinyl or _C 1 -C ₆ haloalkylsulfonyl,
R ² is a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , —CHO, —C (O) OH, —C (O) NH ₂ , —C (S) NH ₂ , —S ( _{_{_{O) 2 NH 2, C 1}}} ~C 6 _alkyl, C 1 -C ₆ _haloalkyl, C 1 -C ₆ _alkoxy, C 1 -C ₆ _haloalkoxy, C 1 -C ₆ _alkylthio, C 1 -C ₆ alkylsulfinyl, C ₁ -C ₆ _{alkylsulfonyl,} C 1 -C ₆ represents _{haloalkylthio,} a C 1 -C ₆ haloalkylsulfinyl or _C 1 -C ₆ haloalkylsulfonyl, when n is 2 or more integer, each of ^{R 2} are each They may be the same or different from each other,
R ³ is a hydrogen atom, a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , —CHO, —C (O) OH, —C (O) NH ₂ , —C (S) NH ₂ , _{_{_{-S (O) 2 NH 2,}}} C 1 ~C 6 _alkyl, C 3 -C ₆ _cycloalkyl, C 2 -C ₆ _alkenyl, C 2 -C ₆ _alkynyl, C 1 -C ₆ _haloalkyl, C 1 -C ₆ _alkoxy, C 1 -C ₆ _haloalkoxy, C 1 -C ₆ _alkylthio, C 1 -C ₆ _{alkylsulfinyl,} C 1 -C ₆ _{alkylsulfonyl,} C 1 -C ₆ _{haloalkylthio,} C 1 -C ₆ haloalkylsulfinyl, C ₁ -C ₆ haloalkylsulfonyl, _cyano, C 1 -C ₆ _{alkoxycarbonyl,} C 1 -C ₆ _{alkylcarbonyl,} C 1 -C ₆ alkylaminocarbonyl or di _(C 1 -C ₆ A It represents Kill) aminocarbonyl,
D1-15, D1-16 and D1-17 each represent a ring represented by the following structural formula;

Ｘ^１は、Ｒ^５によって任意に置換された（Ｃ_１〜Ｃ_６）アルキルを表し、
Ｘ^１ａは、水素原子、Ｃ_１〜Ｃ_６アルキル、Ｒ^５ａによって任意に置換された（Ｃ_１〜Ｃ_６）アルキル、Ｃ_２〜Ｃ_６アルケニル、Ｒ^５ａによって任意に置換された（Ｃ_２〜Ｃ_６）アルケニル、−ＯＨ、−ＯＲ^６ａ、−ＳＨ、−Ｓ（Ｏ）_ｇＲ^６ａ、−Ｃ（Ｏ）Ｒ^７ａ、−Ｃ（Ｏ）ＯＲ^６ａ、−Ｃ（Ｏ）Ｎ（Ｒ^８ａ）Ｒ^９ａ、−Ｃ（Ｓ）Ｎ（Ｒ^８ａ）Ｒ^９ａ、Ｄ２−３２、Ｄ２−３３、Ｄ２−３４、Ｄ２−３６、Ｄ２−３７、Ｄ２−３８、Ｄ２−８１、Ｄ２−８２、Ｄ２−８４、Ｄ２−８５、Ｄ２−８７、Ｄ２−９２、Ｄ２−９３、Ｄ２−９５、Ｄ２−９６又はＤ２−９８を表し、
Ｄ２−３２、Ｄ２−３３、Ｄ２−３４、Ｄ２−３６、Ｄ２−３７、Ｄ２−３８、Ｄ２−８１、Ｄ２−８２、Ｄ２−８４、Ｄ２−８５、Ｄ２−８７、Ｄ２−９２、Ｄ２−９３、Ｄ２−９５、Ｄ２−９６及びＤ２−９８は、それぞれ下記の構造式で表される環を表し、 X ¹ represents (C ₁ -C ₆ ) alkyl optionally substituted with R ⁵ ;
X ^1a represents a hydrogen _atom, C 1 -C ₆ ^alkyl, optionally substituted by ^{R 5a} _(C 1 ~C ₆₎ _alkyl, C 2 -C ₆ ^alkenyl, optionally substituted by ^{R 5a} _(C 2 ~ C ₆₎ ^{_{^{^{alkenyl, -OH, -OR 6a, -SH,}}}} -S (O) g R 6a, -C (O) R 7a, -C (O) OR 6a, -C (O) N (R 8a) ^{^{^{R 9a, -C (S) N}}} (R 8a) R 9a, D2-32, D2-33, D2-34, D2-36, D2-37, D2-38, D2-81, D2-82, D2- 84, D2-85, D2-87, D2-92, D2-93, D2-95, D2-96 or D2-98,
D2-32, D2-33, D2-34, D2-36, D2-37, D2-38, D2-81, D2-82, D2-84, D2-85, D2-87, D2-92, D2- 93, D2-95, D2-96 and D2-98 each represent a ring represented by the following structural formula;

Ｒ^５は、−Ｓ（Ｏ）_ｒＲ^１１を表し、
Ｒ^５ａは、ハロゲン原子、シアノ、−ＯＨ，−ＯＲ^１１ａ、−ＳＨ、−Ｓ（Ｏ）_ｒＲ^１１ａ、−Ｃ（Ｒ^１２ａ）＝ＮＯＨ又は−Ｃ（Ｒ^１２ａ）＝ＮＯＲ^１１ａを表し、
Ｒ^６ａは、Ｃ_１〜Ｃ_６アルキルを表し、
Ｒ^７ａは、水素原子又はＣ_１〜Ｃ_６アルキルを表し、
Ｒ^８ａ及びＲ^９ａは、各々独立して水素原子又はＣ_１〜Ｃ_６アルキルを表し、
Ｒ^１１は、Ｃ_１〜Ｃ_６アルキル又はＲ^１４によって任意に置換された（Ｃ_１〜Ｃ_６）アルキルを表し、
Ｒ^１１ａは、Ｃ_１〜Ｃ_６アルキル又はＲ^１４ａによって任意に置換された（Ｃ_１〜Ｃ_６）アルキルを表し、
Ｒ^１２ａは、水素原子又はＣ_１〜Ｃ_６アルキルを表し、
Ｒ^１４は、ハロゲン原子、Ｃ_３〜Ｃ_６シクロアルキル、−ＯＨ，−ＯＲ^１５、−ＳＨ又は−Ｓ（Ｏ）_ｒＲ^１５を表し、
Ｒ^１４ａは、ハロゲン原子、Ｃ_３〜Ｃ_６シクロアルキル、−ＯＨ，−ＯＲ^１５ａ、−ＳＨ又は−Ｓ（Ｏ）_ｒＲ^１５ａを表し、
Ｒ^１５及びＲ^１５ａは、各々独立してＣ_１〜Ｃ_６アルキルを表し、
Ｘ^２及びＸ^２ｂは、各々独立してハロゲン原子、シアノ、ニトロ、−ＯＨ、−ＳＨ、−ＮＨ_２、Ｃ_１〜Ｃ_６アルキル、Ｃ_２〜Ｃ_６アルケニル、Ｃ_２〜Ｃ_６アルキニル又はＣ_３〜Ｃ_８シクロアルキルを表し、
ｎ及びｔ１は、各々独立して０〜３の整数を表し、
ｐ２は、０〜２の整数を表し、
ｔ４は、０〜４の整数を表し、
ｕ５は、０〜５の整数を表し、
ｕ７は、０〜７の整数を表し、
ｕ９は、０〜９の整数を表し、
ｍ１及びｍ２は、各々独立して０又は１の整数を表し、
ｇ及びｒは、各々独立して０、１又は２の整数を表す。］で表されるチアゾール誘導体又はその塩。 R ⁵ represents —S (O) _r R ¹¹ ,
R ^5a represents a halogen atom, cyano, —OH, —OR ^11a , —SH, —S (O) _r R ^11a , —C (R ^12a ) = NOH or —C (R ^12a ) = NOR ^11a ,
R ^6a represents C ₁ -C ₆ alkyl;
R ^7a represents a hydrogen atom or C ₁ -C ₆ alkyl;
R ^8a and R ^9a each independently represent a hydrogen atom or C ₁ -C ₆ alkyl;
R ¹¹ represents C ₁ -C ₆ alkyl or (C ₁ -C ₆ ) alkyl optionally substituted by R ¹⁴ ,
R ^11a represents C ₁ -C ₆ alkyl or (C ₁ -C ₆ ) alkyl optionally substituted with R ^14a ,
R ^12a represents a hydrogen atom or C ₁ -C ₆ alkyl;
R ¹⁴ represents a halogen atom, C ₃ -C ₆ cycloalkyl, —OH, —OR ¹⁵ , —SH or —S (O) _r R ¹⁵ ;
R ^14a represents a halogen atom, C ₃ -C ₆ cycloalkyl, —OH, —OR ^15a , —SH or —S (O) _r R ^15a ,
R ¹⁵ and R ^15a each independently represent C ₁ -C ₆ alkyl;
X ² and X ^2b are each independently a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , C ₁ -C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ alkynyl or C ₃ -C ₈ cycloalkyl,
n and t1 each independently represents an integer of 0 to 3,
p2 represents an integer of 0 to 2,
t4 represents an integer of 0 to 4,
u5 represents an integer of 0 to 5;
u7 represents an integer of 0 to 7,
u9 represents an integer of 0 to 9,
m1 and m2 each independently represent an integer of 0 or 1,
g and r each independently represents an integer of 0, 1 or 2. Or a salt thereof.

〔２〕
Ａ^１は、ＣＲ^１を表し、
Ｒ^１及びＲ^３は、各々独立して水素原子、ハロゲン原子又はＣ_１〜Ｃ_６アルキルを表し、
Ｒ^２は、ハロゲン原子又はＣ_１〜Ｃ_６アルキルを表す上記〔１〕記載のチアゾール誘導体又はその塩。 [2]
A ¹ represents CR ¹
R ¹ and R ³ each independently represent a hydrogen atom, a halogen atom or C ₁ -C ₆ alkyl;
R ² is a thiazole derivative or a salt thereof according to the above [1], wherein R ² represents a halogen atom or C ₁ -C ₆ alkyl.

〔３〕
Ａ^２は、Ｄ１−１５又はＤ１−１７を表し、
Ｒ^１は、水素原子を表し、
Ｒ^３は、Ｃ_１〜Ｃ_６アルキルを表し、
Ｘ^１は、Ｒ^５によって任意に置換された（Ｃ_１〜Ｃ_６）アルキルを表し、
Ｘ^１ａは、水素原子、Ｃ_１〜Ｃ_６アルキル又はＲ^５ａによって任意に置換された（Ｃ_１〜Ｃ_６）アルキルを表し、
Ｒ^５は、−Ｓ（Ｏ）_ｒＲ^１１を表し、
Ｒ^５ａは、ハロゲン原子を表し、
Ｒ^１１は、Ｃ_１〜Ｃ_６アルキルを表し、
ｍ１及びｎは、０を表し、
ｐ２は、１の整数を表す上記〔２〕記載のチアゾール誘導体又はその塩。 [3]
A ² represents D1-15 or D1-17,
R ¹ represents a hydrogen atom,
R ³ represents C ₁ -C ₆ alkyl,
X ¹ represents (C ₁ -C ₆ ) alkyl optionally substituted with R ⁵ ;
X ^1a represents a hydrogen atom, C ₁ -C ₆ alkyl or (C ₁ -C ₆ ) alkyl optionally substituted with R ^5a ,
R ⁵ represents —S (O) _r R ¹¹ ,
R ^5a represents a halogen atom,
R ¹¹ represents C ₁ -C ₆ alkyl,
m1 and n represent 0;
p2 is the thiazole derivative or the salt thereof according to the above [2], wherein the integer represents 1.

〔４〕
上記〔１〕〜〔３〕記載のチアゾール誘導体及びそれらの塩から選ばれる１種又は２種以上を有効成分として含有する有害生物防除剤。 [4]
A pest control agent comprising one or more selected from the thiazole derivatives described in the above [1] to [3] and salts thereof as an active ingredient.

〔５〕
上記〔１〕〜〔３〕記載のチアゾール誘導体及びそれらの塩から選ばれる１種又は２種以上を有効成分として含有する農薬。 [5]
An agrochemical containing as an active ingredient one or more selected from the thiazole derivatives described in the above [1] to [3] and salts thereof.

〔６〕
上記〔１〕〜〔３〕記載のチアゾール誘導体及びそれらの塩から選ばれる１種又は２種以上を有効成分として含有する哺乳動物又は鳥類の内部もしくは外部寄生虫防除剤。 [6]
A mammal or avian internal or ectoparasite control agent comprising one or more selected from the thiazole derivatives described in the above [1] to [3] and salts thereof as an active ingredient.

〔７〕
上記〔１〕〜〔３〕記載のチアゾール誘導体及びそれらの塩から選ばれる１種又は２種以上を有効成分として含有する殺虫剤又は殺ダニ剤。 [7]
An insecticide or acaricide containing as an active ingredient one or more selected from the thiazole derivatives described in [1] to [3] above and salts thereof.

〔８〕
上記〔１〕〜〔３〕記載のチアゾール誘導体及びそれらの塩から選ばれる１種又は２種以上を有効成分として含有する土壌処理剤。 [8]
A soil treatment agent containing one or more selected from the thiazole derivatives according to the above [1] to [3] and salts thereof as an active ingredient.

〔９〕
土壌処理方法が土壌潅注処理である上記〔８〕記載の土壌処理剤。 [9]
The soil treatment agent according to the above [8], wherein the soil treatment method is soil irrigation treatment.

本発明化合物は多くの農業害虫、ハダニ類、哺乳動物又は鳥類の内部もしくは外部寄生虫に対して優れた殺虫・殺ダニ活性を有し、既存の殺虫剤に対して抵抗性を獲得した害虫に対しても十分な防除効果を発揮する。さらに、ホ乳類、魚類及び益虫に対してほとんど悪影響を及ぼさず、低残留性で環境に対する負荷も軽い。 The compound of the present invention has excellent insecticidal / miticidal activity against many agricultural pests, spider mites, mammals or birds, or against insects that have acquired resistance to existing insecticides. Even against this, it exhibits a sufficient control effect. Furthermore, it has little adverse effect on mammals, fish and beneficial insects, has low persistence, and has a light environmental impact.

従って、本発明は有用な新規有害生物防除剤を提供することができる。 Therefore, the present invention can provide a useful novel pest control agent.

本発明に包含される化合物には、置換基の種類によってはＥ−体及びＺ−体の幾何異性体が存在する場合があるが、本発明はこれらＥ−体、Ｚ−体又はＥ−体及びＺ−体を任意の割合で含む混合物を包含するものである。また、本発明に包含される化合物は、１個又は２個以上の不斉炭素原子の存在に起因する光学活性体が存在するが、本発明は全ての光学活性体又はラセミ体を包含する。 The compounds included in the present invention may have geometrical isomers of E-form and Z-form depending on the type of substituent, and the present invention is not limited to these E-form, Z-form or E-form. And a mixture containing the Z-form in an arbitrary ratio. In addition, the compounds included in the present invention include optically active substances resulting from the presence of one or more asymmetric carbon atoms, but the present invention includes all optically active substances or racemates.

本発明に包含される化合物のうちで、常法に従って酸付加塩にすることができるものは、例えば、フッ化水素酸、塩酸、臭化水素酸、ヨウ化水素酸等のハロゲン化水素酸の塩、硝酸、硫酸、燐酸、塩素酸、過塩素酸等の無機酸の塩、メタンスルホン酸、エタンスルホン酸、トリフルオロメタンスルホン酸、ベンゼンスルホン酸、ｐ−トルエンスルホン酸等のスルホン酸の塩、ギ酸、酢酸、プロピオン酸、トリフルオロ酢酸、フマール酸、酒石酸、蓚酸、マレイン酸、リンゴ酸、コハク酸、安息香酸、マンデル酸、アスコルビン酸、乳酸、グルコン酸、クエン酸等のカルボン酸の塩又はグルタミン酸、アスパラギン酸等のアミノ酸の塩とすることができる。 Among the compounds included in the present invention, those that can be converted into acid addition salts according to a conventional method include, for example, hydrohalic acids such as hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, and the like. Salts of inorganic acids such as salts, nitric acid, sulfuric acid, phosphoric acid, chloric acid, perchloric acid, salts of sulfonic acids such as methanesulfonic acid, ethanesulfonic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, Salts of carboxylic acids such as formic acid, acetic acid, propionic acid, trifluoroacetic acid, fumaric acid, tartaric acid, succinic acid, maleic acid, malic acid, succinic acid, benzoic acid, mandelic acid, ascorbic acid, lactic acid, gluconic acid, citric acid, etc. A salt of an amino acid such as glutamic acid or aspartic acid can be used.

或いは、本発明に包含される化合物のうちで、常法に従って金属塩にすることができるものは、例えば、リチウム、ナトリウム、カリウムといったアルカリ金属の塩、カルシウム、バリウム、マグネシウムといったアルカリ土類金属の塩又はアルミニウムの塩とすることができる。 Alternatively, among the compounds included in the present invention, those that can be converted into a metal salt according to a conventional method include, for example, alkali metal salts such as lithium, sodium, and potassium, and alkaline earth metals such as calcium, barium, and magnesium. It can be a salt or a salt of aluminum.

次に、本明細書において示した各置換基の具体例を以下に示す。ここで、ｎ−はノルマル、ｉ−はイソ、ｓ−はセカンダリー及びｔｅｒｔ−はターシャリーを各々意味し、Ｐｈはフェニルを意味する。 Next, specific examples of each substituent shown in the present specification are shown below. Here, n- represents normal, i- represents iso, s- represents secondary, and tert- represents tertiary, and Ph represents phenyl.

本明細書におけるハロゲン原子としては、フッ素原子、塩素原子、臭素原子及びヨウ素原子が挙げられる。尚、本明細書中「ハロ」の表記もこれらのハロゲン原子を表す。 Examples of the halogen atom in the present specification include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom. In the present specification, the notation “halo” also represents these halogen atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキルの表記は、炭素原子数がａ〜ｂ個よりなる直鎖状又は分岐鎖状の炭化水素基を表し、例えばメチル基、エチル基、ｎ−プロピル基、ｉ−プロピル基、ｎ−ブチル基、ｉ−ブチル基、ｓ−ブチル基、ｔｅｒｔ−ブチル基、ｎ−ペンチル基、１，１−ジメチルプロピル基、ｎ−ヘキシル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkyl in the present specification represents a linear or branched hydrocarbon group having a carbon number of _a to _b , for example, methyl group, ethyl group, n-propyl group, Specific examples include i-propyl group, n-butyl group, i-butyl group, s-butyl group, tert-butyl group, n-pentyl group, 1,1-dimethylpropyl group, n-hexyl group, and the like. Each selected range of carbon atoms is selected.

本明細書におけるＣ_ａ〜Ｃ_ｂハロアルキルの表記は、炭素原子に結合した水素原子が、ハロゲン原子によって任意に置換された、炭素原子数がａ〜ｂ個よりなる直鎖状又は分岐鎖状の炭化水素基を表し、このとき、２個以上のハロゲン原子によって置換されている場合、それらのハロゲン原子は互いに同一でも、又は互いに相異なっていてもよい。例えばフルオロメチル基、クロロメチル基、ブロモメチル基、ヨードメチル基、ジフルオロメチル基、ジクロロメチル基、トリフルオロメチル基、クロロジフルオロメチル基、トリクロロメチル基、ブロモジフルオロメチル基、２−フルオロエチル基、２−クロロエチル基、２−ブロモエチル基、２，２−ジフルオロエチル基、２，２，２−トリフルオロエチル基、２−クロロ−２，２−ジフルオロエチル基、２，２，２−トリクロロエチル基、１，１，２，２−テトラフルオロエチル基、２−クロロ−１，１，２−トリフルオロエチル基、ペンタフルオロエチル基、３，３，３−トリフルオロプロピル基、２，２，３，３，３−ペンタフルオロプロピル基、１，１，２，３，３，３−ヘキサフルオロプロピル基、ヘプタフルオロプロピル基、２，２，２−トリフルオロ−１−（トリフルオロメチル）エチル基、１，２，２，２−テトラフルオロ−１−（トリフルオロメチル）エチル基、２，２，３，３，４，４，４−ヘプタフルオロブチル基、ノナフルオロブチル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C _a -C _b haloalkyl is represented by a linear or branched chain having _a to _b carbon atoms in which a hydrogen atom bonded to a carbon atom is optionally substituted with a halogen atom. Represents a hydrocarbon group, and when substituted by two or more halogen atoms, the halogen atoms may be the same as or different from each other. For example, fluoromethyl group, chloromethyl group, bromomethyl group, iodomethyl group, difluoromethyl group, dichloromethyl group, trifluoromethyl group, chlorodifluoromethyl group, trichloromethyl group, bromodifluoromethyl group, 2-fluoroethyl group, 2- Chloroethyl group, 2-bromoethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, 2-chloro-2,2-difluoroethyl group, 2,2,2-trichloroethyl group, 1 , 1,2,2-tetrafluoroethyl group, 2-chloro-1,1,2-trifluoroethyl group, pentafluoroethyl group, 3,3,3-trifluoropropyl group, 2,2,3,3 , 3-pentafluoropropyl group, 1,1,2,3,3,3-hexafluoropropyl group, heptafluoropropyl group 2,2,2-trifluoro-1- (trifluoromethyl) ethyl group, 1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethyl group, 2,2,3,3,4, Specific examples include 4,4-heptafluorobutyl group, nonafluorobutyl group and the like, and each is selected within the range of the number of carbon atoms designated.

本明細書におけるＣ_ａ〜Ｃ_ｂシクロアルキルの表記は、炭素原子数がａ〜ｂ個よりなる環状の炭化水素基を表し、３員環から６員環までの単環又は複合環構造を形成することが出来る。また、各々の環は指定の炭素原子数の範囲でアルキル基によって任意に置換されていてもよい。例えばシクロプロピル基、１−メチルシクロプロピル基、２−メチルシクロプロピル基、２，２−ジメチルシクロプロピル基、シクロブチル基、シクロペンチル基、シクロヘキシル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C _a -C _b cycloalkyl represents a cyclic hydrocarbon group having a carbon number of _a to _b , and forms a monocyclic or complex ring structure having 3 to 6 members. I can do it. Each ring may be optionally substituted with an alkyl group within the range of the specified number of carbon atoms. Specific examples include, for example, cyclopropyl group, 1-methylcyclopropyl group, 2-methylcyclopropyl group, 2,2-dimethylcyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group and the like. Selected in a range of numbers.

本明細書におけるＣ_ａ〜Ｃ_ｂアルケニルの表記は、炭素原子数がａ〜ｂ個よりなる直鎖状又は分岐鎖状で、且つ分子内に１個又は２個以上の二重結合を有する不飽和炭化水素基を表し、例えばビニル基、１−プロペニル基、２−プロペニル基、１−メチルエテニル基、２−ブテニル基、２−メチル−２−プロペニル基、３−メチル−２−ブテニル基、１，１−ジメチル−２−プロペニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C _a -C _b alkenyl is a linear or branched chain composed of _a to _b carbon atoms and has one or more double bonds in the molecule. Represents a saturated hydrocarbon group, for example, vinyl group, 1-propenyl group, 2-propenyl group, 1-methylethenyl group, 2-butenyl group, 2-methyl-2-propenyl group, 3-methyl-2-butenyl group, 1 , 1-dimethyl-2-propenyl group and the like are listed as specific examples, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキニルの表記は、炭素原子数がａ〜ｂ個よりなる直鎖状又は分岐鎖状で、且つ分子内に１個又は２個以上の三重結合を有する不飽和炭化水素基を表し、例えばエチニル基、１−プロピニル基、２−プロピニル基、１−ブチニル基、２−ブチニル基、３−ブチニル基、１，１−ジメチル−２−プロピニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, C _a -C _b alkynyl is a linear or branched chain composed of _a to _b carbon atoms and has one or more triple bonds in the molecule. Represents a hydrocarbon group, for example, ethynyl group, 1-propynyl group, 2-propynyl group, 1-butynyl group, 2-butynyl group, 3-butynyl group, 1,1-dimethyl-2-propynyl group, etc. Each of which is selected for each specified number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルコキシの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル−Ｏ−基を表し、例えばメトキシ基、エトキシ基、ｎ−プロピルオキシ基、ｉ−プロピルオキシ基、ｎ−ブチルオキシ基、ｉ−ブチルオキシ基、ｓ−ブチルオキシ基、ｔｅｒｔ−ブチルオキシ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkoxy in the present specification represents an alkyl-O— group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, methoxy group, ethoxy group, n-propyloxy group, Specific examples include an i-propyloxy group, an n-butyloxy group, an i-butyloxy group, an s-butyloxy group, a tert-butyloxy group, and the like, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂハロアルコキシの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるハロアルキル−Ｏ−基を表し、例えばジフルオロメトキシ基、トリフルオロメトキシ基、クロロジフルオロメトキシ基、ブロモジフルオロメトキシ基、２−フルオロエトキシ基、２−クロロエトキシ基、２，２，２−トリフルオロエトキシ基、１，１，２，２，−テトラフルオロエトキシ基、２−クロロ−１，１，２−トリフルオロエトキシ基、１，１，２，３，３，３−ヘキサフルオロプロピルオキシ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b haloalkoxy in the present specification represents a haloalkyl-O— group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, difluoromethoxy group, trifluoromethoxy group, chlorodifluoro Methoxy group, bromodifluoromethoxy group, 2-fluoroethoxy group, 2-chloroethoxy group, 2,2,2-trifluoroethoxy group, 1,1,2,2, -tetrafluoroethoxy group, 2-chloro-1 Specific examples include 1,2,2-trifluoroethoxy group, 1,1,2,3,3,3-hexafluoropropyloxy group and the like, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキルチオの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル−Ｓ−基を表し、例えばメチルチオ基、エチルチオ基、ｎ−プロピルチオ基、ｉ−プロピルチオ基、ｎ−ブチルチオ基、ｉ−ブチルチオ基、ｓ−ブチルチオ基、ｔｅｒｔ−ブチルチオ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkylthio in the present specification represents an alkyl-S-group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, methylthio group, ethylthio group, n-propylthio group, i Specific examples include -propylthio group, n-butylthio group, i-butylthio group, s-butylthio group, tert-butylthio group and the like, which are selected within the range of the number of carbon atoms specified.

本明細書におけるＣ_ａ〜Ｃ_ｂハロアルキルチオの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるハロアルキル−Ｓ−基を表し、例えばジフルオロメチルチオ基、トリフルオロメチルチオ基、クロロジフルオロメチルチオ基、ブロモジフルオロメチルチオ基、２，２，２−トリフルオロエチルチオ基、１，１，２，２−テトラフルオロエチルチオ基、２−クロロ−１，１，２−トリフルオロエチルチオ基、ペンタフルオロエチルチオ基、１，１，２，３，３，３−ヘキサフルオロプロピルチオ基、ヘプタフルオロプロピルチオ基、１，２，２，２−テトラフルオロ−１−（トリフルオロメチル）エチルチオ基、ノナフルオロブチルチオ基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b haloalkylthio in the present specification represents a haloalkyl-S-group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, difluoromethylthio group, trifluoromethylthio group, chlorodifluoro Methylthio group, bromodifluoromethylthio group, 2,2,2-trifluoroethylthio group, 1,1,2,2-tetrafluoroethylthio group, 2-chloro-1,1,2-trifluoroethylthio group, Pentafluoroethylthio group, 1,1,2,3,3,3-hexafluoropropylthio group, heptafluoropropylthio group, 1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethylthio group , Nonafluorobutylthio group and the like are given as specific examples, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキルスルフィニルの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル−Ｓ（Ｏ）−基を表し、例えばメチルスルフィニル基、エチルスルフィニル基、ｎ−プロピルスルフィニル基、ｉ−プロピルスルフィニル基、ｎ−ブチルスルフィニル基、ｉ−ブチルスルフィニル基、ｓ−ブチルスルフィニル基、ｔｅｒｔ−ブチルスルフィニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkylsulfinyl in the present specification represents an alkyl-S (O) -group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, methylsulfinyl group, ethylsulfinyl group, Specific examples include n-propylsulfinyl group, i-propylsulfinyl group, n-butylsulfinyl group, i-butylsulfinyl group, s-butylsulfinyl group, tert-butylsulfinyl group and the like. The range is selected.

本明細書におけるＣ_ａ〜Ｃ_ｂハロアルキルスルフィニルの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるハロアルキル−Ｓ（Ｏ）−基を表し、例えばジフルオロメチルスルフィニル基、トリフルオロメチルスルフィニル基、クロロジフルオロメチルスルフィニル基、ブロモジフルオロメチルスルフィニル基、２，２，２−トリフルオロエチルスルフィニル基、１，２，２，２−テトラフルオロ−１−（トリフルオロメチル）エチルスルフィニル基、ノナフルオロブチルスルフィニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b haloalkylsulfinyl in the present specification represents a haloalkyl-S (O) -group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, difluoromethylsulfinyl group, trifluoromethyl Sulfinyl group, chlorodifluoromethylsulfinyl group, bromodifluoromethylsulfinyl group, 2,2,2-trifluoroethylsulfinyl group, 1,2,2,2-tetrafluoro-1- (trifluoromethyl) ethylsulfinyl group, nona Specific examples include a fluorobutylsulfinyl group and the like, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキルスルホニルの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル−ＳＯ_２−基を表し、例えばメチルスルホニル基、エチルスルホニル基、ｎ−プロピルスルホニル基、ｉ−プロピルスルホニル基、ｎ−ブチルスルホニル基、ｉ−ブチルスルホニル基、ｓ−ブチルスルホニル基、ｔｅｒｔ−ブチルスルホニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkylsulfonyl in the present specification represents an alkyl-SO ₂ -group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, methylsulfonyl group, ethylsulfonyl group, n- Specific examples include a propylsulfonyl group, an i-propylsulfonyl group, an n-butylsulfonyl group, an i-butylsulfonyl group, an s-butylsulfonyl group, a tert-butylsulfonyl group, and the range of each designated number of carbon atoms. Selected.

本明細書におけるＣ_ａ〜Ｃ_ｂハロアルキルスルホニルの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるハロアルキル−ＳＯ_２−基を表し、例えばジフルオロメチルスルホニル基、トリフルオロメチルスルホニル基、クロロジフルオロメチルスルホニル基、ブロモジフルオロメチルスルホニル基、２，２，２−トリフルオロエチルスルホニル基、１，１，２，２−テトラフルオロエチルスルホニル基、２−クロロ−１，１，２−トリフルオロエチルスルホニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b haloalkylsulfonyl in the present specification represents a haloalkyl-SO ₂ -group having the above-mentioned meaning consisting of _a to _b carbon atoms, such as a difluoromethylsulfonyl group or a trifluoromethylsulfonyl group. Chlorodifluoromethylsulfonyl group, bromodifluoromethylsulfonyl group, 2,2,2-trifluoroethylsulfonyl group, 1,1,2,2-tetrafluoroethylsulfonyl group, 2-chloro-1,1,2-trimethyl Specific examples include a fluoroethylsulfonyl group and the like, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキルカルボニルの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル−Ｃ（Ｏ）−基を表し、例えばアセチル基、プロピオニル基、ブチリル基、イソブチリル基、バレリル基、イソバレリル基、２−メチルブタノイル基、ピバロイル基、ヘキサノイル基、ヘプタノイル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkylcarbonyl in the present specification represents an alkyl-C (O) -group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, acetyl group, propionyl group, butyryl group. , Isobutyryl group, valeryl group, isovaleryl group, 2-methylbutanoyl group, pivaloyl group, hexanoyl group, heptanoyl group, and the like, and specific examples thereof are selected within the range of the number of carbon atoms designated.

本明細書におけるＣ_ａ〜Ｃ_ｂアルコキシカルボニルの表記は、炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル−Ｏ−Ｃ（Ｏ）−基を表し、例えばメトキシカルボニル基、エトキシカルボニル基、ｎ−プロピルオキシカルボニル基、ｉ−プロピルオキシカルボニル基、ｎ−ブトキシカルボニル基、ｉ−ブトキシカルボニル基、ｔｅｒｔ−ブトキシカルボニル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkoxycarbonyl in the present specification represents an alkyl-O—C (O) — group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, methoxycarbonyl group, ethoxycarbonyl Group, n-propyloxycarbonyl group, i-propyloxycarbonyl group, n-butoxycarbonyl group, i-butoxycarbonyl group, tert-butoxycarbonyl group and the like, and specific ranges of the number of carbon atoms are designated. Selected.

本明細書におけるＣ_ａ〜Ｃ_ｂアルキルアミノカルボニルの表記は、水素原子の一方が炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル基によって置換されたカルバモイル基を表し、例えばメチルカルバモイル基、エチルカルバモイル基、ｎ−プロピルカルバモイル基、ｉ−プロピルカルバモイル基、ｎ−ブチルカルバモイル基、ｉ−ブチルカルバモイル基、ｓ−ブチルカルバモイル基、ｔｅｒｔ−ブチルカルバモイル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 The notation of C _a -C _b alkylaminocarbonyl in the present specification represents a carbamoyl group in which one of the hydrogen atoms is substituted with an alkyl group having the above-mentioned meaning consisting of _a to _b carbon atoms, for example, methylcarbamoyl Group, ethylcarbamoyl group, n-propylcarbamoyl group, i-propylcarbamoyl group, n-butylcarbamoyl group, i-butylcarbamoyl group, s-butylcarbamoyl group, tert-butylcarbamoyl group, etc. Is selected within the range of the specified number of carbon atoms.

本明細書におけるジ（Ｃ_ａ〜Ｃ_ｂアルキル）アミノカルボニルの表記は、水素原子が両方とも、それぞれ同一でも又は互いに相異なっていてもよい炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル基によって置換されたカルバモイル基を表し、例えばＮ，Ｎ−ジメチルカルバモイル基、Ｎ−エチル−Ｎ−メチルカルバモイル基、Ｎ，Ｎ−ジエチルカルバモイル基、Ｎ，Ｎ−ジ（ｎ−プロピル）カルバモイル基、Ｎ，Ｎ−ジ（ｎ−ブチル）カルバモイル基等が具体例として挙げられ、各々の指定の炭素原子数の範囲で選択される。 In the present specification, the notation of di (C _a -C _b alkyl) aminocarbonyl means in the above meaning that the number of carbon atoms which may be the same or different from each other is _a to _b. Represents a carbamoyl group substituted by an alkyl group, such as N, N-dimethylcarbamoyl group, N-ethyl-N-methylcarbamoyl group, N, N-diethylcarbamoyl group, N, N-di (n-propyl) carbamoyl Specific examples include a group, an N, N-di (n-butyl) carbamoyl group, and the like, and each is selected within the range of the designated number of carbon atoms.

本明細書におけるＲ^５によって任意に置換された（Ｃ_ａ〜Ｃ_ｂ）アルキル、Ｒ^５ａによって任意に置換された（Ｃ_ａ〜Ｃ_ｂ）アルキル、Ｒ^１４によって任意に置換された（Ｃ_ａ〜Ｃ_ｂ）アルキル又はＲ^１４ａによって任意に置換された（Ｃ_ａ〜Ｃ_ｂ）アルキル等の表記は、任意のＲ^５、Ｒ^５ａ、Ｒ^１４又はＲ^１４ａによって、炭素原子に結合した水素原子が任意に置換された炭素原子数がａ〜ｂ個よりなる前記の意味であるアルキル基を表し、各々の指定の炭素原子数の範囲で選択される。このとき、それぞれの（Ｃ_ａ〜Ｃ_ｂ）アルキル基上の置換基Ｒ^５、Ｒ^５ａ、Ｒ^１４又はＲ^１４ａが２個以上存在するとき、それぞれのＲ^５、Ｒ^５ａ、Ｒ^１４又はＲ^１４ａは互いに同一でも異なってもよい。 Optionally substituted by ^{R 5} in this specification _(C a _~C _b) ^alkyl, optionally substituted by ^{R 5a} _(C ^a _~C _b) ^alkyl, optionally substituted by ^{R 14} _(C a ~ The notation such as C _b ) alkyl or (C _a -C _b ) alkyl optionally substituted by R ^14a is any R ⁵ , R ^5a , R ¹⁴ or R ^14a , and a hydrogen atom bonded to a carbon atom is arbitrary Represents an alkyl group having the above meaning consisting of a to b carbon atoms, and is selected within the range of the respective designated number of carbon atoms. At this time, when two or more substituents R ⁵ , R ^5a , R ¹⁴ or R ^14a on each (C _a -C _b ) alkyl group are present, each R ⁵ , R ^5a , R ¹⁴ or R ^{14a is present.} May be the same as or different from each other.

本明細書におけるＲ^５ａによって任意に置換された（Ｃ_ａ〜Ｃ_ｂ）アルケニル等の表記は、任意のＲ^５ａによって、炭素原子に結合した水素原子が任意に置換された炭素原子数がａ〜ｂ個よりなる前記の意味であるアルケニル基を表し、各々の指定の炭素原子数の範囲で選択される。このとき、それぞれの（Ｃ_ａ〜Ｃ_ｂ）アルケニル基上の置換基Ｒ^５ａが２個以上存在するとき、それぞれのＲ^５ａは互いに同一でも異なってもよい。 Notation such as _(C a ~C _b) alkenyl optionally substituted by R ^5a herein, by any R ^5a, carbon atoms bonded to hydrogen atoms are optionally substituted carbon atoms a~ It represents an alkenyl group having the above-mentioned meaning consisting of b, and is selected within the range of each designated number of carbon atoms. At this time, when there are two or more substituents R ^5a on each (C _a -C _b ) alkenyl group, each R ^5a may be the same as or different from each other.

本発明化合物は、例えば以下の方法により製造することができる。 The compound of the present invention can be produced, for example, by the following method.

製造法Ａ Manufacturing method A

式（８）［式中Ａ^１、Ｒ^２、Ｒ^３及びｎは前記と同じ意味を表し、Ｒ^５０は、水素原子又は同一若しくは異なってもよいＣ_１〜Ｃ_６アルキルを表すか、２つのＲ^５０が一緒になって−ＣＨ_２ＣＨ_２−又は−Ｃ（ＣＨ_３）_２Ｃ（ＣＨ_３）_２−を形成してもよい。］で表される化合物と、式（７）で表される化合物［式中Ｘ^１及びｐ２は前記と同じ意味を表し、Ｗ^１はハロゲン原子又はＣ_１〜Ｃ_４ハロアルキルスルホネート基（例えばトリフルオロメタンスルホニルオキシ基）、Ｐ^１はＣ^１〜Ｃ^６アルキル基（例えばターシャリーブチル基）、アルコキシアルキル基（例えばメトキシメチル基）又は置換ベンジル基（例えばパラメトキシベンジル基）を表す］とを反応させることにより、式（２）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｐ^１、ｐ２及びｎは前記と同じ意味を表す。］で表される本発明化合物を製造することができる。 Formula (8) [wherein A ¹ , R ² , R ³ and n represent the same meaning as described above, and R ⁵⁰ represents a hydrogen atom or C ₁ -C ₆ alkyl which may be the same or different, or two R ⁵⁰ together may form —CH ₂ CH ₂ — or —C (CH ₃ ) ₂ C (CH ₃ ) ₂ —. And a compound represented by formula (7) [wherein X ¹ and p2 represent the same meaning as described above, and W ¹ represents a halogen atom or a C _{1 to} C ₄ haloalkylsulfonate group (for example, trifluoromethane). A sulfonyloxy group), P ¹ represents a C ¹ -C ⁶ alkyl group (eg, tertiary butyl group), an alkoxyalkyl group (eg, methoxymethyl group) or a substituted benzyl group (eg, paramethoxybenzyl group)] Thus, formula (2) [wherein A ¹ , R ² , R ³ , X ¹ , P ¹ , p 2 and n represent the same meaning as described above. This invention compound represented by this can be manufactured.

式（７）で表される化合物のあるものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の公知の方法に準じて合成することができる。 Some of the compounds represented by formula (7) are known compounds, and some are available as commercial products. Others can be synthesized according to known methods described in the literature.

式（８）で表される化合物の量は、式（７）で表される化合物1当量に対して０．８〜５当量の範囲で用いることができる。 The amount of the compound represented by the formula (8) can be used in the range of 0.8 to 5 equivalents relative to 1 equivalent of the compound represented by the formula (7).

本反応で使用できる触媒としては、例えば、パラジウム−炭素、塩化パラジウム、酢酸パラジウム、ビス（トリフェニルホスフィン）パラジウムジクロリド、テトラキス（トリフェニルホスフィン）パラジウム等のパラジウム触媒及び金属銅、酢酸銅（１価）、酢酸銅（２価）、酸化銅（１価）、酸化銅（２価）、ヨウ化銅等の銅触媒が挙げられる。触媒の使用量は、式（８）で表される化合物１当量に対して、０．００１〜１．０当量、好ましくは０．０１〜０．５当量、さらに好ましくは０．０５〜０．２当量の範囲である。 Examples of the catalyst that can be used in this reaction include palladium catalysts such as palladium-carbon, palladium chloride, palladium acetate, bis (triphenylphosphine) palladium dichloride, tetrakis (triphenylphosphine) palladium, and metal copper, copper acetate (monovalent). ), Copper acetate (divalent), copper oxide (monovalent), copper oxide (divalent), copper iodide and the like. The usage-amount of a catalyst is 0.001-1.0 equivalent with respect to 1 equivalent of compounds represented by Formula (8), Preferably it is 0.01-0.5 equivalent, More preferably, it is 0.05-0. The range is 2 equivalents.

使用する塩基としては、例えば、ピリジン、ジイソプロピルエチルアミン、トリエチルアミン等の三級アミン化合物、例えば水酸化ナトリウム水酸化カリウム、炭酸ナトリウム、炭酸カリウム、炭酸セシウム、炭酸水素ナトリウム等の無機塩基等が挙げられる。塩基の使用量は式（７）で表される化合物１当量に対して、０．１〜１０．０当量の範囲である。 Examples of the base to be used include tertiary amine compounds such as pyridine, diisopropylethylamine, and triethylamine, and inorganic bases such as sodium hydroxide, sodium carbonate, potassium carbonate, cesium carbonate, and sodium bicarbonate. The usage-amount of a base is the range of 0.1-10.0 equivalent with respect to 1 equivalent of compounds represented by Formula (7).

本反応は、無溶媒で実施することができるが、溶媒を用いてもよい。例えば、Ｎ，Ｎ−ジメチルホルムアミド、Ｎ，Ｎ−ジメチルアセトアミド、アセトニトリル、ジメチルスルホキシド、１，３−ジメチル−２−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、２−プロパノール、エチレングリコール等のアルコール類、ジエチルエーテル、テトラヒドロフラン、ジフェニルエーテル等のエーテル類、ベンゼン、トルエン、キシレン等の芳香族炭化水素類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、ｎ−ヘキサン等の脂肪族炭化水素類が挙げられる。これらの溶媒は単独で用いても、これらの内の２種類以上を混合して用いてもよい。
反応温度は、０℃〜使用する溶媒の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常５分から１００時間の範囲で任意に設定できる。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, dimethyl sulfoxide, 1,3-dimethyl-2-imidazolinone, water, methanol, ethanol, propanol, 2-propanol, ethylene glycol Alcohols such as diethyl ether, tetrahydrofuran and diphenyl ether, aromatic hydrocarbons such as benzene, toluene and xylene, halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, pentane and n-hexane And aliphatic hydrocarbons. These solvents may be used alone or as a mixture of two or more thereof.
The reaction temperature can be set to any temperature from 0 ° C. to the reflux temperature of the solvent to be used, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but usually ranges from 5 minutes to 100 hours. Can be set.

製造法Ｂ Manufacturing method B

次いで、式（２）で表される化合物を酸と反応させることにより、式（３）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、ｐ２及びｎは前記と同じ意味を表す。］で表される本発明化合物を得ることができる。 Next, by reacting the compound represented by the formula (2) with an acid, the formula (3) [wherein A ¹ , R ² , R ³ , X ¹ , p2 and n represent the same meaning as described above. This invention compound represented by this can be obtained.

酸としては、塩酸、硫酸、ｐ−トルエンスルホン酸、トリフルオロ酢酸等を用いることができる。 As the acid, hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, trifluoroacetic acid and the like can be used.

製造法Ｃ Manufacturing method C

次いで、式（３）で表される化合物を公知の式（６）［式中Ｘ^１ａは前記と同じ意味を表し、Ｊ^ａはハロゲン原子、−ＯＨ、−ＯＳＯ_２ＣＨ_３、−ＯＳＯ_２ＣＦ_３等の脱離基を表す。］と反応させることにより、式（４）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｘ^１ａ、ｐ２及びｎは前記と同じ意味を表す。］及び（５）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｘ^１ａ、ｐ２及びｎは前記と同じ意味を表す。］で表される本発明化合物を得ることができる。 Next, the compound represented by the formula (3) is converted into a known formula (6) [wherein X ^1a represents the same meaning as described above, J ^a represents ^a halogen atom, —OH, —OSO ₂ CH ₃ , —OSO ₂ CF Represents a leaving group such as ₃ ; ], The compound represented by formula (4) [wherein A ¹ , R ² , R ³ , X ¹ , X ^1a , p2 and n have the same meaning as described above]. ] And (5) [wherein ^{^{^{^{A 1, R 2, R 3}}}} , X 1, X 1a, p2 and n are as defined above. This invention compound represented by this can be obtained.

式（６）で表される化合物のあるものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の公知の方法に準じて合成することができる。 Some of the compounds represented by formula (6) are known compounds, and some of them are available as commercial products. Others can be synthesized according to known methods described in the literature.

式（６）で表される化合物の量は、式（３）で表される化合物1当量に対して０．８〜５当量の範囲で用いることができる。必要ならば塩酸、硫酸、ｐ−トルエンスルホン酸等の酸、炭酸カリウム、トリエチルアミン、ピリジン、４−（ジメチルアミノ）ピリジン、水素化ナトリウム、水酸化ナトリウム、水酸化カリウム等の塩基を使用することができ、又は、ジエチルアゾジカルボキシレート等とトリフェニルホスフィン等を使用する光延反応を使用することができる。 The amount of the compound represented by formula (6) can be used in the range of 0.8 to 5 equivalents relative to 1 equivalent of the compound represented by formula (3). If necessary, an acid such as hydrochloric acid, sulfuric acid, p-toluenesulfonic acid, a base such as potassium carbonate, triethylamine, pyridine, 4- (dimethylamino) pyridine, sodium hydride, sodium hydroxide, potassium hydroxide may be used. Or Mitsunobu reaction using diethyl azodicarboxylate or the like and triphenylphosphine or the like can be used.

製造法Ｄ Manufacturing method D

式（４−１）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｘ^１ａ、ｐ２及びｎは前記と同じ意味を表し、ｒは０を表す。］で表される化合物を酸化剤と反応させることにより、式（４−２）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｘ^１ａ、ｐ２及びｎは前記と同じ意味を表し、ｒは１又は２の整数を表す。］で表される本発明化合物を得ることができる。 Formula (4-1) [wherein A ¹ , R ² , R ³ , X ¹ , X ^1a , p2 and n represent the same meaning as described above, and r represents 0. The compound represented by formula (4-2) [wherein A ¹ , R ² , R ³ , X ¹ , X ^1a , p2 and n represent the same meaning as described above] r represents an integer of 1 or 2. This invention compound represented by this can be obtained.

酸化剤としては、例えば、過酸化水素、メタ−クロロ過安息香酸、クメンヒドロペルオキシド、マグネシウムモノペルオキシフタレート、オキソン、過ホウ酸ナトリウム、過マンガン酸カリウム、過ヨウ素酸ナトリウム、次亜塩素酸ナトリウム等が挙げられる。酸化剤の使用量は、式（４−１）で表される化合物１当量に対して、０．１〜１０当量の範囲である。 Examples of the oxidizing agent include hydrogen peroxide, meta-chloroperbenzoic acid, cumene hydroperoxide, magnesium monoperoxyphthalate, oxone, sodium perborate, potassium permanganate, sodium periodate, sodium hypochlorite and the like. Is mentioned. The usage-amount of an oxidizing agent is the range of 0.1-10 equivalent with respect to 1 equivalent of compounds represented by Formula (4-1).

本反応で使用できる触媒としては、例えば、タングステン酸ナトリウム、五酸化バナジウム、トリクロロルテニウム等が挙げられる。触媒の使用量は、式（４−１）で表される化合物１当量に対して、０．００１〜１．０当量、好ましくは０．０１〜０．５当量の範囲である。 Examples of the catalyst that can be used in this reaction include sodium tungstate, vanadium pentoxide, trichlororuthenium, and the like. The usage-amount of a catalyst is 0.001-1.0 equivalent with respect to 1 equivalent of compounds represented by Formula (4-1), Preferably it is the range of 0.01-0.5 equivalent.

本反応は、無溶媒で実施することができるが、溶媒を用いてもよい。例えば、Ｎ，Ｎ−ジメチルホルムアミド、Ｎ，Ｎ−ジメチルアセトアミド、アセトニトリル、１，３−ジメチル−２−イミダゾリノン、水等の極性溶媒、メタノール、エタノール、プロパノール、２−プロパノール、エチレングリコール等のアルコール類、塩化メチレン、クロロホルム、四塩化炭素等のハロゲン化炭化水素類、ペンタン、ｎ−ヘキサン等の脂肪族炭化水素、酢酸、蟻酸等の脂肪酸類が挙げられる。これらの溶媒は単独で用いても、これらの内の２種類以上を混合して用いてもよい。
反応温度は、−７８℃〜使用する溶媒の還流温度までの任意の温度を設定することができ、反応時間は、反応基質の濃度、反応温度によって変化するが、通常５分から１００時間の範囲で任意に設定できる。 This reaction can be carried out without solvent, but a solvent may be used. For example, polar solvents such as N, N-dimethylformamide, N, N-dimethylacetamide, acetonitrile, 1,3-dimethyl-2-imidazolinone, water, alcohols such as methanol, ethanol, propanol, 2-propanol, and ethylene glycol , Halogenated hydrocarbons such as methylene chloride, chloroform and carbon tetrachloride, aliphatic hydrocarbons such as pentane and n-hexane, and fatty acids such as acetic acid and formic acid. These solvents may be used alone or as a mixture of two or more thereof.
The reaction temperature can be set to any temperature from −78 ° C. to the reflux temperature of the solvent used, and the reaction time varies depending on the concentration of the reaction substrate and the reaction temperature, but is usually in the range of 5 minutes to 100 hours. Can be set arbitrarily.

製造法Ｅ Manufacturing method E

式（５−１）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｘ^１ａ、ｐ２及びｎは前記と同じ意味を表し、ｒは０を表す。］で表される化合物を酸化剤と反応させることにより、式（５−２）［式中Ａ^１、Ｒ^２、Ｒ^３、Ｘ^１、Ｘ^１ａ、ｐ２及びｎは前記と同じ意味を表し、ｒは１又は２の整数を表す。］で表される本発明化合物を得ることができる。 Formula (5-1) [wherein A ¹ , R ² , R ³ , X ¹ , X ^1a , p2 and n represent the same meaning as described above, and r represents 0. The compound represented by formula (5-2) [wherein A ¹ , R ² , R ³ , X ¹ , X ^1a , p2 and n represent the same meaning as described above] r represents an integer of 1 or 2. This invention compound represented by this can be obtained.

酸化剤としては、例えば、過酸化水素、メタ−クロロ過安息香酸、クメンヒドロペルオキシド、マグネシウムモノペルオキシフタレート、オキソン、過ホウ酸ナトリウム、過マンガン酸カリウム、過ヨウ素酸ナトリウム、次亜塩素酸ナトリウム等が挙げられる。酸化剤の使用量は、式（５−１）で表される化合物１当量に対して、０．１〜１０当量の範囲である。 Examples of the oxidizing agent include hydrogen peroxide, meta-chloroperbenzoic acid, cumene hydroperoxide, magnesium monoperoxyphthalate, oxone, sodium perborate, potassium permanganate, sodium periodate, sodium hypochlorite and the like. Is mentioned. The usage-amount of an oxidizing agent is the range of 0.1-10 equivalent with respect to 1 equivalent of compounds represented by Formula (5-1).

本反応で使用できる触媒としては、例えば、タングステン酸ナトリウム、五酸化バナジウム、トリクロロルテニウム等が挙げられる。触媒の使用量は、式（５−１）で表される化合物１当量に対して、０．００１〜１．０当量、好ましくは０．０１〜０．５当量の範囲である。 Examples of the catalyst that can be used in this reaction include sodium tungstate, vanadium pentoxide, trichlororuthenium, and the like. The usage-amount of a catalyst is 0.001-1.0 equivalent with respect to 1 equivalent of compounds represented by Formula (5-1), Preferably it is the range of 0.01-0.5 equivalent.

製造法Ａ乃至製造法Ｅの反応は必要であれば窒素、アルゴン等の不活性ガス雰囲気下で実施しても良い。 The reaction of production method A to production method E may be carried out in an inert gas atmosphere such as nitrogen or argon if necessary.

製造法Ａ乃至製造法Ｅの反応において、反応終了後の反応混合物は、直接濃縮、又は有機溶媒に溶解し、水洗後濃縮、又は氷水に投入、有機溶媒抽出後濃縮といった通常の後処理を行ない、目的の本発明化合物を得ることができる。また、精製の必要が生じたときには、再結晶、カラムクロマトグラフ、薄層クロマトグラフ、液体クロマトグラフ分取等の任意の精製方法によって分離、精製することができる。 In the reaction of production method A to production method E, the reaction mixture after completion of the reaction is directly concentrated or dissolved in an organic solvent, concentrated after washing with water, or poured into ice water, concentrated after extraction with an organic solvent, and then subjected to normal post-treatment. The objective compound of the present invention can be obtained. Moreover, when the necessity for purification arises, it can be separated and purified by any purification method such as recrystallization, column chromatograph, thin layer chromatograph, liquid chromatographic fractionation and the like.

製造法Ａで用いられる式（８）で表される化合物は、例えば以下のようにして合成することができる。 The compound represented by the formula (8) used in the production method A can be synthesized, for example, as follows.

反応式１ Reaction formula 1

式（９）[式中Ａ^１、Ｒ^２、Ｒ^３及びｎは前記と同じ意味を表し、Ｙ^１は、ハロゲン原子を表す。]で表される化合物は、ジャーナルオブメディシナルケミストリー２００６年、４９巻、１７３０頁等の公知の方法により合成することができる。 Formula (9) [wherein A ¹ , R ² , R ³ and n represent the same meaning as described above, and Y ¹ represents a halogen atom. ] Can be synthesized by a known method such as Journal of Medicinal Chemistry 2006, 49, 1730.

すなわち、式（９）で表される化合物を、文献既知の公知の方法、例えばジャーナルオブオーガニックケミストリー２０１２年，７７巻，３５４３頁等に記載の方法に準じて、公知化合物であるＢ（ＯＲ^５０）_３［式中Ｒ^５０は、水素原子又は同一若しくは異なってもよいＣ_１〜Ｃ_６アルキルを表すか、或いは、２つのＲ^５０が一緒になって−ＣＨ_２ＣＨ_２−又は−Ｃ（ＣＨ_３）_２Ｃ（ＣＨ_３）_２−を形成してもよい。］又は−［Ｂ（ＯＲ^５０）_２］_２［式中Ｒ^５０は前記と同じ意味を表す。］で表される化合物と、パラジウムなどの遷移金属触媒及び塩基の存在下で反応させることにより、式（８）［式中Ａ^１、Ｒ^２、Ｒ^３及びｎは前記と同じ意味を表し、Ｒ^５０は、水素原子又は同一若しくは異なってもよいＣ_１〜Ｃ_６アルキルを表すか、２つのＲ^５０が一緒になって−ＣＨ_２ＣＨ_２−又は−Ｃ（ＣＨ_３）_２Ｃ（ＣＨ_３）_２−を形成してもよい。］で表される化合物を製造することができる。 That is, the compound represented by the formula (9) is converted into a known compound B (OR ⁵⁰ ) according to a known method known in the literature, for example, the method described in Journal of Organic Chemistry 2012, Vol. 77, page 3543. ₃ [wherein R ⁵⁰ represents a hydrogen atom or C _{1 to} C ₆ alkyl which may be the same or different, or two R ⁵⁰ together represent —CH ₂ CH ₂ — or —C (CH ₃ ) ₂ C (CH ₃ ) ₂ — may be formed. ] Or-[B (OR ⁵⁰ ) ₂ ] ₂ [wherein R ⁵⁰ represents the same meaning as described above.] ] In the presence of a transition metal catalyst such as palladium and a base, wherein A ¹ , R ² , R ³ and n represent the same meaning as described above, R ⁵⁰ represents a hydrogen atom or C _{1 to} C ₆ alkyl, which may be the same or different, or two R ⁵⁰ together represent —CH ₂ CH ₂ — or —C (CH ₃ ) ₂ C (CH ₃ ) _2- may be formed. The compound represented by this can be manufactured.

ここで用いられる、Ｂ（ＯＲ^５０）_３又は−［Ｂ（ＯＲ^５０）_２］_２で表される化合物の或るものは公知化合物であり、一部は市販品として入手できる。また、それ以外のものも文献記載の公知の方法に準じて合成することができる。 Some of the compounds represented by B (OR ⁵⁰ ) ₃ or-[B (OR ⁵⁰ ) ₂ ] ₂ used here are known compounds, and some of them are commercially available. Others can be synthesized according to known methods described in the literature.

本発明に包含される活性化合物としては、具体的に例えば第１表に示す化合物が挙げられる。但し、第１表の化合物は例示のためのものであって、本発明はこれらのみに限定されるものではない。尚、表中、Ｍｅと記載される置換基はメチル基を表し、以下、Ｅｔとの記載はエチル基を表し、ｎ−Ｐｒ及びＰｒ−ｎはノルマルプロピル基を、ｉ−Ｐｒ及びＰｒ−ｉはイソプロピル基を、ｃ−Ｐｒ及びＰｒ−ｃはシクロプロピル基を、ｎ−Ｂｕ及びＢｕ−ｎはノルマルブチル基を、ｓ−Ｂｕ及びＢｕ−ｓはセカンダリーブチル基を、ｉ−Ｂｕ及びＢｕ−ｉはイソブチル基を、ｔ−Ｂｕ及びＢｕ−ｔはターシャリーブチル基を、ｃ−Ｂｕ及びＢｕ−ｃはシクロブチル基を、ｎ−Ｐｅｎ及びＰｅｎ−ｎはノルマルペンチル基を、ｃ−Ｐｅｎ及びＰｅｎ−ｃはシクロペンチル基を、ｎ−Ｈｅｘ及びＨｅｘ−ｎはノルマルヘキシル基を、ｃ−Ｈｅｘ及びＨｅｘ−ｃはシクロヘキシル基を、Ｈｅｐｔはヘプチル基を、Ｏｃｔはオクチル基を、Ｐｈはフェニル基をそれぞれ表す。 Specific examples of the active compound included in the present invention include compounds shown in Table 1. However, the compounds in Table 1 are for illustrative purposes, and the present invention is not limited thereto. In the table, the substituent described as Me represents a methyl group, hereinafter, Et represents an ethyl group, n-Pr and Pr-n represent normal propyl groups, i-Pr and Pr-i. Is an isopropyl group, c-Pr and Pr-c are cyclopropyl groups, n-Bu and Bu-n are normal butyl groups, s-Bu and Bu-s are secondary butyl groups, i-Bu and Bu- i is an isobutyl group, t-Bu and Bu-t are tertiary butyl groups, c-Bu and Bu-c are cyclobutyl groups, n-Pen and Pen-n are normal pentyl groups, c-Pen and Pen -C represents a cyclopentyl group, n-Hex and Hex-n represent a normal hexyl group, c-Hex and Hex-c represent a cyclohexyl group, Hept represents a heptyl group, Oct represents an octyl group, and Ph represents a hexyl group. It represents a sulfonyl group, respectively.

表中、Ｄ２−３２ａ、Ｄ２−３３ａ、Ｄ２−３４ａ、Ｄ２−３６ａ、Ｄ２−３７ａ、Ｄ２−３８ａ及びＤ２−９２ａで表される構造は下記の構造を表す。 In the table, the structures represented by D2-32a, D2-33a, D2-34a, D2-36a, D2-37a, D2-38a, and D2-92a represent the following structures.

第１表 Table 1

――――――――――――――――――
X^1a X¹
――――――――――――――――――
H CH₂SMe
H CH₂SEt
H CH₂SCF₃
H CH₂SCH₂CF₃
H CH₂S(O)Me
H CH₂S(O)Et
H CH₂S(O)CF₃
H CH₂S(O)CH₂CF₃
H CH₂S(O)₂Me
H CH₂S(O)₂Et
H CH₂S(O)₂CF₃
H CH₂S(O)₂CH₂CF₃
H CH(Me)SMe
H CH(Me)SEt
H CH(Me)SCF₃
H CH(Me)SCH₂CF₃
H CH(Me)S(O)Me
H CH(Me)S(O)Et
H CH(Me)S(O)CF₃
H CH(Me)S(O)CH₂CF₃
H CH(Me)S(O)₂Me
H CH(Me)S(O)₂Et
H CH(Me)S(O)₂CF₃
H CH(Me)S(O)₂CH₂CF₃
H CH(Et)SMe
H CH(Et)SEt
H CH(Et)SCF₃
H CH(Et)SCH₂CF₃
H CH(Et)S(O)Me
H CH(Et)S(O)Et
H CH(Et)S(O)CF₃
H CH(Et)S(O)CH₂CF₃
H CH(Et)S(O)₂Me
H CH(Et)S(O)₂Et
H CH(Et)S(O)₂CF₃
H CH(Et)S(O)₂CH₂CF₃
H CH(n-Pr)SMe
H CH(n-Pr)SEt
H CH(n-Pr)SCF₃
H CH(n-Pr)SCH₂CF₃
H CH(n-Pr)S(O)Me
H CH(n-Pr)S(O)Et
H CH(n-Pr)S(O)CF₃
H CH(n-Pr)S(O)CH₂CF₃
H CH(n-Pr)S(O)₂Me
H CH(n-Pr)S(O)₂Et
H CH(n-Pr)S(O)₂CF₃
H CH(n-Pr)S(O)₂CH₂CF₃
H CH(i-Pr)SMe
H CH(i-Pr)SEt
H CH(i-Pr)SCF₃
H CH(i-Pr)SCH₂CF₃
H CH(i-Pr)S(O)Me
H CH(i-Pr)S(O)Et
H CH(i-Pr)S(O)CF₃
H CH(i-Pr)S(O)CH₂CF₃
H CH(i-Pr)S(O)₂Me
H CH(i-Pr)S(O)₂Et
H CH(i-Pr)S(O)₂CF₃
H CH(i-Pr)S(O)₂CH₂CF₃
H CH(n-Bu)SMe
H CH(n-Bu)SEt
H CH(n-Bu)SCF₃
H CH(n-Bu)SCH₂CF₃
H CH(n-Bu)S(O)Me
H CH(n-Bu)S(O)Et
H CH(n-Bu)S(O)CF₃
H CH(n-Bu)S(O)CH₂CF₃
H CH(n-Bu)S(O)₂Me
H CH(n-Bu)S(O)₂Et
H CH(n-Bu)S(O)₂CF₃
H CH(n-Bu)S(O)₂CH₂CF₃
H CH(i-Bu)SMe
H CH(i-Bu)SEt
H CH(i-Bu)SCF₃
H CH(i-Bu)SCH₂CF₃
H CH(i-Bu)S(O)Me
H CH(i-Bu)S(O)Et
H CH(i-Bu)S(O)CF₃
H CH(i-Bu)S(O)CH₂CF₃
H CH(i-Bu)S(O)₂Me
H CH(i-Bu)S(O)₂Et
H CH(i-Bu)S(O)₂CF₃
H CH(i-Bu)S(O)₂CH₂CF₃
H CH(s-Bu)SMe
H CH(s-Bu)SEt
H CH(s-Bu)SCF₃
H CH(s-Bu)SCH₂CF₃
H CH(s-Bu)S(O)Me
H CH(s-Bu)S(O)Et
H CH(s-Bu)S(O)CF₃
H CH(s-Bu)S(O)CH₂CF₃
H CH(s-Bu)S(O)₂Me
H CH(s-Bu)S(O)₂Et
H CH(s-Bu)S(O)₂CF₃
H CH(s-Bu)S(O)₂CH₂CF₃
H CH(t-Bu)SMe
H CH(t-Bu)SEt
H CH(t-Bu)SCF₃
H CH(t-Bu)SCH₂CF₃
H CH(t-Bu)S(O)Me
H CH(t-Bu)S(O)Et
H CH(t-Bu)S(O)CF₃
H CH(t-Bu)S(O)CH₂CF₃
H CH(t-Bu)S(O)₂Me
H CH(t-Bu)S(O)₂Et
H CH(t-Bu)S(O)₂CF₃
H CH(t-Bu)S(O)₂CH₂CF₃
H CH(CF₃)SMe
H CH(CF₃)SEt
H CH(CF₃)SCF₃
H CH(CF₃)SCH₂CF₃
H CH(CF₃)S(O)Me
H CH(CF₃)S(O)Et
H CH(CF₃)S(O)CF₃
H CH(CF₃)S(O)CH₂CF₃
H CH(CF₃)S(O)₂Me
H CH(CF₃)S(O)₂Et
H CH(CF₃)S(O)₂CF₃
H CH(CF₃)S(O)₂CH₂CF₃
H CH₂CH₂SMe
H CH₂CH₂SEt
H CH₂CH₂SCF₃
H CH₂CH₂SCH₂CF₃
H CH₂CH₂S(O)Me
H CH₂CH₂S(O)Et
H CH₂CH₂S(O)CF₃
H CH₂CH₂S(O)CH₂CF₃
H CH₂CH₂S(O)₂Me
H CH₂CH₂S(O)₂Et
H CH₂CH₂S(O)₂CF₃
H CH₂CH₂S(O)₂CH₂CF₃
H CH(Me)CH₂SMe
H CH(Me)CH₂SEt
H CH(Me)CH₂SCF₃
H CH(Me)CH₂SCH₂CF₃
H CH(Me)CH₂S(O)Me
H CH(Me)CH₂S(O)Et
H CH(Me)CH₂S(O)CF₃
H CH(Me)CH₂S(O)CH₂CF₃
H CH(Me)CH₂S(O)₂Me
H CH(Me)CH₂S(O)₂Et
H CH(Me)CH₂S(O)₂CF₃
H CH(Me)CH₂S(O)₂CH₂CF₃
H CH(Et)CH₂SMe
H CH(Et)CH₂SEt
H CH(Et)CH₂SCF₃
H CH(Et)CH₂SCH₂CF₃
H CH(Et)CH₂S(O)Me
H CH(Et)CH₂S(O)Et
H CH(Et)CH₂S(O)CF₃
H CH(Et)CH₂S(O)CH₂CF₃
H CH(Et)CH₂S(O)₂Me
H CH(Et)CH₂S(O)₂Et
H CH(Et)CH₂S(O)₂CF₃
H CH(Et)CH₂S(O)₂CH₂CF₃
H C(Me)₂CH₂SMe
H C(Me)₂CH₂SEt
H C(Me)₂CH₂SCF₃
H C(Me)₂CH₂SCH₂CF₃
H C(Me)₂CH₂S(O)Me
H C(Me)₂CH₂S(O)Et
H C(Me)₂CH₂S(O)CF₃
H C(Me)₂CH₂S(O)CH₂CF₃
H C(Me)₂CH₂S(O)₂Me
H C(Me)₂CH₂S(O)₂Et
H C(Me)₂CH₂S(O)₂CF₃
H C(Me)₂CH₂S(O)₂CH₂CF₃
H CH₂CH(Me)SMe
H CH₂CH(Me)SEt
H CH₂CH(Me)SCF₃
H CH₂CH(Me)SCH₂CF₃
H CH₂CH(Me)S(O)Me
H CH₂CH(Me)S(O)Et
H CH₂CH(Me)S(O)CF₃
H CH₂CH(Me)S(O)CH₂CF₃
H CH₂CH(Me)S(O)₂Me
H CH₂CH(Me)S(O)₂Et
H CH₂CH(Me)S(O)₂CF₃
H CH₂CH(Me)S(O)₂CH₂CF₃
H CH₂CH(Et)SMe
H CH₂CH(Et)SEt
H CH₂CH(Et)SCF₃
H CH₂CH(Et)SCH₂CF₃
H CH₂CH(Et)S(O)Me
H CH₂CH(Et)S(O)Et
H CH₂CH(Et)S(O)CF₃
H CH₂CH(Et)S(O)CH₂CF₃
H CH₂CH(Et)S(O)₂Me
H CH₂CH(Et)S(O)₂Et
H CH₂CH(Et)S(O)₂CF₃
H CH₂CH(Et)S(O)₂CH₂CF₃
H CH(Me)CH(Me)SMe
H CH(Me)CH(Me)SEt
H CH(Me)CH(Me)SCF₃
H CH(Me)CH(Me)SCH₂CF₃
H CH(Me)CH(Me)S(O)Me
H CH(Me)CH(Me)S(O)Et
H CH(Me)CH(Me)S(O)CF₃
H CH(Me)CH(Me)S(O)CH₂CF₃
H CH(Me)CH(Me)S(O)₂Me
H CH(Me)CH(Me)S(O)₂Et
H CH(Me)CH(Me)S(O)₂CF₃
H CH(Me)CH(Me)S(O)₂CH₂CF₃
Me CH₂SMe
Me CH₂SEt
Me CH₂SCF₃
Me CH₂SCH₂CF₃
Me CH₂S(O)Me
Me CH₂S(O)Et
Me CH₂S(O)CF₃
Me CH₂S(O)CH₂CF₃
Me CH₂S(O)₂Me
Me CH₂S(O)₂Et
Me CH₂S(O)₂CF₃
Me CH₂S(O)₂CH₂CF₃
Me CH(Me)SMe
Me CH(Me)SEt
Me CH(Me)SCF₃
Me CH(Me)SCH₂CF₃
Me CH(Me)S(O)Me
Me CH(Me)S(O)Et
Me CH(Me)S(O)CF₃
Me CH(Me)S(O)CH₂CF₃
Me CH(Me)S(O)₂Me
Me CH(Me)S(O)₂Et
Me CH(Me)S(O)₂CF₃
Me CH(Me)S(O)₂CH₂CF₃
Me CH(Et)SMe
Me CH(Et)SEt
Me CH(Et)SCF₃
Me CH(Et)SCH₂CF₃
Me CH(Et)S(O)Me
Me CH(Et)S(O)Et
Me CH(Et)S(O)CF₃
Me CH(Et)S(O)CH₂CF₃
Me CH(Et)S(O)₂Me
Me CH(Et)S(O)₂Et
Me CH(Et)S(O)₂CF₃
Me CH(Et)S(O)₂CH₂CF₃
Me CH(n-Pr)SMe
Me CH(n-Pr)SEt
Me CH(n-Pr)SCF₃
Me CH(n-Pr)SCH₂CF₃
Me CH(n-Pr)S(O)Me
Me CH(n-Pr)S(O)Et
Me CH(n-Pr)S(O)CF₃
Me CH(n-Pr)S(O)CH₂CF₃
Me CH(n-Pr)S(O)₂Me
Me CH(n-Pr)S(O)₂Et
Me CH(n-Pr)S(O)₂CF₃
Me CH(n-Pr)S(O)₂CH₂CF₃
Me CH(i-Pr)SMe
Me CH(i-Pr)SEt
Me CH(i-Pr)SCF₃
Me CH(i-Pr)SCH₂CF₃
Me CH(i-Pr)S(O)Me
Me CH(i-Pr)S(O)Et
Me CH(i-Pr)S(O)CF₃
Me CH(i-Pr)S(O)CH₂CF₃
Me CH(i-Pr)S(O)₂Me
Me CH(i-Pr)S(O)₂Et
Me CH(i-Pr)S(O)₂CF₃
Me CH(i-Pr)S(O)₂CH₂CF₃
Me CH(n-Bu)SMe
Me CH(n-Bu)SEt
Me CH(n-Bu)SCF₃
Me CH(n-Bu)SCH₂CF₃
Me CH(n-Bu)S(O)Me
Me CH(n-Bu)S(O)Et
Me CH(n-Bu)S(O)CF₃
Me CH(n-Bu)S(O)CH₂CF₃
Me CH(n-Bu)S(O)₂Me
Me CH(n-Bu)S(O)₂Et
Me CH(n-Bu)S(O)₂CF₃
Me CH(n-Bu)S(O)₂CH₂CF₃
Me CH(i-Bu)SMe
Me CH(i-Bu)SEt
Me CH(i-Bu)SCF₃
Me CH(i-Bu)SCH₂CF₃
Me CH(i-Bu)S(O)Me
Me CH(i-Bu)S(O)Et
Me CH(i-Bu)S(O)CF₃
Me CH(i-Bu)S(O)CH₂CF₃
Me CH(i-Bu)S(O)₂Me
Me CH(i-Bu)S(O)₂Et
Me CH(i-Bu)S(O)₂CF₃
Me CH(i-Bu)S(O)₂CH₂CF₃
Me CH(s-Bu)SMe
Me CH(s-Bu)SEt
Me CH(s-Bu)SCF₃
Me CH(s-Bu)SCH₂CF₃
Me CH(s-Bu)S(O)Me
Me CH(s-Bu)S(O)Et
Me CH(s-Bu)S(O)CF₃
Me CH(s-Bu)S(O)CH₂CF₃
Me CH(s-Bu)S(O)₂Me
Me CH(s-Bu)S(O)₂Et
Me CH(s-Bu)S(O)₂CF₃
Me CH(s-Bu)S(O)₂CH₂CF₃
Me CH(t-Bu)SMe
Me CH(t-Bu)SEt
Me CH(t-Bu)SCF₃
Me CH(t-Bu)SCH₂CF₃
Me CH(t-Bu)S(O)Me
Me CH(t-Bu)S(O)Et
Me CH(t-Bu)S(O)CF₃
Me CH(t-Bu)S(O)CH₂CF₃
Me CH(t-Bu)S(O)₂Me
Me CH(t-Bu)S(O)₂Et
Me CH(t-Bu)S(O)₂CF₃
Me CH(t-Bu)S(O)₂CH₂CF₃
Me CH(CF₃)SMe
Me CH(CF₃)SEt
Me CH(CF₃)SCF₃
Me CH(CF₃)SCH₂CF₃
Me CH(CF₃)S(O)Me
Me CH(CF₃)S(O)Et
Me CH(CF₃)S(O)CF₃
Me CH(CF₃)S(O)CH₂CF₃
Me CH(CF₃)S(O)₂Me
Me CH(CF₃)S(O)₂Et
Me CH(CF₃)S(O)₂CF₃
Me CH(CF₃)S(O)₂CH₂CF₃
Me CH₂CH₂SMe
Me CH₂CH₂SEt
Me CH₂CH₂SCF₃
Me CH₂CH₂SCH₂CF₃
Me CH₂CH₂S(O)Me
Me CH₂CH₂S(O)Et
Me CH₂CH₂S(O)CF₃
Me CH₂CH₂S(O)CH₂CF₃
Me CH₂CH₂S(O)₂Me
Me CH₂CH₂S(O)₂Et
Me CH₂CH₂S(O)₂CF₃
Me CH₂CH₂S(O)₂CH₂CF₃
Me CH(Me)CH₂SMe
Me CH(Me)CH₂SEt
Me CH(Me)CH₂SCF₃
Me CH(Me)CH₂SCH₂CF₃
Me CH(Me)CH₂S(O)Me
Me CH(Me)CH₂S(O)Et
Me CH(Me)CH₂S(O)CF₃
Me CH(Me)CH₂S(O)CH₂CF₃
Me CH(Me)CH₂S(O)₂Me
Me CH(Me)CH₂S(O)₂Et
Me CH(Me)CH₂S(O)₂CF₃
Me CH(Me)CH₂S(O)₂CH₂CF₃
Me CH(Et)CH₂SMe
Me CH(Et)CH₂SEt
Me CH(Et)CH₂SCF₃
Me CH(Et)CH₂SCH₂CF₃
Me CH(Et)CH₂S(O)Me
Me CH(Et)CH₂S(O)Et
Me CH(Et)CH₂S(O)CF₃
Me CH(Et)CH₂S(O)CH₂CF₃
Me CH(Et)CH₂S(O)₂Me
Me CH(Et)CH₂S(O)₂Et
Me CH(Et)CH₂S(O)₂CF₃
Me CH(Et)CH₂S(O)₂CH₂CF₃
Me C(Me)₂CH₂SMe
Me C(Me)₂CH₂SEt
Me C(Me)₂CH₂SCF₃
Me C(Me)₂CH₂SCH₂CF₃
Me C(Me)₂CH₂S(O)Me
Me C(Me)₂CH₂S(O)Et
Me C(Me)₂CH₂S(O)CF₃
Me C(Me)₂CH₂S(O)CH₂CF₃
Me C(Me)₂CH₂S(O)₂Me
Me C(Me)₂CH₂S(O)₂Et
Me C(Me)₂CH₂S(O)₂CF₃
Me C(Me)₂CH₂S(O)₂CH₂CF₃
Me CH₂CH(Me)SMe
Me CH₂CH(Me)SEt
Me CH₂CH(Me)SCF₃
Me CH₂CH(Me)SCH₂CF₃
Me CH₂CH(Me)S(O)Me
Me CH₂CH(Me)S(O)Et
Me CH₂CH(Me)S(O)CF₃
Me CH₂CH(Me)S(O)CH₂CF₃
Me CH₂CH(Me)S(O)₂Me
Me CH₂CH(Me)S(O)₂Et
Me CH₂CH(Me)S(O)₂CF₃
Me CH₂CH(Me)S(O)₂CH₂CF₃
Me CH₂CH(Et)SMe
Me CH₂CH(Et)SEt
Me CH₂CH(Et)SCF₃
Me CH₂CH(Et)SCH₂CF₃
Me CH₂CH(Et)S(O)Me
Me CH₂CH(Et)S(O)Et
Me CH₂CH(Et)S(O)CF₃
Me CH₂CH(Et)S(O)CH₂CF₃
Me CH₂CH(Et)S(O)₂Me
Me CH₂CH(Et)S(O)₂Et
Me CH₂CH(Et)S(O)₂CF₃
Me CH₂CH(Et)S(O)₂CH₂CF₃
Me CH(Me)CH(Me)SMe
Me CH(Me)CH(Me)SEt
Me CH(Me)CH(Me)SCF₃
Me CH(Me)CH(Me)SCH₂CF₃
Me CH(Me)CH(Me)S(O)Me
Me CH(Me)CH(Me)S(O)Et
Me CH(Me)CH(Me)S(O)CF₃
Me CH(Me)CH(Me)S(O)CH₂CF₃
Me CH(Me)CH(Me)S(O)₂Me
Me CH(Me)CH(Me)S(O)₂Et
Me CH(Me)CH(Me)S(O)₂CF₃
Me CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂CF₃ CH₂SMe
CH₂CF₃ CH₂SEt
CH₂CF₃ CH₂SCF₃
CH₂CF₃ CH₂SCH₂CF₃
CH₂CF₃ CH₂S(O)Me
CH₂CF₃ CH₂S(O)Et
CH₂CF₃ CH₂S(O)CF₃
CH₂CF₃ CH₂S(O)CH₂CF₃
CH₂CF₃ CH₂S(O)₂Me
CH₂CF₃ CH₂S(O)₂Et
CH₂CF₃ CH₂S(O)₂CF₃
CH₂CF₃ CH₂S(O)₂CH₂CF₃
CH₂CF₃ CH(Me)SMe
CH₂CF₃ CH(Me)SEt
CH₂CF₃ CH(Me)SCF₃
CH₂CF₃ CH(Me)SCH₂CF₃
CH₂CF₃ CH(Me)S(O)Me
CH₂CF₃ CH(Me)S(O)Et
CH₂CF₃ CH(Me)S(O)CF₃
CH₂CF₃ CH(Me)S(O)CH₂CF₃
CH₂CF₃ CH(Me)S(O)₂Me
CH₂CF₃ CH(Me)S(O)₂Et
CH₂CF₃ CH(Me)S(O)₂CF₃
CH₂CF₃ CH(Me)S(O)₂CH₂CF₃
CH₂CF₃ CH(Et)SMe
CH₂CF₃ CH(Et)SEt
CH₂CF₃ CH(Et)SCF₃
CH₂CF₃ CH(Et)SCH₂CF₃
CH₂CF₃ CH(Et)S(O)Me
CH₂CF₃ CH(Et)S(O)Et
CH₂CF₃ CH(Et)S(O)CF₃
CH₂CF₃ CH(Et)S(O)CH₂CF₃
CH₂CF₃ CH(Et)S(O)₂Me
CH₂CF₃ CH(Et)S(O)₂Et
CH₂CF₃ CH(Et)S(O)₂CF₃
CH₂CF₃ CH(Et)S(O)₂CH₂CF₃
CH₂CF₃ CH(n-Pr)SMe
CH₂CF₃ CH(n-Pr)SEt
CH₂CF₃ CH(n-Pr)SCF₃
CH₂CF₃ CH(n-Pr)SCH₂CF₃
CH₂CF₃ CH(n-Pr)S(O)Me
CH₂CF₃ CH(n-Pr)S(O)Et
CH₂CF₃ CH(n-Pr)S(O)CF₃
CH₂CF₃ CH(n-Pr)S(O)CH₂CF₃
CH₂CF₃ CH(n-Pr)S(O)₂Me
CH₂CF₃ CH(n-Pr)S(O)₂Et
CH₂CF₃ CH(n-Pr)S(O)₂CF₃
CH₂CF₃ CH(n-Pr)S(O)₂CH₂CF₃
CH₂CF₃ CH(i-Pr)SMe
CH₂CF₃ CH(i-Pr)SEt
CH₂CF₃ CH(i-Pr)SCF₃
CH₂CF₃ CH(i-Pr)SCH₂CF₃
CH₂CF₃ CH(i-Pr)S(O)Me
CH₂CF₃ CH(i-Pr)S(O)Et
CH₂CF₃ CH(i-Pr)S(O)CF₃
CH₂CF₃ CH(i-Pr)S(O)CH₂CF₃
CH₂CF₃ CH(i-Pr)S(O)₂Me
CH₂CF₃ CH(i-Pr)S(O)₂Et
CH₂CF₃ CH(i-Pr)S(O)₂CF₃
CH₂CF₃ CH(i-Pr)S(O)₂CH₂CF₃
CH₂CF₃ CH(n-Bu)SMe
CH₂CF₃ CH(n-Bu)SEt
CH₂CF₃ CH(n-Bu)SCF₃
CH₂CF₃ CH(n-Bu)SCH₂CF₃
CH₂CF₃ CH(n-Bu)S(O)Me
CH₂CF₃ CH(n-Bu)S(O)Et
CH₂CF₃ CH(n-Bu)S(O)CF₃
CH₂CF₃ CH(n-Bu)S(O)CH₂CF₃
CH₂CF₃ CH(n-Bu)S(O)₂Me
CH₂CF₃ CH(n-Bu)S(O)₂Et
CH₂CF₃ CH(n-Bu)S(O)₂CF₃
CH₂CF₃ CH(n-Bu)S(O)₂CH₂CF₃
CH₂CF₃ CH(i-Bu)SMe
CH₂CF₃ CH(i-Bu)SEt
CH₂CF₃ CH(i-Bu)SCF₃
CH₂CF₃ CH(i-Bu)SCH₂CF₃
CH₂CF₃ CH(i-Bu)S(O)Me
CH₂CF₃ CH(i-Bu)S(O)Et
CH₂CF₃ CH(i-Bu)S(O)CF₃
CH₂CF₃ CH(i-Bu)S(O)CH₂CF₃
CH₂CF₃ CH(i-Bu)S(O)₂Me
CH₂CF₃ CH(i-Bu)S(O)₂Et
CH₂CF₃ CH(i-Bu)S(O)₂CF₃
CH₂CF₃ CH(i-Bu)S(O)₂CH₂CF₃
CH₂CF₃ CH(s-Bu)SMe
CH₂CF₃ CH(s-Bu)SEt
CH₂CF₃ CH(s-Bu)SCF₃
CH₂CF₃ CH(s-Bu)SCH₂CF₃
CH₂CF₃ CH(s-Bu)S(O)Me
CH₂CF₃ CH(s-Bu)S(O)Et
CH₂CF₃ CH(s-Bu)S(O)CF₃
CH₂CF₃ CH(s-Bu)S(O)CH₂CF₃
CH₂CF₃ CH(s-Bu)S(O)₂Me
CH₂CF₃ CH(s-Bu)S(O)₂Et
CH₂CF₃ CH(s-Bu)S(O)₂CF₃
CH₂CF₃ CH(s-Bu)S(O)₂CH₂CF₃
CH₂CF₃ CH(t-Bu)SMe
CH₂CF₃ CH(t-Bu)SEt
CH₂CF₃ CH(t-Bu)SCF₃
CH₂CF₃ CH(t-Bu)SCH₂CF₃
CH₂CF₃ CH(t-Bu)S(O)Me
CH₂CF₃ CH(t-Bu)S(O)Et
CH₂CF₃ CH(t-Bu)S(O)CF₃
CH₂CF₃ CH(t-Bu)S(O)CH₂CF₃
CH₂CF₃ CH(t-Bu)S(O)₂Me
CH₂CF₃ CH(t-Bu)S(O)₂Et
CH₂CF₃ CH(t-Bu)S(O)₂CF₃
CH₂CF₃ CH(t-Bu)S(O)₂CH₂CF₃
CH₂CF₃ CH(CF₃)SMe
CH₂CF₃ CH(CF₃)SEt
CH₂CF₃ CH(CF₃)SCF₃
CH₂CF₃ CH(CF₃)SCH₂CF₃
CH₂CF₃ CH(CF₃)S(O)Me
CH₂CF₃ CH(CF₃)S(O)Et
CH₂CF₃ CH(CF₃)S(O)CF₃
CH₂CF₃ CH(CF₃)S(O)CH₂CF₃
CH₂CF₃ CH(CF₃)S(O)₂Me
CH₂CF₃ CH(CF₃)S(O)₂Et
CH₂CF₃ CH(CF₃)S(O)₂CF₃
CH₂CF₃ CH(CF₃)S(O)₂CH₂CF₃
CH₂CF₃ CH₂CH₂SMe
CH₂CF₃ CH₂CH₂SEt
CH₂CF₃ CH₂CH₂SCF₃
CH₂CF₃ CH₂CH₂SCH₂CF₃
CH₂CF₃ CH₂CH₂S(O)Me
CH₂CF₃ CH₂CH₂S(O)Et
CH₂CF₃ CH₂CH₂S(O)CF₃
CH₂CF₃ CH₂CH₂S(O)CH₂CF₃
CH₂CF₃ CH₂CH₂S(O)₂Me
CH₂CF₃ CH₂CH₂S(O)₂Et
CH₂CF₃ CH₂CH₂S(O)₂CF₃
CH₂CF₃ CH₂CH₂S(O)₂CH₂CF₃
CH₂CF₃ CH(Me)CH₂SMe
CH₂CF₃ CH(Me)CH₂SEt
CH₂CF₃ CH(Me)CH₂SCF₃
CH₂CF₃ CH(Me)CH₂SCH₂CF₃
CH₂CF₃ CH(Me)CH₂S(O)Me
CH₂CF₃ CH(Me)CH₂S(O)Et
CH₂CF₃ CH(Me)CH₂S(O)CF₃
CH₂CF₃ CH(Me)CH₂S(O)CH₂CF₃
CH₂CF₃ CH(Me)CH₂S(O)₂Me
CH₂CF₃ CH(Me)CH₂S(O)₂Et
CH₂CF₃ CH(Me)CH₂S(O)₂CF₃
CH₂CF₃ CH(Me)CH₂S(O)₂CH₂CF₃
CH₂CF₃ CH(Et)CH₂SMe
CH₂CF₃ CH(Et)CH₂SEt
CH₂CF₃ CH(Et)CH₂SCF₃
CH₂CF₃ CH(Et)CH₂SCH₂CF₃
CH₂CF₃ CH(Et)CH₂S(O)Me
CH₂CF₃ CH(Et)CH₂S(O)Et
CH₂CF₃ CH(Et)CH₂S(O)CF₃
CH₂CF₃ CH(Et)CH₂S(O)CH₂CF₃
CH₂CF₃ CH(Et)CH₂S(O)₂Me
CH₂CF₃ CH(Et)CH₂S(O)₂Et
CH₂CF₃ CH(Et)CH₂S(O)₂CF₃
CH₂CF₃ CH(Et)CH₂S(O)₂CH₂CF₃
CH₂CF₃ C(Me)₂CH₂SMe
CH₂CF₃ C(Me)₂CH₂SEt
CH₂CF₃ C(Me)₂CH₂SCF₃
CH₂CF₃ C(Me)₂CH₂SCH₂CF₃
CH₂CF₃ C(Me)₂CH₂S(O)Me
CH₂CF₃ C(Me)₂CH₂S(O)Et
CH₂CF₃ C(Me)₂CH₂S(O)CF₃
CH₂CF₃ C(Me)₂CH₂S(O)CH₂CF₃
CH₂CF₃ C(Me)₂CH₂S(O)₂Me
CH₂CF₃ C(Me)₂CH₂S(O)₂Et
CH₂CF₃ C(Me)₂CH₂S(O)₂CF₃
CH₂CF₃ C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂CF₃ CH₂CH(Me)SMe
CH₂CF₃ CH₂CH(Me)SEt
CH₂CF₃ CH₂CH(Me)SCF₃
CH₂CF₃ CH₂CH(Me)SCH₂CF₃
CH₂CF₃ CH₂CH(Me)S(O)Me
CH₂CF₃ CH₂CH(Me)S(O)Et
CH₂CF₃ CH₂CH(Me)S(O)CF₃
CH₂CF₃ CH₂CH(Me)S(O)CH₂CF₃
CH₂CF₃ CH₂CH(Me)S(O)₂Me
CH₂CF₃ CH₂CH(Me)S(O)₂Et
CH₂CF₃ CH₂CH(Me)S(O)₂CF₃
CH₂CF₃ CH₂CH(Me)S(O)₂CH₂CF₃
CH₂CF₃ CH₂CH(Et)SMe
CH₂CF₃ CH₂CH(Et)SEt
CH₂CF₃ CH₂CH(Et)SCF₃
CH₂CF₃ CH₂CH(Et)SCH₂CF₃
CH₂CF₃ CH₂CH(Et)S(O)Me
CH₂CF₃ CH₂CH(Et)S(O)Et
CH₂CF₃ CH₂CH(Et)S(O)CF₃
CH₂CF₃ CH₂CH(Et)S(O)CH₂CF₃
CH₂CF₃ CH₂CH(Et)S(O)₂Me
CH₂CF₃ CH₂CH(Et)S(O)₂Et
CH₂CF₃ CH₂CH(Et)S(O)₂CF₃
CH₂CF₃ CH₂CH(Et)S(O)₂CH₂CF₃
CH₂CF₃ CH(Me)CH(Me)SMe
CH₂CF₃ CH(Me)CH(Me)SEt
CH₂CF₃ CH(Me)CH(Me)SCF₃
CH₂CF₃ CH(Me)CH(Me)SCH₂CF₃
CH₂CF₃ CH(Me)CH(Me)S(O)Me
CH₂CF₃ CH(Me)CH(Me)S(O)Et
CH₂CF₃ CH(Me)CH(Me)S(O)CF₃
CH₂CF₃ CH(Me)CH(Me)S(O)CH₂CF₃
CH₂CF₃ CH(Me)CH(Me)S(O)₂Me
CH₂CF₃ CH(Me)CH(Me)S(O)₂Et
CH₂CF₃ CH(Me)CH(Me)S(O)₂CF₃
CH₂CF₃ CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂CN CH₂SMe
CH₂CN CH₂SEt
CH₂CN CH₂SCF₃
CH₂CN CH₂SCH₂CF₃
CH₂CN CH₂S(O)Me
CH₂CN CH₂S(O)Et
CH₂CN CH₂S(O)CF₃
CH₂CN CH₂S(O)CH₂CF₃
CH₂CN CH₂S(O)₂Me
CH₂CN CH₂S(O)₂Et
CH₂CN CH₂S(O)₂CF₃
CH₂CN CH₂S(O)₂CH₂CF₃
CH₂CN CH(Me)SMe
CH₂CN CH(Me)SEt
CH₂CN CH(Me)SCF₃
CH₂CN CH(Me)SCH₂CF₃
CH₂CN CH(Me)S(O)Me
CH₂CN CH(Me)S(O)Et
CH₂CN CH(Me)S(O)CF₃
CH₂CN CH(Me)S(O)CH₂CF₃
CH₂CN CH(Me)S(O)₂Me
CH₂CN CH(Me)S(O)₂Et
CH₂CN CH(Me)S(O)₂CF₃
CH₂CN CH(Me)S(O)₂CH₂CF₃
CH₂CN CH(Et)SMe
CH₂CN CH(Et)SEt
CH₂CN CH(Et)SCF₃
CH₂CN CH(Et)SCH₂CF₃
CH₂CN CH(Et)S(O)Me
CH₂CN CH(Et)S(O)Et
CH₂CN CH(Et)S(O)CF₃
CH₂CN CH(Et)S(O)CH₂CF₃
CH₂CN CH(Et)S(O)₂Me
CH₂CN CH(Et)S(O)₂Et
CH₂CN CH(Et)S(O)₂CF₃
CH₂CN CH(Et)S(O)₂CH₂CF₃
CH₂CN CH(n-Pr)SMe
CH₂CN CH(n-Pr)SEt
CH₂CN CH(n-Pr)SCF₃
CH₂CN CH(n-Pr)SCH₂CF₃
CH₂CN CH(n-Pr)S(O)Me
CH₂CN CH(n-Pr)S(O)Et
CH₂CN CH(n-Pr)S(O)CF₃
CH₂CN CH(n-Pr)S(O)CH₂CF₃
CH₂CN CH(n-Pr)S(O)₂Me
CH₂CN CH(n-Pr)S(O)₂Et
CH₂CN CH(n-Pr)S(O)₂CF₃
CH₂CN CH(n-Pr)S(O)₂CH₂CF₃
CH₂CN CH(i-Pr)SMe
CH₂CN CH(i-Pr)SEt
CH₂CN CH(i-Pr)SCF₃
CH₂CN CH(i-Pr)SCH₂CF₃
CH₂CN CH(i-Pr)S(O)Me
CH₂CN CH(i-Pr)S(O)Et
CH₂CN CH(i-Pr)S(O)CF₃
CH₂CN CH(i-Pr)S(O)CH₂CF₃
CH₂CN CH(i-Pr)S(O)₂Me
CH₂CN CH(i-Pr)S(O)₂Et
CH₂CN CH(i-Pr)S(O)₂CF₃
CH₂CN CH(i-Pr)S(O)₂CH₂CF₃
CH₂CN CH(n-Bu)SMe
CH₂CN CH(n-Bu)SEt
CH₂CN CH(n-Bu)SCF₃
CH₂CN CH(n-Bu)SCH₂CF₃
CH₂CN CH(n-Bu)S(O)Me
CH₂CN CH(n-Bu)S(O)Et
CH₂CN CH(n-Bu)S(O)CF₃
CH₂CN CH(n-Bu)S(O)CH₂CF₃
CH₂CN CH(n-Bu)S(O)₂Me
CH₂CN CH(n-Bu)S(O)₂Et
CH₂CN CH(n-Bu)S(O)₂CF₃
CH₂CN CH(n-Bu)S(O)₂CH₂CF₃
CH₂CN CH(i-Bu)SMe
CH₂CN CH(i-Bu)SEt
CH₂CN CH(i-Bu)SCF₃
CH₂CN CH(i-Bu)SCH₂CF₃
CH₂CN CH(i-Bu)S(O)Me
CH₂CN CH(i-Bu)S(O)Et
CH₂CN CH(i-Bu)S(O)CF₃
CH₂CN CH(i-Bu)S(O)CH₂CF₃
CH₂CN CH(i-Bu)S(O)₂Me
CH₂CN CH(i-Bu)S(O)₂Et
CH₂CN CH(i-Bu)S(O)₂CF₃
CH₂CN CH(i-Bu)S(O)₂CH₂CF₃
CH₂CN CH(s-Bu)SMe
CH₂CN CH(s-Bu)SEt
CH₂CN CH(s-Bu)SCF₃
CH₂CN CH(s-Bu)SCH₂CF₃
CH₂CN CH(s-Bu)S(O)Me
CH₂CN CH(s-Bu)S(O)Et
CH₂CN CH(s-Bu)S(O)CF₃
CH₂CN CH(s-Bu)S(O)CH₂CF₃
CH₂CN CH(s-Bu)S(O)₂Me
CH₂CN CH(s-Bu)S(O)₂Et
CH₂CN CH(s-Bu)S(O)₂CF₃
CH₂CN CH(s-Bu)S(O)₂CH₂CF₃
CH₂CN CH(t-Bu)SMe
CH₂CN CH(t-Bu)SEt
CH₂CN CH(t-Bu)SCF₃
CH₂CN CH(t-Bu)SCH₂CF₃
CH₂CN CH(t-Bu)S(O)Me
CH₂CN CH(t-Bu)S(O)Et
CH₂CN CH(t-Bu)S(O)CF₃
CH₂CN CH(t-Bu)S(O)CH₂CF₃
CH₂CN CH(t-Bu)S(O)₂Me
CH₂CN CH(t-Bu)S(O)₂Et
CH₂CN CH(t-Bu)S(O)₂CF₃
CH₂CN CH(t-Bu)S(O)₂CH₂CF₃
CH₂CN CH(CF₃)SMe
CH₂CN CH(CF₃)SEt
CH₂CN CH(CF₃)SCF₃
CH₂CN CH(CF₃)SCH₂CF₃
CH₂CN CH(CF₃)S(O)Me
CH₂CN CH(CF₃)S(O)Et
CH₂CN CH(CF₃)S(O)CF₃
CH₂CN CH(CF₃)S(O)CH₂CF₃
CH₂CN CH(CF₃)S(O)₂Me
CH₂CN CH(CF₃)S(O)₂Et
CH₂CN CH(CF₃)S(O)₂CF₃
CH₂CN CH(CF₃)S(O)₂CH₂CF₃
CH₂CN CH₂CH₂SMe
CH₂CN CH₂CH₂SEt
CH₂CN CH₂CH₂SCF₃
CH₂CN CH₂CH₂SCH₂CF₃
CH₂CN CH₂CH₂S(O)Me
CH₂CN CH₂CH₂S(O)Et
CH₂CN CH₂CH₂S(O)CF₃
CH₂CN CH₂CH₂S(O)CH₂CF₃
CH₂CN CH₂CH₂S(O)₂Me
CH₂CN CH₂CH₂S(O)₂Et
CH₂CN CH₂CH₂S(O)₂CF₃
CH₂CN CH₂CH₂S(O)₂CH₂CF₃
CH₂CN CH(Me)CH₂SMe
CH₂CN CH(Me)CH₂SEt
CH₂CN CH(Me)CH₂SCF₃
CH₂CN CH(Me)CH₂SCH₂CF₃
CH₂CN CH(Me)CH₂S(O)Me
CH₂CN CH(Me)CH₂S(O)Et
CH₂CN CH(Me)CH₂S(O)CF₃
CH₂CN CH(Me)CH₂S(O)CH₂CF₃
CH₂CN CH(Me)CH₂S(O)₂Me
CH₂CN CH(Me)CH₂S(O)₂Et
CH₂CN CH(Me)CH₂S(O)₂CF₃
CH₂CN CH(Me)CH₂S(O)₂CH₂CF₃
CH₂CN CH(Et)CH₂SMe
CH₂CN CH(Et)CH₂SEt
CH₂CN CH(Et)CH₂SCF₃
CH₂CN CH(Et)CH₂SCH₂CF₃
CH₂CN CH(Et)CH₂S(O)Me
CH₂CN CH(Et)CH₂S(O)Et
CH₂CN CH(Et)CH₂S(O)CF₃
CH₂CN CH(Et)CH₂S(O)CH₂CF₃
CH₂CN CH(Et)CH₂S(O)₂Me
CH₂CN CH(Et)CH₂S(O)₂Et
CH₂CN CH(Et)CH₂S(O)₂CF₃
CH₂CN CH(Et)CH₂S(O)₂CH₂CF₃
CH₂CN C(Me)₂CH₂SMe
CH₂CN C(Me)₂CH₂SEt
CH₂CN C(Me)₂CH₂SCF₃
CH₂CN C(Me)₂CH₂SCH₂CF₃
CH₂CN C(Me)₂CH₂S(O)Me
CH₂CN C(Me)₂CH₂S(O)Et
CH₂CN C(Me)₂CH₂S(O)CF₃
CH₂CN C(Me)₂CH₂S(O)CH₂CF₃
CH₂CN C(Me)₂CH₂S(O)₂Me
CH₂CN C(Me)₂CH₂S(O)₂Et
CH₂CN C(Me)₂CH₂S(O)₂CF₃
CH₂CN C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂CN CH₂CH(Me)SMe
CH₂CN CH₂CH(Me)SEt
CH₂CN CH₂CH(Me)SCF₃
CH₂CN CH₂CH(Me)SCH₂CF₃
CH₂CN CH₂CH(Me)S(O)Me
CH₂CN CH₂CH(Me)S(O)Et
CH₂CN CH₂CH(Me)S(O)CF₃
CH₂CN CH₂CH(Me)S(O)CH₂CF₃
CH₂CN CH₂CH(Me)S(O)₂Me
CH₂CN CH₂CH(Me)S(O)₂Et
CH₂CN CH₂CH(Me)S(O)₂CF₃
CH₂CN CH₂CH(Me)S(O)₂CH₂CF₃
CH₂CN CH₂CH(Et)SMe
CH₂CN CH₂CH(Et)SEt
CH₂CN CH₂CH(Et)SCF₃
CH₂CN CH₂CH(Et)SCH₂CF₃
CH₂CN CH₂CH(Et)S(O)Me
CH₂CN CH₂CH(Et)S(O)Et
CH₂CN CH₂CH(Et)S(O)CF₃
CH₂CN CH₂CH(Et)S(O)CH₂CF₃
CH₂CN CH₂CH(Et)S(O)₂Me
CH₂CN CH₂CH(Et)S(O)₂Et
CH₂CN CH₂CH(Et)S(O)₂CF₃
CH₂CN CH₂CH(Et)S(O)₂CH₂CF₃
CH₂CN CH(Me)CH(Me)SMe
CH₂CN CH(Me)CH(Me)SEt
CH₂CN CH(Me)CH(Me)SCF₃
CH₂CN CH(Me)CH(Me)SCH₂CF₃
CH₂CN CH(Me)CH(Me)S(O)Me
CH₂CN CH(Me)CH(Me)S(O)Et
CH₂CN CH(Me)CH(Me)S(O)CF₃
CH₂CN CH(Me)CH(Me)S(O)CH₂CF₃
CH₂CN CH(Me)CH(Me)S(O)₂Me
CH₂CN CH(Me)CH(Me)S(O)₂Et
CH₂CN CH(Me)CH(Me)S(O)₂CF₃
CH₂CN CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH₂SMe
CH₂CH=CH₂ CH₂SEt
CH₂CH=CH₂ CH₂SCF₃
CH₂CH=CH₂ CH₂SCH₂CF₃
CH₂CH=CH₂ CH₂S(O)Me
CH₂CH=CH₂ CH₂S(O)Et
CH₂CH=CH₂ CH₂S(O)CF₃
CH₂CH=CH₂ CH₂S(O)CH₂CF₃
CH₂CH=CH₂ CH₂S(O)₂Me
CH₂CH=CH₂ CH₂S(O)₂Et
CH₂CH=CH₂ CH₂S(O)₂CF₃
CH₂CH=CH₂ CH₂S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(Me)SMe
CH₂CH=CH₂ CH(Me)SEt
CH₂CH=CH₂ CH(Me)SCF₃
CH₂CH=CH₂ CH(Me)SCH₂CF₃
CH₂CH=CH₂ CH(Me)S(O)Me
CH₂CH=CH₂ CH(Me)S(O)Et
CH₂CH=CH₂ CH(Me)S(O)CF₃
CH₂CH=CH₂ CH(Me)S(O)CH₂CF₃
CH₂CH=CH₂ CH(Me)S(O)₂Me
CH₂CH=CH₂ CH(Me)S(O)₂Et
CH₂CH=CH₂ CH(Me)S(O)₂CF₃
CH₂CH=CH₂ CH(Me)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(Et)SMe
CH₂CH=CH₂ CH(Et)SEt
CH₂CH=CH₂ CH(Et)SCF₃
CH₂CH=CH₂ CH(Et)SCH₂CF₃
CH₂CH=CH₂ CH(Et)S(O)Me
CH₂CH=CH₂ CH(Et)S(O)Et
CH₂CH=CH₂ CH(Et)S(O)CF₃
CH₂CH=CH₂ CH(Et)S(O)CH₂CF₃
CH₂CH=CH₂ CH(Et)S(O)₂Me
CH₂CH=CH₂ CH(Et)S(O)₂Et
CH₂CH=CH₂ CH(Et)S(O)₂CF₃
CH₂CH=CH₂ CH(Et)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(n-Pr)SMe
CH₂CH=CH₂ CH(n-Pr)SEt
CH₂CH=CH₂ CH(n-Pr)SCF₃
CH₂CH=CH₂ CH(n-Pr)SCH₂CF₃
CH₂CH=CH₂ CH(n-Pr)S(O)Me
CH₂CH=CH₂ CH(n-Pr)S(O)Et
CH₂CH=CH₂ CH(n-Pr)S(O)CF₃
CH₂CH=CH₂ CH(n-Pr)S(O)CH₂CF₃
CH₂CH=CH₂ CH(n-Pr)S(O)₂Me
CH₂CH=CH₂ CH(n-Pr)S(O)₂Et
CH₂CH=CH₂ CH(n-Pr)S(O)₂CF₃
CH₂CH=CH₂ CH(n-Pr)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(i-Pr)SMe
CH₂CH=CH₂ CH(i-Pr)SEt
CH₂CH=CH₂ CH(i-Pr)SCF₃
CH₂CH=CH₂ CH(i-Pr)SCH₂CF₃
CH₂CH=CH₂ CH(i-Pr)S(O)Me
CH₂CH=CH₂ CH(i-Pr)S(O)Et
CH₂CH=CH₂ CH(i-Pr)S(O)CF₃
CH₂CH=CH₂ CH(i-Pr)S(O)CH₂CF₃
CH₂CH=CH₂ CH(i-Pr)S(O)₂Me
CH₂CH=CH₂ CH(i-Pr)S(O)₂Et
CH₂CH=CH₂ CH(i-Pr)S(O)₂CF₃
CH₂CH=CH₂ CH(i-Pr)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(n-Bu)SMe
CH₂CH=CH₂ CH(n-Bu)SEt
CH₂CH=CH₂ CH(n-Bu)SCF₃
CH₂CH=CH₂ CH(n-Bu)SCH₂CF₃
CH₂CH=CH₂ CH(n-Bu)S(O)Me
CH₂CH=CH₂ CH(n-Bu)S(O)Et
CH₂CH=CH₂ CH(n-Bu)S(O)CF₃
CH₂CH=CH₂ CH(n-Bu)S(O)CH₂CF₃
CH₂CH=CH₂ CH(n-Bu)S(O)₂Me
CH₂CH=CH₂ CH(n-Bu)S(O)₂Et
CH₂CH=CH₂ CH(n-Bu)S(O)₂CF₃
CH₂CH=CH₂ CH(n-Bu)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(i-Bu)SMe
CH₂CH=CH₂ CH(i-Bu)SEt
CH₂CH=CH₂ CH(i-Bu)SCF₃
CH₂CH=CH₂ CH(i-Bu)SCH₂CF₃
CH₂CH=CH₂ CH(i-Bu)S(O)Me
CH₂CH=CH₂ CH(i-Bu)S(O)Et
CH₂CH=CH₂ CH(i-Bu)S(O)CF₃
CH₂CH=CH₂ CH(i-Bu)S(O)CH₂CF₃
CH₂CH=CH₂ CH(i-Bu)S(O)₂Me
CH₂CH=CH₂ CH(i-Bu)S(O)₂Et
CH₂CH=CH₂ CH(i-Bu)S(O)₂CF₃
CH₂CH=CH₂ CH(i-Bu)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(s-Bu)SMe
CH₂CH=CH₂ CH(s-Bu)SEt
CH₂CH=CH₂ CH(s-Bu)SCF₃
CH₂CH=CH₂ CH(s-Bu)SCH₂CF₃
CH₂CH=CH₂ CH(s-Bu)S(O)Me
CH₂CH=CH₂ CH(s-Bu)S(O)Et
CH₂CH=CH₂ CH(s-Bu)S(O)CF₃
CH₂CH=CH₂ CH(s-Bu)S(O)CH₂CF₃
CH₂CH=CH₂ CH(s-Bu)S(O)₂Me
CH₂CH=CH₂ CH(s-Bu)S(O)₂Et
CH₂CH=CH₂ CH(s-Bu)S(O)₂CF₃
CH₂CH=CH₂ CH(s-Bu)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(t-Bu)SMe
CH₂CH=CH₂ CH(t-Bu)SEt
CH₂CH=CH₂ CH(t-Bu)SCF₃
CH₂CH=CH₂ CH(t-Bu)SCH₂CF₃
CH₂CH=CH₂ CH(t-Bu)S(O)Me
CH₂CH=CH₂ CH(t-Bu)S(O)Et
CH₂CH=CH₂ CH(t-Bu)S(O)CF₃
CH₂CH=CH₂ CH(t-Bu)S(O)CH₂CF₃
CH₂CH=CH₂ CH(t-Bu)S(O)₂Me
CH₂CH=CH₂ CH(t-Bu)S(O)₂Et
CH₂CH=CH₂ CH(t-Bu)S(O)₂CF₃
CH₂CH=CH₂ CH(t-Bu)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(CF₃)SMe
CH₂CH=CH₂ CH(CF₃)SEt
CH₂CH=CH₂ CH(CF₃)SCF₃
CH₂CH=CH₂ CH(CF₃)SCH₂CF₃
CH₂CH=CH₂ CH(CF₃)S(O)Me
CH₂CH=CH₂ CH(CF₃)S(O)Et
CH₂CH=CH₂ CH(CF₃)S(O)CF₃
CH₂CH=CH₂ CH(CF₃)S(O)CH₂CF₃
CH₂CH=CH₂ CH(CF₃)S(O)₂Me
CH₂CH=CH₂ CH(CF₃)S(O)₂Et
CH₂CH=CH₂ CH(CF₃)S(O)₂CF₃
CH₂CH=CH₂ CH(CF₃)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH₂CH₂SMe
CH₂CH=CH₂ CH₂CH₂SEt
CH₂CH=CH₂ CH₂CH₂SCF₃
CH₂CH=CH₂ CH₂CH₂SCH₂CF₃
CH₂CH=CH₂ CH₂CH₂S(O)Me
CH₂CH=CH₂ CH₂CH₂S(O)Et
CH₂CH=CH₂ CH₂CH₂S(O)CF₃
CH₂CH=CH₂ CH₂CH₂S(O)CH₂CF₃
CH₂CH=CH₂ CH₂CH₂S(O)₂Me
CH₂CH=CH₂ CH₂CH₂S(O)₂Et
CH₂CH=CH₂ CH₂CH₂S(O)₂CF₃
CH₂CH=CH₂ CH₂CH₂S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(Me)CH₂SMe
CH₂CH=CH₂ CH(Me)CH₂SEt
CH₂CH=CH₂ CH(Me)CH₂SCF₃
CH₂CH=CH₂ CH(Me)CH₂SCH₂CF₃
CH₂CH=CH₂ CH(Me)CH₂S(O)Me
CH₂CH=CH₂ CH(Me)CH₂S(O)Et
CH₂CH=CH₂ CH(Me)CH₂S(O)CF₃
CH₂CH=CH₂ CH(Me)CH₂S(O)CH₂CF₃
CH₂CH=CH₂ CH(Me)CH₂S(O)₂Me
CH₂CH=CH₂ CH(Me)CH₂S(O)₂Et
CH₂CH=CH₂ CH(Me)CH₂S(O)₂CF₃
CH₂CH=CH₂ CH(Me)CH₂S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(Et)CH₂SMe
CH₂CH=CH₂ CH(Et)CH₂SEt
CH₂CH=CH₂ CH(Et)CH₂SCF₃
CH₂CH=CH₂ CH(Et)CH₂SCH₂CF₃
CH₂CH=CH₂ CH(Et)CH₂S(O)Me
CH₂CH=CH₂ CH(Et)CH₂S(O)Et
CH₂CH=CH₂ CH(Et)CH₂S(O)CF₃
CH₂CH=CH₂ CH(Et)CH₂S(O)CH₂CF₃
CH₂CH=CH₂ CH(Et)CH₂S(O)₂Me
CH₂CH=CH₂ CH(Et)CH₂S(O)₂Et
CH₂CH=CH₂ CH(Et)CH₂S(O)₂CF₃
CH₂CH=CH₂ CH(Et)CH₂S(O)₂CH₂CF₃
CH₂CH=CH₂ C(Me)₂CH₂SMe
CH₂CH=CH₂ C(Me)₂CH₂SEt
CH₂CH=CH₂ C(Me)₂CH₂SCF₃
CH₂CH=CH₂ C(Me)₂CH₂SCH₂CF₃
CH₂CH=CH₂ C(Me)₂CH₂S(O)Me
CH₂CH=CH₂ C(Me)₂CH₂S(O)Et
CH₂CH=CH₂ C(Me)₂CH₂S(O)CF₃
CH₂CH=CH₂ C(Me)₂CH₂S(O)CH₂CF₃
CH₂CH=CH₂ C(Me)₂CH₂S(O)₂Me
CH₂CH=CH₂ C(Me)₂CH₂S(O)₂Et
CH₂CH=CH₂ C(Me)₂CH₂S(O)₂CF₃
CH₂CH=CH₂ C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂CH=CH₂ CH₂CH(Me)SMe
CH₂CH=CH₂ CH₂CH(Me)SEt
CH₂CH=CH₂ CH₂CH(Me)SCF₃
CH₂CH=CH₂ CH₂CH(Me)SCH₂CF₃
CH₂CH=CH₂ CH₂CH(Me)S(O)Me
CH₂CH=CH₂ CH₂CH(Me)S(O)Et
CH₂CH=CH₂ CH₂CH(Me)S(O)CF₃
CH₂CH=CH₂ CH₂CH(Me)S(O)CH₂CF₃
CH₂CH=CH₂ CH₂CH(Me)S(O)₂Me
CH₂CH=CH₂ CH₂CH(Me)S(O)₂Et
CH₂CH=CH₂ CH₂CH(Me)S(O)₂CF₃
CH₂CH=CH₂ CH₂CH(Me)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH₂CH(Et)SMe
CH₂CH=CH₂ CH₂CH(Et)SEt
CH₂CH=CH₂ CH₂CH(Et)SCF₃
CH₂CH=CH₂ CH₂CH(Et)SCH₂CF₃
CH₂CH=CH₂ CH₂CH(Et)S(O)Me
CH₂CH=CH₂ CH₂CH(Et)S(O)Et
CH₂CH=CH₂ CH₂CH(Et)S(O)CF₃
CH₂CH=CH₂ CH₂CH(Et)S(O)CH₂CF₃
CH₂CH=CH₂ CH₂CH(Et)S(O)₂Me
CH₂CH=CH₂ CH₂CH(Et)S(O)₂Et
CH₂CH=CH₂ CH₂CH(Et)S(O)₂CF₃
CH₂CH=CH₂ CH₂CH(Et)S(O)₂CH₂CF₃
CH₂CH=CH₂ CH(Me)CH(Me)SMe
CH₂CH=CH₂ CH(Me)CH(Me)SEt
CH₂CH=CH₂ CH(Me)CH(Me)SCF₃
CH₂CH=CH₂ CH(Me)CH(Me)SCH₂CF₃
CH₂CH=CH₂ CH(Me)CH(Me)S(O)Me
CH₂CH=CH₂ CH(Me)CH(Me)S(O)Et
CH₂CH=CH₂ CH(Me)CH(Me)S(O)CF₃
CH₂CH=CH₂ CH(Me)CH(Me)S(O)CH₂CF₃
CH₂CH=CH₂ CH(Me)CH(Me)S(O)₂Me
CH₂CH=CH₂ CH(Me)CH(Me)S(O)₂Et
CH₂CH=CH₂ CH(Me)CH(Me)S(O)₂CF₃
CH₂CH=CH₂ CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH₂SMe
CH₂CH(OMe)₂ CH₂SEt
CH₂CH(OMe)₂ CH₂SCF₃
CH₂CH(OMe)₂ CH₂SCH₂CF₃
CH₂CH(OMe)₂ CH₂S(O)Me
CH₂CH(OMe)₂ CH₂S(O)Et
CH₂CH(OMe)₂ CH₂S(O)CF₃
CH₂CH(OMe)₂ CH₂S(O)CH₂CF₃
CH₂CH(OMe)₂ CH₂S(O)₂Me
CH₂CH(OMe)₂ CH₂S(O)₂Et
CH₂CH(OMe)₂ CH₂S(O)₂CF₃
CH₂CH(OMe)₂ CH₂S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(Me)SMe
CH₂CH(OMe)₂ CH(Me)SEt
CH₂CH(OMe)₂ CH(Me)SCF₃
CH₂CH(OMe)₂ CH(Me)SCH₂CF₃
CH₂CH(OMe)₂ CH(Me)S(O)Me
CH₂CH(OMe)₂ CH(Me)S(O)Et
CH₂CH(OMe)₂ CH(Me)S(O)CF₃
CH₂CH(OMe)₂ CH(Me)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(Me)S(O)₂Me
CH₂CH(OMe)₂ CH(Me)S(O)₂Et
CH₂CH(OMe)₂ CH(Me)S(O)₂CF₃
CH₂CH(OMe)₂ CH(Me)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(Et)SMe
CH₂CH(OMe)₂ CH(Et)SEt
CH₂CH(OMe)₂ CH(Et)SCF₃
CH₂CH(OMe)₂ CH(Et)SCH₂CF₃
CH₂CH(OMe)₂ CH(Et)S(O)Me
CH₂CH(OMe)₂ CH(Et)S(O)Et
CH₂CH(OMe)₂ CH(Et)S(O)CF₃
CH₂CH(OMe)₂ CH(Et)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(Et)S(O)₂Me
CH₂CH(OMe)₂ CH(Et)S(O)₂Et
CH₂CH(OMe)₂ CH(Et)S(O)₂CF₃
CH₂CH(OMe)₂ CH(Et)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(n-Pr)SMe
CH₂CH(OMe)₂ CH(n-Pr)SEt
CH₂CH(OMe)₂ CH(n-Pr)SCF₃
CH₂CH(OMe)₂ CH(n-Pr)SCH₂CF₃
CH₂CH(OMe)₂ CH(n-Pr)S(O)Me
CH₂CH(OMe)₂ CH(n-Pr)S(O)Et
CH₂CH(OMe)₂ CH(n-Pr)S(O)CF₃
CH₂CH(OMe)₂ CH(n-Pr)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(n-Pr)S(O)₂Me
CH₂CH(OMe)₂ CH(n-Pr)S(O)₂Et
CH₂CH(OMe)₂ CH(n-Pr)S(O)₂CF₃
CH₂CH(OMe)₂ CH(n-Pr)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(i-Pr)SMe
CH₂CH(OMe)₂ CH(i-Pr)SEt
CH₂CH(OMe)₂ CH(i-Pr)SCF₃
CH₂CH(OMe)₂ CH(i-Pr)SCH₂CF₃
CH₂CH(OMe)₂ CH(i-Pr)S(O)Me
CH₂CH(OMe)₂ CH(i-Pr)S(O)Et
CH₂CH(OMe)₂ CH(i-Pr)S(O)CF₃
CH₂CH(OMe)₂ CH(i-Pr)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(i-Pr)S(O)₂Me
CH₂CH(OMe)₂ CH(i-Pr)S(O)₂Et
CH₂CH(OMe)₂ CH(i-Pr)S(O)₂CF₃
CH₂CH(OMe)₂ CH(i-Pr)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(n-Bu)SMe
CH₂CH(OMe)₂ CH(n-Bu)SEt
CH₂CH(OMe)₂ CH(n-Bu)SCF₃
CH₂CH(OMe)₂ CH(n-Bu)SCH₂CF₃
CH₂CH(OMe)₂ CH(n-Bu)S(O)Me
CH₂CH(OMe)₂ CH(n-Bu)S(O)Et
CH₂CH(OMe)₂ CH(n-Bu)S(O)CF₃
CH₂CH(OMe)₂ CH(n-Bu)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(n-Bu)S(O)₂Me
CH₂CH(OMe)₂ CH(n-Bu)S(O)₂Et
CH₂CH(OMe)₂ CH(n-Bu)S(O)₂CF₃
CH₂CH(OMe)₂ CH(n-Bu)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(i-Bu)SMe
CH₂CH(OMe)₂ CH(i-Bu)SEt
CH₂CH(OMe)₂ CH(i-Bu)SCF₃
CH₂CH(OMe)₂ CH(i-Bu)SCH₂CF₃
CH₂CH(OMe)₂ CH(i-Bu)S(O)Me
CH₂CH(OMe)₂ CH(i-Bu)S(O)Et
CH₂CH(OMe)₂ CH(i-Bu)S(O)CF₃
CH₂CH(OMe)₂ CH(i-Bu)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(i-Bu)S(O)₂Me
CH₂CH(OMe)₂ CH(i-Bu)S(O)₂Et
CH₂CH(OMe)₂ CH(i-Bu)S(O)₂CF₃
CH₂CH(OMe)₂ CH(i-Bu)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(s-Bu)SMe
CH₂CH(OMe)₂ CH(s-Bu)SEt
CH₂CH(OMe)₂ CH(s-Bu)SCF₃
CH₂CH(OMe)₂ CH(s-Bu)SCH₂CF₃
CH₂CH(OMe)₂ CH(s-Bu)S(O)Me
CH₂CH(OMe)₂ CH(s-Bu)S(O)Et
CH₂CH(OMe)₂ CH(s-Bu)S(O)CF₃
CH₂CH(OMe)₂ CH(s-Bu)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(s-Bu)S(O)₂Me
CH₂CH(OMe)₂ CH(s-Bu)S(O)₂Et
CH₂CH(OMe)₂ CH(s-Bu)S(O)₂CF₃
CH₂CH(OMe)₂ CH(s-Bu)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(t-Bu)SMe
CH₂CH(OMe)₂ CH(t-Bu)SEt
CH₂CH(OMe)₂ CH(t-Bu)SCF₃
CH₂CH(OMe)₂ CH(t-Bu)SCH₂CF₃
CH₂CH(OMe)₂ CH(t-Bu)S(O)Me
CH₂CH(OMe)₂ CH(t-Bu)S(O)Et
CH₂CH(OMe)₂ CH(t-Bu)S(O)CF₃
CH₂CH(OMe)₂ CH(t-Bu)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(t-Bu)S(O)₂Me
CH₂CH(OMe)₂ CH(t-Bu)S(O)₂Et
CH₂CH(OMe)₂ CH(t-Bu)S(O)₂CF₃
CH₂CH(OMe)₂ CH(t-Bu)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(CF₃)SMe
CH₂CH(OMe)₂ CH(CF₃)SEt
CH₂CH(OMe)₂ CH(CF₃)SCF₃
CH₂CH(OMe)₂ CH(CF₃)SCH₂CF₃
CH₂CH(OMe)₂ CH(CF₃)S(O)Me
CH₂CH(OMe)₂ CH(CF₃)S(O)Et
CH₂CH(OMe)₂ CH(CF₃)S(O)CF₃
CH₂CH(OMe)₂ CH(CF₃)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(CF₃)S(O)₂Me
CH₂CH(OMe)₂ CH(CF₃)S(O)₂Et
CH₂CH(OMe)₂ CH(CF₃)S(O)₂CF₃
CH₂CH(OMe)₂ CH(CF₃)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH₂CH₂SMe
CH₂CH(OMe)₂ CH₂CH₂SEt
CH₂CH(OMe)₂ CH₂CH₂SCF₃
CH₂CH(OMe)₂ CH₂CH₂SCH₂CF₃
CH₂CH(OMe)₂ CH₂CH₂S(O)Me
CH₂CH(OMe)₂ CH₂CH₂S(O)Et
CH₂CH(OMe)₂ CH₂CH₂S(O)CF₃
CH₂CH(OMe)₂ CH₂CH₂S(O)CH₂CF₃
CH₂CH(OMe)₂ CH₂CH₂S(O)₂Me
CH₂CH(OMe)₂ CH₂CH₂S(O)₂Et
CH₂CH(OMe)₂ CH₂CH₂S(O)₂CF₃
CH₂CH(OMe)₂ CH₂CH₂S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(Me)CH₂SMe
CH₂CH(OMe)₂ CH(Me)CH₂SEt
CH₂CH(OMe)₂ CH(Me)CH₂SCF₃
CH₂CH(OMe)₂ CH(Me)CH₂SCH₂CF₃
CH₂CH(OMe)₂ CH(Me)CH₂S(O)Me
CH₂CH(OMe)₂ CH(Me)CH₂S(O)Et
CH₂CH(OMe)₂ CH(Me)CH₂S(O)CF₃
CH₂CH(OMe)₂ CH(Me)CH₂S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(Me)CH₂S(O)₂Me
CH₂CH(OMe)₂ CH(Me)CH₂S(O)₂Et
CH₂CH(OMe)₂ CH(Me)CH₂S(O)₂CF₃
CH₂CH(OMe)₂ CH(Me)CH₂S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(Et)CH₂SMe
CH₂CH(OMe)₂ CH(Et)CH₂SEt
CH₂CH(OMe)₂ CH(Et)CH₂SCF₃
CH₂CH(OMe)₂ CH(Et)CH₂SCH₂CF₃
CH₂CH(OMe)₂ CH(Et)CH₂S(O)Me
CH₂CH(OMe)₂ CH(Et)CH₂S(O)Et
CH₂CH(OMe)₂ CH(Et)CH₂S(O)CF₃
CH₂CH(OMe)₂ CH(Et)CH₂S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(Et)CH₂S(O)₂Me
CH₂CH(OMe)₂ CH(Et)CH₂S(O)₂Et
CH₂CH(OMe)₂ CH(Et)CH₂S(O)₂CF₃
CH₂CH(OMe)₂ CH(Et)CH₂S(O)₂CH₂CF₃
CH₂CH(OMe)₂ C(Me)₂CH₂SMe
CH₂CH(OMe)₂ C(Me)₂CH₂SEt
CH₂CH(OMe)₂ C(Me)₂CH₂SCF₃
CH₂CH(OMe)₂ C(Me)₂CH₂SCH₂CF₃
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)Me
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)Et
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)CF₃
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)CH₂CF₃
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)₂Me
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)₂Et
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)₂CF₃
CH₂CH(OMe)₂ C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH₂CH(Me)SMe
CH₂CH(OMe)₂ CH₂CH(Me)SEt
CH₂CH(OMe)₂ CH₂CH(Me)SCF₃
CH₂CH(OMe)₂ CH₂CH(Me)SCH₂CF₃
CH₂CH(OMe)₂ CH₂CH(Me)S(O)Me
CH₂CH(OMe)₂ CH₂CH(Me)S(O)Et
CH₂CH(OMe)₂ CH₂CH(Me)S(O)CF₃
CH₂CH(OMe)₂ CH₂CH(Me)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH₂CH(Me)S(O)₂Me
CH₂CH(OMe)₂ CH₂CH(Me)S(O)₂Et
CH₂CH(OMe)₂ CH₂CH(Me)S(O)₂CF₃
CH₂CH(OMe)₂ CH₂CH(Me)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH₂CH(Et)SMe
CH₂CH(OMe)₂ CH₂CH(Et)SEt
CH₂CH(OMe)₂ CH₂CH(Et)SCF₃
CH₂CH(OMe)₂ CH₂CH(Et)SCH₂CF₃
CH₂CH(OMe)₂ CH₂CH(Et)S(O)Me
CH₂CH(OMe)₂ CH₂CH(Et)S(O)Et
CH₂CH(OMe)₂ CH₂CH(Et)S(O)CF₃
CH₂CH(OMe)₂ CH₂CH(Et)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH₂CH(Et)S(O)₂Me
CH₂CH(OMe)₂ CH₂CH(Et)S(O)₂Et
CH₂CH(OMe)₂ CH₂CH(Et)S(O)₂CF₃
CH₂CH(OMe)₂ CH₂CH(Et)S(O)₂CH₂CF₃
CH₂CH(OMe)₂ CH(Me)CH(Me)SMe
CH₂CH(OMe)₂ CH(Me)CH(Me)SEt
CH₂CH(OMe)₂ CH(Me)CH(Me)SCF₃
CH₂CH(OMe)₂ CH(Me)CH(Me)SCH₂CF₃
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)Me
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)Et
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)CF₃
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)CH₂CF₃
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)₂Me
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)₂Et
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)₂CF₃
CH₂CH(OMe)₂ CH(Me)CH(Me)S(O)₂CH₂CF₃
CH(Me)OEt CH₂SMe
CH(Me)OEt CH₂SEt
CH(Me)OEt CH₂SCF₃
CH(Me)OEt CH₂SCH₂CF₃
CH(Me)OEt CH₂S(O)Me
CH(Me)OEt CH₂S(O)Et
CH(Me)OEt CH₂S(O)CF₃
CH(Me)OEt CH₂S(O)CH₂CF₃
CH(Me)OEt CH₂S(O)₂Me
CH(Me)OEt CH₂S(O)₂Et
CH(Me)OEt CH₂S(O)₂CF₃
CH(Me)OEt CH₂S(O)₂CH₂CF₃
CH(Me)OEt CH(Me)SMe
CH(Me)OEt CH(Me)SEt
CH(Me)OEt CH(Me)SCF₃
CH(Me)OEt CH(Me)SCH₂CF₃
CH(Me)OEt CH(Me)S(O)Me
CH(Me)OEt CH(Me)S(O)Et
CH(Me)OEt CH(Me)S(O)CF₃
CH(Me)OEt CH(Me)S(O)CH₂CF₃
CH(Me)OEt CH(Me)S(O)₂Me
CH(Me)OEt CH(Me)S(O)₂Et
CH(Me)OEt CH(Me)S(O)₂CF₃
CH(Me)OEt CH(Me)S(O)₂CH₂CF₃
CH(Me)OEt CH(Et)SMe
CH(Me)OEt CH(Et)SEt
CH(Me)OEt CH(Et)SCF₃
CH(Me)OEt CH(Et)SCH₂CF₃
CH(Me)OEt CH(Et)S(O)Me
CH(Me)OEt CH(Et)S(O)Et
CH(Me)OEt CH(Et)S(O)CF₃
CH(Me)OEt CH(Et)S(O)CH₂CF₃
CH(Me)OEt CH(Et)S(O)₂Me
CH(Me)OEt CH(Et)S(O)₂Et
CH(Me)OEt CH(Et)S(O)₂CF₃
CH(Me)OEt CH(Et)S(O)₂CH₂CF₃
CH(Me)OEt CH(n-Pr)SMe
CH(Me)OEt CH(n-Pr)SEt
CH(Me)OEt CH(n-Pr)SCF₃
CH(Me)OEt CH(n-Pr)SCH₂CF₃
CH(Me)OEt CH(n-Pr)S(O)Me
CH(Me)OEt CH(n-Pr)S(O)Et
CH(Me)OEt CH(n-Pr)S(O)CF₃
CH(Me)OEt CH(n-Pr)S(O)CH₂CF₃
CH(Me)OEt CH(n-Pr)S(O)₂Me
CH(Me)OEt CH(n-Pr)S(O)₂Et
CH(Me)OEt CH(n-Pr)S(O)₂CF₃
CH(Me)OEt CH(n-Pr)S(O)₂CH₂CF₃
CH(Me)OEt CH(i-Pr)SMe
CH(Me)OEt CH(i-Pr)SEt
CH(Me)OEt CH(i-Pr)SCF₃
CH(Me)OEt CH(i-Pr)SCH₂CF₃
CH(Me)OEt CH(i-Pr)S(O)Me
CH(Me)OEt CH(i-Pr)S(O)Et
CH(Me)OEt CH(i-Pr)S(O)CF₃
CH(Me)OEt CH(i-Pr)S(O)CH₂CF₃
CH(Me)OEt CH(i-Pr)S(O)₂Me
CH(Me)OEt CH(i-Pr)S(O)₂Et
CH(Me)OEt CH(i-Pr)S(O)₂CF₃
CH(Me)OEt CH(i-Pr)S(O)₂CH₂CF₃
CH(Me)OEt CH(n-Bu)SMe
CH(Me)OEt CH(n-Bu)SEt
CH(Me)OEt CH(n-Bu)SCF₃
CH(Me)OEt CH(n-Bu)SCH₂CF₃
CH(Me)OEt CH(n-Bu)S(O)Me
CH(Me)OEt CH(n-Bu)S(O)Et
CH(Me)OEt CH(n-Bu)S(O)CF₃
CH(Me)OEt CH(n-Bu)S(O)CH₂CF₃
CH(Me)OEt CH(n-Bu)S(O)₂Me
CH(Me)OEt CH(n-Bu)S(O)₂Et
CH(Me)OEt CH(n-Bu)S(O)₂CF₃
CH(Me)OEt CH(n-Bu)S(O)₂CH₂CF₃
CH(Me)OEt CH(i-Bu)SMe
CH(Me)OEt CH(i-Bu)SEt
CH(Me)OEt CH(i-Bu)SCF₃
CH(Me)OEt CH(i-Bu)SCH₂CF₃
CH(Me)OEt CH(i-Bu)S(O)Me
CH(Me)OEt CH(i-Bu)S(O)Et
CH(Me)OEt CH(i-Bu)S(O)CF₃
CH(Me)OEt CH(i-Bu)S(O)CH₂CF₃
CH(Me)OEt CH(i-Bu)S(O)₂Me
CH(Me)OEt CH(i-Bu)S(O)₂Et
CH(Me)OEt CH(i-Bu)S(O)₂CF₃
CH(Me)OEt CH(i-Bu)S(O)₂CH₂CF₃
CH(Me)OEt CH(s-Bu)SMe
CH(Me)OEt CH(s-Bu)SEt
CH(Me)OEt CH(s-Bu)SCF₃
CH(Me)OEt CH(s-Bu)SCH₂CF₃
CH(Me)OEt CH(s-Bu)S(O)Me
CH(Me)OEt CH(s-Bu)S(O)Et
CH(Me)OEt CH(s-Bu)S(O)CF₃
CH(Me)OEt CH(s-Bu)S(O)CH₂CF₃
CH(Me)OEt CH(s-Bu)S(O)₂Me
CH(Me)OEt CH(s-Bu)S(O)₂Et
CH(Me)OEt CH(s-Bu)S(O)₂CF₃
CH(Me)OEt CH(s-Bu)S(O)₂CH₂CF₃
CH(Me)OEt CH(t-Bu)SMe
CH(Me)OEt CH(t-Bu)SEt
CH(Me)OEt CH(t-Bu)SCF₃
CH(Me)OEt CH(t-Bu)SCH₂CF₃
CH(Me)OEt CH(t-Bu)S(O)Me
CH(Me)OEt CH(t-Bu)S(O)Et
CH(Me)OEt CH(t-Bu)S(O)CF₃
CH(Me)OEt CH(t-Bu)S(O)CH₂CF₃
CH(Me)OEt CH(t-Bu)S(O)₂Me
CH(Me)OEt CH(t-Bu)S(O)₂Et
CH(Me)OEt CH(t-Bu)S(O)₂CF₃
CH(Me)OEt CH(t-Bu)S(O)₂CH₂CF₃
CH(Me)OEt CH(CF₃)SMe
CH(Me)OEt CH(CF₃)SEt
CH(Me)OEt CH(CF₃)SCF₃
CH(Me)OEt CH(CF₃)SCH₂CF₃
CH(Me)OEt CH(CF₃)S(O)Me
CH(Me)OEt CH(CF₃)S(O)Et
CH(Me)OEt CH(CF₃)S(O)CF₃
CH(Me)OEt CH(CF₃)S(O)CH₂CF₃
CH(Me)OEt CH(CF₃)S(O)₂Me
CH(Me)OEt CH(CF₃)S(O)₂Et
CH(Me)OEt CH(CF₃)S(O)₂CF₃
CH(Me)OEt CH(CF₃)S(O)₂CH₂CF₃
CH(Me)OEt CH₂CH₂SMe
CH(Me)OEt CH₂CH₂SEt
CH(Me)OEt CH₂CH₂SCF₃
CH(Me)OEt CH₂CH₂SCH₂CF₃
CH(Me)OEt CH₂CH₂S(O)Me
CH(Me)OEt CH₂CH₂S(O)Et
CH(Me)OEt CH₂CH₂S(O)CF₃
CH(Me)OEt CH₂CH₂S(O)CH₂CF₃
CH(Me)OEt CH₂CH₂S(O)₂Me
CH(Me)OEt CH₂CH₂S(O)₂Et
CH(Me)OEt CH₂CH₂S(O)₂CF₃
CH(Me)OEt CH₂CH₂S(O)₂CH₂CF₃
CH(Me)OEt CH(Me)CH₂SMe
CH(Me)OEt CH(Me)CH₂SEt
CH(Me)OEt CH(Me)CH₂SCF₃
CH(Me)OEt CH(Me)CH₂SCH₂CF₃
CH(Me)OEt CH(Me)CH₂S(O)Me
CH(Me)OEt CH(Me)CH₂S(O)Et
CH(Me)OEt CH(Me)CH₂S(O)CF₃
CH(Me)OEt CH(Me)CH₂S(O)CH₂CF₃
CH(Me)OEt CH(Me)CH₂S(O)₂Me
CH(Me)OEt CH(Me)CH₂S(O)₂Et
CH(Me)OEt CH(Me)CH₂S(O)₂CF₃
CH(Me)OEt CH(Me)CH₂S(O)₂CH₂CF₃
CH(Me)OEt CH(Et)CH₂SMe
CH(Me)OEt CH(Et)CH₂SEt
CH(Me)OEt CH(Et)CH₂SCF₃
CH(Me)OEt CH(Et)CH₂SCH₂CF₃
CH(Me)OEt CH(Et)CH₂S(O)Me
CH(Me)OEt CH(Et)CH₂S(O)Et
CH(Me)OEt CH(Et)CH₂S(O)CF₃
CH(Me)OEt CH(Et)CH₂S(O)CH₂CF₃
CH(Me)OEt CH(Et)CH₂S(O)₂Me
CH(Me)OEt CH(Et)CH₂S(O)₂Et
CH(Me)OEt CH(Et)CH₂S(O)₂CF₃
CH(Me)OEt CH(Et)CH₂S(O)₂CH₂CF₃
CH(Me)OEt C(Me)₂CH₂SMe
CH(Me)OEt C(Me)₂CH₂SEt
CH(Me)OEt C(Me)₂CH₂SCF₃
CH(Me)OEt C(Me)₂CH₂SCH₂CF₃
CH(Me)OEt C(Me)₂CH₂S(O)Me
CH(Me)OEt C(Me)₂CH₂S(O)Et
CH(Me)OEt C(Me)₂CH₂S(O)CF₃
CH(Me)OEt C(Me)₂CH₂S(O)CH₂CF₃
CH(Me)OEt C(Me)₂CH₂S(O)₂Me
CH(Me)OEt C(Me)₂CH₂S(O)₂Et
CH(Me)OEt C(Me)₂CH₂S(O)₂CF₃
CH(Me)OEt C(Me)₂CH₂S(O)₂CH₂CF₃
CH(Me)OEt CH₂CH(Me)SMe
CH(Me)OEt CH₂CH(Me)SEt
CH(Me)OEt CH₂CH(Me)SCF₃
CH(Me)OEt CH₂CH(Me)SCH₂CF₃
CH(Me)OEt CH₂CH(Me)S(O)Me
CH(Me)OEt CH₂CH(Me)S(O)Et
CH(Me)OEt CH₂CH(Me)S(O)CF₃
CH(Me)OEt CH₂CH(Me)S(O)CH₂CF₃
CH(Me)OEt CH₂CH(Me)S(O)₂Me
CH(Me)OEt CH₂CH(Me)S(O)₂Et
CH(Me)OEt CH₂CH(Me)S(O)₂CF₃
CH(Me)OEt CH₂CH(Me)S(O)₂CH₂CF₃
CH(Me)OEt CH₂CH(Et)SMe
CH(Me)OEt CH₂CH(Et)SEt
CH(Me)OEt CH₂CH(Et)SCF₃
CH(Me)OEt CH₂CH(Et)SCH₂CF₃
CH(Me)OEt CH₂CH(Et)S(O)Me
CH(Me)OEt CH₂CH(Et)S(O)Et
CH(Me)OEt CH₂CH(Et)S(O)CF₃
CH(Me)OEt CH₂CH(Et)S(O)CH₂CF₃
CH(Me)OEt CH₂CH(Et)S(O)₂Me
CH(Me)OEt CH₂CH(Et)S(O)₂Et
CH(Me)OEt CH₂CH(Et)S(O)₂CF₃
CH(Me)OEt CH₂CH(Et)S(O)₂CH₂CF₃
CH(Me)OEt CH(Me)CH(Me)SMe
CH(Me)OEt CH(Me)CH(Me)SEt
CH(Me)OEt CH(Me)CH(Me)SCF₃
CH(Me)OEt CH(Me)CH(Me)SCH₂CF₃
CH(Me)OEt CH(Me)CH(Me)S(O)Me
CH(Me)OEt CH(Me)CH(Me)S(O)Et
CH(Me)OEt CH(Me)CH(Me)S(O)CF₃
CH(Me)OEt CH(Me)CH(Me)S(O)CH₂CF₃
CH(Me)OEt CH(Me)CH(Me)S(O)₂Me
CH(Me)OEt CH(Me)CH(Me)S(O)₂Et
CH(Me)OEt CH(Me)CH(Me)S(O)₂CF₃
CH(Me)OEt CH(Me)CH(Me)S(O)₂CH₂CF₃
S(O)₂Me CH₂SMe
S(O)₂Me CH₂SEt
S(O)₂Me CH₂SCF₃
S(O)₂Me CH₂SCH₂CF₃
S(O)₂Me CH₂S(O)Me
S(O)₂Me CH₂S(O)Et
S(O)₂Me CH₂S(O)CF₃
S(O)₂Me CH₂S(O)CH₂CF₃
S(O)₂Me CH₂S(O)₂Me
S(O)₂Me CH₂S(O)₂Et
S(O)₂Me CH₂S(O)₂CF₃
S(O)₂Me CH₂S(O)₂CH₂CF₃
S(O)₂Me CH(Me)SMe
S(O)₂Me CH(Me)SEt
S(O)₂Me CH(Me)SCF₃
S(O)₂Me CH(Me)SCH₂CF₃
S(O)₂Me CH(Me)S(O)Me
S(O)₂Me CH(Me)S(O)Et
S(O)₂Me CH(Me)S(O)CF₃
S(O)₂Me CH(Me)S(O)CH₂CF₃
S(O)₂Me CH(Me)S(O)₂Me
S(O)₂Me CH(Me)S(O)₂Et
S(O)₂Me CH(Me)S(O)₂CF₃
S(O)₂Me CH(Me)S(O)₂CH₂CF₃
S(O)₂Me CH(Et)SMe
S(O)₂Me CH(Et)SEt
S(O)₂Me CH(Et)SCF₃
S(O)₂Me CH(Et)SCH₂CF₃
S(O)₂Me CH(Et)S(O)Me
S(O)₂Me CH(Et)S(O)Et
S(O)₂Me CH(Et)S(O)CF₃
S(O)₂Me CH(Et)S(O)CH₂CF₃
S(O)₂Me CH(Et)S(O)₂Me
S(O)₂Me CH(Et)S(O)₂Et
S(O)₂Me CH(Et)S(O)₂CF₃
S(O)₂Me CH(Et)S(O)₂CH₂CF₃
S(O)₂Me CH(n-Pr)SMe
S(O)₂Me CH(n-Pr)SEt
S(O)₂Me CH(n-Pr)SCF₃
S(O)₂Me CH(n-Pr)SCH₂CF₃
S(O)₂Me CH(n-Pr)S(O)Me
S(O)₂Me CH(n-Pr)S(O)Et
S(O)₂Me CH(n-Pr)S(O)CF₃
S(O)₂Me CH(n-Pr)S(O)CH₂CF₃
S(O)₂Me CH(n-Pr)S(O)₂Me
S(O)₂Me CH(n-Pr)S(O)₂Et
S(O)₂Me CH(n-Pr)S(O)₂CF₃
S(O)₂Me CH(n-Pr)S(O)₂CH₂CF₃
S(O)₂Me CH(i-Pr)SMe
S(O)₂Me CH(i-Pr)SEt
S(O)₂Me CH(i-Pr)SCF₃
S(O)₂Me CH(i-Pr)SCH₂CF₃
S(O)₂Me CH(i-Pr)S(O)Me
S(O)₂Me CH(i-Pr)S(O)Et
S(O)₂Me CH(i-Pr)S(O)CF₃
S(O)₂Me CH(i-Pr)S(O)CH₂CF₃
S(O)₂Me CH(i-Pr)S(O)₂Me
S(O)₂Me CH(i-Pr)S(O)₂Et
S(O)₂Me CH(i-Pr)S(O)₂CF₃
S(O)₂Me CH(i-Pr)S(O)₂CH₂CF₃
S(O)₂Me CH(n-Bu)SMe
S(O)₂Me CH(n-Bu)SEt
S(O)₂Me CH(n-Bu)SCF₃
S(O)₂Me CH(n-Bu)SCH₂CF₃
S(O)₂Me CH(n-Bu)S(O)Me
S(O)₂Me CH(n-Bu)S(O)Et
S(O)₂Me CH(n-Bu)S(O)CF₃
S(O)₂Me CH(n-Bu)S(O)CH₂CF₃
S(O)₂Me CH(n-Bu)S(O)₂Me
S(O)₂Me CH(n-Bu)S(O)₂Et
S(O)₂Me CH(n-Bu)S(O)₂CF₃
S(O)₂Me CH(n-Bu)S(O)₂CH₂CF₃
S(O)₂Me CH(i-Bu)SMe
S(O)₂Me CH(i-Bu)SEt
S(O)₂Me CH(i-Bu)SCF₃
S(O)₂Me CH(i-Bu)SCH₂CF₃
S(O)₂Me CH(i-Bu)S(O)Me
S(O)₂Me CH(i-Bu)S(O)Et
S(O)₂Me CH(i-Bu)S(O)CF₃
S(O)₂Me CH(i-Bu)S(O)CH₂CF₃
S(O)₂Me CH(i-Bu)S(O)₂Me
S(O)₂Me CH(i-Bu)S(O)₂Et
S(O)₂Me CH(i-Bu)S(O)₂CF₃
S(O)₂Me CH(i-Bu)S(O)₂CH₂CF₃
S(O)₂Me CH(s-Bu)SMe
S(O)₂Me CH(s-Bu)SEt
S(O)₂Me CH(s-Bu)SCF₃
S(O)₂Me CH(s-Bu)SCH₂CF₃
S(O)₂Me CH(s-Bu)S(O)Me
S(O)₂Me CH(s-Bu)S(O)Et
S(O)₂Me CH(s-Bu)S(O)CF₃
S(O)₂Me CH(s-Bu)S(O)CH₂CF₃
S(O)₂Me CH(s-Bu)S(O)₂Me
S(O)₂Me CH(s-Bu)S(O)₂Et
S(O)₂Me CH(s-Bu)S(O)₂CF₃
S(O)₂Me CH(s-Bu)S(O)₂CH₂CF₃
S(O)₂Me CH(t-Bu)SMe
S(O)₂Me CH(t-Bu)SEt
S(O)₂Me CH(t-Bu)SCF₃
S(O)₂Me CH(t-Bu)SCH₂CF₃
S(O)₂Me CH(t-Bu)S(O)Me
S(O)₂Me CH(t-Bu)S(O)Et
S(O)₂Me CH(t-Bu)S(O)CF₃
S(O)₂Me CH(t-Bu)S(O)CH₂CF₃
S(O)₂Me CH(t-Bu)S(O)₂Me
S(O)₂Me CH(t-Bu)S(O)₂Et
S(O)₂Me CH(t-Bu)S(O)₂CF₃
S(O)₂Me CH(t-Bu)S(O)₂CH₂CF₃
S(O)₂Me CH(CF₃)SMe
S(O)₂Me CH(CF₃)SEt
S(O)₂Me CH(CF₃)SCF₃
S(O)₂Me CH(CF₃)SCH₂CF₃
S(O)₂Me CH(CF₃)S(O)Me
S(O)₂Me CH(CF₃)S(O)Et
S(O)₂Me CH(CF₃)S(O)CF₃
S(O)₂Me CH(CF₃)S(O)CH₂CF₃
S(O)₂Me CH(CF₃)S(O)₂Me
S(O)₂Me CH(CF₃)S(O)₂Et
S(O)₂Me CH(CF₃)S(O)₂CF₃
S(O)₂Me CH(CF₃)S(O)₂CH₂CF₃
S(O)₂Me CH₂CH₂SMe
S(O)₂Me CH₂CH₂SEt
S(O)₂Me CH₂CH₂SCF₃
S(O)₂Me CH₂CH₂SCH₂CF₃
S(O)₂Me CH₂CH₂S(O)Me
S(O)₂Me CH₂CH₂S(O)Et
S(O)₂Me CH₂CH₂S(O)CF₃
S(O)₂Me CH₂CH₂S(O)CH₂CF₃
S(O)₂Me CH₂CH₂S(O)₂Me
S(O)₂Me CH₂CH₂S(O)₂Et
S(O)₂Me CH₂CH₂S(O)₂CF₃
S(O)₂Me CH₂CH₂S(O)₂CH₂CF₃
S(O)₂Me CH(Me)CH₂SMe
S(O)₂Me CH(Me)CH₂SEt
S(O)₂Me CH(Me)CH₂SCF₃
S(O)₂Me CH(Me)CH₂SCH₂CF₃
S(O)₂Me CH(Me)CH₂S(O)Me
S(O)₂Me CH(Me)CH₂S(O)Et
S(O)₂Me CH(Me)CH₂S(O)CF₃
S(O)₂Me CH(Me)CH₂S(O)CH₂CF₃
S(O)₂Me CH(Me)CH₂S(O)₂Me
S(O)₂Me CH(Me)CH₂S(O)₂Et
S(O)₂Me CH(Me)CH₂S(O)₂CF₃
S(O)₂Me CH(Me)CH₂S(O)₂CH₂CF₃
S(O)₂Me CH(Et)CH₂SMe
S(O)₂Me CH(Et)CH₂SEt
S(O)₂Me CH(Et)CH₂SCF₃
S(O)₂Me CH(Et)CH₂SCH₂CF₃
S(O)₂Me CH(Et)CH₂S(O)Me
S(O)₂Me CH(Et)CH₂S(O)Et
S(O)₂Me CH(Et)CH₂S(O)CF₃
S(O)₂Me CH(Et)CH₂S(O)CH₂CF₃
S(O)₂Me CH(Et)CH₂S(O)₂Me
S(O)₂Me CH(Et)CH₂S(O)₂Et
S(O)₂Me CH(Et)CH₂S(O)₂CF₃
S(O)₂Me CH(Et)CH₂S(O)₂CH₂CF₃
S(O)₂Me C(Me)₂CH₂SMe
S(O)₂Me C(Me)₂CH₂SEt
S(O)₂Me C(Me)₂CH₂SCF₃
S(O)₂Me C(Me)₂CH₂SCH₂CF₃
S(O)₂Me C(Me)₂CH₂S(O)Me
S(O)₂Me C(Me)₂CH₂S(O)Et
S(O)₂Me C(Me)₂CH₂S(O)CF₃
S(O)₂Me C(Me)₂CH₂S(O)CH₂CF₃
S(O)₂Me C(Me)₂CH₂S(O)₂Me
S(O)₂Me C(Me)₂CH₂S(O)₂Et
S(O)₂Me C(Me)₂CH₂S(O)₂CF₃
S(O)₂Me C(Me)₂CH₂S(O)₂CH₂CF₃
S(O)₂Me CH₂CH(Me)SMe
S(O)₂Me CH₂CH(Me)SEt
S(O)₂Me CH₂CH(Me)SCF₃
S(O)₂Me CH₂CH(Me)SCH₂CF₃
S(O)₂Me CH₂CH(Me)S(O)Me
S(O)₂Me CH₂CH(Me)S(O)Et
S(O)₂Me CH₂CH(Me)S(O)CF₃
S(O)₂Me CH₂CH(Me)S(O)CH₂CF₃
S(O)₂Me CH₂CH(Me)S(O)₂Me
S(O)₂Me CH₂CH(Me)S(O)₂Et
S(O)₂Me CH₂CH(Me)S(O)₂CF₃
S(O)₂Me CH₂CH(Me)S(O)₂CH₂CF₃
S(O)₂Me CH₂CH(Et)SMe
S(O)₂Me CH₂CH(Et)SEt
S(O)₂Me CH₂CH(Et)SCF₃
S(O)₂Me CH₂CH(Et)SCH₂CF₃
S(O)₂Me CH₂CH(Et)S(O)Me
S(O)₂Me CH₂CH(Et)S(O)Et
S(O)₂Me CH₂CH(Et)S(O)CF₃
S(O)₂Me CH₂CH(Et)S(O)CH₂CF₃
S(O)₂Me CH₂CH(Et)S(O)₂Me
S(O)₂Me CH₂CH(Et)S(O)₂Et
S(O)₂Me CH₂CH(Et)S(O)₂CF₃
S(O)₂Me CH₂CH(Et)S(O)₂CH₂CF₃
S(O)₂Me CH(Me)CH(Me)SMe
S(O)₂Me CH(Me)CH(Me)SEt
S(O)₂Me CH(Me)CH(Me)SCF₃
S(O)₂Me CH(Me)CH(Me)SCH₂CF₃
S(O)₂Me CH(Me)CH(Me)S(O)Me
S(O)₂Me CH(Me)CH(Me)S(O)Et
S(O)₂Me CH(Me)CH(Me)S(O)CF₃
S(O)₂Me CH(Me)CH(Me)S(O)CH₂CF₃
S(O)₂Me CH(Me)CH(Me)S(O)₂Me
S(O)₂Me CH(Me)CH(Me)S(O)₂Et
S(O)₂Me CH(Me)CH(Me)S(O)₂CF₃
S(O)₂Me CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-32a CH₂SMe
D2-32a CH₂SEt
D2-32a CH₂SCF₃
D2-32a CH₂SCH₂CF₃
D2-32a CH₂S(O)Me
D2-32a CH₂S(O)Et
D2-32a CH₂S(O)CF₃
D2-32a CH₂S(O)CH₂CF₃
D2-32a CH₂S(O)₂Me
D2-32a CH₂S(O)₂Et
D2-32a CH₂S(O)₂CF₃
D2-32a CH₂S(O)₂CH₂CF₃
D2-32a CH(Me)SMe
D2-32a CH(Me)SEt
D2-32a CH(Me)SCF₃
D2-32a CH(Me)SCH₂CF₃
D2-32a CH(Me)S(O)Me
D2-32a CH(Me)S(O)Et
D2-32a CH(Me)S(O)CF₃
D2-32a CH(Me)S(O)CH₂CF₃
D2-32a CH(Me)S(O)₂Me
D2-32a CH(Me)S(O)₂Et
D2-32a CH(Me)S(O)₂CF₃
D2-32a CH(Me)S(O)₂CH₂CF₃
D2-32a CH(Et)SMe
D2-32a CH(Et)SEt
D2-32a CH(Et)SCF₃
D2-32a CH(Et)SCH₂CF₃
D2-32a CH(Et)S(O)Me
D2-32a CH(Et)S(O)Et
D2-32a CH(Et)S(O)CF₃
D2-32a CH(Et)S(O)CH₂CF₃
D2-32a CH(Et)S(O)₂Me
D2-32a CH(Et)S(O)₂Et
D2-32a CH(Et)S(O)₂CF₃
D2-32a CH(Et)S(O)₂CH₂CF₃
D2-32a CH(n-Pr)SMe
D2-32a CH(n-Pr)SEt
D2-32a CH(n-Pr)SCF₃
D2-32a CH(n-Pr)SCH₂CF₃
D2-32a CH(n-Pr)S(O)Me
D2-32a CH(n-Pr)S(O)Et
D2-32a CH(n-Pr)S(O)CF₃
D2-32a CH(n-Pr)S(O)CH₂CF₃
D2-32a CH(n-Pr)S(O)₂Me
D2-32a CH(n-Pr)S(O)₂Et
D2-32a CH(n-Pr)S(O)₂CF₃
D2-32a CH(n-Pr)S(O)₂CH₂CF₃
D2-32a CH(i-Pr)SMe
D2-32a CH(i-Pr)SEt
D2-32a CH(i-Pr)SCF₃
D2-32a CH(i-Pr)SCH₂CF₃
D2-32a CH(i-Pr)S(O)Me
D2-32a CH(i-Pr)S(O)Et
D2-32a CH(i-Pr)S(O)CF₃
D2-32a CH(i-Pr)S(O)CH₂CF₃
D2-32a CH(i-Pr)S(O)₂Me
D2-32a CH(i-Pr)S(O)₂Et
D2-32a CH(i-Pr)S(O)₂CF₃
D2-32a CH(i-Pr)S(O)₂CH₂CF₃
D2-32a CH(n-Bu)SMe
D2-32a CH(n-Bu)SEt
D2-32a CH(n-Bu)SCF₃
D2-32a CH(n-Bu)SCH₂CF₃
D2-32a CH(n-Bu)S(O)Me
D2-32a CH(n-Bu)S(O)Et
D2-32a CH(n-Bu)S(O)CF₃
D2-32a CH(n-Bu)S(O)CH₂CF₃
D2-32a CH(n-Bu)S(O)₂Me
D2-32a CH(n-Bu)S(O)₂Et
D2-32a CH(n-Bu)S(O)₂CF₃
D2-32a CH(n-Bu)S(O)₂CH₂CF₃
D2-32a CH(i-Bu)SMe
D2-32a CH(i-Bu)SEt
D2-32a CH(i-Bu)SCF₃
D2-32a CH(i-Bu)SCH₂CF₃
D2-32a CH(i-Bu)S(O)Me
D2-32a CH(i-Bu)S(O)Et
D2-32a CH(i-Bu)S(O)CF₃
D2-32a CH(i-Bu)S(O)CH₂CF₃
D2-32a CH(i-Bu)S(O)₂Me
D2-32a CH(i-Bu)S(O)₂Et
D2-32a CH(i-Bu)S(O)₂CF₃
D2-32a CH(i-Bu)S(O)₂CH₂CF₃
D2-32a CH(s-Bu)SMe
D2-32a CH(s-Bu)SEt
D2-32a CH(s-Bu)SCF₃
D2-32a CH(s-Bu)SCH₂CF₃
D2-32a CH(s-Bu)S(O)Me
D2-32a CH(s-Bu)S(O)Et
D2-32a CH(s-Bu)S(O)CF₃
D2-32a CH(s-Bu)S(O)CH₂CF₃
D2-32a CH(s-Bu)S(O)₂Me
D2-32a CH(s-Bu)S(O)₂Et
D2-32a CH(s-Bu)S(O)₂CF₃
D2-32a CH(s-Bu)S(O)₂CH₂CF₃
D2-32a CH(t-Bu)SMe
D2-32a CH(t-Bu)SEt
D2-32a CH(t-Bu)SCF₃
D2-32a CH(t-Bu)SCH₂CF₃
D2-32a CH(t-Bu)S(O)Me
D2-32a CH(t-Bu)S(O)Et
D2-32a CH(t-Bu)S(O)CF₃
D2-32a CH(t-Bu)S(O)CH₂CF₃
D2-32a CH(t-Bu)S(O)₂Me
D2-32a CH(t-Bu)S(O)₂Et
D2-32a CH(t-Bu)S(O)₂CF₃
D2-32a CH(t-Bu)S(O)₂CH₂CF₃
D2-32a CH(CF₃)SMe
D2-32a CH(CF₃)SEt
D2-32a CH(CF₃)SCF₃
D2-32a CH(CF₃)SCH₂CF₃
D2-32a CH(CF₃)S(O)Me
D2-32a CH(CF₃)S(O)Et
D2-32a CH(CF₃)S(O)CF₃
D2-32a CH(CF₃)S(O)CH₂CF₃
D2-32a CH(CF₃)S(O)₂Me
D2-32a CH(CF₃)S(O)₂Et
D2-32a CH(CF₃)S(O)₂CF₃
D2-32a CH(CF₃)S(O)₂CH₂CF₃
D2-32a CH₂CH₂SMe
D2-32a CH₂CH₂SEt
D2-32a CH₂CH₂SCF₃
D2-32a CH₂CH₂SCH₂CF₃
D2-32a CH₂CH₂S(O)Me
D2-32a CH₂CH₂S(O)Et
D2-32a CH₂CH₂S(O)CF₃
D2-32a CH₂CH₂S(O)CH₂CF₃
D2-32a CH₂CH₂S(O)₂Me
D2-32a CH₂CH₂S(O)₂Et
D2-32a CH₂CH₂S(O)₂CF₃
D2-32a CH₂CH₂S(O)₂CH₂CF₃
D2-32a CH(Me)CH₂SMe
D2-32a CH(Me)CH₂SEt
D2-32a CH(Me)CH₂SCF₃
D2-32a CH(Me)CH₂SCH₂CF₃
D2-32a CH(Me)CH₂S(O)Me
D2-32a CH(Me)CH₂S(O)Et
D2-32a CH(Me)CH₂S(O)CF₃
D2-32a CH(Me)CH₂S(O)CH₂CF₃
D2-32a CH(Me)CH₂S(O)₂Me
D2-32a CH(Me)CH₂S(O)₂Et
D2-32a CH(Me)CH₂S(O)₂CF₃
D2-32a CH(Me)CH₂S(O)₂CH₂CF₃
D2-32a CH(Et)CH₂SMe
D2-32a CH(Et)CH₂SEt
D2-32a CH(Et)CH₂SCF₃
D2-32a CH(Et)CH₂SCH₂CF₃
D2-32a CH(Et)CH₂S(O)Me
D2-32a CH(Et)CH₂S(O)Et
D2-32a CH(Et)CH₂S(O)CF₃
D2-32a CH(Et)CH₂S(O)CH₂CF₃
D2-32a CH(Et)CH₂S(O)₂Me
D2-32a CH(Et)CH₂S(O)₂Et
D2-32a CH(Et)CH₂S(O)₂CF₃
D2-32a CH(Et)CH₂S(O)₂CH₂CF₃
D2-32a C(Me)₂CH₂SMe
D2-32a C(Me)₂CH₂SEt
D2-32a C(Me)₂CH₂SCF₃
D2-32a C(Me)₂CH₂SCH₂CF₃
D2-32a C(Me)₂CH₂S(O)Me
D2-32a C(Me)₂CH₂S(O)Et
D2-32a C(Me)₂CH₂S(O)CF₃
D2-32a C(Me)₂CH₂S(O)CH₂CF₃
D2-32a C(Me)₂CH₂S(O)₂Me
D2-32a C(Me)₂CH₂S(O)₂Et
D2-32a C(Me)₂CH₂S(O)₂CF₃
D2-32a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-32a CH₂CH(Me)SMe
D2-32a CH₂CH(Me)SEt
D2-32a CH₂CH(Me)SCF₃
D2-32a CH₂CH(Me)SCH₂CF₃
D2-32a CH₂CH(Me)S(O)Me
D2-32a CH₂CH(Me)S(O)Et
D2-32a CH₂CH(Me)S(O)CF₃
D2-32a CH₂CH(Me)S(O)CH₂CF₃
D2-32a CH₂CH(Me)S(O)₂Me
D2-32a CH₂CH(Me)S(O)₂Et
D2-32a CH₂CH(Me)S(O)₂CF₃
D2-32a CH₂CH(Me)S(O)₂CH₂CF₃
D2-32a CH₂CH(Et)SMe
D2-32a CH₂CH(Et)SEt
D2-32a CH₂CH(Et)SCF₃
D2-32a CH₂CH(Et)SCH₂CF₃
D2-32a CH₂CH(Et)S(O)Me
D2-32a CH₂CH(Et)S(O)Et
D2-32a CH₂CH(Et)S(O)CF₃
D2-32a CH₂CH(Et)S(O)CH₂CF₃
D2-32a CH₂CH(Et)S(O)₂Me
D2-32a CH₂CH(Et)S(O)₂Et
D2-32a CH₂CH(Et)S(O)₂CF₃
D2-32a CH₂CH(Et)S(O)₂CH₂CF₃
D2-32a CH(Me)CH(Me)SMe
D2-32a CH(Me)CH(Me)SEt
D2-32a CH(Me)CH(Me)SCF₃
D2-32a CH(Me)CH(Me)SCH₂CF₃
D2-32a CH(Me)CH(Me)S(O)Me
D2-32a CH(Me)CH(Me)S(O)Et
D2-32a CH(Me)CH(Me)S(O)CF₃
D2-32a CH(Me)CH(Me)S(O)CH₂CF₃
D2-32a CH(Me)CH(Me)S(O)₂Me
D2-32a CH(Me)CH(Me)S(O)₂Et
D2-32a CH(Me)CH(Me)S(O)₂CF₃
D2-32a CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-33a CH₂SMe
D2-33a CH₂SEt
D2-33a CH₂SCF₃
D2-33a CH₂SCH₂CF₃
D2-33a CH₂S(O)Me
D2-33a CH₂S(O)Et
D2-33a CH₂S(O)CF₃
D2-33a CH₂S(O)CH₂CF₃
D2-33a CH₂S(O)₂Me
D2-33a CH₂S(O)₂Et
D2-33a CH₂S(O)₂CF₃
D2-33a CH₂S(O)₂CH₂CF₃
D2-33a CH(Me)SMe
D2-33a CH(Me)SEt
D2-33a CH(Me)SCF₃
D2-33a CH(Me)SCH₂CF₃
D2-33a CH(Me)S(O)Me
D2-33a CH(Me)S(O)Et
D2-33a CH(Me)S(O)CF₃
D2-33a CH(Me)S(O)CH₂CF₃
D2-33a CH(Me)S(O)₂Me
D2-33a CH(Me)S(O)₂Et
D2-33a CH(Me)S(O)₂CF₃
D2-33a CH(Me)S(O)₂CH₂CF₃
D2-33a CH(Et)SMe
D2-33a CH(Et)SEt
D2-33a CH(Et)SCF₃
D2-33a CH(Et)SCH₂CF₃
D2-33a CH(Et)S(O)Me
D2-33a CH(Et)S(O)Et
D2-33a CH(Et)S(O)CF₃
D2-33a CH(Et)S(O)CH₂CF₃
D2-33a CH(Et)S(O)₂Me
D2-33a CH(Et)S(O)₂Et
D2-33a CH(Et)S(O)₂CF₃
D2-33a CH(Et)S(O)₂CH₂CF₃
D2-33a CH(n-Pr)SMe
D2-33a CH(n-Pr)SEt
D2-33a CH(n-Pr)SCF₃
D2-33a CH(n-Pr)SCH₂CF₃
D2-33a CH(n-Pr)S(O)Me
D2-33a CH(n-Pr)S(O)Et
D2-33a CH(n-Pr)S(O)CF₃
D2-33a CH(n-Pr)S(O)CH₂CF₃
D2-33a CH(n-Pr)S(O)₂Me
D2-33a CH(n-Pr)S(O)₂Et
D2-33a CH(n-Pr)S(O)₂CF₃
D2-33a CH(n-Pr)S(O)₂CH₂CF₃
D2-33a CH(i-Pr)SMe
D2-33a CH(i-Pr)SEt
D2-33a CH(i-Pr)SCF₃
D2-33a CH(i-Pr)SCH₂CF₃
D2-33a CH(i-Pr)S(O)Me
D2-33a CH(i-Pr)S(O)Et
D2-33a CH(i-Pr)S(O)CF₃
D2-33a CH(i-Pr)S(O)CH₂CF₃
D2-33a CH(i-Pr)S(O)₂Me
D2-33a CH(i-Pr)S(O)₂Et
D2-33a CH(i-Pr)S(O)₂CF₃
D2-33a CH(i-Pr)S(O)₂CH₂CF₃
D2-33a CH(n-Bu)SMe
D2-33a CH(n-Bu)SEt
D2-33a CH(n-Bu)SCF₃
D2-33a CH(n-Bu)SCH₂CF₃
D2-33a CH(n-Bu)S(O)Me
D2-33a CH(n-Bu)S(O)Et
D2-33a CH(n-Bu)S(O)CF₃
D2-33a CH(n-Bu)S(O)CH₂CF₃
D2-33a CH(n-Bu)S(O)₂Me
D2-33a CH(n-Bu)S(O)₂Et
D2-33a CH(n-Bu)S(O)₂CF₃
D2-33a CH(n-Bu)S(O)₂CH₂CF₃
D2-33a CH(i-Bu)SMe
D2-33a CH(i-Bu)SEt
D2-33a CH(i-Bu)SCF₃
D2-33a CH(i-Bu)SCH₂CF₃
D2-33a CH(i-Bu)S(O)Me
D2-33a CH(i-Bu)S(O)Et
D2-33a CH(i-Bu)S(O)CF₃
D2-33a CH(i-Bu)S(O)CH₂CF₃
D2-33a CH(i-Bu)S(O)₂Me
D2-33a CH(i-Bu)S(O)₂Et
D2-33a CH(i-Bu)S(O)₂CF₃
D2-33a CH(i-Bu)S(O)₂CH₂CF₃
D2-33a CH(s-Bu)SMe
D2-33a CH(s-Bu)SEt
D2-33a CH(s-Bu)SCF₃
D2-33a CH(s-Bu)SCH₂CF₃
D2-33a CH(s-Bu)S(O)Me
D2-33a CH(s-Bu)S(O)Et
D2-33a CH(s-Bu)S(O)CF₃
D2-33a CH(s-Bu)S(O)CH₂CF₃
D2-33a CH(s-Bu)S(O)₂Me
D2-33a CH(s-Bu)S(O)₂Et
D2-33a CH(s-Bu)S(O)₂CF₃
D2-33a CH(s-Bu)S(O)₂CH₂CF₃
D2-33a CH(t-Bu)SMe
D2-33a CH(t-Bu)SEt
D2-33a CH(t-Bu)SCF₃
D2-33a CH(t-Bu)SCH₂CF₃
D2-33a CH(t-Bu)S(O)Me
D2-33a CH(t-Bu)S(O)Et
D2-33a CH(t-Bu)S(O)CF₃
D2-33a CH(t-Bu)S(O)CH₂CF₃
D2-33a CH(t-Bu)S(O)₂Me
D2-33a CH(t-Bu)S(O)₂Et
D2-33a CH(t-Bu)S(O)₂CF₃
D2-33a CH(t-Bu)S(O)₂CH₂CF₃
D2-33a CH(CF₃)SMe
D2-33a CH(CF₃)SEt
D2-33a CH(CF₃)SCF₃
D2-33a CH(CF₃)SCH₂CF₃
D2-33a CH(CF₃)S(O)Me
D2-33a CH(CF₃)S(O)Et
D2-33a CH(CF₃)S(O)CF₃
D2-33a CH(CF₃)S(O)CH₂CF₃
D2-33a CH(CF₃)S(O)₂Me
D2-33a CH(CF₃)S(O)₂Et
D2-33a CH(CF₃)S(O)₂CF₃
D2-33a CH(CF₃)S(O)₂CH₂CF₃
D2-33a CH₂CH₂SMe
D2-33a CH₂CH₂SEt
D2-33a CH₂CH₂SCF₃
D2-33a CH₂CH₂SCH₂CF₃
D2-33a CH₂CH₂S(O)Me
D2-33a CH₂CH₂S(O)Et
D2-33a CH₂CH₂S(O)CF₃
D2-33a CH₂CH₂S(O)CH₂CF₃
D2-33a CH₂CH₂S(O)₂Me
D2-33a CH₂CH₂S(O)₂Et
D2-33a CH₂CH₂S(O)₂CF₃
D2-33a CH₂CH₂S(O)₂CH₂CF₃
D2-33a CH(Me)CH₂SMe
D2-33a CH(Me)CH₂SEt
D2-33a CH(Me)CH₂SCF₃
D2-33a CH(Me)CH₂SCH₂CF₃
D2-33a CH(Me)CH₂S(O)Me
D2-33a CH(Me)CH₂S(O)Et
D2-33a CH(Me)CH₂S(O)CF₃
D2-33a CH(Me)CH₂S(O)CH₂CF₃
D2-33a CH(Me)CH₂S(O)₂Me
D2-33a CH(Me)CH₂S(O)₂Et
D2-33a CH(Me)CH₂S(O)₂CF₃
D2-33a CH(Me)CH₂S(O)₂CH₂CF₃
D2-33a CH(Et)CH₂SMe
D2-33a CH(Et)CH₂SEt
D2-33a CH(Et)CH₂SCF₃
D2-33a CH(Et)CH₂SCH₂CF₃
D2-33a CH(Et)CH₂S(O)Me
D2-33a CH(Et)CH₂S(O)Et
D2-33a CH(Et)CH₂S(O)CF₃
D2-33a CH(Et)CH₂S(O)CH₂CF₃
D2-33a CH(Et)CH₂S(O)₂Me
D2-33a CH(Et)CH₂S(O)₂Et
D2-33a CH(Et)CH₂S(O)₂CF₃
D2-33a CH(Et)CH₂S(O)₂CH₂CF₃
D2-33a C(Me)₂CH₂SMe
D2-33a C(Me)₂CH₂SEt
D2-33a C(Me)₂CH₂SCF₃
D2-33a C(Me)₂CH₂SCH₂CF₃
D2-33a C(Me)₂CH₂S(O)Me
D2-33a C(Me)₂CH₂S(O)Et
D2-33a C(Me)₂CH₂S(O)CF₃
D2-33a C(Me)₂CH₂S(O)CH₂CF₃
D2-33a C(Me)₂CH₂S(O)₂Me
D2-33a C(Me)₂CH₂S(O)₂Et
D2-33a C(Me)₂CH₂S(O)₂CF₃
D2-33a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-33a CH₂CH(Me)SMe
D2-33a CH₂CH(Me)SEt
D2-33a CH₂CH(Me)SCF₃
D2-33a CH₂CH(Me)SCH₂CF₃
D2-33a CH₂CH(Me)S(O)Me
D2-33a CH₂CH(Me)S(O)Et
D2-33a CH₂CH(Me)S(O)CF₃
D2-33a CH₂CH(Me)S(O)CH₂CF₃
D2-33a CH₂CH(Me)S(O)₂Me
D2-33a CH₂CH(Me)S(O)₂Et
D2-33a CH₂CH(Me)S(O)₂CF₃
D2-33a CH₂CH(Me)S(O)₂CH₂CF₃
D2-33a CH₂CH(Et)SMe
D2-33a CH₂CH(Et)SEt
D2-33a CH₂CH(Et)SCF₃
D2-33a CH₂CH(Et)SCH₂CF₃
D2-33a CH₂CH(Et)S(O)Me
D2-33a CH₂CH(Et)S(O)Et
D2-33a CH₂CH(Et)S(O)CF₃
D2-33a CH₂CH(Et)S(O)CH₂CF₃
D2-33a CH₂CH(Et)S(O)₂Me
D2-33a CH₂CH(Et)S(O)₂Et
D2-33a CH₂CH(Et)S(O)₂CF₃
D2-33a CH₂CH(Et)S(O)₂CH₂CF₃
D2-33a CH(Me)CH(Me)SMe
D2-33a CH(Me)CH(Me)SEt
D2-33a CH(Me)CH(Me)SCF₃
D2-33a CH(Me)CH(Me)SCH₂CF₃
D2-33a CH(Me)CH(Me)S(O)Me
D2-33a CH(Me)CH(Me)S(O)Et
D2-33a CH(Me)CH(Me)S(O)CF₃
D2-33a CH(Me)CH(Me)S(O)CH₂CF₃
D2-33a CH(Me)CH(Me)S(O)₂Me
D2-33a CH(Me)CH(Me)S(O)₂Et
D2-33a CH(Me)CH(Me)S(O)₂CF₃
D2-33a CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-34a CH₂SMe
D2-34a CH₂SEt
D2-34a CH₂SCF₃
D2-34a CH₂SCH₂CF₃
D2-34a CH₂S(O)Me
D2-34a CH₂S(O)Et
D2-34a CH₂S(O)CF₃
D2-34a CH₂S(O)CH₂CF₃
D2-34a CH₂S(O)₂Me
D2-34a CH₂S(O)₂Et
D2-34a CH₂S(O)₂CF₃
D2-34a CH₂S(O)₂CH₂CF₃
D2-34a CH(Me)SMe
D2-34a CH(Me)SEt
D2-34a CH(Me)SCF₃
D2-34a CH(Me)SCH₂CF₃
D2-34a CH(Me)S(O)Me
D2-34a CH(Me)S(O)Et
D2-34a CH(Me)S(O)CF₃
D2-34a CH(Me)S(O)CH₂CF₃
D2-34a CH(Me)S(O)₂Me
D2-34a CH(Me)S(O)₂Et
D2-34a CH(Me)S(O)₂CF₃
D2-34a CH(Me)S(O)₂CH₂CF₃
D2-34a CH(Et)SMe
D2-34a CH(Et)SEt
D2-34a CH(Et)SCF₃
D2-34a CH(Et)SCH₂CF₃
D2-34a CH(Et)S(O)Me
D2-34a CH(Et)S(O)Et
D2-34a CH(Et)S(O)CF₃
D2-34a CH(Et)S(O)CH₂CF₃
D2-34a CH(Et)S(O)₂Me
D2-34a CH(Et)S(O)₂Et
D2-34a CH(Et)S(O)₂CF₃
D2-34a CH(Et)S(O)₂CH₂CF₃
D2-34a CH(n-Pr)SMe
D2-34a CH(n-Pr)SEt
D2-34a CH(n-Pr)SCF₃
D2-34a CH(n-Pr)SCH₂CF₃
D2-34a CH(n-Pr)S(O)Me
D2-34a CH(n-Pr)S(O)Et
D2-34a CH(n-Pr)S(O)CF₃
D2-34a CH(n-Pr)S(O)CH₂CF₃
D2-34a CH(n-Pr)S(O)₂Me
D2-34a CH(n-Pr)S(O)₂Et
D2-34a CH(n-Pr)S(O)₂CF₃
D2-34a CH(n-Pr)S(O)₂CH₂CF₃
D2-34a CH(i-Pr)SMe
D2-34a CH(i-Pr)SEt
D2-34a CH(i-Pr)SCF₃
D2-34a CH(i-Pr)SCH₂CF₃
D2-34a CH(i-Pr)S(O)Me
D2-34a CH(i-Pr)S(O)Et
D2-34a CH(i-Pr)S(O)CF₃
D2-34a CH(i-Pr)S(O)CH₂CF₃
D2-34a CH(i-Pr)S(O)₂Me
D2-34a CH(i-Pr)S(O)₂Et
D2-34a CH(i-Pr)S(O)₂CF₃
D2-34a CH(i-Pr)S(O)₂CH₂CF₃
D2-34a CH(n-Bu)SMe
D2-34a CH(n-Bu)SEt
D2-34a CH(n-Bu)SCF₃
D2-34a CH(n-Bu)SCH₂CF₃
D2-34a CH(n-Bu)S(O)Me
D2-34a CH(n-Bu)S(O)Et
D2-34a CH(n-Bu)S(O)CF₃
D2-34a CH(n-Bu)S(O)CH₂CF₃
D2-34a CH(n-Bu)S(O)₂Me
D2-34a CH(n-Bu)S(O)₂Et
D2-34a CH(n-Bu)S(O)₂CF₃
D2-34a CH(n-Bu)S(O)₂CH₂CF₃
D2-34a CH(i-Bu)SMe
D2-34a CH(i-Bu)SEt
D2-34a CH(i-Bu)SCF₃
D2-34a CH(i-Bu)SCH₂CF₃
D2-34a CH(i-Bu)S(O)Me
D2-34a CH(i-Bu)S(O)Et
D2-34a CH(i-Bu)S(O)CF₃
D2-34a CH(i-Bu)S(O)CH₂CF₃
D2-34a CH(i-Bu)S(O)₂Me
D2-34a CH(i-Bu)S(O)₂Et
D2-34a CH(i-Bu)S(O)₂CF₃
D2-34a CH(i-Bu)S(O)₂CH₂CF₃
D2-34a CH(s-Bu)SMe
D2-34a CH(s-Bu)SEt
D2-34a CH(s-Bu)SCF₃
D2-34a CH(s-Bu)SCH₂CF₃
D2-34a CH(s-Bu)S(O)Me
D2-34a CH(s-Bu)S(O)Et
D2-34a CH(s-Bu)S(O)CF₃
D2-34a CH(s-Bu)S(O)CH₂CF₃
D2-34a CH(s-Bu)S(O)₂Me
D2-34a CH(s-Bu)S(O)₂Et
D2-34a CH(s-Bu)S(O)₂CF₃
D2-34a CH(s-Bu)S(O)₂CH₂CF₃
D2-34a CH(t-Bu)SMe
D2-34a CH(t-Bu)SEt
D2-34a CH(t-Bu)SCF₃
D2-34a CH(t-Bu)SCH₂CF₃
D2-34a CH(t-Bu)S(O)Me
D2-34a CH(t-Bu)S(O)Et
D2-34a CH(t-Bu)S(O)CF₃
D2-34a CH(t-Bu)S(O)CH₂CF₃
D2-34a CH(t-Bu)S(O)₂Me
D2-34a CH(t-Bu)S(O)₂Et
D2-34a CH(t-Bu)S(O)₂CF₃
D2-34a CH(t-Bu)S(O)₂CH₂CF₃
D2-34a CH(CF₃)SMe
D2-34a CH(CF₃)SEt
D2-34a CH(CF₃)SCF₃
D2-34a CH(CF₃)SCH₂CF₃
D2-34a CH(CF₃)S(O)Me
D2-34a CH(CF₃)S(O)Et
D2-34a CH(CF₃)S(O)CF₃
D2-34a CH(CF₃)S(O)CH₂CF₃
D2-34a CH(CF₃)S(O)₂Me
D2-34a CH(CF₃)S(O)₂Et
D2-34a CH(CF₃)S(O)₂CF₃
D2-34a CH(CF₃)S(O)₂CH₂CF₃
D2-34a CH₂CH₂SMe
D2-34a CH₂CH₂SEt
D2-34a CH₂CH₂SCF₃
D2-34a CH₂CH₂SCH₂CF₃
D2-34a CH₂CH₂S(O)Me
D2-34a CH₂CH₂S(O)Et
D2-34a CH₂CH₂S(O)CF₃
D2-34a CH₂CH₂S(O)CH₂CF₃
D2-34a CH₂CH₂S(O)₂Me
D2-34a CH₂CH₂S(O)₂Et
D2-34a CH₂CH₂S(O)₂CF₃
D2-34a CH₂CH₂S(O)₂CH₂CF₃
D2-34a CH(Me)CH₂SMe
D2-34a CH(Me)CH₂SEt
D2-34a CH(Me)CH₂SCF₃
D2-34a CH(Me)CH₂SCH₂CF₃
D2-34a CH(Me)CH₂S(O)Me
D2-34a CH(Me)CH₂S(O)Et
D2-34a CH(Me)CH₂S(O)CF₃
D2-34a CH(Me)CH₂S(O)CH₂CF₃
D2-34a CH(Me)CH₂S(O)₂Me
D2-34a CH(Me)CH₂S(O)₂Et
D2-34a CH(Me)CH₂S(O)₂CF₃
D2-34a CH(Me)CH₂S(O)₂CH₂CF₃
D2-34a CH(Et)CH₂SMe
D2-34a CH(Et)CH₂SEt
D2-34a CH(Et)CH₂SCF₃
D2-34a CH(Et)CH₂SCH₂CF₃
D2-34a CH(Et)CH₂S(O)Me
D2-34a CH(Et)CH₂S(O)Et
D2-34a CH(Et)CH₂S(O)CF₃
D2-34a CH(Et)CH₂S(O)CH₂CF₃
D2-34a CH(Et)CH₂S(O)₂Me
D2-34a CH(Et)CH₂S(O)₂Et
D2-34a CH(Et)CH₂S(O)₂CF₃
D2-34a CH(Et)CH₂S(O)₂CH₂CF₃
D2-34a C(Me)₂CH₂SMe
D2-34a C(Me)₂CH₂SEt
D2-34a C(Me)₂CH₂SCF₃
D2-34a C(Me)₂CH₂SCH₂CF₃
D2-34a C(Me)₂CH₂S(O)Me
D2-34a C(Me)₂CH₂S(O)Et
D2-34a C(Me)₂CH₂S(O)CF₃
D2-34a C(Me)₂CH₂S(O)CH₂CF₃
D2-34a C(Me)₂CH₂S(O)₂Me
D2-34a C(Me)₂CH₂S(O)₂Et
D2-34a C(Me)₂CH₂S(O)₂CF₃
D2-34a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-34a CH₂CH(Me)SMe
D2-34a CH₂CH(Me)SEt
D2-34a CH₂CH(Me)SCF₃
D2-34a CH₂CH(Me)SCH₂CF₃
D2-34a CH₂CH(Me)S(O)Me
D2-34a CH₂CH(Me)S(O)Et
D2-34a CH₂CH(Me)S(O)CF₃
D2-34a CH₂CH(Me)S(O)CH₂CF₃
D2-34a CH₂CH(Me)S(O)₂Me
D2-34a CH₂CH(Me)S(O)₂Et
D2-34a CH₂CH(Me)S(O)₂CF₃
D2-34a CH₂CH(Me)S(O)₂CH₂CF₃
D2-34a CH₂CH(Et)SMe
D2-34a CH₂CH(Et)SEt
D2-34a CH₂CH(Et)SCF₃
D2-34a CH₂CH(Et)SCH₂CF₃
D2-34a CH₂CH(Et)S(O)Me
D2-34a CH₂CH(Et)S(O)Et
D2-34a CH₂CH(Et)S(O)CF₃
D2-34a CH₂CH(Et)S(O)CH₂CF₃
D2-34a CH₂CH(Et)S(O)₂Me
D2-34a CH₂CH(Et)S(O)₂Et
D2-34a CH₂CH(Et)S(O)₂CF₃
D2-34a CH₂CH(Et)S(O)₂CH₂CF₃
D2-34a CH(Me)CH(Me)SMe
D2-34a CH(Me)CH(Me)SEt
D2-34a CH(Me)CH(Me)SCF₃
D2-34a CH(Me)CH(Me)SCH₂CF₃
D2-34a CH(Me)CH(Me)S(O)Me
D2-34a CH(Me)CH(Me)S(O)Et
D2-34a CH(Me)CH(Me)S(O)CF₃
D2-34a CH(Me)CH(Me)S(O)CH₂CF₃
D2-34a CH(Me)CH(Me)S(O)₂Me
D2-34a CH(Me)CH(Me)S(O)₂Et
D2-34a CH(Me)CH(Me)S(O)₂CF₃
D2-34a CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-36a CH₂SMe
D2-36a CH₂SEt
D2-36a CH₂SCF₃
D2-36a CH₂SCH₂CF₃
D2-36a CH₂S(O)Me
D2-36a CH₂S(O)Et
D2-36a CH₂S(O)CF₃
D2-36a CH₂S(O)CH₂CF₃
D2-36a CH₂S(O)₂Me
D2-36a CH₂S(O)₂Et
D2-36a CH₂S(O)₂CF₃
D2-36a CH₂S(O)₂CH₂CF₃
D2-36a CH(Me)SMe
D2-36a CH(Me)SEt
D2-36a CH(Me)SCF₃
D2-36a CH(Me)SCH₂CF₃
D2-36a CH(Me)S(O)Me
D2-36a CH(Me)S(O)Et
D2-36a CH(Me)S(O)CF₃
D2-36a CH(Me)S(O)CH₂CF₃
D2-36a CH(Me)S(O)₂Me
D2-36a CH(Me)S(O)₂Et
D2-36a CH(Me)S(O)₂CF₃
D2-36a CH(Me)S(O)₂CH₂CF₃
D2-36a CH(Et)SMe
D2-36a CH(Et)SEt
D2-36a CH(Et)SCF₃
D2-36a CH(Et)SCH₂CF₃
D2-36a CH(Et)S(O)Me
D2-36a CH(Et)S(O)Et
D2-36a CH(Et)S(O)CF₃
D2-36a CH(Et)S(O)CH₂CF₃
D2-36a CH(Et)S(O)₂Me
D2-36a CH(Et)S(O)₂Et
D2-36a CH(Et)S(O)₂CF₃
D2-36a CH(Et)S(O)₂CH₂CF₃
D2-36a CH(n-Pr)SMe
D2-36a CH(n-Pr)SEt
D2-36a CH(n-Pr)SCF₃
D2-36a CH(n-Pr)SCH₂CF₃
D2-36a CH(n-Pr)S(O)Me
D2-36a CH(n-Pr)S(O)Et
D2-36a CH(n-Pr)S(O)CF₃
D2-36a CH(n-Pr)S(O)CH₂CF₃
D2-36a CH(n-Pr)S(O)₂Me
D2-36a CH(n-Pr)S(O)₂Et
D2-36a CH(n-Pr)S(O)₂CF₃
D2-36a CH(n-Pr)S(O)₂CH₂CF₃
D2-36a CH(i-Pr)SMe
D2-36a CH(i-Pr)SEt
D2-36a CH(i-Pr)SCF₃
D2-36a CH(i-Pr)SCH₂CF₃
D2-36a CH(i-Pr)S(O)Me
D2-36a CH(i-Pr)S(O)Et
D2-36a CH(i-Pr)S(O)CF₃
D2-36a CH(i-Pr)S(O)CH₂CF₃
D2-36a CH(i-Pr)S(O)₂Me
D2-36a CH(i-Pr)S(O)₂Et
D2-36a CH(i-Pr)S(O)₂CF₃
D2-36a CH(i-Pr)S(O)₂CH₂CF₃
D2-36a CH(n-Bu)SMe
D2-36a CH(n-Bu)SEt
D2-36a CH(n-Bu)SCF₃
D2-36a CH(n-Bu)SCH₂CF₃
D2-36a CH(n-Bu)S(O)Me
D2-36a CH(n-Bu)S(O)Et
D2-36a CH(n-Bu)S(O)CF₃
D2-36a CH(n-Bu)S(O)CH₂CF₃
D2-36a CH(n-Bu)S(O)₂Me
D2-36a CH(n-Bu)S(O)₂Et
D2-36a CH(n-Bu)S(O)₂CF₃
D2-36a CH(n-Bu)S(O)₂CH₂CF₃
D2-36a CH(i-Bu)SMe
D2-36a CH(i-Bu)SEt
D2-36a CH(i-Bu)SCF₃
D2-36a CH(i-Bu)SCH₂CF₃
D2-36a CH(i-Bu)S(O)Me
D2-36a CH(i-Bu)S(O)Et
D2-36a CH(i-Bu)S(O)CF₃
D2-36a CH(i-Bu)S(O)CH₂CF₃
D2-36a CH(i-Bu)S(O)₂Me
D2-36a CH(i-Bu)S(O)₂Et
D2-36a CH(i-Bu)S(O)₂CF₃
D2-36a CH(i-Bu)S(O)₂CH₂CF₃
D2-36a CH(s-Bu)SMe
D2-36a CH(s-Bu)SEt
D2-36a CH(s-Bu)SCF₃
D2-36a CH(s-Bu)SCH₂CF₃
D2-36a CH(s-Bu)S(O)Me
D2-36a CH(s-Bu)S(O)Et
D2-36a CH(s-Bu)S(O)CF₃
D2-36a CH(s-Bu)S(O)CH₂CF₃
D2-36a CH(s-Bu)S(O)₂Me
D2-36a CH(s-Bu)S(O)₂Et
D2-36a CH(s-Bu)S(O)₂CF₃
D2-36a CH(s-Bu)S(O)₂CH₂CF₃
D2-36a CH(t-Bu)SMe
D2-36a CH(t-Bu)SEt
D2-36a CH(t-Bu)SCF₃
D2-36a CH(t-Bu)SCH₂CF₃
D2-36a CH(t-Bu)S(O)Me
D2-36a CH(t-Bu)S(O)Et
D2-36a CH(t-Bu)S(O)CF₃
D2-36a CH(t-Bu)S(O)CH₂CF₃
D2-36a CH(t-Bu)S(O)₂Me
D2-36a CH(t-Bu)S(O)₂Et
D2-36a CH(t-Bu)S(O)₂CF₃
D2-36a CH(t-Bu)S(O)₂CH₂CF₃
D2-36a CH(CF₃)SMe
D2-36a CH(CF₃)SEt
D2-36a CH(CF₃)SCF₃
D2-36a CH(CF₃)SCH₂CF₃
D2-36a CH(CF₃)S(O)Me
D2-36a CH(CF₃)S(O)Et
D2-36a CH(CF₃)S(O)CF₃
D2-36a CH(CF₃)S(O)CH₂CF₃
D2-36a CH(CF₃)S(O)₂Me
D2-36a CH(CF₃)S(O)₂Et
D2-36a CH(CF₃)S(O)₂CF₃
D2-36a CH(CF₃)S(O)₂CH₂CF₃
D2-36a CH₂CH₂SMe
D2-36a CH₂CH₂SEt
D2-36a CH₂CH₂SCF₃
D2-36a CH₂CH₂SCH₂CF₃
D2-36a CH₂CH₂S(O)Me
D2-36a CH₂CH₂S(O)Et
D2-36a CH₂CH₂S(O)CF₃
D2-36a CH₂CH₂S(O)CH₂CF₃
D2-36a CH₂CH₂S(O)₂Me
D2-36a CH₂CH₂S(O)₂Et
D2-36a CH₂CH₂S(O)₂CF₃
D2-36a CH₂CH₂S(O)₂CH₂CF₃
D2-36a CH(Me)CH₂SMe
D2-36a CH(Me)CH₂SEt
D2-36a CH(Me)CH₂SCF₃
D2-36a CH(Me)CH₂SCH₂CF₃
D2-36a CH(Me)CH₂S(O)Me
D2-36a CH(Me)CH₂S(O)Et
D2-36a CH(Me)CH₂S(O)CF₃
D2-36a CH(Me)CH₂S(O)CH₂CF₃
D2-36a CH(Me)CH₂S(O)₂Me
D2-36a CH(Me)CH₂S(O)₂Et
D2-36a CH(Me)CH₂S(O)₂CF₃
D2-36a CH(Me)CH₂S(O)₂CH₂CF₃
D2-36a CH(Et)CH₂SMe
D2-36a CH(Et)CH₂SEt
D2-36a CH(Et)CH₂SCF₃
D2-36a CH(Et)CH₂SCH₂CF₃
D2-36a CH(Et)CH₂S(O)Me
D2-36a CH(Et)CH₂S(O)Et
D2-36a CH(Et)CH₂S(O)CF₃
D2-36a CH(Et)CH₂S(O)CH₂CF₃
D2-36a CH(Et)CH₂S(O)₂Me
D2-36a CH(Et)CH₂S(O)₂Et
D2-36a CH(Et)CH₂S(O)₂CF₃
D2-36a CH(Et)CH₂S(O)₂CH₂CF₃
D2-36a C(Me)₂CH₂SMe
D2-36a C(Me)₂CH₂SEt
D2-36a C(Me)₂CH₂SCF₃
D2-36a C(Me)₂CH₂SCH₂CF₃
D2-36a C(Me)₂CH₂S(O)Me
D2-36a C(Me)₂CH₂S(O)Et
D2-36a C(Me)₂CH₂S(O)CF₃
D2-36a C(Me)₂CH₂S(O)CH₂CF₃
D2-36a C(Me)₂CH₂S(O)₂Me
D2-36a C(Me)₂CH₂S(O)₂Et
D2-36a C(Me)₂CH₂S(O)₂CF₃
D2-36a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-36a CH₂CH(Me)SMe
D2-36a CH₂CH(Me)SEt
D2-36a CH₂CH(Me)SCF₃
D2-36a CH₂CH(Me)SCH₂CF₃
D2-36a CH₂CH(Me)S(O)Me
D2-36a CH₂CH(Me)S(O)Et
D2-36a CH₂CH(Me)S(O)CF₃
D2-36a CH₂CH(Me)S(O)CH₂CF₃
D2-36a CH₂CH(Me)S(O)₂Me
D2-36a CH₂CH(Me)S(O)₂Et
D2-36a CH₂CH(Me)S(O)₂CF₃
D2-36a CH₂CH(Me)S(O)₂CH₂CF₃
D2-36a CH₂CH(Et)SMe
D2-36a CH₂CH(Et)SEt
D2-36a CH₂CH(Et)SCF₃
D2-36a CH₂CH(Et)SCH₂CF₃
D2-36a CH₂CH(Et)S(O)Me
D2-36a CH₂CH(Et)S(O)Et
D2-36a CH₂CH(Et)S(O)CF₃
D2-36a CH₂CH(Et)S(O)CH₂CF₃
D2-36a CH₂CH(Et)S(O)₂Me
D2-36a CH₂CH(Et)S(O)₂Et
D2-36a CH₂CH(Et)S(O)₂CF₃
D2-36a CH₂CH(Et)S(O)₂CH₂CF₃
D2-36a CH(Me)CH(Me)SMe
D2-36a CH(Me)CH(Me)SEt
D2-36a CH(Me)CH(Me)SCF₃
D2-36a CH(Me)CH(Me)SCH₂CF₃
D2-36a CH(Me)CH(Me)S(O)Me
D2-36a CH(Me)CH(Me)S(O)Et
D2-36a CH(Me)CH(Me)S(O)CF₃
D2-36a CH(Me)CH(Me)S(O)CH₂CF₃
D2-36a CH(Me)CH(Me)S(O)₂Me
D2-36a CH(Me)CH(Me)S(O)₂Et
D2-36a CH(Me)CH(Me)S(O)₂CF₃
D2-36a CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-37a CH₂SMe
D2-37a CH₂SEt
D2-37a CH₂SCF₃
D2-37a CH₂SCH₂CF₃
D2-37a CH₂S(O)Me
D2-37a CH₂S(O)Et
D2-37a CH₂S(O)CF₃
D2-37a CH₂S(O)CH₂CF₃
D2-37a CH₂S(O)₂Me
D2-37a CH₂S(O)₂Et
D2-37a CH₂S(O)₂CF₃
D2-37a CH₂S(O)₂CH₂CF₃
D2-37a CH(Me)SMe
D2-37a CH(Me)SEt
D2-37a CH(Me)SCF₃
D2-37a CH(Me)SCH₂CF₃
D2-37a CH(Me)S(O)Me
D2-37a CH(Me)S(O)Et
D2-37a CH(Me)S(O)CF₃
D2-37a CH(Me)S(O)CH₂CF₃
D2-37a CH(Me)S(O)₂Me
D2-37a CH(Me)S(O)₂Et
D2-37a CH(Me)S(O)₂CF₃
D2-37a CH(Me)S(O)₂CH₂CF₃
D2-37a CH(Et)SMe
D2-37a CH(Et)SEt
D2-37a CH(Et)SCF₃
D2-37a CH(Et)SCH₂CF₃
D2-37a CH(Et)S(O)Me
D2-37a CH(Et)S(O)Et
D2-37a CH(Et)S(O)CF₃
D2-37a CH(Et)S(O)CH₂CF₃
D2-37a CH(Et)S(O)₂Me
D2-37a CH(Et)S(O)₂Et
D2-37a CH(Et)S(O)₂CF₃
D2-37a CH(Et)S(O)₂CH₂CF₃
D2-37a CH(n-Pr)SMe
D2-37a CH(n-Pr)SEt
D2-37a CH(n-Pr)SCF₃
D2-37a CH(n-Pr)SCH₂CF₃
D2-37a CH(n-Pr)S(O)Me
D2-37a CH(n-Pr)S(O)Et
D2-37a CH(n-Pr)S(O)CF₃
D2-37a CH(n-Pr)S(O)CH₂CF₃
D2-37a CH(n-Pr)S(O)₂Me
D2-37a CH(n-Pr)S(O)₂Et
D2-37a CH(n-Pr)S(O)₂CF₃
D2-37a CH(n-Pr)S(O)₂CH₂CF₃
D2-37a CH(i-Pr)SMe
D2-37a CH(i-Pr)SEt
D2-37a CH(i-Pr)SCF₃
D2-37a CH(i-Pr)SCH₂CF₃
D2-37a CH(i-Pr)S(O)Me
D2-37a CH(i-Pr)S(O)Et
D2-37a CH(i-Pr)S(O)CF₃
D2-37a CH(i-Pr)S(O)CH₂CF₃
D2-37a CH(i-Pr)S(O)₂Me
D2-37a CH(i-Pr)S(O)₂Et
D2-37a CH(i-Pr)S(O)₂CF₃
D2-37a CH(i-Pr)S(O)₂CH₂CF₃
D2-37a CH(n-Bu)SMe
D2-37a CH(n-Bu)SEt
D2-37a CH(n-Bu)SCF₃
D2-37a CH(n-Bu)SCH₂CF₃
D2-37a CH(n-Bu)S(O)Me
D2-37a CH(n-Bu)S(O)Et
D2-37a CH(n-Bu)S(O)CF₃
D2-37a CH(n-Bu)S(O)CH₂CF₃
D2-37a CH(n-Bu)S(O)₂Me
D2-37a CH(n-Bu)S(O)₂Et
D2-37a CH(n-Bu)S(O)₂CF₃
D2-37a CH(n-Bu)S(O)₂CH₂CF₃
D2-37a CH(i-Bu)SMe
D2-37a CH(i-Bu)SEt
D2-37a CH(i-Bu)SCF₃
D2-37a CH(i-Bu)SCH₂CF₃
D2-37a CH(i-Bu)S(O)Me
D2-37a CH(i-Bu)S(O)Et
D2-37a CH(i-Bu)S(O)CF₃
D2-37a CH(i-Bu)S(O)CH₂CF₃
D2-37a CH(i-Bu)S(O)₂Me
D2-37a CH(i-Bu)S(O)₂Et
D2-37a CH(i-Bu)S(O)₂CF₃
D2-37a CH(i-Bu)S(O)₂CH₂CF₃
D2-37a CH(s-Bu)SMe
D2-37a CH(s-Bu)SEt
D2-37a CH(s-Bu)SCF₃
D2-37a CH(s-Bu)SCH₂CF₃
D2-37a CH(s-Bu)S(O)Me
D2-37a CH(s-Bu)S(O)Et
D2-37a CH(s-Bu)S(O)CF₃
D2-37a CH(s-Bu)S(O)CH₂CF₃
D2-37a CH(s-Bu)S(O)₂Me
D2-37a CH(s-Bu)S(O)₂Et
D2-37a CH(s-Bu)S(O)₂CF₃
D2-37a CH(s-Bu)S(O)₂CH₂CF₃
D2-37a CH(t-Bu)SMe
D2-37a CH(t-Bu)SEt
D2-37a CH(t-Bu)SCF₃
D2-37a CH(t-Bu)SCH₂CF₃
D2-37a CH(t-Bu)S(O)Me
D2-37a CH(t-Bu)S(O)Et
D2-37a CH(t-Bu)S(O)CF₃
D2-37a CH(t-Bu)S(O)CH₂CF₃
D2-37a CH(t-Bu)S(O)₂Me
D2-37a CH(t-Bu)S(O)₂Et
D2-37a CH(t-Bu)S(O)₂CF₃
D2-37a CH(t-Bu)S(O)₂CH₂CF₃
D2-37a CH(CF₃)SMe
D2-37a CH(CF₃)SEt
D2-37a CH(CF₃)SCF₃
D2-37a CH(CF₃)SCH₂CF₃
D2-37a CH(CF₃)S(O)Me
D2-37a CH(CF₃)S(O)Et
D2-37a CH(CF₃)S(O)CF₃
D2-37a CH(CF₃)S(O)CH₂CF₃
D2-37a CH(CF₃)S(O)₂Me
D2-37a CH(CF₃)S(O)₂Et
D2-37a CH(CF₃)S(O)₂CF₃
D2-37a CH(CF₃)S(O)₂CH₂CF₃
D2-37a CH₂CH₂SMe
D2-37a CH₂CH₂SEt
D2-37a CH₂CH₂SCF₃
D2-37a CH₂CH₂SCH₂CF₃
D2-37a CH₂CH₂S(O)Me
D2-37a CH₂CH₂S(O)Et
D2-37a CH₂CH₂S(O)CF₃
D2-37a CH₂CH₂S(O)CH₂CF₃
D2-37a CH₂CH₂S(O)₂Me
D2-37a CH₂CH₂S(O)₂Et
D2-37a CH₂CH₂S(O)₂CF₃
D2-37a CH₂CH₂S(O)₂CH₂CF₃
D2-37a CH(Me)CH₂SMe
D2-37a CH(Me)CH₂SEt
D2-37a CH(Me)CH₂SCF₃
D2-37a CH(Me)CH₂SCH₂CF₃
D2-37a CH(Me)CH₂S(O)Me
D2-37a CH(Me)CH₂S(O)Et
D2-37a CH(Me)CH₂S(O)CF₃
D2-37a CH(Me)CH₂S(O)CH₂CF₃
D2-37a CH(Me)CH₂S(O)₂Me
D2-37a CH(Me)CH₂S(O)₂Et
D2-37a CH(Me)CH₂S(O)₂CF₃
D2-37a CH(Me)CH₂S(O)₂CH₂CF₃
D2-37a CH(Et)CH₂SMe
D2-37a CH(Et)CH₂SEt
D2-37a CH(Et)CH₂SCF₃
D2-37a CH(Et)CH₂SCH₂CF₃
D2-37a CH(Et)CH₂S(O)Me
D2-37a CH(Et)CH₂S(O)Et
D2-37a CH(Et)CH₂S(O)CF₃
D2-37a CH(Et)CH₂S(O)CH₂CF₃
D2-37a CH(Et)CH₂S(O)₂Me
D2-37a CH(Et)CH₂S(O)₂Et
D2-37a CH(Et)CH₂S(O)₂CF₃
D2-37a CH(Et)CH₂S(O)₂CH₂CF₃
D2-37a C(Me)₂CH₂SMe
D2-37a C(Me)₂CH₂SEt
D2-37a C(Me)₂CH₂SCF₃
D2-37a C(Me)₂CH₂SCH₂CF₃
D2-37a C(Me)₂CH₂S(O)Me
D2-37a C(Me)₂CH₂S(O)Et
D2-37a C(Me)₂CH₂S(O)CF₃
D2-37a C(Me)₂CH₂S(O)CH₂CF₃
D2-37a C(Me)₂CH₂S(O)₂Me
D2-37a C(Me)₂CH₂S(O)₂Et
D2-37a C(Me)₂CH₂S(O)₂CF₃
D2-37a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-37a CH₂CH(Me)SMe
D2-37a CH₂CH(Me)SEt
D2-37a CH₂CH(Me)SCF₃
D2-37a CH₂CH(Me)SCH₂CF₃
D2-37a CH₂CH(Me)S(O)Me
D2-37a CH₂CH(Me)S(O)Et
D2-37a CH₂CH(Me)S(O)CF₃
D2-37a CH₂CH(Me)S(O)CH₂CF₃
D2-37a CH₂CH(Me)S(O)₂Me
D2-37a CH₂CH(Me)S(O)₂Et
D2-37a CH₂CH(Me)S(O)₂CF₃
D2-37a CH₂CH(Me)S(O)₂CH₂CF₃
D2-37a CH₂CH(Et)SMe
D2-37a CH₂CH(Et)SEt
D2-37a CH₂CH(Et)SCF₃
D2-37a CH₂CH(Et)SCH₂CF₃
D2-37a CH₂CH(Et)S(O)Me
D2-37a CH₂CH(Et)S(O)Et
D2-37a CH₂CH(Et)S(O)CF₃
D2-37a CH₂CH(Et)S(O)CH₂CF₃
D2-37a CH₂CH(Et)S(O)₂Me
D2-37a CH₂CH(Et)S(O)₂Et
D2-37a CH₂CH(Et)S(O)₂CF₃
D2-37a CH₂CH(Et)S(O)₂CH₂CF₃
D2-37a CH(Me)CH(Me)SMe
D2-37a CH(Me)CH(Me)SEt
D2-37a CH(Me)CH(Me)SCF₃
D2-37a CH(Me)CH(Me)SCH₂CF₃
D2-37a CH(Me)CH(Me)S(O)Me
D2-37a CH(Me)CH(Me)S(O)Et
D2-37a CH(Me)CH(Me)S(O)CF₃
D2-37a CH(Me)CH(Me)S(O)CH₂CF₃
D2-37a CH(Me)CH(Me)S(O)₂Me
D2-37a CH(Me)CH(Me)S(O)₂Et
D2-37a CH(Me)CH(Me)S(O)₂CF₃
D2-37a CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-38a CH₂SMe
D2-38a CH₂SEt
D2-38a CH₂SCF₃
D2-38a CH₂SCH₂CF₃
D2-38a CH₂S(O)Me
D2-38a CH₂S(O)Et
D2-38a CH₂S(O)CF₃
D2-38a CH₂S(O)CH₂CF₃
D2-38a CH₂S(O)₂Me
D2-38a CH₂S(O)₂Et
D2-38a CH₂S(O)₂CF₃
D2-38a CH₂S(O)₂CH₂CF₃
D2-38a CH(Me)SMe
D2-38a CH(Me)SEt
D2-38a CH(Me)SCF₃
D2-38a CH(Me)SCH₂CF₃
D2-38a CH(Me)S(O)Me
D2-38a CH(Me)S(O)Et
D2-38a CH(Me)S(O)CF₃
D2-38a CH(Me)S(O)CH₂CF₃
D2-38a CH(Me)S(O)₂Me
D2-38a CH(Me)S(O)₂Et
D2-38a CH(Me)S(O)₂CF₃
D2-38a CH(Me)S(O)₂CH₂CF₃
D2-38a CH(Et)SMe
D2-38a CH(Et)SEt
D2-38a CH(Et)SCF₃
D2-38a CH(Et)SCH₂CF₃
D2-38a CH(Et)S(O)Me
D2-38a CH(Et)S(O)Et
D2-38a CH(Et)S(O)CF₃
D2-38a CH(Et)S(O)CH₂CF₃
D2-38a CH(Et)S(O)₂Me
D2-38a CH(Et)S(O)₂Et
D2-38a CH(Et)S(O)₂CF₃
D2-38a CH(Et)S(O)₂CH₂CF₃
D2-38a CH(n-Pr)SMe
D2-38a CH(n-Pr)SEt
D2-38a CH(n-Pr)SCF₃
D2-38a CH(n-Pr)SCH₂CF₃
D2-38a CH(n-Pr)S(O)Me
D2-38a CH(n-Pr)S(O)Et
D2-38a CH(n-Pr)S(O)CF₃
D2-38a CH(n-Pr)S(O)CH₂CF₃
D2-38a CH(n-Pr)S(O)₂Me
D2-38a CH(n-Pr)S(O)₂Et
D2-38a CH(n-Pr)S(O)₂CF₃
D2-38a CH(n-Pr)S(O)₂CH₂CF₃
D2-38a CH(i-Pr)SMe
D2-38a CH(i-Pr)SEt
D2-38a CH(i-Pr)SCF₃
D2-38a CH(i-Pr)SCH₂CF₃
D2-38a CH(i-Pr)S(O)Me
D2-38a CH(i-Pr)S(O)Et
D2-38a CH(i-Pr)S(O)CF₃
D2-38a CH(i-Pr)S(O)CH₂CF₃
D2-38a CH(i-Pr)S(O)₂Me
D2-38a CH(i-Pr)S(O)₂Et
D2-38a CH(i-Pr)S(O)₂CF₃
D2-38a CH(i-Pr)S(O)₂CH₂CF₃
D2-38a CH(n-Bu)SMe
D2-38a CH(n-Bu)SEt
D2-38a CH(n-Bu)SCF₃
D2-38a CH(n-Bu)SCH₂CF₃
D2-38a CH(n-Bu)S(O)Me
D2-38a CH(n-Bu)S(O)Et
D2-38a CH(n-Bu)S(O)CF₃
D2-38a CH(n-Bu)S(O)CH₂CF₃
D2-38a CH(n-Bu)S(O)₂Me
D2-38a CH(n-Bu)S(O)₂Et
D2-38a CH(n-Bu)S(O)₂CF₃
D2-38a CH(n-Bu)S(O)₂CH₂CF₃
D2-38a CH(i-Bu)SMe
D2-38a CH(i-Bu)SEt
D2-38a CH(i-Bu)SCF₃
D2-38a CH(i-Bu)SCH₂CF₃
D2-38a CH(i-Bu)S(O)Me
D2-38a CH(i-Bu)S(O)Et
D2-38a CH(i-Bu)S(O)CF₃
D2-38a CH(i-Bu)S(O)CH₂CF₃
D2-38a CH(i-Bu)S(O)₂Me
D2-38a CH(i-Bu)S(O)₂Et
D2-38a CH(i-Bu)S(O)₂CF₃
D2-38a CH(i-Bu)S(O)₂CH₂CF₃
D2-38a CH(s-Bu)SMe
D2-38a CH(s-Bu)SEt
D2-38a CH(s-Bu)SCF₃
D2-38a CH(s-Bu)SCH₂CF₃
D2-38a CH(s-Bu)S(O)Me
D2-38a CH(s-Bu)S(O)Et
D2-38a CH(s-Bu)S(O)CF₃
D2-38a CH(s-Bu)S(O)CH₂CF₃
D2-38a CH(s-Bu)S(O)₂Me
D2-38a CH(s-Bu)S(O)₂Et
D2-38a CH(s-Bu)S(O)₂CF₃
D2-38a CH(s-Bu)S(O)₂CH₂CF₃
D2-38a CH(t-Bu)SMe
D2-38a CH(t-Bu)SEt
D2-38a CH(t-Bu)SCF₃
D2-38a CH(t-Bu)SCH₂CF₃
D2-38a CH(t-Bu)S(O)Me
D2-38a CH(t-Bu)S(O)Et
D2-38a CH(t-Bu)S(O)CF₃
D2-38a CH(t-Bu)S(O)CH₂CF₃
D2-38a CH(t-Bu)S(O)₂Me
D2-38a CH(t-Bu)S(O)₂Et
D2-38a CH(t-Bu)S(O)₂CF₃
D2-38a CH(t-Bu)S(O)₂CH₂CF₃
D2-38a CH(CF₃)SMe
D2-38a CH(CF₃)SEt
D2-38a CH(CF₃)SCF₃
D2-38a CH(CF₃)SCH₂CF₃
D2-38a CH(CF₃)S(O)Me
D2-38a CH(CF₃)S(O)Et
D2-38a CH(CF₃)S(O)CF₃
D2-38a CH(CF₃)S(O)CH₂CF₃
D2-38a CH(CF₃)S(O)₂Me
D2-38a CH(CF₃)S(O)₂Et
D2-38a CH(CF₃)S(O)₂CF₃
D2-38a CH(CF₃)S(O)₂CH₂CF₃
D2-38a CH₂CH₂SMe
D2-38a CH₂CH₂SEt
D2-38a CH₂CH₂SCF₃
D2-38a CH₂CH₂SCH₂CF₃
D2-38a CH₂CH₂S(O)Me
D2-38a CH₂CH₂S(O)Et
D2-38a CH₂CH₂S(O)CF₃
D2-38a CH₂CH₂S(O)CH₂CF₃
D2-38a CH₂CH₂S(O)₂Me
D2-38a CH₂CH₂S(O)₂Et
D2-38a CH₂CH₂S(O)₂CF₃
D2-38a CH₂CH₂S(O)₂CH₂CF₃
D2-38a CH(Me)CH₂SMe
D2-38a CH(Me)CH₂SEt
D2-38a CH(Me)CH₂SCF₃
D2-38a CH(Me)CH₂SCH₂CF₃
D2-38a CH(Me)CH₂S(O)Me
D2-38a CH(Me)CH₂S(O)Et
D2-38a CH(Me)CH₂S(O)CF₃
D2-38a CH(Me)CH₂S(O)CH₂CF₃
D2-38a CH(Me)CH₂S(O)₂Me
D2-38a CH(Me)CH₂S(O)₂Et
D2-38a CH(Me)CH₂S(O)₂CF₃
D2-38a CH(Me)CH₂S(O)₂CH₂CF₃
D2-38a CH(Et)CH₂SMe
D2-38a CH(Et)CH₂SEt
D2-38a CH(Et)CH₂SCF₃
D2-38a CH(Et)CH₂SCH₂CF₃
D2-38a CH(Et)CH₂S(O)Me
D2-38a CH(Et)CH₂S(O)Et
D2-38a CH(Et)CH₂S(O)CF₃
D2-38a CH(Et)CH₂S(O)CH₂CF₃
D2-38a CH(Et)CH₂S(O)₂Me
D2-38a CH(Et)CH₂S(O)₂Et
D2-38a CH(Et)CH₂S(O)₂CF₃
D2-38a CH(Et)CH₂S(O)₂CH₂CF₃
D2-38a C(Me)₂CH₂SMe
D2-38a C(Me)₂CH₂SEt
D2-38a C(Me)₂CH₂SCF₃
D2-38a C(Me)₂CH₂SCH₂CF₃
D2-38a C(Me)₂CH₂S(O)Me
D2-38a C(Me)₂CH₂S(O)Et
D2-38a C(Me)₂CH₂S(O)CF₃
D2-38a C(Me)₂CH₂S(O)CH₂CF₃
D2-38a C(Me)₂CH₂S(O)₂Me
D2-38a C(Me)₂CH₂S(O)₂Et
D2-38a C(Me)₂CH₂S(O)₂CF₃
D2-38a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-38a CH₂CH(Me)SMe
D2-38a CH₂CH(Me)SEt
D2-38a CH₂CH(Me)SCF₃
D2-38a CH₂CH(Me)SCH₂CF₃
D2-38a CH₂CH(Me)S(O)Me
D2-38a CH₂CH(Me)S(O)Et
D2-38a CH₂CH(Me)S(O)CF₃
D2-38a CH₂CH(Me)S(O)CH₂CF₃
D2-38a CH₂CH(Me)S(O)₂Me
D2-38a CH₂CH(Me)S(O)₂Et
D2-38a CH₂CH(Me)S(O)₂CF₃
D2-38a CH₂CH(Me)S(O)₂CH₂CF₃
D2-38a CH₂CH(Et)SMe
D2-38a CH₂CH(Et)SEt
D2-38a CH₂CH(Et)SCF₃
D2-38a CH₂CH(Et)SCH₂CF₃
D2-38a CH₂CH(Et)S(O)Me
D2-38a CH₂CH(Et)S(O)Et
D2-38a CH₂CH(Et)S(O)CF₃
D2-38a CH₂CH(Et)S(O)CH₂CF₃
D2-38a CH₂CH(Et)S(O)₂Me
D2-38a CH₂CH(Et)S(O)₂Et
D2-38a CH₂CH(Et)S(O)₂CF₃
D2-38a CH₂CH(Et)S(O)₂CH₂CF₃
D2-38a CH(Me)CH(Me)SMe
D2-38a CH(Me)CH(Me)SEt
D2-38a CH(Me)CH(Me)SCF₃
D2-38a CH(Me)CH(Me)SCH₂CF₃
D2-38a CH(Me)CH(Me)S(O)Me
D2-38a CH(Me)CH(Me)S(O)Et
D2-38a CH(Me)CH(Me)S(O)CF₃
D2-38a CH(Me)CH(Me)S(O)CH₂CF₃
D2-38a CH(Me)CH(Me)S(O)₂Me
D2-38a CH(Me)CH(Me)S(O)₂Et
D2-38a CH(Me)CH(Me)S(O)₂CF₃
D2-38a CH(Me)CH(Me)S(O)₂CH₂CF₃
D2-92a CH₂SMe
D2-92a CH₂SEt
D2-92a CH₂SCF₃
D2-92a CH₂SCH₂CF₃
D2-92a CH₂S(O)Me
D2-92a CH₂S(O)Et
D2-92a CH₂S(O)CF₃
D2-92a CH₂S(O)CH₂CF₃
D2-92a CH₂S(O)₂Me
D2-92a CH₂S(O)₂Et
D2-92a CH₂S(O)₂CF₃
D2-92a CH₂S(O)₂CH₂CF₃
D2-92a CH(Me)SMe
D2-92a CH(Me)SEt
D2-92a CH(Me)SCF₃
D2-92a CH(Me)SCH₂CF₃
D2-92a CH(Me)S(O)Me
D2-92a CH(Me)S(O)Et
D2-92a CH(Me)S(O)CF₃
D2-92a CH(Me)S(O)CH₂CF₃
D2-92a CH(Me)S(O)₂Me
D2-92a CH(Me)S(O)₂Et
D2-92a CH(Me)S(O)₂CF₃
D2-92a CH(Me)S(O)₂CH₂CF₃
D2-92a CH(Et)SMe
D2-92a CH(Et)SEt
D2-92a CH(Et)SCF₃
D2-92a CH(Et)SCH₂CF₃
D2-92a CH(Et)S(O)Me
D2-92a CH(Et)S(O)Et
D2-92a CH(Et)S(O)CF₃
D2-92a CH(Et)S(O)CH₂CF₃
D2-92a CH(Et)S(O)₂Me
D2-92a CH(Et)S(O)₂Et
D2-92a CH(Et)S(O)₂CF₃
D2-92a CH(Et)S(O)₂CH₂CF₃
D2-92a CH(n-Pr)SMe
D2-92a CH(n-Pr)SEt
D2-92a CH(n-Pr)SCF₃
D2-92a CH(n-Pr)SCH₂CF₃
D2-92a CH(n-Pr)S(O)Me
D2-92a CH(n-Pr)S(O)Et
D2-92a CH(n-Pr)S(O)CF₃
D2-92a CH(n-Pr)S(O)CH₂CF₃
D2-92a CH(n-Pr)S(O)₂Me
D2-92a CH(n-Pr)S(O)₂Et
D2-92a CH(n-Pr)S(O)₂CF₃
D2-92a CH(n-Pr)S(O)₂CH₂CF₃
D2-92a CH(i-Pr)SMe
D2-92a CH(i-Pr)SEt
D2-92a CH(i-Pr)SCF₃
D2-92a CH(i-Pr)SCH₂CF₃
D2-92a CH(i-Pr)S(O)Me
D2-92a CH(i-Pr)S(O)Et
D2-92a CH(i-Pr)S(O)CF₃
D2-92a CH(i-Pr)S(O)CH₂CF₃
D2-92a CH(i-Pr)S(O)₂Me
D2-92a CH(i-Pr)S(O)₂Et
D2-92a CH(i-Pr)S(O)₂CF₃
D2-92a CH(i-Pr)S(O)₂CH₂CF₃
D2-92a CH(n-Bu)SMe
D2-92a CH(n-Bu)SEt
D2-92a CH(n-Bu)SCF₃
D2-92a CH(n-Bu)SCH₂CF₃
D2-92a CH(n-Bu)S(O)Me
D2-92a CH(n-Bu)S(O)Et
D2-92a CH(n-Bu)S(O)CF₃
D2-92a CH(n-Bu)S(O)CH₂CF₃
D2-92a CH(n-Bu)S(O)₂Me
D2-92a CH(n-Bu)S(O)₂Et
D2-92a CH(n-Bu)S(O)₂CF₃
D2-92a CH(n-Bu)S(O)₂CH₂CF₃
D2-92a CH(i-Bu)SMe
D2-92a CH(i-Bu)SEt
D2-92a CH(i-Bu)SCF₃
D2-92a CH(i-Bu)SCH₂CF₃
D2-92a CH(i-Bu)S(O)Me
D2-92a CH(i-Bu)S(O)Et
D2-92a CH(i-Bu)S(O)CF₃
D2-92a CH(i-Bu)S(O)CH₂CF₃
D2-92a CH(i-Bu)S(O)₂Me
D2-92a CH(i-Bu)S(O)₂Et
D2-92a CH(i-Bu)S(O)₂CF₃
D2-92a CH(i-Bu)S(O)₂CH₂CF₃
D2-92a CH(s-Bu)SMe
D2-92a CH(s-Bu)SEt
D2-92a CH(s-Bu)SCF₃
D2-92a CH(s-Bu)SCH₂CF₃
D2-92a CH(s-Bu)S(O)Me
D2-92a CH(s-Bu)S(O)Et
D2-92a CH(s-Bu)S(O)CF₃
D2-92a CH(s-Bu)S(O)CH₂CF₃
D2-92a CH(s-Bu)S(O)₂Me
D2-92a CH(s-Bu)S(O)₂Et
D2-92a CH(s-Bu)S(O)₂CF₃
D2-92a CH(s-Bu)S(O)₂CH₂CF₃
D2-92a CH(t-Bu)SMe
D2-92a CH(t-Bu)SEt
D2-92a CH(t-Bu)SCF₃
D2-92a CH(t-Bu)SCH₂CF₃
D2-92a CH(t-Bu)S(O)Me
D2-92a CH(t-Bu)S(O)Et
D2-92a CH(t-Bu)S(O)CF₃
D2-92a CH(t-Bu)S(O)CH₂CF₃
D2-92a CH(t-Bu)S(O)₂Me
D2-92a CH(t-Bu)S(O)₂Et
D2-92a CH(t-Bu)S(O)₂CF₃
D2-92a CH(t-Bu)S(O)₂CH₂CF₃
D2-92a CH(CF₃)SMe
D2-92a CH(CF₃)SEt
D2-92a CH(CF₃)SCF₃
D2-92a CH(CF₃)SCH₂CF₃
D2-92a CH(CF₃)S(O)Me
D2-92a CH(CF₃)S(O)Et
D2-92a CH(CF₃)S(O)CF₃
D2-92a CH(CF₃)S(O)CH₂CF₃
D2-92a CH(CF₃)S(O)₂Me
D2-92a CH(CF₃)S(O)₂Et
D2-92a CH(CF₃)S(O)₂CF₃
D2-92a CH(CF₃)S(O)₂CH₂CF₃
D2-92a CH₂CH₂SMe
D2-92a CH₂CH₂SEt
D2-92a CH₂CH₂SCF₃
D2-92a CH₂CH₂SCH₂CF₃
D2-92a CH₂CH₂S(O)Me
D2-92a CH₂CH₂S(O)Et
D2-92a CH₂CH₂S(O)CF₃
D2-92a CH₂CH₂S(O)CH₂CF₃
D2-92a CH₂CH₂S(O)₂Me
D2-92a CH₂CH₂S(O)₂Et
D2-92a CH₂CH₂S(O)₂CF₃
D2-92a CH₂CH₂S(O)₂CH₂CF₃
D2-92a CH(Me)CH₂SMe
D2-92a CH(Me)CH₂SEt
D2-92a CH(Me)CH₂SCF₃
D2-92a CH(Me)CH₂SCH₂CF₃
D2-92a CH(Me)CH₂S(O)Me
D2-92a CH(Me)CH₂S(O)Et
D2-92a CH(Me)CH₂S(O)CF₃
D2-92a CH(Me)CH₂S(O)CH₂CF₃
D2-92a CH(Me)CH₂S(O)₂Me
D2-92a CH(Me)CH₂S(O)₂Et
D2-92a CH(Me)CH₂S(O)₂CF₃
D2-92a CH(Me)CH₂S(O)₂CH₂CF₃
D2-92a CH(Et)CH₂SMe
D2-92a CH(Et)CH₂SEt
D2-92a CH(Et)CH₂SCF₃
D2-92a CH(Et)CH₂SCH₂CF₃
D2-92a CH(Et)CH₂S(O)Me
D2-92a CH(Et)CH₂S(O)Et
D2-92a CH(Et)CH₂S(O)CF₃
D2-92a CH(Et)CH₂S(O)CH₂CF₃
D2-92a CH(Et)CH₂S(O)₂Me
D2-92a CH(Et)CH₂S(O)₂Et
D2-92a CH(Et)CH₂S(O)₂CF₃
D2-92a CH(Et)CH₂S(O)₂CH₂CF₃
D2-92a C(Me)₂CH₂SMe
D2-92a C(Me)₂CH₂SEt
D2-92a C(Me)₂CH₂SCF₃
D2-92a C(Me)₂CH₂SCH₂CF₃
D2-92a C(Me)₂CH₂S(O)Me
D2-92a C(Me)₂CH₂S(O)Et
D2-92a C(Me)₂CH₂S(O)CF₃
D2-92a C(Me)₂CH₂S(O)CH₂CF₃
D2-92a C(Me)₂CH₂S(O)₂Me
D2-92a C(Me)₂CH₂S(O)₂Et
D2-92a C(Me)₂CH₂S(O)₂CF₃
D2-92a C(Me)₂CH₂S(O)₂CH₂CF₃
D2-92a CH₂CH(Me)SMe
D2-92a CH₂CH(Me)SEt
D2-92a CH₂CH(Me)SCF₃
D2-92a CH₂CH(Me)SCH₂CF₃
D2-92a CH₂CH(Me)S(O)Me
D2-92a CH₂CH(Me)S(O)Et
D2-92a CH₂CH(Me)S(O)CF₃
D2-92a CH₂CH(Me)S(O)CH₂CF₃
D2-92a CH₂CH(Me)S(O)₂Me
D2-92a CH₂CH(Me)S(O)₂Et
D2-92a CH₂CH(Me)S(O)₂CF₃
D2-92a CH₂CH(Me)S(O)₂CH₂CF₃
D2-92a CH₂CH(Et)SMe
D2-92a CH₂CH(Et)SEt
D2-92a CH₂CH(Et)SCF₃
D2-92a CH₂CH(Et)SCH₂CF₃
D2-92a CH₂CH(Et)S(O)Me
D2-92a CH₂CH(Et)S(O)Et
D2-92a CH₂CH(Et)S(O)CF₃
D2-92a CH₂CH(Et)S(O)CH₂CF₃
D2-92a CH₂CH(Et)S(O)₂Me
D2-92a CH₂CH(Et)S(O)₂Et
D2-92a CH₂CH(Et)S(O)₂CF₃
D2-92a CH₂CH(Et)S(O)₂CH₂CF₃
D2-92a CH(Me)CH(Me)SMe
D2-92a CH(Me)CH(Me)SEt
D2-92a CH(Me)CH(Me)SCF₃
D2-92a CH(Me)CH(Me)SCH₂CF₃
D2-92a CH(Me)CH(Me)S(O)Me
D2-92a CH(Me)CH(Me)S(O)Et
D2-92a CH(Me)CH(Me)S(O)CF₃
D2-92a CH(Me)CH(Me)S(O)CH₂CF₃
D2-92a CH(Me)CH(Me)S(O)₂Me
D2-92a CH(Me)CH(Me)S(O)₂Et
D2-92a CH(Me)CH(Me)S(O)₂CF₃
D2-92a CH(Me)CH(Me)S(O)₂CH₂CF₃
CH(Me)SMe CH₂SMe
CH(Me)SMe CH₂SEt
CH(Me)SMe CH₂SCF₃
CH(Me)SMe CH₂SCH₂CF₃
CH(Me)SMe CH₂S(O)Me
CH(Me)SMe CH₂S(O)Et
CH(Me)SMe CH₂S(O)CF₃
CH(Me)SMe CH₂S(O)CH₂CF₃
CH(Me)SMe CH₂S(O)₂Me
CH(Me)SMe CH₂S(O)₂Et
CH(Me)SMe CH₂S(O)₂CF₃
CH(Me)SMe CH₂S(O)₂CH₂CF₃
CH(Me)SMe CH(Me)SMe
CH(Me)SMe CH(Me)SEt
CH(Me)SMe CH(Me)SCF₃
CH(Me)SMe CH(Me)SCH₂CF₃
CH(Me)SMe CH(Me)S(O)Me
CH(Me)SMe CH(Me)S(O)Et
CH(Me)SMe CH(Me)S(O)CF₃
CH(Me)SMe CH(Me)S(O)CH₂CF₃
CH(Me)SMe CH(Me)S(O)₂Me
CH(Me)SMe CH(Me)S(O)₂Et
CH(Me)SMe CH(Me)S(O)₂CF₃
CH(Me)SMe CH(Me)S(O)₂CH₂CF₃
CH(Me)SMe CH(Et)SMe
CH(Me)SMe CH(Et)SEt
CH(Me)SMe CH(Et)SCF₃
CH(Me)SMe CH(Et)SCH₂CF₃
CH(Me)SMe CH(Et)S(O)Me
CH(Me)SMe CH(Et)S(O)Et
CH(Me)SMe CH(Et)S(O)CF₃
CH(Me)SMe CH(Et)S(O)CH₂CF₃
CH(Me)SMe CH(Et)S(O)₂Me
CH(Me)SMe CH(Et)S(O)₂Et
CH(Me)SMe CH(Et)S(O)₂CF₃
CH(Me)SMe CH(Et)S(O)₂CH₂CF₃
CH(Me)SMe CH(n-Pr)SMe
CH(Me)SMe CH(n-Pr)SEt
CH(Me)SMe CH(n-Pr)SCF₃
CH(Me)SMe CH(n-Pr)SCH₂CF₃
CH(Me)SMe CH(n-Pr)S(O)Me
CH(Me)SMe CH(n-Pr)S(O)Et
CH(Me)SMe CH(n-Pr)S(O)CF₃
CH(Me)SMe CH(n-Pr)S(O)CH₂CF₃
CH(Me)SMe CH(n-Pr)S(O)₂Me
CH(Me)SMe CH(n-Pr)S(O)₂Et
CH(Me)SMe CH(n-Pr)S(O)₂CF₃
CH(Me)SMe CH(n-Pr)S(O)₂CH₂CF₃
CH(Me)SMe CH(i-Pr)SMe
CH(Me)SMe CH(i-Pr)SEt
CH(Me)SMe CH(i-Pr)SCF₃
CH(Me)SMe CH(i-Pr)SCH₂CF₃
CH(Me)SMe CH(i-Pr)S(O)Me
CH(Me)SMe CH(i-Pr)S(O)Et
CH(Me)SMe CH(i-Pr)S(O)CF₃
CH(Me)SMe CH(i-Pr)S(O)CH₂CF₃
CH(Me)SMe CH(i-Pr)S(O)₂Me
CH(Me)SMe CH(i-Pr)S(O)₂Et
CH(Me)SMe CH(i-Pr)S(O)₂CF₃
CH(Me)SMe CH(i-Pr)S(O)₂CH₂CF₃
CH(Me)SMe CH(n-Bu)SMe
CH(Me)SMe CH(n-Bu)SEt
CH(Me)SMe CH(n-Bu)SCF₃
CH(Me)SMe CH(n-Bu)SCH₂CF₃
CH(Me)SMe CH(n-Bu)S(O)Me
CH(Me)SMe CH(n-Bu)S(O)Et
CH(Me)SMe CH(n-Bu)S(O)CF₃
CH(Me)SMe CH(n-Bu)S(O)CH₂CF₃
CH(Me)SMe CH(n-Bu)S(O)₂Me
CH(Me)SMe CH(n-Bu)S(O)₂Et
CH(Me)SMe CH(n-Bu)S(O)₂CF₃
CH(Me)SMe CH(n-Bu)S(O)₂CH₂CF₃
CH(Me)SMe CH(i-Bu)SMe
CH(Me)SMe CH(i-Bu)SEt
CH(Me)SMe CH(i-Bu)SCF₃
CH(Me)SMe CH(i-Bu)SCH₂CF₃
CH(Me)SMe CH(i-Bu)S(O)Me
CH(Me)SMe CH(i-Bu)S(O)Et
CH(Me)SMe CH(i-Bu)S(O)CF₃
CH(Me)SMe CH(i-Bu)S(O)CH₂CF₃
CH(Me)SMe CH(i-Bu)S(O)₂Me
CH(Me)SMe CH(i-Bu)S(O)₂Et
CH(Me)SMe CH(i-Bu)S(O)₂CF₃
CH(Me)SMe CH(i-Bu)S(O)₂CH₂CF₃
CH(Me)SMe CH(s-Bu)SMe
CH(Me)SMe CH(s-Bu)SEt
CH(Me)SMe CH(s-Bu)SCF₃
CH(Me)SMe CH(s-Bu)SCH₂CF₃
CH(Me)SMe CH(s-Bu)S(O)Me
CH(Me)SMe CH(s-Bu)S(O)Et
CH(Me)SMe CH(s-Bu)S(O)CF₃
CH(Me)SMe CH(s-Bu)S(O)CH₂CF₃
CH(Me)SMe CH(s-Bu)S(O)₂Me
CH(Me)SMe CH(s-Bu)S(O)₂Et
CH(Me)SMe CH(s-Bu)S(O)₂CF₃
CH(Me)SMe CH(s-Bu)S(O)₂CH₂CF₃
CH(Me)SMe CH(t-Bu)SMe
CH(Me)SMe CH(t-Bu)SEt
CH(Me)SMe CH(t-Bu)SCF₃
CH(Me)SMe CH(t-Bu)SCH₂CF₃
CH(Me)SMe CH(t-Bu)S(O)Me
CH(Me)SMe CH(t-Bu)S(O)Et
CH(Me)SMe CH(t-Bu)S(O)CF₃
CH(Me)SMe CH(t-Bu)S(O)CH₂CF₃
CH(Me)SMe CH(t-Bu)S(O)₂Me
CH(Me)SMe CH(t-Bu)S(O)₂Et
CH(Me)SMe CH(t-Bu)S(O)₂CF₃
CH(Me)SMe CH(t-Bu)S(O)₂CH₂CF₃
CH(Me)SMe CH(CF₃)SMe
CH(Me)SMe CH(CF₃)SEt
CH(Me)SMe CH(CF₃)SCF₃
CH(Me)SMe CH(CF₃)SCH₂CF₃
CH(Me)SMe CH(CF₃)S(O)Me
CH(Me)SMe CH(CF₃)S(O)Et
CH(Me)SMe CH(CF₃)S(O)CF₃
CH(Me)SMe CH(CF₃)S(O)CH₂CF₃
CH(Me)SMe CH(CF₃)S(O)₂Me
CH(Me)SMe CH(CF₃)S(O)₂Et
CH(Me)SMe CH(CF₃)S(O)₂CF₃
CH(Me)SMe CH(CF₃)S(O)₂CH₂CF₃
CH(Me)SMe CH₂CH₂SMe
CH(Me)SMe CH₂CH₂SEt
CH(Me)SMe CH₂CH₂SCF₃
CH(Me)SMe CH₂CH₂SCH₂CF₃
CH(Me)SMe CH₂CH₂S(O)Me
CH(Me)SMe CH₂CH₂S(O)Et
CH(Me)SMe CH₂CH₂S(O)CF₃
CH(Me)SMe CH₂CH₂S(O)CH₂CF₃
CH(Me)SMe CH₂CH₂S(O)₂Me
CH(Me)SMe CH₂CH₂S(O)₂Et
CH(Me)SMe CH₂CH₂S(O)₂CF₃
CH(Me)SMe CH₂CH₂S(O)₂CH₂CF₃
CH(Me)SMe CH(Me)CH₂SMe
CH(Me)SMe CH(Me)CH₂SEt
CH(Me)SMe CH(Me)CH₂SCF₃
CH(Me)SMe CH(Me)CH₂SCH₂CF₃
CH(Me)SMe CH(Me)CH₂S(O)Me
CH(Me)SMe CH(Me)CH₂S(O)Et
CH(Me)SMe CH(Me)CH₂S(O)CF₃
CH(Me)SMe CH(Me)CH₂S(O)CH₂CF₃
CH(Me)SMe CH(Me)CH₂S(O)₂Me
CH(Me)SMe CH(Me)CH₂S(O)₂Et
CH(Me)SMe CH(Me)CH₂S(O)₂CF₃
CH(Me)SMe CH(Me)CH₂S(O)₂CH₂CF₃
CH(Me)SMe CH(Et)CH₂SMe
CH(Me)SMe CH(Et)CH₂SEt
CH(Me)SMe CH(Et)CH₂SCF₃
CH(Me)SMe CH(Et)CH₂SCH₂CF₃
CH(Me)SMe CH(Et)CH₂S(O)Me
CH(Me)SMe CH(Et)CH₂S(O)Et
CH(Me)SMe CH(Et)CH₂S(O)CF₃
CH(Me)SMe CH(Et)CH₂S(O)CH₂CF₃
CH(Me)SMe CH(Et)CH₂S(O)₂Me
CH(Me)SMe CH(Et)CH₂S(O)₂Et
CH(Me)SMe CH(Et)CH₂S(O)₂CF₃
CH(Me)SMe CH(Et)CH₂S(O)₂CH₂CF₃
CH(Me)SMe C(Me)₂CH₂SMe
CH(Me)SMe C(Me)₂CH₂SEt
CH(Me)SMe C(Me)₂CH₂SCF₃
CH(Me)SMe C(Me)₂CH₂SCH₂CF₃
CH(Me)SMe C(Me)₂CH₂S(O)Me
CH(Me)SMe C(Me)₂CH₂S(O)Et
CH(Me)SMe C(Me)₂CH₂S(O)CF₃
CH(Me)SMe C(Me)₂CH₂S(O)CH₂CF₃
CH(Me)SMe C(Me)₂CH₂S(O)₂Me
CH(Me)SMe C(Me)₂CH₂S(O)₂Et
CH(Me)SMe C(Me)₂CH₂S(O)₂CF₃
CH(Me)SMe C(Me)₂CH₂S(O)₂CH₂CF₃
CH(Me)SMe CH₂CH(Me)SMe
CH(Me)SMe CH₂CH(Me)SEt
CH(Me)SMe CH₂CH(Me)SCF₃
CH(Me)SMe CH₂CH(Me)SCH₂CF₃
CH(Me)SMe CH₂CH(Me)S(O)Me
CH(Me)SMe CH₂CH(Me)S(O)Et
CH(Me)SMe CH₂CH(Me)S(O)CF₃
CH(Me)SMe CH₂CH(Me)S(O)CH₂CF₃
CH(Me)SMe CH₂CH(Me)S(O)₂Me
CH(Me)SMe CH₂CH(Me)S(O)₂Et
CH(Me)SMe CH₂CH(Me)S(O)₂CF₃
CH(Me)SMe CH₂CH(Me)S(O)₂CH₂CF₃
CH(Me)SMe CH₂CH(Et)SMe
CH(Me)SMe CH₂CH(Et)SEt
CH(Me)SMe CH₂CH(Et)SCF₃
CH(Me)SMe CH₂CH(Et)SCH₂CF₃
CH(Me)SMe CH₂CH(Et)S(O)Me
CH(Me)SMe CH₂CH(Et)S(O)Et
CH(Me)SMe CH₂CH(Et)S(O)CF₃
CH(Me)SMe CH₂CH(Et)S(O)CH₂CF₃
CH(Me)SMe CH₂CH(Et)S(O)₂Me
CH(Me)SMe CH₂CH(Et)S(O)₂Et
CH(Me)SMe CH₂CH(Et)S(O)₂CF₃
CH(Me)SMe CH₂CH(Et)S(O)₂CH₂CF₃
CH(Me)SMe CH(Me)CH(Me)SMe
CH(Me)SMe CH(Me)CH(Me)SEt
CH(Me)SMe CH(Me)CH(Me)SCF₃
CH(Me)SMe CH(Me)CH(Me)SCH₂CF₃
CH(Me)SMe CH(Me)CH(Me)S(O)Me
CH(Me)SMe CH(Me)CH(Me)S(O)Et
CH(Me)SMe CH(Me)CH(Me)S(O)CF₃
CH(Me)SMe CH(Me)CH(Me)S(O)CH₂CF₃
CH(Me)SMe CH(Me)CH(Me)S(O)₂Me
CH(Me)SMe CH(Me)CH(Me)S(O)₂Et
CH(Me)SMe CH(Me)CH(Me)S(O)₂CF₃
CH(Me)SMe CH(Me)CH(Me)S(O)₂CH₂CF₃
C(O)Me CH₂SMe
C(O)Me CH₂SEt
C(O)Me CH₂SCF₃
C(O)Me CH₂SCH₂CF₃
C(O)Me CH₂S(O)Me
C(O)Me CH₂S(O)Et
C(O)Me CH₂S(O)CF₃
C(O)Me CH₂S(O)CH₂CF₃
C(O)Me CH₂S(O)₂Me
C(O)Me CH₂S(O)₂Et
C(O)Me CH₂S(O)₂CF₃
C(O)Me CH₂S(O)₂CH₂CF₃
C(O)Me CH(Me)SMe
C(O)Me CH(Me)SEt
C(O)Me CH(Me)SCF₃
C(O)Me CH(Me)SCH₂CF₃
C(O)Me CH(Me)S(O)Me
C(O)Me CH(Me)S(O)Et
C(O)Me CH(Me)S(O)CF₃
C(O)Me CH(Me)S(O)CH₂CF₃
C(O)Me CH(Me)S(O)₂Me
C(O)Me CH(Me)S(O)₂Et
C(O)Me CH(Me)S(O)₂CF₃
C(O)Me CH(Me)S(O)₂CH₂CF₃
C(O)Me CH(Et)SMe
C(O)Me CH(Et)SEt
C(O)Me CH(Et)SCF₃
C(O)Me CH(Et)SCH₂CF₃
C(O)Me CH(Et)S(O)Me
C(O)Me CH(Et)S(O)Et
C(O)Me CH(Et)S(O)CF₃
C(O)Me CH(Et)S(O)CH₂CF₃
C(O)Me CH(Et)S(O)₂Me
C(O)Me CH(Et)S(O)₂Et
C(O)Me CH(Et)S(O)₂CF₃
C(O)Me CH(Et)S(O)₂CH₂CF₃
C(O)Me CH(n-Pr)SMe
C(O)Me CH(n-Pr)SEt
C(O)Me CH(n-Pr)SCF₃
C(O)Me CH(n-Pr)SCH₂CF₃
C(O)Me CH(n-Pr)S(O)Me
C(O)Me CH(n-Pr)S(O)Et
C(O)Me CH(n-Pr)S(O)CF₃
C(O)Me CH(n-Pr)S(O)CH₂CF₃
C(O)Me CH(n-Pr)S(O)₂Me
C(O)Me CH(n-Pr)S(O)₂Et
C(O)Me CH(n-Pr)S(O)₂CF₃
C(O)Me CH(n-Pr)S(O)₂CH₂CF₃
C(O)Me CH(i-Pr)SMe
C(O)Me CH(i-Pr)SEt
C(O)Me CH(i-Pr)SCF₃
C(O)Me CH(i-Pr)SCH₂CF₃
C(O)Me CH(i-Pr)S(O)Me
C(O)Me CH(i-Pr)S(O)Et
C(O)Me CH(i-Pr)S(O)CF₃
C(O)Me CH(i-Pr)S(O)CH₂CF₃
C(O)Me CH(i-Pr)S(O)₂Me
C(O)Me CH(i-Pr)S(O)₂Et
C(O)Me CH(i-Pr)S(O)₂CF₃
C(O)Me CH(i-Pr)S(O)₂CH₂CF₃
C(O)Me CH(n-Bu)SMe
C(O)Me CH(n-Bu)SEt
C(O)Me CH(n-Bu)SCF₃
C(O)Me CH(n-Bu)SCH₂CF₃
C(O)Me CH(n-Bu)S(O)Me
C(O)Me CH(n-Bu)S(O)Et
C(O)Me CH(n-Bu)S(O)CF₃
C(O)Me CH(n-Bu)S(O)CH₂CF₃
C(O)Me CH(n-Bu)S(O)₂Me
C(O)Me CH(n-Bu)S(O)₂Et
C(O)Me CH(n-Bu)S(O)₂CF₃
C(O)Me CH(n-Bu)S(O)₂CH₂CF₃
C(O)Me CH(i-Bu)SMe
C(O)Me CH(i-Bu)SEt
C(O)Me CH(i-Bu)SCF₃
C(O)Me CH(i-Bu)SCH₂CF₃
C(O)Me CH(i-Bu)S(O)Me
C(O)Me CH(i-Bu)S(O)Et
C(O)Me CH(i-Bu)S(O)CF₃
C(O)Me CH(i-Bu)S(O)CH₂CF₃
C(O)Me CH(i-Bu)S(O)₂Me
C(O)Me CH(i-Bu)S(O)₂Et
C(O)Me CH(i-Bu)S(O)₂CF₃
C(O)Me CH(i-Bu)S(O)₂CH₂CF₃
C(O)Me CH(s-Bu)SMe
C(O)Me CH(s-Bu)SEt
C(O)Me CH(s-Bu)SCF₃
C(O)Me CH(s-Bu)SCH₂CF₃
C(O)Me CH(s-Bu)S(O)Me
C(O)Me CH(s-Bu)S(O)Et
C(O)Me CH(s-Bu)S(O)CF₃
C(O)Me CH(s-Bu)S(O)CH₂CF₃
C(O)Me CH(s-Bu)S(O)₂Me
C(O)Me CH(s-Bu)S(O)₂Et
C(O)Me CH(s-Bu)S(O)₂CF₃
C(O)Me CH(s-Bu)S(O)₂CH₂CF₃
C(O)Me CH(t-Bu)SMe
C(O)Me CH(t-Bu)SEt
C(O)Me CH(t-Bu)SCF₃
C(O)Me CH(t-Bu)SCH₂CF₃
C(O)Me CH(t-Bu)S(O)Me
C(O)Me CH(t-Bu)S(O)Et
C(O)Me CH(t-Bu)S(O)CF₃
C(O)Me CH(t-Bu)S(O)CH₂CF₃
C(O)Me CH(t-Bu)S(O)₂Me
C(O)Me CH(t-Bu)S(O)₂Et
C(O)Me CH(t-Bu)S(O)₂CF₃
C(O)Me CH(t-Bu)S(O)₂CH₂CF₃
C(O)Me CH(CF₃)SMe
C(O)Me CH(CF₃)SEt
C(O)Me CH(CF₃)SCF₃
C(O)Me CH(CF₃)SCH₂CF₃
C(O)Me CH(CF₃)S(O)Me
C(O)Me CH(CF₃)S(O)Et
C(O)Me CH(CF₃)S(O)CF₃
C(O)Me CH(CF₃)S(O)CH₂CF₃
C(O)Me CH(CF₃)S(O)₂Me
C(O)Me CH(CF₃)S(O)₂Et
C(O)Me CH(CF₃)S(O)₂CF₃
C(O)Me CH(CF₃)S(O)₂CH₂CF₃
C(O)Me CH₂CH₂SMe
C(O)Me CH₂CH₂SEt
C(O)Me CH₂CH₂SCF₃
C(O)Me CH₂CH₂SCH₂CF₃
C(O)Me CH₂CH₂S(O)Me
C(O)Me CH₂CH₂S(O)Et
C(O)Me CH₂CH₂S(O)CF₃
C(O)Me CH₂CH₂S(O)CH₂CF₃
C(O)Me CH₂CH₂S(O)₂Me
C(O)Me CH₂CH₂S(O)₂Et
C(O)Me CH₂CH₂S(O)₂CF₃
C(O)Me CH₂CH₂S(O)₂CH₂CF₃
C(O)Me CH(Me)CH₂SMe
C(O)Me CH(Me)CH₂SEt
C(O)Me CH(Me)CH₂SCF₃
C(O)Me CH(Me)CH₂SCH₂CF₃
C(O)Me CH(Me)CH₂S(O)Me
C(O)Me CH(Me)CH₂S(O)Et
C(O)Me CH(Me)CH₂S(O)CF₃
C(O)Me CH(Me)CH₂S(O)CH₂CF₃
C(O)Me CH(Me)CH₂S(O)₂Me
C(O)Me CH(Me)CH₂S(O)₂Et
C(O)Me CH(Me)CH₂S(O)₂CF₃
C(O)Me CH(Me)CH₂S(O)₂CH₂CF₃
C(O)Me CH(Et)CH₂SMe
C(O)Me CH(Et)CH₂SEt
C(O)Me CH(Et)CH₂SCF₃
C(O)Me CH(Et)CH₂SCH₂CF₃
C(O)Me CH(Et)CH₂S(O)Me
C(O)Me CH(Et)CH₂S(O)Et
C(O)Me CH(Et)CH₂S(O)CF₃
C(O)Me CH(Et)CH₂S(O)CH₂CF₃
C(O)Me CH(Et)CH₂S(O)₂Me
C(O)Me CH(Et)CH₂S(O)₂Et
C(O)Me CH(Et)CH₂S(O)₂CF₃
C(O)Me CH(Et)CH₂S(O)₂CH₂CF₃
C(O)Me C(Me)₂CH₂SMe
C(O)Me C(Me)₂CH₂SEt
C(O)Me C(Me)₂CH₂SCF₃
C(O)Me C(Me)₂CH₂SCH₂CF₃
C(O)Me C(Me)₂CH₂S(O)Me
C(O)Me C(Me)₂CH₂S(O)Et
C(O)Me C(Me)₂CH₂S(O)CF₃
C(O)Me C(Me)₂CH₂S(O)CH₂CF₃
C(O)Me C(Me)₂CH₂S(O)₂Me
C(O)Me C(Me)₂CH₂S(O)₂Et
C(O)Me C(Me)₂CH₂S(O)₂CF₃
C(O)Me C(Me)₂CH₂S(O)₂CH₂CF₃
C(O)Me CH₂CH(Me)SMe
C(O)Me CH₂CH(Me)SEt
C(O)Me CH₂CH(Me)SCF₃
C(O)Me CH₂CH(Me)SCH₂CF₃
C(O)Me CH₂CH(Me)S(O)Me
C(O)Me CH₂CH(Me)S(O)Et
C(O)Me CH₂CH(Me)S(O)CF₃
C(O)Me CH₂CH(Me)S(O)CH₂CF₃
C(O)Me CH₂CH(Me)S(O)₂Me
C(O)Me CH₂CH(Me)S(O)₂Et
C(O)Me CH₂CH(Me)S(O)₂CF₃
C(O)Me CH₂CH(Me)S(O)₂CH₂CF₃
C(O)Me CH₂CH(Et)SMe
C(O)Me CH₂CH(Et)SEt
C(O)Me CH₂CH(Et)SCF₃
C(O)Me CH₂CH(Et)SCH₂CF₃
C(O)Me CH₂CH(Et)S(O)Me
C(O)Me CH₂CH(Et)S(O)Et
C(O)Me CH₂CH(Et)S(O)CF₃
C(O)Me CH₂CH(Et)S(O)CH₂CF₃
C(O)Me CH₂CH(Et)S(O)₂Me
C(O)Me CH₂CH(Et)S(O)₂Et
C(O)Me CH₂CH(Et)S(O)₂CF₃
C(O)Me CH₂CH(Et)S(O)₂CH₂CF₃
C(O)Me CH(Me)CH(Me)SMe
C(O)Me CH(Me)CH(Me)SEt
C(O)Me CH(Me)CH(Me)SCF₃
C(O)Me CH(Me)CH(Me)SCH₂CF₃
C(O)Me CH(Me)CH(Me)S(O)Me
C(O)Me CH(Me)CH(Me)S(O)Et
C(O)Me CH(Me)CH(Me)S(O)CF₃
C(O)Me CH(Me)CH(Me)S(O)CH₂CF₃
C(O)Me CH(Me)CH(Me)S(O)₂Me
C(O)Me CH(Me)CH(Me)S(O)₂Et
C(O)Me CH(Me)CH(Me)S(O)₂CF₃
C(O)Me CH(Me)CH(Me)S(O)₂CH₂CF₃
C(O)OMe CH₂SMe
C(O)OMe CH₂SEt
C(O)OMe CH₂SCF₃
C(O)OMe CH₂SCH₂CF₃
C(O)OMe CH₂S(O)Me
C(O)OMe CH₂S(O)Et
C(O)OMe CH₂S(O)CF₃
C(O)OMe CH₂S(O)CH₂CF₃
C(O)OMe CH₂S(O)₂Me
C(O)OMe CH₂S(O)₂Et
C(O)OMe CH₂S(O)₂CF₃
C(O)OMe CH₂S(O)₂CH₂CF₃
C(O)OMe CH(Me)SMe
C(O)OMe CH(Me)SEt
C(O)OMe CH(Me)SCF₃
C(O)OMe CH(Me)SCH₂CF₃
C(O)OMe CH(Me)S(O)Me
C(O)OMe CH(Me)S(O)Et
C(O)OMe CH(Me)S(O)CF₃
C(O)OMe CH(Me)S(O)CH₂CF₃
C(O)OMe CH(Me)S(O)₂Me
C(O)OMe CH(Me)S(O)₂Et
C(O)OMe CH(Me)S(O)₂CF₃
C(O)OMe CH(Me)S(O)₂CH₂CF₃
C(O)OMe CH(Et)SMe
C(O)OMe CH(Et)SEt
C(O)OMe CH(Et)SCF₃
C(O)OMe CH(Et)SCH₂CF₃
C(O)OMe CH(Et)S(O)Me
C(O)OMe CH(Et)S(O)Et
C(O)OMe CH(Et)S(O)CF₃
C(O)OMe CH(Et)S(O)CH₂CF₃
C(O)OMe CH(Et)S(O)₂Me
C(O)OMe CH(Et)S(O)₂Et
C(O)OMe CH(Et)S(O)₂CF₃
C(O)OMe CH(Et)S(O)₂CH₂CF₃
C(O)OMe CH(n-Pr)SMe
C(O)OMe CH(n-Pr)SEt
C(O)OMe CH(n-Pr)SCF₃
C(O)OMe CH(n-Pr)SCH₂CF₃
C(O)OMe CH(n-Pr)S(O)Me
C(O)OMe CH(n-Pr)S(O)Et
C(O)OMe CH(n-Pr)S(O)CF₃
C(O)OMe CH(n-Pr)S(O)CH₂CF₃
C(O)OMe CH(n-Pr)S(O)₂Me
C(O)OMe CH(n-Pr)S(O)₂Et
C(O)OMe CH(n-Pr)S(O)₂CF₃
C(O)OMe CH(n-Pr)S(O)₂CH₂CF₃
C(O)OMe CH(i-Pr)SMe
C(O)OMe CH(i-Pr)SEt
C(O)OMe CH(i-Pr)SCF₃
C(O)OMe CH(i-Pr)SCH₂CF₃
C(O)OMe CH(i-Pr)S(O)Me
C(O)OMe CH(i-Pr)S(O)Et
C(O)OMe CH(i-Pr)S(O)CF₃
C(O)OMe CH(i-Pr)S(O)CH₂CF₃
C(O)OMe CH(i-Pr)S(O)₂Me
C(O)OMe CH(i-Pr)S(O)₂Et
C(O)OMe CH(i-Pr)S(O)₂CF₃
C(O)OMe CH(i-Pr)S(O)₂CH₂CF₃
C(O)OMe CH(n-Bu)SMe
C(O)OMe CH(n-Bu)SEt
C(O)OMe CH(n-Bu)SCF₃
C(O)OMe CH(n-Bu)SCH₂CF₃
C(O)OMe CH(n-Bu)S(O)Me
C(O)OMe CH(n-Bu)S(O)Et
C(O)OMe CH(n-Bu)S(O)CF₃
C(O)OMe CH(n-Bu)S(O)CH₂CF₃
C(O)OMe CH(n-Bu)S(O)₂Me
C(O)OMe CH(n-Bu)S(O)₂Et
C(O)OMe CH(n-Bu)S(O)₂CF₃
C(O)OMe CH(n-Bu)S(O)₂CH₂CF₃
C(O)OMe CH(i-Bu)SMe
C(O)OMe CH(i-Bu)SEt
C(O)OMe CH(i-Bu)SCF₃
C(O)OMe CH(i-Bu)SCH₂CF₃
C(O)OMe CH(i-Bu)S(O)Me
C(O)OMe CH(i-Bu)S(O)Et
C(O)OMe CH(i-Bu)S(O)CF₃
C(O)OMe CH(i-Bu)S(O)CH₂CF₃
C(O)OMe CH(i-Bu)S(O)₂Me
C(O)OMe CH(i-Bu)S(O)₂Et
C(O)OMe CH(i-Bu)S(O)₂CF₃
C(O)OMe CH(i-Bu)S(O)₂CH₂CF₃
C(O)OMe CH(s-Bu)SMe
C(O)OMe CH(s-Bu)SEt
C(O)OMe CH(s-Bu)SCF₃
C(O)OMe CH(s-Bu)SCH₂CF₃
C(O)OMe CH(s-Bu)S(O)Me
C(O)OMe CH(s-Bu)S(O)Et
C(O)OMe CH(s-Bu)S(O)CF₃
C(O)OMe CH(s-Bu)S(O)CH₂CF₃
C(O)OMe CH(s-Bu)S(O)₂Me
C(O)OMe CH(s-Bu)S(O)₂Et
C(O)OMe CH(s-Bu)S(O)₂CF₃
C(O)OMe CH(s-Bu)S(O)₂CH₂CF₃
C(O)OMe CH(t-Bu)SMe
C(O)OMe CH(t-Bu)SEt
C(O)OMe CH(t-Bu)SCF₃
C(O)OMe CH(t-Bu)SCH₂CF₃
C(O)OMe CH(t-Bu)S(O)Me
C(O)OMe CH(t-Bu)S(O)Et
C(O)OMe CH(t-Bu)S(O)CF₃
C(O)OMe CH(t-Bu)S(O)CH₂CF₃
C(O)OMe CH(t-Bu)S(O)₂Me
C(O)OMe CH(t-Bu)S(O)₂Et
C(O)OMe CH(t-Bu)S(O)₂CF₃
C(O)OMe CH(t-Bu)S(O)₂CH₂CF₃
C(O)OMe CH(CF₃)SMe
C(O)OMe CH(CF₃)SEt
C(O)OMe CH(CF₃)SCF₃
C(O)OMe CH(CF₃)SCH₂CF₃
C(O)OMe CH(CF₃)S(O)Me
C(O)OMe CH(CF₃)S(O)Et
C(O)OMe CH(CF₃)S(O)CF₃
C(O)OMe CH(CF₃)S(O)CH₂CF₃
C(O)OMe CH(CF₃)S(O)₂Me
C(O)OMe CH(CF₃)S(O)₂Et
C(O)OMe CH(CF₃)S(O)₂CF₃
C(O)OMe CH(CF₃)S(O)₂CH₂CF₃
C(O)OMe CH₂CH₂SMe
C(O)OMe CH₂CH₂SEt
C(O)OMe CH₂CH₂SCF₃
C(O)OMe CH₂CH₂SCH₂CF₃
C(O)OMe CH₂CH₂S(O)Me
C(O)OMe CH₂CH₂S(O)Et
C(O)OMe CH₂CH₂S(O)CF₃
C(O)OMe CH₂CH₂S(O)CH₂CF₃
C(O)OMe CH₂CH₂S(O)₂Me
C(O)OMe CH₂CH₂S(O)₂Et
C(O)OMe CH₂CH₂S(O)₂CF₃
C(O)OMe CH₂CH₂S(O)₂CH₂CF₃
C(O)OMe CH(Me)CH₂SMe
C(O)OMe CH(Me)CH₂SEt
C(O)OMe CH(Me)CH₂SCF₃
C(O)OMe CH(Me)CH₂SCH₂CF₃
C(O)OMe CH(Me)CH₂S(O)Me
C(O)OMe CH(Me)CH₂S(O)Et
C(O)OMe CH(Me)CH₂S(O)CF₃
C(O)OMe CH(Me)CH₂S(O)CH₂CF₃
C(O)OMe CH(Me)CH₂S(O)₂Me
C(O)OMe CH(Me)CH₂S(O)₂Et
C(O)OMe CH(Me)CH₂S(O)₂CF₃
C(O)OMe CH(Me)CH₂S(O)₂CH₂CF₃
C(O)OMe CH(Et)CH₂SMe
C(O)OMe CH(Et)CH₂SEt
C(O)OMe CH(Et)CH₂SCF₃
C(O)OMe CH(Et)CH₂SCH₂CF₃
C(O)OMe CH(Et)CH₂S(O)Me
C(O)OMe CH(Et)CH₂S(O)Et
C(O)OMe CH(Et)CH₂S(O)CF₃
C(O)OMe CH(Et)CH₂S(O)CH₂CF₃
C(O)OMe CH(Et)CH₂S(O)₂Me
C(O)OMe CH(Et)CH₂S(O)₂Et
C(O)OMe CH(Et)CH₂S(O)₂CF₃
C(O)OMe CH(Et)CH₂S(O)₂CH₂CF₃
C(O)OMe C(Me)₂CH₂SMe
C(O)OMe C(Me)₂CH₂SEt
C(O)OMe C(Me)₂CH₂SCF₃
C(O)OMe C(Me)₂CH₂SCH₂CF₃
C(O)OMe C(Me)₂CH₂S(O)Me
C(O)OMe C(Me)₂CH₂S(O)Et
C(O)OMe C(Me)₂CH₂S(O)CF₃
C(O)OMe C(Me)₂CH₂S(O)CH₂CF₃
C(O)OMe C(Me)₂CH₂S(O)₂Me
C(O)OMe C(Me)₂CH₂S(O)₂Et
C(O)OMe C(Me)₂CH₂S(O)₂CF₃
C(O)OMe C(Me)₂CH₂S(O)₂CH₂CF₃
C(O)OMe CH₂CH(Me)SMe
C(O)OMe CH₂CH(Me)SEt
C(O)OMe CH₂CH(Me)SCF₃
C(O)OMe CH₂CH(Me)SCH₂CF₃
C(O)OMe CH₂CH(Me)S(O)Me
C(O)OMe CH₂CH(Me)S(O)Et
C(O)OMe CH₂CH(Me)S(O)CF₃
C(O)OMe CH₂CH(Me)S(O)CH₂CF₃
C(O)OMe CH₂CH(Me)S(O)₂Me
C(O)OMe CH₂CH(Me)S(O)₂Et
C(O)OMe CH₂CH(Me)S(O)₂CF₃
C(O)OMe CH₂CH(Me)S(O)₂CH₂CF₃
C(O)OMe CH₂CH(Et)SMe
C(O)OMe CH₂CH(Et)SEt
C(O)OMe CH₂CH(Et)SCF₃
C(O)OMe CH₂CH(Et)SCH₂CF₃
C(O)OMe CH₂CH(Et)S(O)Me
C(O)OMe CH₂CH(Et)S(O)Et
C(O)OMe CH₂CH(Et)S(O)CF₃
C(O)OMe CH₂CH(Et)S(O)CH₂CF₃
C(O)OMe CH₂CH(Et)S(O)₂Me
C(O)OMe CH₂CH(Et)S(O)₂Et
C(O)OMe CH₂CH(Et)S(O)₂CF₃
C(O)OMe CH₂CH(Et)S(O)₂CH₂CF₃
C(O)OMe CH(Me)CH(Me)SMe
C(O)OMe CH(Me)CH(Me)SEt
C(O)OMe CH(Me)CH(Me)SCF₃
C(O)OMe CH(Me)CH(Me)SCH₂CF₃
C(O)OMe CH(Me)CH(Me)S(O)Me
C(O)OMe CH(Me)CH(Me)S(O)Et
C(O)OMe CH(Me)CH(Me)S(O)CF₃
C(O)OMe CH(Me)CH(Me)S(O)CH₂CF₃
C(O)OMe CH(Me)CH(Me)S(O)₂Me
C(O)OMe CH(Me)CH(Me)S(O)₂Et
C(O)OMe CH(Me)CH(Me)S(O)₂CF₃
C(O)OMe CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂OMe CH₂SMe
CH₂OMe CH₂SEt
CH₂OMe CH₂SCF₃
CH₂OMe CH₂SCH₂CF₃
CH₂OMe CH₂S(O)Me
CH₂OMe CH₂S(O)Et
CH₂OMe CH₂S(O)CF₃
CH₂OMe CH₂S(O)CH₂CF₃
CH₂OMe CH₂S(O)₂Me
CH₂OMe CH₂S(O)₂Et
CH₂OMe CH₂S(O)₂CF₃
CH₂OMe CH₂S(O)₂CH₂CF₃
CH₂OMe CH(Me)SMe
CH₂OMe CH(Me)SEt
CH₂OMe CH(Me)SCF₃
CH₂OMe CH(Me)SCH₂CF₃
CH₂OMe CH(Me)S(O)Me
CH₂OMe CH(Me)S(O)Et
CH₂OMe CH(Me)S(O)CF₃
CH₂OMe CH(Me)S(O)CH₂CF₃
CH₂OMe CH(Me)S(O)₂Me
CH₂OMe CH(Me)S(O)₂Et
CH₂OMe CH(Me)S(O)₂CF₃
CH₂OMe CH(Me)S(O)₂CH₂CF₃
CH₂OMe CH(Et)SMe
CH₂OMe CH(Et)SEt
CH₂OMe CH(Et)SCF₃
CH₂OMe CH(Et)SCH₂CF₃
CH₂OMe CH(Et)S(O)Me
CH₂OMe CH(Et)S(O)Et
CH₂OMe CH(Et)S(O)CF₃
CH₂OMe CH(Et)S(O)CH₂CF₃
CH₂OMe CH(Et)S(O)₂Me
CH₂OMe CH(Et)S(O)₂Et
CH₂OMe CH(Et)S(O)₂CF₃
CH₂OMe CH(Et)S(O)₂CH₂CF₃
CH₂OMe CH(n-Pr)SMe
CH₂OMe CH(n-Pr)SEt
CH₂OMe CH(n-Pr)SCF₃
CH₂OMe CH(n-Pr)SCH₂CF₃
CH₂OMe CH(n-Pr)S(O)Me
CH₂OMe CH(n-Pr)S(O)Et
CH₂OMe CH(n-Pr)S(O)CF₃
CH₂OMe CH(n-Pr)S(O)CH₂CF₃
CH₂OMe CH(n-Pr)S(O)₂Me
CH₂OMe CH(n-Pr)S(O)₂Et
CH₂OMe CH(n-Pr)S(O)₂CF₃
CH₂OMe CH(n-Pr)S(O)₂CH₂CF₃
CH₂OMe CH(i-Pr)SMe
CH₂OMe CH(i-Pr)SEt
CH₂OMe CH(i-Pr)SCF₃
CH₂OMe CH(i-Pr)SCH₂CF₃
CH₂OMe CH(i-Pr)S(O)Me
CH₂OMe CH(i-Pr)S(O)Et
CH₂OMe CH(i-Pr)S(O)CF₃
CH₂OMe CH(i-Pr)S(O)CH₂CF₃
CH₂OMe CH(i-Pr)S(O)₂Me
CH₂OMe CH(i-Pr)S(O)₂Et
CH₂OMe CH(i-Pr)S(O)₂CF₃
CH₂OMe CH(i-Pr)S(O)₂CH₂CF₃
CH₂OMe CH(n-Bu)SMe
CH₂OMe CH(n-Bu)SEt
CH₂OMe CH(n-Bu)SCF₃
CH₂OMe CH(n-Bu)SCH₂CF₃
CH₂OMe CH(n-Bu)S(O)Me
CH₂OMe CH(n-Bu)S(O)Et
CH₂OMe CH(n-Bu)S(O)CF₃
CH₂OMe CH(n-Bu)S(O)CH₂CF₃
CH₂OMe CH(n-Bu)S(O)₂Me
CH₂OMe CH(n-Bu)S(O)₂Et
CH₂OMe CH(n-Bu)S(O)₂CF₃
CH₂OMe CH(n-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(i-Bu)SMe
CH₂OMe CH(i-Bu)SEt
CH₂OMe CH(i-Bu)SCF₃
CH₂OMe CH(i-Bu)SCH₂CF₃
CH₂OMe CH(i-Bu)S(O)Me
CH₂OMe CH(i-Bu)S(O)Et
CH₂OMe CH(i-Bu)S(O)CF₃
CH₂OMe CH(i-Bu)S(O)CH₂CF₃
CH₂OMe CH(i-Bu)S(O)₂Me
CH₂OMe CH(i-Bu)S(O)₂Et
CH₂OMe CH(i-Bu)S(O)₂CF₃
CH₂OMe CH(i-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(s-Bu)SMe
CH₂OMe CH(s-Bu)SEt
CH₂OMe CH(s-Bu)SCF₃
CH₂OMe CH(s-Bu)SCH₂CF₃
CH₂OMe CH(s-Bu)S(O)Me
CH₂OMe CH(s-Bu)S(O)Et
CH₂OMe CH(s-Bu)S(O)CF₃
CH₂OMe CH(s-Bu)S(O)CH₂CF₃
CH₂OMe CH(s-Bu)S(O)₂Me
CH₂OMe CH(s-Bu)S(O)₂Et
CH₂OMe CH(s-Bu)S(O)₂CF₃
CH₂OMe CH(s-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(t-Bu)SMe
CH₂OMe CH(t-Bu)SEt
CH₂OMe CH(t-Bu)SCF₃
CH₂OMe CH(t-Bu)SCH₂CF₃
CH₂OMe CH(t-Bu)S(O)Me
CH₂OMe CH(t-Bu)S(O)Et
CH₂OMe CH(t-Bu)S(O)CF₃
CH₂OMe CH(t-Bu)S(O)CH₂CF₃
CH₂OMe CH(t-Bu)S(O)₂Me
CH₂OMe CH(t-Bu)S(O)₂Et
CH₂OMe CH(t-Bu)S(O)₂CF₃
CH₂OMe CH(t-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(CF₃)SMe
CH₂OMe CH(CF₃)SEt
CH₂OMe CH(CF₃)SCF₃
CH₂OMe CH(CF₃)SCH₂CF₃
CH₂OMe CH(CF₃)S(O)Me
CH₂OMe CH(CF₃)S(O)Et
CH₂OMe CH(CF₃)S(O)CF₃
CH₂OMe CH(CF₃)S(O)CH₂CF₃
CH₂OMe CH(CF₃)S(O)₂Me
CH₂OMe CH(CF₃)S(O)₂Et
CH₂OMe CH(CF₃)S(O)₂CF₃
CH₂OMe CH(CF₃)S(O)₂CH₂CF₃
CH₂OMe CH₂CH₂SMe
CH₂OMe CH₂CH₂SEt
CH₂OMe CH₂CH₂SCF₃
CH₂OMe CH₂CH₂SCH₂CF₃
CH₂OMe CH₂CH₂S(O)Me
CH₂OMe CH₂CH₂S(O)Et
CH₂OMe CH₂CH₂S(O)CF₃
CH₂OMe CH₂CH₂S(O)CH₂CF₃
CH₂OMe CH₂CH₂S(O)₂Me
CH₂OMe CH₂CH₂S(O)₂Et
CH₂OMe CH₂CH₂S(O)₂CF₃
CH₂OMe CH₂CH₂S(O)₂CH₂CF₃
CH₂OMe CH(Me)CH₂SMe
CH₂OMe CH(Me)CH₂SEt
CH₂OMe CH(Me)CH₂SCF₃
CH₂OMe CH(Me)CH₂SCH₂CF₃
CH₂OMe CH(Me)CH₂S(O)Me
CH₂OMe CH(Me)CH₂S(O)Et
CH₂OMe CH(Me)CH₂S(O)CF₃
CH₂OMe CH(Me)CH₂S(O)CH₂CF₃
CH₂OMe CH(Me)CH₂S(O)₂Me
CH₂OMe CH(Me)CH₂S(O)₂Et
CH₂OMe CH(Me)CH₂S(O)₂CF₃
CH₂OMe CH(Me)CH₂S(O)₂CH₂CF₃
CH₂OMe CH(Et)CH₂SMe
CH₂OMe CH(Et)CH₂SEt
CH₂OMe CH(Et)CH₂SCF₃
CH₂OMe CH(Et)CH₂SCH₂CF₃
CH₂OMe CH(Et)CH₂S(O)Me
CH₂OMe CH(Et)CH₂S(O)Et
CH₂OMe CH(Et)CH₂S(O)CF₃
CH₂OMe CH(Et)CH₂S(O)CH₂CF₃
CH₂OMe CH(Et)CH₂S(O)₂Me
CH₂OMe CH(Et)CH₂S(O)₂Et
CH₂OMe CH(Et)CH₂S(O)₂CF₃
CH₂OMe CH(Et)CH₂S(O)₂CH₂CF₃
CH₂OMe C(Me)₂CH₂SMe
CH₂OMe C(Me)₂CH₂SEt
CH₂OMe C(Me)₂CH₂SCF₃
CH₂OMe C(Me)₂CH₂SCH₂CF₃
CH₂OMe C(Me)₂CH₂S(O)Me
CH₂OMe C(Me)₂CH₂S(O)Et
CH₂OMe C(Me)₂CH₂S(O)CF₃
CH₂OMe C(Me)₂CH₂S(O)CH₂CF₃
CH₂OMe C(Me)₂CH₂S(O)₂Me
CH₂OMe C(Me)₂CH₂S(O)₂Et
CH₂OMe C(Me)₂CH₂S(O)₂CF₃
CH₂OMe C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂OMe CH₂CH(Me)SMe
CH₂OMe CH₂CH(Me)SEt
CH₂OMe CH₂CH(Me)SCF₃
CH₂OMe CH₂CH(Me)SCH₂CF₃
CH₂OMe CH₂CH(Me)S(O)Me
CH₂OMe CH₂CH(Me)S(O)Et
CH₂OMe CH₂CH(Me)S(O)CF₃
CH₂OMe CH₂CH(Me)S(O)CH₂CF₃
CH₂OMe CH₂CH(Me)S(O)₂Me
CH₂OMe CH₂CH(Me)S(O)₂Et
CH₂OMe CH₂CH(Me)S(O)₂CF₃
CH₂OMe CH₂CH(Me)S(O)₂CH₂CF₃
CH₂OMe CH₂CH(Et)SMe
CH₂OMe CH₂CH(Et)SEt
CH₂OMe CH₂CH(Et)SCF₃
CH₂OMe CH₂CH(Et)SCH₂CF₃
CH₂OMe CH₂CH(Et)S(O)Me
CH₂OMe CH₂CH(Et)S(O)Et
CH₂OMe CH₂CH(Et)S(O)CF₃
CH₂OMe CH₂CH(Et)S(O)CH₂CF₃
CH₂OMe CH₂CH(Et)S(O)₂Me
CH₂OMe CH₂CH(Et)S(O)₂Et
CH₂OMe CH₂CH(Et)S(O)₂CF₃
CH₂OMe CH₂CH(Et)S(O)₂CH₂CF₃
CH₂OMe CH(Me)CH(Me)SMe
CH₂OMe CH(Me)CH(Me)SEt
CH₂OMe CH(Me)CH(Me)SCF₃
CH₂OMe CH(Me)CH(Me)SCH₂CF₃
CH₂OMe CH(Me)CH(Me)S(O)Me
CH₂OMe CH(Me)CH(Me)S(O)Et
CH₂OMe CH(Me)CH(Me)S(O)CF₃
CH₂OMe CH(Me)CH(Me)S(O)CH₂CF₃
CH₂OMe CH(Me)CH(Me)S(O)₂Me
CH₂OMe CH(Me)CH(Me)S(O)₂Et
CH₂OMe CH(Me)CH(Me)S(O)₂CF₃
CH₂OMe CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂SMe CH₂SMe
CH₂SEt CH₂SMe
CH₂S(O)Me CH₂SMe
CH₂S(O)Et CH₂SMe
CH₂S(O)₂Me CH₂SMe
CH₂S(O)₂Et CH₂SMe
CH(Me)SMe CH₂SMe
CH(Me)SEt CH₂SMe
CH(Me)S(O)Me CH₂SMe
CH(Me)S(O)Et CH₂SMe
CH(Me)S(O)₂Me CH₂SMe
CH(Me)S(O)₂Et CH₂SMe
CH(Et)SMe CH₂SMe
CH(Et)SEt CH₂SMe
CH(Et)S(O)Me CH₂SMe
CH(Et)S(O)Et CH₂SMe
CH(Et)S(O)₂Me CH₂SMe
CH(Et)S(O)₂Et CH₂SMe
CH(n-Pr)SMe CH₂SMe
CH(n-Pr)SEt CH₂SMe
CH(n-Pr)S(O)Me CH₂SMe
CH(n-Pr)S(O)Et CH₂SMe
CH(n-Pr)S(O)₂Me CH₂SMe
CH(n-Pr)S(O)₂Et CH₂SMe
CH(i-Pr)SMe CH₂SMe
CH(i-Pr)SEt CH₂SMe
CH(i-Pr)S(O)Me CH₂SMe
CH(i-Pr)S(O)Et CH₂SMe
CH(i-Pr)S(O)₂Me CH₂SMe
CH(i-Pr)S(O)₂Et CH₂SMe
CH(n-Bu)SMe CH₂SMe
CH(n-Bu)SEt CH₂SMe
CH(n-Bu)S(O)Me CH₂SMe
CH(n-Bu)S(O)Et CH₂SMe
CH(n-Bu)S(O)₂Me CH₂SMe
CH(n-Bu)S(O)₂Et CH₂SMe
CH(i-Bu)SMe CH₂SMe
CH(i-Bu)SEt CH₂SMe
CH(i-Bu)S(O)Me CH₂SMe
CH(i-Bu)S(O)Et CH₂SMe
CH(i-Bu)S(O)₂Me CH₂SMe
CH(i-Bu)S(O)₂Et CH₂SMe
CH(s-Bu)SMe CH₂SMe
CH(s-Bu)SEt CH₂SMe
CH(s-Bu)S(O)Me CH₂SMe
CH(s-Bu)S(O)Et CH₂SMe
CH(s-Bu)S(O)₂Me CH₂SMe
CH(s-Bu)S(O)₂Et CH₂SMe
CH(t-Bu)SMe CH₂SMe
CH(t-Bu)SEt CH₂SMe
CH(t-Bu)S(O)Me CH₂SMe
CH(t-Bu)S(O)Et CH₂SMe
CH(t-Bu)S(O)₂Me CH₂SMe
CH(t-Bu)S(O)₂Et CH₂SMe
CH₂CH₂SMe CH₂SMe
CH₂CH₂SEt CH₂SMe
CH₂CH₂S(O)₂Me CH₂SMe
CH₂CH₂S(O)₂Et CH₂SMe
CH(Me)CH₂SMe CH₂SMe
CH(Me)CH₂SEt CH₂SMe
CH(Me)CH₂S(O)Me CH₂SMe
CH(Me)CH₂S(O)Et CH₂SMe
CH(Me)CH₂S(O)₂Me CH₂SMe
CH(Me)CH₂S(O)₂Et CH₂SMe
CH(Et)CH₂SMe CH₂SMe
CH(Et)CH₂SEt CH₂SMe
CH(Et)CH₂S(O)Me CH₂SMe
CH(Et)CH₂S(O)Et CH₂SMe
CH(Et)CH₂S(O)₂Me CH₂SMe
CH(Et)CH₂S(O)₂Et CH₂SMe
C(Me)₂CH₂SMe CH₂SMe
C(Me)₂CH₂SEt CH₂SMe
C(Me)₂CH₂S(O)Me CH₂SMe
C(Me)₂CH₂S(O)Et CH₂SMe
C(Me)₂CH₂S(O)₂Me CH₂SMe
C(Me)₂CH₂S(O)₂Et CH₂SMe
CH₂CH(Me)SMe CH₂SMe
CH₂CH(Me)SEt CH₂SMe
CH₂CH(Me)S(O)Me CH₂SMe
CH₂CH(Me)S(O)Et CH₂SMe
CH₂CH(Me)S(O)₂Me CH₂SMe
CH₂CH(Me)S(O)₂Et CH₂SMe
CH₂CH(Et)SMe CH₂SMe
CH₂CH(Et)SEt CH₂SMe
CH₂CH(Et)S(O)Me CH₂SMe
CH₂CH(Et)S(O)Et CH₂SMe
CH₂CH(Et)S(O)₂Me CH₂SMe
CH₂CH(Et)S(O)₂Et CH₂SMe
CH(Me)CH(Me)SMe CH₂SMe
CH(Me)CH(Me)SEt CH₂SMe
CH(Me)CH(Me)S(O)Me CH₂SMe
CH(Me)CH(Me)S(O)Et CH₂SMe
CH(Me)CH(Me)S(O)₂Me CH₂SMe
CH(Me)CH(Me)S(O)₂Et CH₂SMe
CH₂SMe CH₂S(O)Me
CH₂SEt CH₂S(O)Me
CH₂S(O)Me CH₂S(O)Me
CH₂S(O)Et CH₂S(O)Me
CH₂S(O)₂Me CH₂S(O)Me
CH₂S(O)₂Et CH₂S(O)Me
CH(Me)SMe CH₂S(O)Me
CH(Me)SEt CH₂S(O)Me
CH(Me)S(O)Me CH₂S(O)Me
CH(Me)S(O)Et CH₂S(O)Me
CH(Me)S(O)₂Me CH₂S(O)Me
CH(Me)S(O)₂Et CH₂S(O)Me
CH(Et)SMe CH₂S(O)Me
CH(Et)SEt CH₂S(O)Me
CH(Et)S(O)Me CH₂S(O)Me
CH(Et)S(O)Et CH₂S(O)Me
CH(Et)S(O)₂Me CH₂S(O)Me
CH(Et)S(O)₂Et CH₂S(O)Me
CH(n-Pr)SMe CH₂S(O)Me
CH(n-Pr)SEt CH₂S(O)Me
CH(n-Pr)S(O)Me CH₂S(O)Me
CH(n-Pr)S(O)Et CH₂S(O)Me
CH(n-Pr)S(O)₂Me CH₂S(O)Me
CH(n-Pr)S(O)₂Et CH₂S(O)Me
CH(i-Pr)SMe CH₂S(O)Me
CH(i-Pr)SEt CH₂S(O)Me
CH(i-Pr)S(O)Me CH₂S(O)Me
CH(i-Pr)S(O)Et CH₂S(O)Me
CH(i-Pr)S(O)₂Me CH₂S(O)Me
CH(i-Pr)S(O)₂Et CH₂S(O)Me
CH(n-Bu)SMe CH₂S(O)Me
CH(n-Bu)SEt CH₂S(O)Me
CH(n-Bu)S(O)Me CH₂S(O)Me
CH(n-Bu)S(O)Et CH₂S(O)Me
CH(n-Bu)S(O)₂Me CH₂S(O)Me
CH(n-Bu)S(O)₂Et CH₂S(O)Me
CH(i-Bu)SMe CH₂S(O)Me
CH(i-Bu)SEt CH₂S(O)Me
CH(i-Bu)S(O)Me CH₂S(O)Me
CH(i-Bu)S(O)Et CH₂S(O)Me
CH(i-Bu)S(O)₂Me CH₂S(O)Me
CH(i-Bu)S(O)₂Et CH₂S(O)Me
CH(s-Bu)SMe CH₂S(O)Me
CH(s-Bu)SEt CH₂S(O)Me
CH(s-Bu)S(O)Me CH₂S(O)Me
CH(s-Bu)S(O)Et CH₂S(O)Me
CH(s-Bu)S(O)₂Me CH₂S(O)Me
CH(s-Bu)S(O)₂Et CH₂S(O)Me
CH(t-Bu)SMe CH₂S(O)Me
CH(t-Bu)SEt CH₂S(O)Me
CH(t-Bu)S(O)Me CH₂S(O)Me
CH(t-Bu)S(O)Et CH₂S(O)Me
CH(t-Bu)S(O)₂Me CH₂S(O)Me
CH(t-Bu)S(O)₂Et CH₂S(O)Me
CH₂CH₂SMe CH₂S(O)Me
CH₂CH₂SEt CH₂S(O)Me
CH₂CH₂S(O)₂Me CH₂S(O)Me
CH₂CH₂S(O)₂Et CH₂S(O)Me
CH(Me)CH₂SMe CH₂S(O)Me
CH(Me)CH₂SEt CH₂S(O)Me
CH(Me)CH₂S(O)Me CH₂S(O)Me
CH(Me)CH₂S(O)Et CH₂S(O)Me
CH(Me)CH₂S(O)₂Me CH₂S(O)Me
CH(Me)CH₂S(O)₂Et CH₂S(O)Me
CH(Et)CH₂SMe CH₂S(O)Me
CH(Et)CH₂SEt CH₂S(O)Me
CH(Et)CH₂S(O)Me CH₂S(O)Me
CH(Et)CH₂S(O)Et CH₂S(O)Me
CH(Et)CH₂S(O)₂Me CH₂S(O)Me
CH(Et)CH₂S(O)₂Et CH₂S(O)Me
C(Me)₂CH₂SMe CH₂S(O)Me
C(Me)₂CH₂SEt CH₂S(O)Me
C(Me)₂CH₂S(O)Me CH₂S(O)Me
C(Me)₂CH₂S(O)Et CH₂S(O)Me
C(Me)₂CH₂S(O)₂Me CH₂S(O)Me
C(Me)₂CH₂S(O)₂Et CH₂S(O)Me
CH₂CH(Me)SMe CH₂S(O)Me
CH₂CH(Me)SEt CH₂S(O)Me
CH₂CH(Me)S(O)Me CH₂S(O)Me
CH₂CH(Me)S(O)Et CH₂S(O)Me
CH₂CH(Me)S(O)₂Me CH₂S(O)Me
CH₂CH(Me)S(O)₂Et CH₂S(O)Me
CH₂CH(Et)SMe CH₂S(O)Me
CH₂CH(Et)SEt CH₂S(O)Me
CH₂CH(Et)S(O)Me CH₂S(O)Me
CH₂CH(Et)S(O)Et CH₂S(O)Me
CH₂CH(Et)S(O)₂Me CH₂S(O)Me
CH₂CH(Et)S(O)₂Et CH₂S(O)Me
CH(Me)CH(Me)SMe CH₂S(O)Me
CH(Me)CH(Me)SEt CH₂S(O)Me
CH(Me)CH(Me)S(O)Me CH₂S(O)Me
CH(Me)CH(Me)S(O)Et CH₂S(O)Me
CH(Me)CH(Me)S(O)₂Me CH₂S(O)Me
CH(Me)CH(Me)S(O)₂Et CH₂S(O)Me
CH₂SMe CH₂S(O)₂Me
CH₂SEt CH₂S(O)₂Me
CH₂S(O)Me CH₂S(O)₂Me
CH₂S(O)Et CH₂S(O)₂Me
CH₂S(O)₂Me CH₂S(O)₂Me
CH₂S(O)₂Et CH₂S(O)₂Me
CH(Me)SMe CH₂S(O)₂Me
CH(Me)SEt CH₂S(O)₂Me
CH(Me)S(O)Me CH₂S(O)₂Me
CH(Me)S(O)Et CH₂S(O)₂Me
CH(Me)S(O)₂Me CH₂S(O)₂Me
CH(Me)S(O)₂Et CH₂S(O)₂Me
CH(Et)SMe CH₂S(O)₂Me
CH(Et)SEt CH₂S(O)₂Me
CH(Et)S(O)Me CH₂S(O)₂Me
CH(Et)S(O)Et CH₂S(O)₂Me
CH(Et)S(O)₂Me CH₂S(O)₂Me
CH(Et)S(O)₂Et CH₂S(O)₂Me
CH(n-Pr)SMe CH₂S(O)₂Me
CH(n-Pr)SEt CH₂S(O)₂Me
CH(n-Pr)S(O)Me CH₂S(O)₂Me
CH(n-Pr)S(O)Et CH₂S(O)₂Me
CH(n-Pr)S(O)₂Me CH₂S(O)₂Me
CH(n-Pr)S(O)₂Et CH₂S(O)₂Me
CH(i-Pr)SMe CH₂S(O)₂Me
CH(i-Pr)SEt CH₂S(O)₂Me
CH(i-Pr)S(O)Me CH₂S(O)₂Me
CH(i-Pr)S(O)Et CH₂S(O)₂Me
CH(i-Pr)S(O)₂Me CH₂S(O)₂Me
CH(i-Pr)S(O)₂Et CH₂S(O)₂Me
CH(n-Bu)SMe CH₂S(O)₂Me
CH(n-Bu)SEt CH₂S(O)₂Me
CH(n-Bu)S(O)Me CH₂S(O)₂Me
CH(n-Bu)S(O)Et CH₂S(O)₂Me
CH(n-Bu)S(O)₂Me CH₂S(O)₂Me
CH(n-Bu)S(O)₂Et CH₂S(O)₂Me
CH(i-Bu)SMe CH₂S(O)₂Me
CH(i-Bu)SEt CH₂S(O)₂Me
CH(i-Bu)S(O)Me CH₂S(O)₂Me
CH(i-Bu)S(O)Et CH₂S(O)₂Me
CH(i-Bu)S(O)₂Me CH₂S(O)₂Me
CH(i-Bu)S(O)₂Et CH₂S(O)₂Me
CH(s-Bu)SMe CH₂S(O)₂Me
CH(s-Bu)SEt CH₂S(O)₂Me
CH(s-Bu)S(O)Me CH₂S(O)₂Me
CH(s-Bu)S(O)Et CH₂S(O)₂Me
CH(s-Bu)S(O)₂Me CH₂S(O)₂Me
CH(s-Bu)S(O)₂Et CH₂S(O)₂Me
CH(t-Bu)SMe CH₂S(O)₂Me
CH(t-Bu)SEt CH₂S(O)₂Me
CH(t-Bu)S(O)Me CH₂S(O)₂Me
CH(t-Bu)S(O)Et CH₂S(O)₂Me
CH(t-Bu)S(O)₂Me CH₂S(O)₂Me
CH(t-Bu)S(O)₂Et CH₂S(O)₂Me
CH₂CH₂SMe CH₂S(O)₂Me
CH₂CH₂SEt CH₂S(O)₂Me
CH₂CH₂S(O)₂Me CH₂S(O)₂Me
CH₂CH₂S(O)₂Et CH₂S(O)₂Me
CH(Me)CH₂SMe CH₂S(O)₂Me
CH(Me)CH₂SEt CH₂S(O)₂Me
CH(Me)CH₂S(O)Me CH₂S(O)₂Me
CH(Me)CH₂S(O)Et CH₂S(O)₂Me
CH(Me)CH₂S(O)₂Me CH₂S(O)₂Me
CH(Me)CH₂S(O)₂Et CH₂S(O)₂Me
CH(Et)CH₂SMe CH₂S(O)₂Me
CH(Et)CH₂SEt CH₂S(O)₂Me
CH(Et)CH₂S(O)Me CH₂S(O)₂Me
CH(Et)CH₂S(O)Et CH₂S(O)₂Me
CH(Et)CH₂S(O)₂Me CH₂S(O)₂Me
CH(Et)CH₂S(O)₂Et CH₂S(O)₂Me
C(Me)₂CH₂SMe CH₂S(O)₂Me
C(Me)₂CH₂SEt CH₂S(O)₂Me
C(Me)₂CH₂S(O)Me CH₂S(O)₂Me
C(Me)₂CH₂S(O)Et CH₂S(O)₂Me
C(Me)₂CH₂S(O)₂Me CH₂S(O)₂Me
C(Me)₂CH₂S(O)₂Et CH₂S(O)₂Me
CH₂CH(Me)SMe CH₂S(O)₂Me
CH₂CH(Me)SEt CH₂S(O)₂Me
CH₂CH(Me)S(O)Me CH₂S(O)₂Me
CH₂CH(Me)S(O)Et CH₂S(O)₂Me
CH₂CH(Me)S(O)₂Me CH₂S(O)₂Me
CH₂CH(Me)S(O)₂Et CH₂S(O)₂Me
CH₂CH(Et)SMe CH₂S(O)₂Me
CH₂CH(Et)SEt CH₂S(O)₂Me
CH₂CH(Et)S(O)Me CH₂S(O)₂Me
CH₂CH(Et)S(O)Et CH₂S(O)₂Me
CH₂CH(Et)S(O)₂Me CH₂S(O)₂Me
CH₂CH(Et)S(O)₂Et CH₂S(O)₂Me
CH(Me)CH(Me)SMe CH₂S(O)₂Me
CH(Me)CH(Me)SEt CH₂S(O)₂Me
CH(Me)CH(Me)S(O)Me CH₂S(O)₂Me
CH(Me)CH(Me)S(O)Et CH₂S(O)₂Me
CH(Me)CH(Me)S(O)₂Me CH₂S(O)₂Me
CH(Me)CH(Me)S(O)₂Et CH₂S(O)₂Me
CH₂SMe SMe
CH₂SEt SMe
CH₂S(O)Me SMe
CH₂S(O)Et SMe
CH₂S(O)₂Me SMe
CH₂S(O)₂Et SMe
CH(Me)SMe SMe
CH(Me)SEt SMe
CH(Me)S(O)Me SMe
CH(Me)S(O)Et SMe
CH(Me)S(O)₂Me SMe
CH(Me)S(O)₂Et SMe
CH(Et)SMe SMe
CH(Et)SEt SMe
CH(Et)S(O)Me SMe
CH(Et)S(O)Et SMe
CH(Et)S(O)₂Me SMe
CH(Et)S(O)₂Et SMe
CH(n-Pr)SMe SMe
CH(n-Pr)SEt SMe
CH(n-Pr)S(O)Me SMe
CH(n-Pr)S(O)Et SMe
CH(n-Pr)S(O)₂Me SMe
CH(n-Pr)S(O)₂Et SMe
CH(i-Pr)SMe SMe
CH(i-Pr)SEt SMe
CH(i-Pr)S(O)Me SMe
CH(i-Pr)S(O)Et SMe
CH(i-Pr)S(O)₂Me SMe
CH(i-Pr)S(O)₂Et SMe
CH(n-Bu)SMe SMe
CH(n-Bu)SEt SMe
CH(n-Bu)S(O)Me SMe
CH(n-Bu)S(O)Et SMe
CH(n-Bu)S(O)₂Me SMe
CH(n-Bu)S(O)₂Et SMe
CH(i-Bu)SMe SMe
CH(i-Bu)SEt SMe
CH(i-Bu)S(O)Me SMe
CH(i-Bu)S(O)Et SMe
CH(i-Bu)S(O)₂Me SMe
CH(i-Bu)S(O)₂Et SMe
CH(s-Bu)SMe SMe
CH(s-Bu)SEt SMe
CH(s-Bu)S(O)Me SMe
CH(s-Bu)S(O)Et SMe
CH(s-Bu)S(O)₂Me SMe
CH(s-Bu)S(O)₂Et SMe
CH(t-Bu)SMe SMe
CH(t-Bu)SEt SMe
CH(t-Bu)S(O)Me SMe
CH(t-Bu)S(O)Et SMe
CH(t-Bu)S(O)₂Me SMe
CH(t-Bu)S(O)₂Et SMe
CH₂CH₂SMe SMe
CH₂CH₂SEt SMe
CH₂CH₂S(O)₂Me SMe
CH₂CH₂S(O)₂Et SMe
CH(Me)CH₂SMe SMe
CH(Me)CH₂SEt SMe
CH(Me)CH₂S(O)Me SMe
CH(Me)CH₂S(O)Et SMe
CH(Me)CH₂S(O)₂Me SMe
CH(Me)CH₂S(O)₂Et SMe
CH(Et)CH₂SMe SMe
CH(Et)CH₂SEt SMe
CH(Et)CH₂S(O)Me SMe
CH(Et)CH₂S(O)Et SMe
CH(Et)CH₂S(O)₂Me SMe
CH(Et)CH₂S(O)₂Et SMe
C(Me)₂CH₂SMe SMe
C(Me)₂CH₂SEt SMe
C(Me)₂CH₂S(O)Me SMe
C(Me)₂CH₂S(O)Et SMe
C(Me)₂CH₂S(O)₂Me SMe
C(Me)₂CH₂S(O)₂Et SMe
CH₂CH(Me)SMe SMe
CH₂CH(Me)SEt SMe
CH₂CH(Me)S(O)Me SMe
CH₂CH(Me)S(O)Et SMe
CH₂CH(Me)S(O)₂Me SMe
CH₂CH(Me)S(O)₂Et SMe
CH₂CH(Et)SMe SMe
CH₂CH(Et)SEt SMe
CH₂CH(Et)S(O)Me SMe
CH₂CH(Et)S(O)Et SMe
CH₂CH(Et)S(O)₂Me SMe
CH₂CH(Et)S(O)₂Et SMe
CH(Me)CH(Me)SMe SMe
CH(Me)CH(Me)SEt SMe
CH(Me)CH(Me)S(O)Me SMe
CH(Me)CH(Me)S(O)Et SMe
CH(Me)CH(Me)S(O)₂Me SMe
CH(Me)CH(Me)S(O)₂Et SMe
CH₂SMe S(O)Me
CH₂SEt S(O)Me
CH₂S(O)Me S(O)Me
CH₂S(O)Et S(O)Me
CH₂S(O)₂Me S(O)Me
CH₂S(O)₂Et S(O)Me
CH(Me)SMe S(O)Me
CH(Me)SEt S(O)Me
CH(Me)S(O)Me S(O)Me
CH(Me)S(O)Et S(O)Me
CH(Me)S(O)₂Me S(O)Me
CH(Me)S(O)₂Et S(O)Me
CH(Et)SMe S(O)Me
CH(Et)SEt S(O)Me
CH(Et)S(O)Me S(O)Me
CH(Et)S(O)Et S(O)Me
CH(Et)S(O)₂Me S(O)Me
CH(Et)S(O)₂Et S(O)Me
CH(n-Pr)SMe S(O)Me
CH(n-Pr)SEt S(O)Me
CH(n-Pr)S(O)Me S(O)Me
CH(n-Pr)S(O)Et S(O)Me
CH(n-Pr)S(O)₂Me S(O)Me
CH(n-Pr)S(O)₂Et S(O)Me
CH(i-Pr)SMe S(O)Me
CH(i-Pr)SEt S(O)Me
CH(i-Pr)S(O)Me S(O)Me
CH(i-Pr)S(O)Et S(O)Me
CH(i-Pr)S(O)₂Me S(O)Me
CH(i-Pr)S(O)₂Et S(O)Me
CH(n-Bu)SMe S(O)Me
CH(n-Bu)SEt S(O)Me
CH(n-Bu)S(O)Me S(O)Me
CH(n-Bu)S(O)Et S(O)Me
CH(n-Bu)S(O)₂Me S(O)Me
CH(n-Bu)S(O)₂Et S(O)Me
CH(i-Bu)SMe S(O)Me
CH(i-Bu)SEt S(O)Me
CH(i-Bu)S(O)Me S(O)Me
CH(i-Bu)S(O)Et S(O)Me
CH(i-Bu)S(O)₂Me S(O)Me
CH(i-Bu)S(O)₂Et S(O)Me
CH(s-Bu)SMe S(O)Me
CH(s-Bu)SEt S(O)Me
CH(s-Bu)S(O)Me S(O)Me
CH(s-Bu)S(O)Et S(O)Me
CH(s-Bu)S(O)₂Me S(O)Me
CH(s-Bu)S(O)₂Et S(O)Me
CH(t-Bu)SMe S(O)Me
CH(t-Bu)SEt S(O)Me
CH(t-Bu)S(O)Me S(O)Me
CH(t-Bu)S(O)Et S(O)Me
CH(t-Bu)S(O)₂Me S(O)Me
CH(t-Bu)S(O)₂Et S(O)Me
CH₂CH₂SMe S(O)Me
CH₂CH₂SEt S(O)Me
CH₂CH₂S(O)₂Me S(O)Me
CH₂CH₂S(O)₂Et S(O)Me
CH(Me)CH₂SMe S(O)Me
CH(Me)CH₂SEt S(O)Me
CH(Me)CH₂S(O)Me S(O)Me
CH(Me)CH₂S(O)Et S(O)Me
CH(Me)CH₂S(O)₂Me S(O)Me
CH(Me)CH₂S(O)₂Et S(O)Me
CH(Et)CH₂SMe S(O)Me
CH(Et)CH₂SEt S(O)Me
CH(Et)CH₂S(O)Me S(O)Me
CH(Et)CH₂S(O)Et S(O)Me
CH(Et)CH₂S(O)₂Me S(O)Me
CH(Et)CH₂S(O)₂Et S(O)Me
C(Me)₂CH₂SMe S(O)Me
C(Me)₂CH₂SEt S(O)Me
C(Me)₂CH₂S(O)Me S(O)Me
C(Me)₂CH₂S(O)Et S(O)Me
C(Me)₂CH₂S(O)₂Me S(O)Me
C(Me)₂CH₂S(O)₂Et S(O)Me
CH₂CH(Me)SMe S(O)Me
CH₂CH(Me)SEt S(O)Me
CH₂CH(Me)S(O)Me S(O)Me
CH₂CH(Me)S(O)Et S(O)Me
CH₂CH(Me)S(O)₂Me S(O)Me
CH₂CH(Me)S(O)₂Et S(O)Me
CH₂CH(Et)SMe S(O)Me
CH₂CH(Et)SEt S(O)Me
CH₂CH(Et)S(O)Me S(O)Me
CH₂CH(Et)S(O)Et S(O)Me
CH₂CH(Et)S(O)₂Me S(O)Me
CH₂CH(Et)S(O)₂Et S(O)Me
CH(Me)CH(Me)SMe S(O)Me
CH(Me)CH(Me)SEt S(O)Me
CH(Me)CH(Me)S(O)Me S(O)Me
CH(Me)CH(Me)S(O)Et S(O)Me
CH(Me)CH(Me)S(O)₂Me S(O)Me
CH(Me)CH(Me)S(O)₂Et S(O)Me
CH₂SMe S(O)₂Me
CH₂SEt S(O)₂Me
CH₂S(O)Me S(O)₂Me
CH₂S(O)Et S(O)₂Me
CH₂S(O)₂Me S(O)₂Me
CH₂S(O)₂Et S(O)₂Me
CH(Me)SMe S(O)₂Me
CH(Me)SEt S(O)₂Me
CH(Me)S(O)Me S(O)₂Me
CH(Me)S(O)Et S(O)₂Me
CH(Me)S(O)₂Me S(O)₂Me
CH(Me)S(O)₂Et S(O)₂Me
CH(Et)SMe S(O)₂Me
CH(Et)SEt S(O)₂Me
CH(Et)S(O)Me S(O)₂Me
CH(Et)S(O)Et S(O)₂Me
CH(Et)S(O)₂Me S(O)₂Me
CH(Et)S(O)₂Et S(O)₂Me
CH(n-Pr)SMe S(O)₂Me
CH(n-Pr)SEt S(O)₂Me
CH(n-Pr)S(O)Me S(O)₂Me
CH(n-Pr)S(O)Et S(O)₂Me
CH(n-Pr)S(O)₂Me S(O)₂Me
CH(n-Pr)S(O)₂Et S(O)₂Me
CH(i-Pr)SMe S(O)₂Me
CH(i-Pr)SEt S(O)₂Me
CH(i-Pr)S(O)Me S(O)₂Me
CH(i-Pr)S(O)Et S(O)₂Me
CH(i-Pr)S(O)₂Me S(O)₂Me
CH(i-Pr)S(O)₂Et S(O)₂Me
CH(n-Bu)SMe S(O)₂Me
CH(n-Bu)SEt S(O)₂Me
CH(n-Bu)S(O)Me S(O)₂Me
CH(n-Bu)S(O)Et S(O)₂Me
CH(n-Bu)S(O)₂Me S(O)₂Me
CH(n-Bu)S(O)₂Et S(O)₂Me
CH(i-Bu)SMe S(O)₂Me
CH(i-Bu)SEt S(O)₂Me
CH(i-Bu)S(O)Me S(O)₂Me
CH(i-Bu)S(O)Et S(O)₂Me
CH(i-Bu)S(O)₂Me S(O)₂Me
CH(i-Bu)S(O)₂Et S(O)₂Me
CH(s-Bu)SMe S(O)₂Me
CH(s-Bu)SEt S(O)₂Me
CH(s-Bu)S(O)Me S(O)₂Me
CH(s-Bu)S(O)Et S(O)₂Me
CH(s-Bu)S(O)₂Me S(O)₂Me
CH(s-Bu)S(O)₂Et S(O)₂Me
CH(t-Bu)SMe S(O)₂Me
CH(t-Bu)SEt S(O)₂Me
CH(t-Bu)S(O)Me S(O)₂Me
CH(t-Bu)S(O)Et S(O)₂Me
CH(t-Bu)S(O)₂Me S(O)₂Me
CH(t-Bu)S(O)₂Et S(O)₂Me
CH₂CH₂SMe S(O)₂Me
CH₂CH₂SEt S(O)₂Me
CH₂CH₂S(O)₂Me S(O)₂Me
CH₂CH₂S(O)₂Et S(O)₂Me
CH(Me)CH₂SMe S(O)₂Me
CH(Me)CH₂SEt S(O)₂Me
CH(Me)CH₂S(O)Me S(O)₂Me
CH(Me)CH₂S(O)Et S(O)₂Me
CH(Me)CH₂S(O)₂Me S(O)₂Me
CH(Me)CH₂S(O)₂Et S(O)₂Me
CH(Et)CH₂SMe S(O)₂Me
CH(Et)CH₂SEt S(O)₂Me
CH(Et)CH₂S(O)Me S(O)₂Me
CH(Et)CH₂S(O)Et S(O)₂Me
CH(Et)CH₂S(O)₂Me S(O)₂Me
CH(Et)CH₂S(O)₂Et S(O)₂Me
C(Me)₂CH₂SMe S(O)₂Me
C(Me)₂CH₂SEt S(O)₂Me
C(Me)₂CH₂S(O)Me S(O)₂Me
C(Me)₂CH₂S(O)Et S(O)₂Me
C(Me)₂CH₂S(O)₂Me S(O)₂Me
C(Me)₂CH₂S(O)₂Et S(O)₂Me
CH₂CH(Me)SMe S(O)₂Me
CH₂CH(Me)SEt S(O)₂Me
CH₂CH(Me)S(O)Me S(O)₂Me
CH₂CH(Me)S(O)Et S(O)₂Me
CH₂CH(Me)S(O)₂Me S(O)₂Me
CH₂CH(Me)S(O)₂Et S(O)₂Me
CH₂CH(Et)SMe S(O)₂Me
CH₂CH(Et)SEt S(O)₂Me
CH₂CH(Et)S(O)Me S(O)₂Me
CH₂CH(Et)S(O)Et S(O)₂Me
CH₂CH(Et)S(O)₂Me S(O)₂Me
CH₂CH(Et)S(O)₂Et S(O)₂Me
CH(Me)CH(Me)SMe S(O)₂Me
CH(Me)CH(Me)SEt S(O)₂Me
CH(Me)CH(Me)S(O)Me S(O)₂Me
CH(Me)CH(Me)S(O)Et S(O)₂Me
CH(Me)CH(Me)S(O)₂Me S(O)₂Me
CH(Me)CH(Me)S(O)₂Et S(O)₂Me
CH₂SMe H
CH₂SEt H
CH₂S(O)Me H
CH₂S(O)Et H
CH₂S(O)₂Me H
CH₂S(O)₂Et H
CH(Me)SMe H
CH(Me)SEt H
CH(Me)S(O)Me H
CH(Me)S(O)Et H
CH(Me)S(O)₂Me H
CH(Me)S(O)₂Et H
CH(Et)SMe H
CH(Et)SEt H
CH(Et)S(O)Me H
CH(Et)S(O)Et H
CH(Et)S(O)₂Me H
CH(Et)S(O)₂Et H
CH(n-Pr)SMe H
CH(n-Pr)SEt H
CH(n-Pr)S(O)Me H
CH(n-Pr)S(O)Et H
CH(n-Pr)S(O)₂Me H
CH(n-Pr)S(O)₂Et H
CH(i-Pr)SMe H
CH(i-Pr)SEt H
CH(i-Pr)S(O)Me H
CH(i-Pr)S(O)Et H
CH(i-Pr)S(O)₂Me H
CH(i-Pr)S(O)₂Et H
CH(n-Bu)SMe H
CH(n-Bu)SEt H
CH(n-Bu)S(O)Me H
CH(n-Bu)S(O)Et H
CH(n-Bu)S(O)₂Me H
CH(n-Bu)S(O)₂Et H
CH(i-Bu)SMe H
CH(i-Bu)SEt H
CH(i-Bu)S(O)Me H
CH(i-Bu)S(O)Et H
CH(i-Bu)S(O)₂Me H
CH(i-Bu)S(O)₂Et H
CH(s-Bu)SMe H
CH(s-Bu)SEt H
CH(s-Bu)S(O)Me H
CH(s-Bu)S(O)Et H
CH(s-Bu)S(O)₂Me H
CH(s-Bu)S(O)₂Et H
CH(t-Bu)SMe H
CH(t-Bu)SEt H
CH(t-Bu)S(O)Me H
CH(t-Bu)S(O)Et H
CH(t-Bu)S(O)₂Me H
CH(t-Bu)S(O)₂Et H
CH₂CH₂SMe H
CH₂CH₂SEt H
CH₂CH₂S(O)₂Me H
CH₂CH₂S(O)₂Et H
CH(Me)CH₂SMe H
CH(Me)CH₂SEt H
CH(Me)CH₂S(O)Me H
CH(Me)CH₂S(O)Et H
CH(Me)CH₂S(O)₂Me H
CH(Me)CH₂S(O)₂Et H
CH(Et)CH₂SMe H
CH(Et)CH₂SEt H
CH(Et)CH₂S(O)Me H
CH(Et)CH₂S(O)Et H
CH(Et)CH₂S(O)₂Me H
CH(Et)CH₂S(O)₂Et H
C(Me)₂CH₂SMe H
C(Me)₂CH₂SEt H
C(Me)₂CH₂S(O)Me H
C(Me)₂CH₂S(O)Et H
C(Me)₂CH₂S(O)₂Me H
C(Me)₂CH₂S(O)₂Et H
CH₂CH(Me)SMe H
CH₂CH(Me)SEt H
CH₂CH(Me)S(O)Me H
CH₂CH(Me)S(O)Et H
CH₂CH(Me)S(O)₂Me H
CH₂CH(Me)S(O)₂Et H
CH₂CH(Et)SMe H
CH₂CH(Et)SEt H
CH₂CH(Et)S(O)Me H
CH₂CH(Et)S(O)Et H
CH₂CH(Et)S(O)₂Me H
CH₂CH(Et)S(O)₂Et H
CH(Me)CH(Me)SMe H
CH(Me)CH(Me)SEt H
CH(Me)CH(Me)S(O)Me H
CH(Me)CH(Me)S(O)Et H
CH(Me)CH(Me)S(O)₂Me H
CH(Me)CH(Me)S(O)₂Et H
CH₂SMe Me
CH₂SEt Me
CH₂S(O)Me Me
CH₂S(O)Et Me
CH₂S(O)₂Me Me
CH₂S(O)₂Et Me
CH(Me)SMe Me
CH(Me)SEt Me
CH(Me)S(O)Me Me
CH(Me)S(O)Et Me
CH(Me)S(O)₂Me Me
CH(Me)S(O)₂Et Me
CH(Et)SMe Me
CH(Et)SEt Me
CH(Et)S(O)Me Me
CH(Et)S(O)Et Me
CH(Et)S(O)₂Me Me
CH(Et)S(O)₂Et Me
CH(n-Pr)SMe Me
CH(n-Pr)SEt Me
CH(n-Pr)S(O)Me Me
CH(n-Pr)S(O)Et Me
CH(n-Pr)S(O)₂Me Me
CH(n-Pr)S(O)₂Et Me
CH(i-Pr)SMe Me
CH(i-Pr)SEt Me
CH(i-Pr)S(O)Me Me
CH(i-Pr)S(O)Et Me
CH(i-Pr)S(O)₂Me Me
CH(i-Pr)S(O)₂Et Me
CH(n-Bu)SMe Me
CH(n-Bu)SEt Me
CH(n-Bu)S(O)Me Me
CH(n-Bu)S(O)Et Me
CH(n-Bu)S(O)₂Me Me
CH(n-Bu)S(O)₂Et Me
CH(i-Bu)SMe Me
CH(i-Bu)SEt Me
CH(i-Bu)S(O)Me Me
CH(i-Bu)S(O)Et Me
CH(i-Bu)S(O)₂Me Me
CH(i-Bu)S(O)₂Et Me
CH(s-Bu)SMe Me
CH(s-Bu)SEt Me
CH(s-Bu)S(O)Me Me
CH(s-Bu)S(O)Et Me
CH(s-Bu)S(O)₂Me Me
CH(s-Bu)S(O)₂Et Me
CH(t-Bu)SMe Me
CH(t-Bu)SEt Me
CH(t-Bu)S(O)Me Me
CH(t-Bu)S(O)Et Me
CH(t-Bu)S(O)₂Me Me
CH(t-Bu)S(O)₂Et Me
CH₂CH₂SMe Me
CH₂CH₂SEt Me
CH₂CH₂S(O)₂Me Me
CH₂CH₂S(O)₂Et Me
CH(Me)CH₂SMe Me
CH(Me)CH₂SEt Me
CH(Me)CH₂S(O)Me Me
CH(Me)CH₂S(O)Et Me
CH(Me)CH₂S(O)₂Me Me
CH(Me)CH₂S(O)₂Et Me
CH(Et)CH₂SMe Me
CH(Et)CH₂SEt Me
CH(Et)CH₂S(O)Me Me
CH(Et)CH₂S(O)Et Me
CH(Et)CH₂S(O)₂Me Me
CH(Et)CH₂S(O)₂Et Me
C(Me)₂CH₂SMe Me
C(Me)₂CH₂SEt Me
C(Me)₂CH₂S(O)Me Me
C(Me)₂CH₂S(O)Et Me
C(Me)₂CH₂S(O)₂Me Me
C(Me)₂CH₂S(O)₂Et Me
CH₂CH(Me)SMe Me
CH₂CH(Me)SEt Me
CH₂CH(Me)S(O)Me Me
CH₂CH(Me)S(O)Et Me
CH₂CH(Me)S(O)₂Me Me
CH₂CH(Me)S(O)₂Et Me
CH₂CH(Et)SMe Me
CH₂CH(Et)SEt Me
CH₂CH(Et)S(O)Me Me
CH₂CH(Et)S(O)Et Me
CH₂CH(Et)S(O)₂Me Me
CH₂CH(Et)S(O)₂Et Me
CH(Me)CH(Me)SMe Me
CH(Me)CH(Me)SEt Me
CH(Me)CH(Me)S(O)Me Me
CH(Me)CH(Me)S(O)Et Me
CH(Me)CH(Me)S(O)₂Me Me
CH(Me)CH(Me)S(O)₂Et Me
CH₂SMe CF₃
CH₂SEt CF₃
CH₂S(O)Me CF₃
CH₂S(O)Et CF₃
CH₂S(O)₂Me CF₃
CH₂S(O)₂Et CF₃
CH(Me)SMe CF₃
CH(Me)SEt CF₃
CH(Me)S(O)Me CF₃
CH(Me)S(O)Et CF₃
CH(Me)S(O)₂Me CF₃
CH(Me)S(O)₂Et CF₃
CH(Et)SMe CF₃
CH(Et)SEt CF₃
CH(Et)S(O)Me CF₃
CH(Et)S(O)Et CF₃
CH(Et)S(O)₂Me CF₃
CH(Et)S(O)₂Et CF₃
CH(n-Pr)SMe CF₃
CH(n-Pr)SEt CF₃
CH(n-Pr)S(O)Me CF₃
CH(n-Pr)S(O)Et CF₃
CH(n-Pr)S(O)₂Me CF₃
CH(n-Pr)S(O)₂Et CF₃
CH(i-Pr)SMe CF₃
CH(i-Pr)SEt CF₃
CH(i-Pr)S(O)Me CF₃
CH(i-Pr)S(O)Et CF₃
CH(i-Pr)S(O)₂Me CF₃
CH(i-Pr)S(O)₂Et CF₃
CH(n-Bu)SMe CF₃
CH(n-Bu)SEt CF₃
CH(n-Bu)S(O)Me CF₃
CH(n-Bu)S(O)Et CF₃
CH(n-Bu)S(O)₂Me CF₃
CH(n-Bu)S(O)₂Et CF₃
CH(i-Bu)SMe CF₃
CH(i-Bu)SEt CF₃
CH(i-Bu)S(O)Me CF₃
CH(i-Bu)S(O)Et CF₃
CH(i-Bu)S(O)₂Me CF₃
CH(i-Bu)S(O)₂Et CF₃
CH(s-Bu)SMe CF₃
CH(s-Bu)SEt CF₃
CH(s-Bu)S(O)Me CF₃
CH(s-Bu)S(O)Et CF₃
CH(s-Bu)S(O)₂Me CF₃
CH(s-Bu)S(O)₂Et CF₃
CH(t-Bu)SMe CF₃
CH(t-Bu)SEt CF₃
CH(t-Bu)S(O)Me CF₃
CH(t-Bu)S(O)Et CF₃
CH(t-Bu)S(O)₂Me CF₃
CH(t-Bu)S(O)₂Et CF₃
CH₂CH₂SMe CF₃
CH₂CH₂SEt CF₃
CH₂CH₂S(O)₂Me CF₃
CH₂CH₂S(O)₂Et CF₃
CH(Me)CH₂SMe CF₃
CH(Me)CH₂SEt CF₃
CH(Me)CH₂S(O)Me CF₃
CH(Me)CH₂S(O)Et CF₃
CH(Me)CH₂S(O)₂Me CF₃
CH(Me)CH₂S(O)₂Et CF₃
CH(Et)CH₂SMe CF₃
CH(Et)CH₂SEt CF₃
CH(Et)CH₂S(O)Me CF₃
CH(Et)CH₂S(O)Et CF₃
CH(Et)CH₂S(O)₂Me CF₃
CH(Et)CH₂S(O)₂Et CF₃
C(Me)₂CH₂SMe CF₃
C(Me)₂CH₂SEt CF₃
C(Me)₂CH₂S(O)Me CF₃
C(Me)₂CH₂S(O)Et CF₃
C(Me)₂CH₂S(O)₂Me CF₃
C(Me)₂CH₂S(O)₂Et CF₃
CH₂CH(Me)SMe CF₃
CH₂CH(Me)SEt CF₃
CH₂CH(Me)S(O)Me CF₃
CH₂CH(Me)S(O)Et CF₃
CH₂CH(Me)S(O)₂Me CF₃
CH₂CH(Me)S(O)₂Et CF₃
CH₂CH(Et)SMe CF₃
CH₂CH(Et)SEt CF₃
CH₂CH(Et)S(O)Me CF₃
CH₂CH(Et)S(O)Et CF₃
CH₂CH(Et)S(O)₂Me CF₃
CH₂CH(Et)S(O)₂Et CF₃
CH(Me)CH(Me)SMe CF₃
CH(Me)CH(Me)SEt CF₃
CH(Me)CH(Me)S(O)Me CF₃
CH(Me)CH(Me)S(O)Et CF₃
CH(Me)CH(Me)S(O)₂Me CF₃
CH(Me)CH(Me)S(O)₂Et CF₃
CH₂SMe CN
CH₂SEt CN
CH₂S(O)Me CN
CH₂S(O)Et CN
CH₂S(O)₂Me CN
CH₂S(O)₂Et CN
CH(Me)SMe CN
CH(Me)SEt CN
CH(Me)S(O)Me CN
CH(Me)S(O)Et CN
CH(Me)S(O)₂Me CN
CH(Me)S(O)₂Et CN
CH(Et)SMe CN
CH(Et)SEt CN
CH(Et)S(O)Me CN
CH(Et)S(O)Et CN
CH(Et)S(O)₂Me CN
CH(Et)S(O)₂Et CN
CH(n-Pr)SMe CN
CH(n-Pr)SEt CN
CH(n-Pr)S(O)Me CN
CH(n-Pr)S(O)Et CN
CH(n-Pr)S(O)₂Me CN
CH(n-Pr)S(O)₂Et CN
CH(i-Pr)SMe CN
CH(i-Pr)SEt CN
CH(i-Pr)S(O)Me CN
CH(i-Pr)S(O)Et CN
CH(i-Pr)S(O)₂Me CN
CH(i-Pr)S(O)₂Et CN
CH(n-Bu)SMe CN
CH(n-Bu)SEt CN
CH(n-Bu)S(O)Me CN
CH(n-Bu)S(O)Et CN
CH(n-Bu)S(O)₂Me CN
CH(n-Bu)S(O)₂Et CN
CH(i-Bu)SMe CN
CH(i-Bu)SEt CN
CH(i-Bu)S(O)Me CN
CH(i-Bu)S(O)Et CN
CH(i-Bu)S(O)₂Me CN
CH(i-Bu)S(O)₂Et CN
CH(s-Bu)SMe CN
CH(s-Bu)SEt CN
CH(s-Bu)S(O)Me CN
CH(s-Bu)S(O)Et CN
CH(s-Bu)S(O)₂Me CN
CH(s-Bu)S(O)₂Et CN
CH(t-Bu)SMe CN
CH(t-Bu)SEt CN
CH(t-Bu)S(O)Me CN
CH(t-Bu)S(O)Et CN
CH(t-Bu)S(O)₂Me CN
CH(t-Bu)S(O)₂Et CN
CH₂CH₂SMe CN
CH₂CH₂SEt CN
CH₂CH₂S(O)₂Me CN
CH₂CH₂S(O)₂Et CN
CH(Me)CH₂SMe CN
CH(Me)CH₂SEt CN
CH(Me)CH₂S(O)Me CN
CH(Me)CH₂S(O)Et CN
CH(Me)CH₂S(O)₂Me CN
CH(Me)CH₂S(O)₂Et CN
CH(Et)CH₂SMe CN
CH(Et)CH₂SEt CN
CH(Et)CH₂S(O)Me CN
CH(Et)CH₂S(O)Et CN
CH(Et)CH₂S(O)₂Me CN
CH(Et)CH₂S(O)₂Et CN
C(Me)₂CH₂SMe CN
C(Me)₂CH₂SEt CN
C(Me)₂CH₂S(O)Me CN
C(Me)₂CH₂S(O)Et CN
C(Me)₂CH₂S(O)₂Me CN
C(Me)₂CH₂S(O)₂Et CN
CH₂CH(Me)SMe CN
CH₂CH(Me)SEt CN
CH₂CH(Me)S(O)Me CN
CH₂CH(Me)S(O)Et CN
CH₂CH(Me)S(O)₂Me CN
CH₂CH(Me)S(O)₂Et CN
CH₂CH(Et)SMe CN
CH₂CH(Et)SEt CN
CH₂CH(Et)S(O)Me CN
CH₂CH(Et)S(O)Et CN
CH₂CH(Et)S(O)₂Me CN
CH₂CH(Et)S(O)₂Et CN
CH(Me)CH(Me)SMe CN
CH(Me)CH(Me)SEt CN
CH(Me)CH(Me)S(O)Me CN
CH(Me)CH(Me)S(O)Et CN
CH(Me)CH(Me)S(O)₂Me CN
CH(Me)CH(Me)S(O)₂Et CN
CH₂SMe Cl
CH₂SEt Cl
CH₂S(O)Me Cl
CH₂S(O)Et Cl
CH₂S(O)₂Me Cl
CH₂S(O)₂Et Cl
CH(Me)SMe Cl
CH(Me)SEt Cl
CH(Me)S(O)Me Cl
CH(Me)S(O)Et Cl
CH(Me)S(O)₂Me Cl
CH(Me)S(O)₂Et Cl
CH(Et)SMe Cl
CH(Et)SEt Cl
CH(Et)S(O)Me Cl
CH(Et)S(O)Et Cl
CH(Et)S(O)₂Me Cl
CH(Et)S(O)₂Et Cl
CH(n-Pr)SMe Cl
CH(n-Pr)SEt Cl
CH(n-Pr)S(O)Me Cl
CH(n-Pr)S(O)Et Cl
CH(n-Pr)S(O)₂Me Cl
CH(n-Pr)S(O)₂Et Cl
CH(i-Pr)SMe Cl
CH(i-Pr)SEt Cl
CH(i-Pr)S(O)Me Cl
CH(i-Pr)S(O)Et Cl
CH(i-Pr)S(O)₂Me Cl
CH(i-Pr)S(O)₂Et Cl
CH(n-Bu)SMe Cl
CH(n-Bu)SEt Cl
CH(n-Bu)S(O)Me Cl
CH(n-Bu)S(O)Et Cl
CH(n-Bu)S(O)₂Me Cl
CH(n-Bu)S(O)₂Et Cl
CH(i-Bu)SMe Cl
CH(i-Bu)SEt Cl
CH(i-Bu)S(O)Me Cl
CH(i-Bu)S(O)Et Cl
CH(i-Bu)S(O)₂Me Cl
CH(i-Bu)S(O)₂Et Cl
CH(s-Bu)SMe Cl
CH(s-Bu)SEt Cl
CH(s-Bu)S(O)Me Cl
CH(s-Bu)S(O)Et Cl
CH(s-Bu)S(O)₂Me Cl
CH(s-Bu)S(O)₂Et Cl
CH(t-Bu)SMe Cl
CH(t-Bu)SEt Cl
CH(t-Bu)S(O)Me Cl
CH(t-Bu)S(O)Et Cl
CH(t-Bu)S(O)₂Me Cl
CH(t-Bu)S(O)₂Et Cl
CH₂CH₂SMe Cl
CH₂CH₂SEt Cl
CH₂CH₂S(O)₂Me Cl
CH₂CH₂S(O)₂Et Cl
CH(Me)CH₂SMe Cl
CH(Me)CH₂SEt Cl
CH(Me)CH₂S(O)Me Cl
CH(Me)CH₂S(O)Et Cl
CH(Me)CH₂S(O)₂Me Cl
CH(Me)CH₂S(O)₂Et Cl
CH(Et)CH₂SMe Cl
CH(Et)CH₂SEt Cl
CH(Et)CH₂S(O)Me Cl
CH(Et)CH₂S(O)Et Cl
CH(Et)CH₂S(O)₂Me Cl
CH(Et)CH₂S(O)₂Et Cl
C(Me)₂CH₂SMe Cl
C(Me)₂CH₂SEt Cl
C(Me)₂CH₂S(O)Me Cl
C(Me)₂CH₂S(O)Et Cl
C(Me)₂CH₂S(O)₂Me Cl
C(Me)₂CH₂S(O)₂Et Cl
CH₂CH(Me)SMe Cl
CH₂CH(Me)SEt Cl
CH₂CH(Me)S(O)Me Cl
CH₂CH(Me)S(O)Et Cl
CH₂CH(Me)S(O)₂Me Cl
CH₂CH(Me)S(O)₂Et Cl
CH₂CH(Et)SMe Cl
CH₂CH(Et)SEt Cl
CH₂CH(Et)S(O)Me Cl
CH₂CH(Et)S(O)Et Cl
CH₂CH(Et)S(O)₂Me Cl
CH₂CH(Et)S(O)₂Et Cl
CH(Me)CH(Me)SMe Cl
CH(Me)CH(Me)SEt Cl
CH(Me)CH(Me)S(O)Me Cl
CH(Me)CH(Me)S(O)Et Cl
CH(Me)CH(Me)S(O)₂Me Cl
CH(Me)CH(Me)S(O)₂Et Cl
CH₂SMe C(O)OMe
CH₂SEt C(O)OMe
CH₂S(O)Me C(O)OMe
CH₂S(O)Et C(O)OMe
CH₂S(O)₂Me C(O)OMe
CH₂S(O)₂Et C(O)OMe
CH(Me)SMe C(O)OMe
CH(Me)SEt C(O)OMe
CH(Me)S(O)Me C(O)OMe
CH(Me)S(O)Et C(O)OMe
CH(Me)S(O)₂Me C(O)OMe
CH(Me)S(O)₂Et C(O)OMe
CH(Et)SMe C(O)OMe
CH(Et)SEt C(O)OMe
CH(Et)S(O)Me C(O)OMe
CH(Et)S(O)Et C(O)OMe
CH(Et)S(O)₂Me C(O)OMe
CH(Et)S(O)₂Et C(O)OMe
CH(n-Pr)SMe C(O)OMe
CH(n-Pr)SEt C(O)OMe
CH(n-Pr)S(O)Me C(O)OMe
CH(n-Pr)S(O)Et C(O)OMe
CH(n-Pr)S(O)₂Me C(O)OMe
CH(n-Pr)S(O)₂Et C(O)OMe
CH(i-Pr)SMe C(O)OMe
CH(i-Pr)SEt C(O)OMe
CH(i-Pr)S(O)Me C(O)OMe
CH(i-Pr)S(O)Et C(O)OMe
CH(i-Pr)S(O)₂Me C(O)OMe
CH(i-Pr)S(O)₂Et C(O)OMe
CH(n-Bu)SMe C(O)OMe
CH(n-Bu)SEt C(O)OMe
CH(n-Bu)S(O)Me C(O)OMe
CH(n-Bu)S(O)Et C(O)OMe
CH(n-Bu)S(O)₂Me C(O)OMe
CH(n-Bu)S(O)₂Et C(O)OMe
CH(i-Bu)SMe C(O)OMe
CH(i-Bu)SEt C(O)OMe
CH(i-Bu)S(O)Me C(O)OMe
CH(i-Bu)S(O)Et C(O)OMe
CH(i-Bu)S(O)₂Me C(O)OMe
CH(i-Bu)S(O)₂Et C(O)OMe
CH(s-Bu)SMe C(O)OMe
CH(s-Bu)SEt C(O)OMe
CH(s-Bu)S(O)Me C(O)OMe
CH(s-Bu)S(O)Et C(O)OMe
CH(s-Bu)S(O)₂Me C(O)OMe
CH(s-Bu)S(O)₂Et C(O)OMe
CH(t-Bu)SMe C(O)OMe
CH(t-Bu)SEt C(O)OMe
CH(t-Bu)S(O)Me C(O)OMe
CH(t-Bu)S(O)Et C(O)OMe
CH(t-Bu)S(O)₂Me C(O)OMe
CH(t-Bu)S(O)₂Et C(O)OMe
CH₂CH₂SMe C(O)OMe
CH₂CH₂SEt C(O)OMe
CH₂CH₂S(O)₂Me C(O)OMe
CH₂CH₂S(O)₂Et C(O)OMe
CH(Me)CH₂SMe C(O)OMe
CH(Me)CH₂SEt C(O)OMe
CH(Me)CH₂S(O)Me C(O)OMe
CH(Me)CH₂S(O)Et C(O)OMe
CH(Me)CH₂S(O)₂Me C(O)OMe
CH(Me)CH₂S(O)₂Et C(O)OMe
CH(Et)CH₂SMe C(O)OMe
CH(Et)CH₂SEt C(O)OMe
CH(Et)CH₂S(O)Me C(O)OMe
CH(Et)CH₂S(O)Et C(O)OMe
CH(Et)CH₂S(O)₂Me C(O)OMe
CH(Et)CH₂S(O)₂Et C(O)OMe
C(Me)₂CH₂SMe C(O)OMe
C(Me)₂CH₂SEt C(O)OMe
C(Me)₂CH₂S(O)Me C(O)OMe
C(Me)₂CH₂S(O)Et C(O)OMe
C(Me)₂CH₂S(O)₂Me C(O)OMe
C(Me)₂CH₂S(O)₂Et C(O)OMe
CH₂CH(Me)SMe C(O)OMe
CH₂CH(Me)SEt C(O)OMe
CH₂CH(Me)S(O)Me C(O)OMe
CH₂CH(Me)S(O)Et C(O)OMe
CH₂CH(Me)S(O)₂Me C(O)OMe
CH₂CH(Me)S(O)₂Et C(O)OMe
CH₂CH(Et)SMe C(O)OMe
CH₂CH(Et)SEt C(O)OMe
CH₂CH(Et)S(O)Me C(O)OMe
CH₂CH(Et)S(O)Et C(O)OMe
CH₂CH(Et)S(O)₂Me C(O)OMe
CH₂CH(Et)S(O)₂Et C(O)OMe
CH(Me)CH(Me)SMe C(O)OMe
CH(Me)CH(Me)SEt C(O)OMe
CH(Me)CH(Me)S(O)Me C(O)OMe
CH(Me)CH(Me)S(O)Et C(O)OMe
CH(Me)CH(Me)S(O)₂Me C(O)OMe
CH(Me)CH(Me)S(O)₂Et C(O)OMe
CH₂OMe CH₂SMe
CH₂OMe CH₂SEt
CH₂OMe CH₂SCF₃
CH₂OMe CH₂SCH₂CF₃
CH₂OMe CH₂S(O)Me
CH₂OMe CH₂S(O)Et
CH₂OMe CH₂S(O)CF₃
CH₂OMe CH₂S(O)CH₂CF₃
CH₂OMe CH₂S(O)₂Me
CH₂OMe CH₂S(O)₂Et
CH₂OMe CH₂S(O)₂CF₃
CH₂OMe CH₂S(O)₂CH₂CF₃
CH₂OMe CH(Me)SMe
CH₂OMe CH(Me)SEt
CH₂OMe CH(Me)SCF₃
CH₂OMe CH(Me)SCH₂CF₃
CH₂OMe CH(Me)S(O)Me
CH₂OMe CH(Me)S(O)Et
CH₂OMe CH(Me)S(O)CF₃
CH₂OMe CH(Me)S(O)CH₂CF₃
CH₂OMe CH(Me)S(O)₂Me
CH₂OMe CH(Me)S(O)₂Et
CH₂OMe CH(Me)S(O)₂CF₃
CH₂OMe CH(Me)S(O)₂CH₂CF₃
CH₂OMe CH(Et)SMe
CH₂OMe CH(Et)SEt
CH₂OMe CH(Et)SCF₃
CH₂OMe CH(Et)SCH₂CF₃
CH₂OMe CH(Et)S(O)Me
CH₂OMe CH(Et)S(O)Et
CH₂OMe CH(Et)S(O)CF₃
CH₂OMe CH(Et)S(O)CH₂CF₃
CH₂OMe CH(Et)S(O)₂Me
CH₂OMe CH(Et)S(O)₂Et
CH₂OMe CH(Et)S(O)₂CF₃
CH₂OMe CH(Et)S(O)₂CH₂CF₃
CH₂OMe CH(n-Pr)SMe
CH₂OMe CH(n-Pr)SEt
CH₂OMe CH(n-Pr)SCF₃
CH₂OMe CH(n-Pr)SCH₂CF₃
CH₂OMe CH(n-Pr)S(O)Me
CH₂OMe CH(n-Pr)S(O)Et
CH₂OMe CH(n-Pr)S(O)CF₃
CH₂OMe CH(n-Pr)S(O)CH₂CF₃
CH₂OMe CH(n-Pr)S(O)₂Me
CH₂OMe CH(n-Pr)S(O)₂Et
CH₂OMe CH(n-Pr)S(O)₂CF₃
CH₂OMe CH(n-Pr)S(O)₂CH₂CF₃
CH₂OMe CH(i-Pr)SMe
CH₂OMe CH(i-Pr)SEt
CH₂OMe CH(i-Pr)SCF₃
CH₂OMe CH(i-Pr)SCH₂CF₃
CH₂OMe CH(i-Pr)S(O)Me
CH₂OMe CH(i-Pr)S(O)Et
CH₂OMe CH(i-Pr)S(O)CF₃
CH₂OMe CH(i-Pr)S(O)CH₂CF₃
CH₂OMe CH(i-Pr)S(O)₂Me
CH₂OMe CH(i-Pr)S(O)₂Et
CH₂OMe CH(i-Pr)S(O)₂CF₃
CH₂OMe CH(i-Pr)S(O)₂CH₂CF₃
CH₂OMe CH(n-Bu)SMe
CH₂OMe CH(n-Bu)SEt
CH₂OMe CH(n-Bu)SCF₃
CH₂OMe CH(n-Bu)SCH₂CF₃
CH₂OMe CH(n-Bu)S(O)Me
CH₂OMe CH(n-Bu)S(O)Et
CH₂OMe CH(n-Bu)S(O)CF₃
CH₂OMe CH(n-Bu)S(O)CH₂CF₃
CH₂OMe CH(n-Bu)S(O)₂Me
CH₂OMe CH(n-Bu)S(O)₂Et
CH₂OMe CH(n-Bu)S(O)₂CF₃
CH₂OMe CH(n-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(i-Bu)SMe
CH₂OMe CH(i-Bu)SEt
CH₂OMe CH(i-Bu)SCF₃
CH₂OMe CH(i-Bu)SCH₂CF₃
CH₂OMe CH(i-Bu)S(O)Me
CH₂OMe CH(i-Bu)S(O)Et
CH₂OMe CH(i-Bu)S(O)CF₃
CH₂OMe CH(i-Bu)S(O)CH₂CF₃
CH₂OMe CH(i-Bu)S(O)₂Me
CH₂OMe CH(i-Bu)S(O)₂Et
CH₂OMe CH(i-Bu)S(O)₂CF₃
CH₂OMe CH(i-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(s-Bu)SMe
CH₂OMe CH(s-Bu)SEt
CH₂OMe CH(s-Bu)SCF₃
CH₂OMe CH(s-Bu)SCH₂CF₃
CH₂OMe CH(s-Bu)S(O)Me
CH₂OMe CH(s-Bu)S(O)Et
CH₂OMe CH(s-Bu)S(O)CF₃
CH₂OMe CH(s-Bu)S(O)CH₂CF₃
CH₂OMe CH(s-Bu)S(O)₂Me
CH₂OMe CH(s-Bu)S(O)₂Et
CH₂OMe CH(s-Bu)S(O)₂CF₃
CH₂OMe CH(s-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(t-Bu)SMe
CH₂OMe CH(t-Bu)SEt
CH₂OMe CH(t-Bu)SCF₃
CH₂OMe CH(t-Bu)SCH₂CF₃
CH₂OMe CH(t-Bu)S(O)Me
CH₂OMe CH(t-Bu)S(O)Et
CH₂OMe CH(t-Bu)S(O)CF₃
CH₂OMe CH(t-Bu)S(O)CH₂CF₃
CH₂OMe CH(t-Bu)S(O)₂Me
CH₂OMe CH(t-Bu)S(O)₂Et
CH₂OMe CH(t-Bu)S(O)₂CF₃
CH₂OMe CH(t-Bu)S(O)₂CH₂CF₃
CH₂OMe CH(CF₃)SMe
CH₂OMe CH(CF₃)SEt
CH₂OMe CH(CF₃)SCF₃
CH₂OMe CH(CF₃)SCH₂CF₃
CH₂OMe CH(CF₃)S(O)Me
CH₂OMe CH(CF₃)S(O)Et
CH₂OMe CH(CF₃)S(O)CF₃
CH₂OMe CH(CF₃)S(O)CH₂CF₃
CH₂OMe CH(CF₃)S(O)₂Me
CH₂OMe CH(CF₃)S(O)₂Et
CH₂OMe CH(CF₃)S(O)₂CF₃
CH₂OMe CH(CF₃)S(O)₂CH₂CF₃
CH₂OMe CH₂CH₂SMe
CH₂OMe CH₂CH₂SEt
CH₂OMe CH₂CH₂SCF₃
CH₂OMe CH₂CH₂SCH₂CF₃
CH₂OMe CH₂CH₂S(O)Me
CH₂OMe CH₂CH₂S(O)Et
CH₂OMe CH₂CH₂S(O)CF₃
CH₂OMe CH₂CH₂S(O)CH₂CF₃
CH₂OMe CH₂CH₂S(O)₂Me
CH₂OMe CH₂CH₂S(O)₂Et
CH₂OMe CH₂CH₂S(O)₂CF₃
CH₂OMe CH₂CH₂S(O)₂CH₂CF₃
CH₂OMe CH(Me)CH₂SMe
CH₂OMe CH(Me)CH₂SEt
CH₂OMe CH(Me)CH₂SCF₃
CH₂OMe CH(Me)CH₂SCH₂CF₃
CH₂OMe CH(Me)CH₂S(O)Me
CH₂OMe CH(Me)CH₂S(O)Et
CH₂OMe CH(Me)CH₂S(O)CF₃
CH₂OMe CH(Me)CH₂S(O)CH₂CF₃
CH₂OMe CH(Me)CH₂S(O)₂Me
CH₂OMe CH(Me)CH₂S(O)₂Et
CH₂OMe CH(Me)CH₂S(O)₂CF₃
CH₂OMe CH(Me)CH₂S(O)₂CH₂CF₃
CH₂OMe CH(Et)CH₂SMe
CH₂OMe CH(Et)CH₂SEt
CH₂OMe CH(Et)CH₂SCF₃
CH₂OMe CH(Et)CH₂SCH₂CF₃
CH₂OMe CH(Et)CH₂S(O)Me
CH₂OMe CH(Et)CH₂S(O)Et
CH₂OMe CH(Et)CH₂S(O)CF₃
CH₂OMe CH(Et)CH₂S(O)CH₂CF₃
CH₂OMe CH(Et)CH₂S(O)₂Me
CH₂OMe CH(Et)CH₂S(O)₂Et
CH₂OMe CH(Et)CH₂S(O)₂CF₃
CH₂OMe CH(Et)CH₂S(O)₂CH₂CF₃
CH₂OMe C(Me)₂CH₂SMe
CH₂OMe C(Me)₂CH₂SEt
CH₂OMe C(Me)₂CH₂SCF₃
CH₂OMe C(Me)₂CH₂SCH₂CF₃
CH₂OMe C(Me)₂CH₂S(O)Me
CH₂OMe C(Me)₂CH₂S(O)Et
CH₂OMe C(Me)₂CH₂S(O)CF₃
CH₂OMe C(Me)₂CH₂S(O)CH₂CF₃
CH₂OMe C(Me)₂CH₂S(O)₂Me
CH₂OMe C(Me)₂CH₂S(O)₂Et
CH₂OMe C(Me)₂CH₂S(O)₂CF₃
CH₂OMe C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂OMe CH₂CH(Me)SMe
CH₂OMe CH₂CH(Me)SEt
CH₂OMe CH₂CH(Me)SCF₃
CH₂OMe CH₂CH(Me)SCH₂CF₃
CH₂OMe CH₂CH(Me)S(O)Me
CH₂OMe CH₂CH(Me)S(O)Et
CH₂OMe CH₂CH(Me)S(O)CF₃
CH₂OMe CH₂CH(Me)S(O)CH₂CF₃
CH₂OMe CH₂CH(Me)S(O)₂Me
CH₂OMe CH₂CH(Me)S(O)₂Et
CH₂OMe CH₂CH(Me)S(O)₂CF₃
CH₂OMe CH₂CH(Me)S(O)₂CH₂CF₃
CH₂OMe CH₂CH(Et)SMe
CH₂OMe CH₂CH(Et)SEt
CH₂OMe CH₂CH(Et)SCF₃
CH₂OMe CH₂CH(Et)SCH₂CF₃
CH₂OMe CH₂CH(Et)S(O)Me
CH₂OMe CH₂CH(Et)S(O)Et
CH₂OMe CH₂CH(Et)S(O)CF₃
CH₂OMe CH₂CH(Et)S(O)CH₂CF₃
CH₂OMe CH₂CH(Et)S(O)₂Me
CH₂OMe CH₂CH(Et)S(O)₂Et
CH₂OMe CH₂CH(Et)S(O)₂CF₃
CH₂OMe CH₂CH(Et)S(O)₂CH₂CF₃
CH₂OMe CH(Me)CH(Me)SMe
CH₂OMe CH(Me)CH(Me)SEt
CH₂OMe CH(Me)CH(Me)SCF₃
CH₂OMe CH(Me)CH(Me)SCH₂CF₃
CH₂OMe CH(Me)CH(Me)S(O)Me
CH₂OMe CH(Me)CH(Me)S(O)Et
CH₂OMe CH(Me)CH(Me)S(O)CF₃
CH₂OMe CH(Me)CH(Me)S(O)CH₂CF₃
CH₂OMe CH(Me)CH(Me)S(O)₂Me
CH₂OMe CH(Me)CH(Me)S(O)₂Et
CH₂OMe CH(Me)CH(Me)S(O)₂CF₃
CH₂OMe CH(Me)CH(Me)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH₂SMe
CH₂C(=NOMe)Me CH₂SEt
CH₂C(=NOMe)Me CH₂SCF₃
CH₂C(=NOMe)Me CH₂SCH₂CF₃
CH₂C(=NOMe)Me CH₂S(O)Me
CH₂C(=NOMe)Me CH₂S(O)Et
CH₂C(=NOMe)Me CH₂S(O)CF₃
CH₂C(=NOMe)Me CH₂S(O)CH₂CF₃
CH₂C(=NOMe)Me CH₂S(O)₂Me
CH₂C(=NOMe)Me CH₂S(O)₂Et
CH₂C(=NOMe)Me CH₂S(O)₂CF₃
CH₂C(=NOMe)Me CH₂S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(Me)SMe
CH₂C(=NOMe)Me CH(Me)SEt
CH₂C(=NOMe)Me CH(Me)SCF₃
CH₂C(=NOMe)Me CH(Me)SCH₂CF₃
CH₂C(=NOMe)Me CH(Me)S(O)Me
CH₂C(=NOMe)Me CH(Me)S(O)Et
CH₂C(=NOMe)Me CH(Me)S(O)CF₃
CH₂C(=NOMe)Me CH(Me)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(Me)S(O)₂Me
CH₂C(=NOMe)Me CH(Me)S(O)₂Et
CH₂C(=NOMe)Me CH(Me)S(O)₂CF₃
CH₂C(=NOMe)Me CH(Me)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(Et)SMe
CH₂C(=NOMe)Me CH(Et)SEt
CH₂C(=NOMe)Me CH(Et)SCF₃
CH₂C(=NOMe)Me CH(Et)SCH₂CF₃
CH₂C(=NOMe)Me CH(Et)S(O)Me
CH₂C(=NOMe)Me CH(Et)S(O)Et
CH₂C(=NOMe)Me CH(Et)S(O)CF₃
CH₂C(=NOMe)Me CH(Et)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(Et)S(O)₂Me
CH₂C(=NOMe)Me CH(Et)S(O)₂Et
CH₂C(=NOMe)Me CH(Et)S(O)₂CF₃
CH₂C(=NOMe)Me CH(Et)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(n-Pr)SMe
CH₂C(=NOMe)Me CH(n-Pr)SEt
CH₂C(=NOMe)Me CH(n-Pr)SCF₃
CH₂C(=NOMe)Me CH(n-Pr)SCH₂CF₃
CH₂C(=NOMe)Me CH(n-Pr)S(O)Me
CH₂C(=NOMe)Me CH(n-Pr)S(O)Et
CH₂C(=NOMe)Me CH(n-Pr)S(O)CF₃
CH₂C(=NOMe)Me CH(n-Pr)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(n-Pr)S(O)₂Me
CH₂C(=NOMe)Me CH(n-Pr)S(O)₂Et
CH₂C(=NOMe)Me CH(n-Pr)S(O)₂CF₃
CH₂C(=NOMe)Me CH(n-Pr)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(i-Pr)SMe
CH₂C(=NOMe)Me CH(i-Pr)SEt
CH₂C(=NOMe)Me CH(i-Pr)SCF₃
CH₂C(=NOMe)Me CH(i-Pr)SCH₂CF₃
CH₂C(=NOMe)Me CH(i-Pr)S(O)Me
CH₂C(=NOMe)Me CH(i-Pr)S(O)Et
CH₂C(=NOMe)Me CH(i-Pr)S(O)CF₃
CH₂C(=NOMe)Me CH(i-Pr)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(i-Pr)S(O)₂Me
CH₂C(=NOMe)Me CH(i-Pr)S(O)₂Et
CH₂C(=NOMe)Me CH(i-Pr)S(O)₂CF₃
CH₂C(=NOMe)Me CH(i-Pr)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(n-Bu)SMe
CH₂C(=NOMe)Me CH(n-Bu)SEt
CH₂C(=NOMe)Me CH(n-Bu)SCF₃
CH₂C(=NOMe)Me CH(n-Bu)SCH₂CF₃
CH₂C(=NOMe)Me CH(n-Bu)S(O)Me
CH₂C(=NOMe)Me CH(n-Bu)S(O)Et
CH₂C(=NOMe)Me CH(n-Bu)S(O)CF₃
CH₂C(=NOMe)Me CH(n-Bu)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(n-Bu)S(O)₂Me
CH₂C(=NOMe)Me CH(n-Bu)S(O)₂Et
CH₂C(=NOMe)Me CH(n-Bu)S(O)₂CF₃
CH₂C(=NOMe)Me CH(n-Bu)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(i-Bu)SMe
CH₂C(=NOMe)Me CH(i-Bu)SEt
CH₂C(=NOMe)Me CH(i-Bu)SCF₃
CH₂C(=NOMe)Me CH(i-Bu)SCH₂CF₃
CH₂C(=NOMe)Me CH(i-Bu)S(O)Me
CH₂C(=NOMe)Me CH(i-Bu)S(O)Et
CH₂C(=NOMe)Me CH(i-Bu)S(O)CF₃
CH₂C(=NOMe)Me CH(i-Bu)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(i-Bu)S(O)₂Me
CH₂C(=NOMe)Me CH(i-Bu)S(O)₂Et
CH₂C(=NOMe)Me CH(i-Bu)S(O)₂CF₃
CH₂C(=NOMe)Me CH(i-Bu)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(s-Bu)SMe
CH₂C(=NOMe)Me CH(s-Bu)SEt
CH₂C(=NOMe)Me CH(s-Bu)SCF₃
CH₂C(=NOMe)Me CH(s-Bu)SCH₂CF₃
CH₂C(=NOMe)Me CH(s-Bu)S(O)Me
CH₂C(=NOMe)Me CH(s-Bu)S(O)Et
CH₂C(=NOMe)Me CH(s-Bu)S(O)CF₃
CH₂C(=NOMe)Me CH(s-Bu)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(s-Bu)S(O)₂Me
CH₂C(=NOMe)Me CH(s-Bu)S(O)₂Et
CH₂C(=NOMe)Me CH(s-Bu)S(O)₂CF₃
CH₂C(=NOMe)Me CH(s-Bu)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(t-Bu)SMe
CH₂C(=NOMe)Me CH(t-Bu)SEt
CH₂C(=NOMe)Me CH(t-Bu)SCF₃
CH₂C(=NOMe)Me CH(t-Bu)SCH₂CF₃
CH₂C(=NOMe)Me CH(t-Bu)S(O)Me
CH₂C(=NOMe)Me CH(t-Bu)S(O)Et
CH₂C(=NOMe)Me CH(t-Bu)S(O)CF₃
CH₂C(=NOMe)Me CH(t-Bu)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(t-Bu)S(O)₂Me
CH₂C(=NOMe)Me CH(t-Bu)S(O)₂Et
CH₂C(=NOMe)Me CH(t-Bu)S(O)₂CF₃
CH₂C(=NOMe)Me CH(t-Bu)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(CF₃)SMe
CH₂C(=NOMe)Me CH(CF₃)SEt
CH₂C(=NOMe)Me CH(CF₃)SCF₃
CH₂C(=NOMe)Me CH(CF₃)SCH₂CF₃
CH₂C(=NOMe)Me CH(CF₃)S(O)Me
CH₂C(=NOMe)Me CH(CF₃)S(O)Et
CH₂C(=NOMe)Me CH(CF₃)S(O)CF₃
CH₂C(=NOMe)Me CH(CF₃)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(CF₃)S(O)₂Me
CH₂C(=NOMe)Me CH(CF₃)S(O)₂Et
CH₂C(=NOMe)Me CH(CF₃)S(O)₂CF₃
CH₂C(=NOMe)Me CH(CF₃)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH₂CH₂SMe
CH₂C(=NOMe)Me CH₂CH₂SEt
CH₂C(=NOMe)Me CH₂CH₂SCF₃
CH₂C(=NOMe)Me CH₂CH₂SCH₂CF₃
CH₂C(=NOMe)Me CH₂CH₂S(O)Me
CH₂C(=NOMe)Me CH₂CH₂S(O)Et
CH₂C(=NOMe)Me CH₂CH₂S(O)CF₃
CH₂C(=NOMe)Me CH₂CH₂S(O)CH₂CF₃
CH₂C(=NOMe)Me CH₂CH₂S(O)₂Me
CH₂C(=NOMe)Me CH₂CH₂S(O)₂Et
CH₂C(=NOMe)Me CH₂CH₂S(O)₂CF₃
CH₂C(=NOMe)Me CH₂CH₂S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(Me)CH₂SMe
CH₂C(=NOMe)Me CH(Me)CH₂SEt
CH₂C(=NOMe)Me CH(Me)CH₂SCF₃
CH₂C(=NOMe)Me CH(Me)CH₂SCH₂CF₃
CH₂C(=NOMe)Me CH(Me)CH₂S(O)Me
CH₂C(=NOMe)Me CH(Me)CH₂S(O)Et
CH₂C(=NOMe)Me CH(Me)CH₂S(O)CF₃
CH₂C(=NOMe)Me CH(Me)CH₂S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(Me)CH₂S(O)₂Me
CH₂C(=NOMe)Me CH(Me)CH₂S(O)₂Et
CH₂C(=NOMe)Me CH(Me)CH₂S(O)₂CF₃
CH₂C(=NOMe)Me CH(Me)CH₂S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(Et)CH₂SMe
CH₂C(=NOMe)Me CH(Et)CH₂SEt
CH₂C(=NOMe)Me CH(Et)CH₂SCF₃
CH₂C(=NOMe)Me CH(Et)CH₂SCH₂CF₃
CH₂C(=NOMe)Me CH(Et)CH₂S(O)Me
CH₂C(=NOMe)Me CH(Et)CH₂S(O)Et
CH₂C(=NOMe)Me CH(Et)CH₂S(O)CF₃
CH₂C(=NOMe)Me CH(Et)CH₂S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(Et)CH₂S(O)₂Me
CH₂C(=NOMe)Me CH(Et)CH₂S(O)₂Et
CH₂C(=NOMe)Me CH(Et)CH₂S(O)₂CF₃
CH₂C(=NOMe)Me CH(Et)CH₂S(O)₂CH₂CF₃
CH₂C(=NOMe)Me C(Me)₂CH₂SMe
CH₂C(=NOMe)Me C(Me)₂CH₂SEt
CH₂C(=NOMe)Me C(Me)₂CH₂SCF₃
CH₂C(=NOMe)Me C(Me)₂CH₂SCH₂CF₃
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)Me
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)Et
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)CF₃
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)CH₂CF₃
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)₂Me
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)₂Et
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)₂CF₃
CH₂C(=NOMe)Me C(Me)₂CH₂S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH₂CH(Me)SMe
CH₂C(=NOMe)Me CH₂CH(Me)SEt
CH₂C(=NOMe)Me CH₂CH(Me)SCF₃
CH₂C(=NOMe)Me CH₂CH(Me)SCH₂CF₃
CH₂C(=NOMe)Me CH₂CH(Me)S(O)Me
CH₂C(=NOMe)Me CH₂CH(Me)S(O)Et
CH₂C(=NOMe)Me CH₂CH(Me)S(O)CF₃
CH₂C(=NOMe)Me CH₂CH(Me)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH₂CH(Me)S(O)₂Me
CH₂C(=NOMe)Me CH₂CH(Me)S(O)₂Et
CH₂C(=NOMe)Me CH₂CH(Me)S(O)₂CF₃
CH₂C(=NOMe)Me CH₂CH(Me)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH₂CH(Et)SMe
CH₂C(=NOMe)Me CH₂CH(Et)SEt
CH₂C(=NOMe)Me CH₂CH(Et)SCF₃
CH₂C(=NOMe)Me CH₂CH(Et)SCH₂CF₃
CH₂C(=NOMe)Me CH₂CH(Et)S(O)Me
CH₂C(=NOMe)Me CH₂CH(Et)S(O)Et
CH₂C(=NOMe)Me CH₂CH(Et)S(O)CF₃
CH₂C(=NOMe)Me CH₂CH(Et)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH₂CH(Et)S(O)₂Me
CH₂C(=NOMe)Me CH₂CH(Et)S(O)₂Et
CH₂C(=NOMe)Me CH₂CH(Et)S(O)₂CF₃
CH₂C(=NOMe)Me CH₂CH(Et)S(O)₂CH₂CF₃
CH₂C(=NOMe)Me CH(Me)CH(Me)SMe
CH₂C(=NOMe)Me CH(Me)CH(Me)SEt
CH₂C(=NOMe)Me CH(Me)CH(Me)SCF₃
CH₂C(=NOMe)Me CH(Me)CH(Me)SCH₂CF₃
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)Me
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)Et
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)CF₃
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)CH₂CF₃
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)₂Me
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)₂Et
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)₂CF₃
CH₂C(=NOMe)Me CH(Me)CH(Me)S(O)₂CH₂CF₃
――――――――――――――――――
本発明化合物は、農園芸作物及び樹木などを加害する所謂農業害虫、家畜・家禽類に寄生する所謂家畜害虫、家屋等の人間の生活環境で様々な悪影響を与える所謂衛生害虫、倉庫に貯蔵された穀物等を加害する所謂貯穀害虫等としての昆虫類、及び同様の場面で発生、加害するダニ類、甲殻類、軟体動物、線虫類の何れの有害生物も低濃度で有効に防除できる。 ――――――――――――――――――
X^1a          X¹
――――――――――――――――――
H CH₂SMe
H CH₂SEt
H CH₂SCF_Three
H CH₂SCH₂CF_Three
H CH₂S (O) Me
H CH₂S (O) Et
H CH₂S (O) CF_Three
H CH₂S (O) CH₂CF_Three
H CH₂S (O)₂Me
H CH₂S (O)₂Et
H CH₂S (O)₂CF_Three
H CH₂S (O)₂CH₂CF_Three
H CH (Me) SMe
H CH (Me) SEt
H CH (Me) SCF_Three
H CH (Me) SCH₂CF_Three
H CH (Me) S (O) Me
H CH (Me) S (O) Et
H CH (Me) S (O) CF_Three
H CH (Me) S (O) CH₂CF_Three
H CH (Me) S (O)₂Me
H CH (Me) S (O)₂Et
H CH (Me) S (O)₂CF_Three
H CH (Me) S (O)₂CH₂CF_Three
H CH (Et) SMe
H CH (Et) SEt
H CH (Et) SCF_Three
H CH (Et) SCH₂CF_Three
H CH (Et) S (O) Me
H CH (Et) S (O) Et
H CH (Et) S (O) CF_Three
H CH (Et) S (O) CH₂CF_Three
H CH (Et) S (O)₂Me
H CH (Et) S (O)₂Et
H CH (Et) S (O)₂CF_Three
H CH (Et) S (O)₂CH₂CF_Three
H CH (n-Pr) SMe
H CH (n-Pr) SEt
H CH (n-Pr) SCF_Three
H CH (n-Pr) SCH₂CF_Three
H CH (n-Pr) S (O) Me
H CH (n-Pr) S (O) Et
H CH (n-Pr) S (O) CF_Three
H CH (n-Pr) S (O) CH₂CF_Three
H CH (n-Pr) S (O)₂Me
H CH (n-Pr) S (O)₂Et
H CH (n-Pr) S (O)₂CF_Three
H CH (n-Pr) S (O)₂CH₂CF_Three
H CH (i-Pr) SMe
H CH (i-Pr) SEt
H CH (i-Pr) SCF_Three
H CH (i-Pr) SCH₂CF_Three
H CH (i-Pr) S (O) Me
H CH (i-Pr) S (O) Et
H CH (i-Pr) S (O) CF_Three
H CH (i-Pr) S (O) CH₂CF_Three
H CH (i-Pr) S (O)₂Me
H CH (i-Pr) S (O)₂Et
H CH (i-Pr) S (O)₂CF_Three
H CH (i-Pr) S (O)₂CH₂CF_Three
H CH (n-Bu) SMe
H CH (n-Bu) SEt
H CH (n-Bu) SCF_Three
H CH (n-Bu) SCH₂CF_Three
H CH (n-Bu) S (O) Me
H CH (n-Bu) S (O) Et
H CH (n-Bu) S (O) CF_Three
H CH (n-Bu) S (O) CH₂CF_Three
H CH (n-Bu) S (O)₂Me
H CH (n-Bu) S (O)₂Et
H CH (n-Bu) S (O)₂CF_Three
H CH (n-Bu) S (O)₂CH₂CF_Three
H CH (i-Bu) SMe
H CH (i-Bu) SEt
H CH (i-Bu) SCF_Three
H CH (i-Bu) SCH₂CF_Three
H CH (i-Bu) S (O) Me
H CH (i-Bu) S (O) Et
H CH (i-Bu) S (O) CF_Three
H CH (i-Bu) S (O) CH₂CF_Three
H CH (i-Bu) S (O)₂Me
H CH (i-Bu) S (O)₂Et
H CH (i-Bu) S (O)₂CF_Three
H CH (i-Bu) S (O)₂CH₂CF_Three
H CH (s-Bu) SMe
H CH (s-Bu) SEt
H CH (s-Bu) SCF_Three
H CH (s-Bu) SCH₂CF_Three
H CH (s-Bu) S (O) Me
H CH (s-Bu) S (O) Et
H CH (s-Bu) S (O) CF_Three
H CH (s-Bu) S (O) CH₂CF_Three
H CH (s-Bu) S (O)₂Me
H CH (s-Bu) S (O)₂Et
H CH (s-Bu) S (O)₂CF_Three
H CH (s-Bu) S (O)₂CH₂CF_Three
H CH (t-Bu) SMe
H CH (t-Bu) SEt
H CH (t-Bu) SCF_Three
H CH (t-Bu) SCH₂CF_Three
H CH (t-Bu) S (O) Me
H CH (t-Bu) S (O) Et
H CH (t-Bu) S (O) CF_Three
H CH (t-Bu) S (O) CH₂CF_Three
H CH (t-Bu) S (O)₂Me
H CH (t-Bu) S (O)₂Et
H CH (t-Bu) S (O)₂CF_Three
H CH (t-Bu) S (O)₂CH₂CF_Three
H CH (CF_ThreeSMe
H CH (CF_Three) SEt
H CH (CF_Three) SCF_Three
H CH (CF_Three) SCH₂CF_Three
H CH (CF_Three) S (O) Me
H CH (CF_Three) S (O) Et
H CH (CF_Three) S (O) CF_Three
H CH (CF_Three) S (O) CH₂CF_Three
H CH (CF_Three) S (O)₂Me
H CH (CF_Three) S (O)₂Et
H CH (CF_Three) S (O)₂CF_Three
H CH (CF_Three) S (O)₂CH₂CF_Three
H CH₂CH₂SMe
H CH₂CH₂SEt
H CH₂CH₂SCF_Three
H CH₂CH₂SCH₂CF_Three
H CH₂CH₂S (O) Me
H CH₂CH₂S (O) Et
H CH₂CH₂S (O) CF_Three
H CH₂CH₂S (O) CH₂CF_Three
H CH₂CH₂S (O)₂Me
H CH₂CH₂S (O)₂Et
H CH₂CH₂S (O)₂CF_Three
H CH₂CH₂S (O)₂CH₂CF_Three
H CH (Me) CH₂SMe
H CH (Me) CH₂SEt
H CH (Me) CH₂SCF_Three
H CH (Me) CH₂SCH₂CF_Three
H CH (Me) CH₂S (O) Me
H CH (Me) CH₂S (O) Et
H CH (Me) CH₂S (O) CF_Three
H CH (Me) CH₂S (O) CH₂CF_Three
H CH (Me) CH₂S (O)₂Me
H CH (Me) CH₂S (O)₂Et
H CH (Me) CH₂S (O)₂CF_Three
H CH (Me) CH₂S (O)₂CH₂CF_Three
H CH (Et) CH₂SMe
H CH (Et) CH₂SEt
H CH (Et) CH₂SCF_Three
H CH (Et) CH₂SCH₂CF_Three
H CH (Et) CH₂S (O) Me
H CH (Et) CH₂S (O) Et
H CH (Et) CH₂S (O) CF_Three
H CH (Et) CH₂S (O) CH₂CF_Three
H CH (Et) CH₂S (O)₂Me
H CH (Et) CH₂S (O)₂Et
H CH (Et) CH₂S (O)₂CF_Three
H CH (Et) CH₂S (O)₂CH₂CF_Three
H C (Me)₂CH₂SMe
H C (Me)₂CH₂SEt
H C (Me)₂CH₂SCF_Three
H C (Me)₂CH₂SCH₂CF_Three
H C (Me)₂CH₂S (O) Me
H C (Me)₂CH₂S (O) Et
H C (Me)₂CH₂S (O) CF_Three
H C (Me)₂CH₂S (O) CH₂CF_Three
H C (Me)₂CH₂S (O)₂Me
H C (Me)₂CH₂S (O)₂Et
H C (Me)₂CH₂S (O)₂CF_Three
H C (Me)₂CH₂S (O)₂CH₂CF_Three
H CH₂CH (Me) SMe
H CH₂CH (Me) SEt
H CH₂CH (Me) SCF_Three
H CH₂CH (Me) SCH₂CF_Three
H CH₂CH (Me) S (O) Me
H CH₂CH (Me) S (O) Et
H CH₂CH (Me) S (O) CF_Three
H CH₂CH (Me) S (O) CH₂CF_Three
H CH₂CH (Me) S (O)₂Me
H CH₂CH (Me) S (O)₂Et
H CH₂CH (Me) S (O)₂CF_Three
H CH₂CH (Me) S (O)₂CH₂CF_Three
H CH₂CH (Et) SMe
H CH₂CH (Et) SEt
H CH₂CH (Et) SCF_Three
H CH₂CH (Et) SCH₂CF_Three
H CH₂CH (Et) S (O) Me
H CH₂CH (Et) S (O) Et
H CH₂CH (Et) S (O) CF_Three
H CH₂CH (Et) S (O) CH₂CF_Three
H CH₂CH (Et) S (O)₂Me
H CH₂CH (Et) S (O)₂Et
H CH₂CH (Et) S (O)₂CF_Three
H CH₂CH (Et) S (O)₂CH₂CF_Three
H CH (Me) CH (Me) SMe
H CH (Me) CH (Me) SEt
H CH (Me) CH (Me) SCF_Three
H CH (Me) CH (Me) SCH₂CF_Three
H CH (Me) CH (Me) S (O) Me
H CH (Me) CH (Me) S (O) Et
H CH (Me) CH (Me) S (O) CF_Three
H CH (Me) CH (Me) S (O) CH₂CF_Three
H CH (Me) CH (Me) S (O)₂Me
H CH (Me) CH (Me) S (O)₂Et
H CH (Me) CH (Me) S (O)₂CF_Three
H CH (Me) CH (Me) S (O)₂CH₂CF_Three
Me CH₂SMe
Me CH₂SEt
Me CH₂SCF_Three
Me CH₂SCH₂CF_Three
Me CH₂S (O) Me
Me CH₂S (O) Et
Me CH₂S (O) CF_Three
Me CH₂S (O) CH₂CF_Three
Me CH₂S (O)₂Me
Me CH₂S (O)₂Et
Me CH₂S (O)₂CF_Three
Me CH₂S (O)₂CH₂CF_Three
Me CH (Me) SMe
Me CH (Me) SEt
Me CH (Me) SCF_Three
Me CH (Me) SCH₂CF_Three
Me CH (Me) S (O) Me
Me CH (Me) S (O) Et
Me CH (Me) S (O) CF_Three
Me CH (Me) S (O) CH₂CF_Three
Me CH (Me) S (O)₂Me
Me CH (Me) S (O)₂Et
Me CH (Me) S (O)₂CF_Three
Me CH (Me) S (O)₂CH₂CF_Three
Me CH (Et) SMe
Me CH (Et) SEt
Me CH (Et) SCF_Three
Me CH (Et) SCH₂CF_Three
Me CH (Et) S (O) Me
Me CH (Et) S (O) Et
Me CH (Et) S (O) CF_Three
Me CH (Et) S (O) CH₂CF_Three
Me CH (Et) S (O)₂Me
Me CH (Et) S (O)₂Et
Me CH (Et) S (O)₂CF_Three
Me CH (Et) S (O)₂CH₂CF_Three
Me CH (n-Pr) SMe
Me CH (n-Pr) SEt
Me CH (n-Pr) SCF_Three
Me CH (n-Pr) SCH₂CF_Three
Me CH (n-Pr) S (O) Me
Me CH (n-Pr) S (O) Et
Me CH (n-Pr) S (O) CF_Three
Me CH (n-Pr) S (O) CH₂CF_Three
Me CH (n-Pr) S (O)₂Me
Me CH (n-Pr) S (O)₂Et
Me CH (n-Pr) S (O)₂CF_Three
Me CH (n-Pr) S (O)₂CH₂CF_Three
Me CH (i-Pr) SMe
Me CH (i-Pr) SEt
Me CH (i-Pr) SCF_Three
Me CH (i-Pr) SCH₂CF_Three
Me CH (i-Pr) S (O) Me
Me CH (i-Pr) S (O) Et
Me CH (i-Pr) S (O) CF_Three
Me CH (i-Pr) S (O) CH₂CF_Three
Me CH (i-Pr) S (O)₂Me
Me CH (i-Pr) S (O)₂Et
Me CH (i-Pr) S (O)₂CF_Three
Me CH (i-Pr) S (O)₂CH₂CF_Three
Me CH (n-Bu) SMe
Me CH (n-Bu) SEt
Me CH (n-Bu) SCF_Three
Me CH (n-Bu) SCH₂CF_Three
Me CH (n-Bu) S (O) Me
Me CH (n-Bu) S (O) Et
Me CH (n-Bu) S (O) CF_Three
Me CH (n-Bu) S (O) CH₂CF_Three
Me CH (n-Bu) S (O)₂Me
Me CH (n-Bu) S (O)₂Et
Me CH (n-Bu) S (O)₂CF_Three
Me CH (n-Bu) S (O)₂CH₂CF_Three
Me CH (i-Bu) SMe
Me CH (i-Bu) SEt
Me CH (i-Bu) SCF_Three
Me CH (i-Bu) SCH₂CF_Three
Me CH (i-Bu) S (O) Me
Me CH (i-Bu) S (O) Et
Me CH (i-Bu) S (O) CF_Three
Me CH (i-Bu) S (O) CH₂CF_Three
Me CH (i-Bu) S (O)₂Me
Me CH (i-Bu) S (O)₂Et
Me CH (i-Bu) S (O)₂CF_Three
Me CH (i-Bu) S (O)₂CH₂CF_Three
Me CH (s-Bu) SMe
Me CH (s-Bu) SEt
Me CH (s-Bu) SCF_Three
Me CH (s-Bu) SCH₂CF_Three
Me CH (s-Bu) S (O) Me
Me CH (s-Bu) S (O) Et
Me CH (s-Bu) S (O) CF_Three
Me CH (s-Bu) S (O) CH₂CF_Three
Me CH (s-Bu) S (O)₂Me
Me CH (s-Bu) S (O)₂Et
Me CH (s-Bu) S (O)₂CF_Three
Me CH (s-Bu) S (O)₂CH₂CF_Three
Me CH (t-Bu) SMe
Me CH (t-Bu) SEt
Me CH (t-Bu) SCF_Three
Me CH (t-Bu) SCH₂CF_Three
Me CH (t-Bu) S (O) Me
Me CH (t-Bu) S (O) Et
Me CH (t-Bu) S (O) CF_Three
Me CH (t-Bu) S (O) CH₂CF_Three
Me CH (t-Bu) S (O)₂Me
Me CH (t-Bu) S (O)₂Et
Me CH (t-Bu) S (O)₂CF_Three
Me CH (t-Bu) S (O)₂CH₂CF_Three
Me CH (CF_ThreeSMe
Me CH (CF_Three) SEt
Me CH (CF_Three) SCF_Three
Me CH (CF_Three) SCH₂CF_Three
Me CH (CF_Three) S (O) Me
Me CH (CF_Three) S (O) Et
Me CH (CF_Three) S (O) CF_Three
Me CH (CF_Three) S (O) CH₂CF_Three
Me CH (CF_Three) S (O)₂Me
Me CH (CF_Three) S (O)₂Et
Me CH (CF_Three) S (O)₂CF_Three
Me CH (CF_Three) S (O)₂CH₂CF_Three
Me CH₂CH₂SMe
Me CH₂CH₂SEt
Me CH₂CH₂SCF_Three
Me CH₂CH₂SCH₂CF_Three
Me CH₂CH₂S (O) Me
Me CH₂CH₂S (O) Et
Me CH₂CH₂S (O) CF_Three
Me CH₂CH₂S (O) CH₂CF_Three
Me CH₂CH₂S (O)₂Me
Me CH₂CH₂S (O)₂Et
Me CH₂CH₂S (O)₂CF_Three
Me CH₂CH₂S (O)₂CH₂CF_Three
Me CH (Me) CH₂SMe
Me CH (Me) CH₂SEt
Me CH (Me) CH₂SCF_Three
Me CH (Me) CH₂SCH₂CF_Three
Me CH (Me) CH₂S (O) Me
Me CH (Me) CH₂S (O) Et
Me CH (Me) CH₂S (O) CF_Three
Me CH (Me) CH₂S (O) CH₂CF_Three
Me CH (Me) CH₂S (O)₂Me
Me CH (Me) CH₂S (O)₂Et
Me CH (Me) CH₂S (O)₂CF_Three
Me CH (Me) CH₂S (O)₂CH₂CF_Three
Me CH (Et) CH₂SMe
Me CH (Et) CH₂SEt
Me CH (Et) CH₂SCF_Three
Me CH (Et) CH₂SCH₂CF_Three
Me CH (Et) CH₂S (O) Me
Me CH (Et) CH₂S (O) Et
Me CH (Et) CH₂S (O) CF_Three
Me CH (Et) CH₂S (O) CH₂CF_Three
Me CH (Et) CH₂S (O)₂Me
Me CH (Et) CH₂S (O)₂Et
Me CH (Et) CH₂S (O)₂CF_Three
Me CH (Et) CH₂S (O)₂CH₂CF_Three
Me C (Me)₂CH₂SMe
Me C (Me)₂CH₂SEt
Me C (Me)₂CH₂SCF_Three
Me C (Me)₂CH₂SCH₂CF_Three
Me C (Me)₂CH₂S (O) Me
Me C (Me)₂CH₂S (O) Et
Me C (Me)₂CH₂S (O) CF_Three
Me C (Me)₂CH₂S (O) CH₂CF_Three
Me C (Me)₂CH₂S (O)₂Me
Me C (Me)₂CH₂S (O)₂Et
Me C (Me)₂CH₂S (O)₂CF_Three
Me C (Me)₂CH₂S (O)₂CH₂CF_Three
Me CH₂CH (Me) SMe
Me CH₂CH (Me) SEt
Me CH₂CH (Me) SCF_Three
Me CH₂CH (Me) SCH₂CF_Three
Me CH₂CH (Me) S (O) Me
Me CH₂CH (Me) S (O) Et
Me CH₂CH (Me) S (O) CF_Three
Me CH₂CH (Me) S (O) CH₂CF_Three
Me CH₂CH (Me) S (O)₂Me
Me CH₂CH (Me) S (O)₂Et
Me CH₂CH (Me) S (O)₂CF_Three
Me CH₂CH (Me) S (O)₂CH₂CF_Three
Me CH₂CH (Et) SMe
Me CH₂CH (Et) SEt
Me CH₂CH (Et) SCF_Three
Me CH₂CH (Et) SCH₂CF_Three
Me CH₂CH (Et) S (O) Me
Me CH₂CH (Et) S (O) Et
Me CH₂CH (Et) S (O) CF_Three
Me CH₂CH (Et) S (O) CH₂CF_Three
Me CH₂CH (Et) S (O)₂Me
Me CH₂CH (Et) S (O)₂Et
Me CH₂CH (Et) S (O)₂CF_Three
Me CH₂CH (Et) S (O)₂CH₂CF_Three
Me CH (Me) CH (Me) SMe
Me CH (Me) CH (Me) SEt
Me CH (Me) CH (Me) SCF_Three
Me CH (Me) CH (Me) SCH₂CF_Three
Me CH (Me) CH (Me) S (O) Me
Me CH (Me) CH (Me) S (O) Et
Me CH (Me) CH (Me) S (O) CF_Three
Me CH (Me) CH (Me) S (O) CH₂CF_Three
Me CH (Me) CH (Me) S (O)₂Me
Me CH (Me) CH (Me) S (O)₂Et
Me CH (Me) CH (Me) S (O)₂CF_Three
Me CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂CF_Three        CH₂SMe
CH₂CF_Three        CH₂SEt
CH₂CF_Three        CH₂SCF_Three
CH₂CF_Three        CH₂SCH₂CF_Three
CH₂CF_Three        CH₂S (O) Me
CH₂CF_Three        CH₂S (O) Et
CH₂CF_Three        CH₂S (O) CF_Three
CH₂CF_Three        CH₂S (O) CH₂CF_Three
CH₂CF_Three        CH₂S (O)₂Me
CH₂CF_Three        CH₂S (O)₂Et
CH₂CF_Three        CH₂S (O)₂CF_Three
CH₂CF_Three        CH₂S (O)₂CH₂CF_Three
CH₂CF_Three        CH (Me) SMe
CH₂CF_Three        CH (Me) SEt
CH₂CF_Three        CH (Me) SCF_Three
CH₂CF_Three        CH (Me) SCH₂CF_Three
CH₂CF_Three        CH (Me) S (O) Me
CH₂CF_Three        CH (Me) S (O) Et
CH₂CF_Three        CH (Me) S (O) CF_Three
CH₂CF_Three        CH (Me) S (O) CH₂CF_Three
CH₂CF_Three        CH (Me) S (O)₂Me
CH₂CF_Three        CH (Me) S (O)₂Et
CH₂CF_Three        CH (Me) S (O)₂CF_Three
CH₂CF_Three        CH (Me) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (Et) SMe
CH₂CF_Three        CH (Et) SEt
CH₂CF_Three        CH (Et) SCF_Three
CH₂CF_Three        CH (Et) SCH₂CF_Three
CH₂CF_Three        CH (Et) S (O) Me
CH₂CF_Three        CH (Et) S (O) Et
CH₂CF_Three        CH (Et) S (O) CF_Three
CH₂CF_Three        CH (Et) S (O) CH₂CF_Three
CH₂CF_Three        CH (Et) S (O)₂Me
CH₂CF_Three        CH (Et) S (O)₂Et
CH₂CF_Three        CH (Et) S (O)₂CF_Three
CH₂CF_Three        CH (Et) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (n-Pr) SMe
CH₂CF_Three        CH (n-Pr) SEt
CH₂CF_Three        CH (n-Pr) SCF_Three
CH₂CF_Three        CH (n-Pr) SCH₂CF_Three
CH₂CF_Three        CH (n-Pr) S (O) Me
CH₂CF_Three        CH (n-Pr) S (O) Et
CH₂CF_Three        CH (n-Pr) S (O) CF_Three
CH₂CF_Three        CH (n-Pr) S (O) CH₂CF_Three
CH₂CF_Three        CH (n-Pr) S (O)₂Me
CH₂CF_Three        CH (n-Pr) S (O)₂Et
CH₂CF_Three        CH (n-Pr) S (O)₂CF_Three
CH₂CF_Three        CH (n-Pr) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (i-Pr) SMe
CH₂CF_Three        CH (i-Pr) SEt
CH₂CF_Three        CH (i-Pr) SCF_Three
CH₂CF_Three        CH (i-Pr) SCH₂CF_Three
CH₂CF_Three        CH (i-Pr) S (O) Me
CH₂CF_Three        CH (i-Pr) S (O) Et
CH₂CF_Three        CH (i-Pr) S (O) CF_Three
CH₂CF_Three        CH (i-Pr) S (O) CH₂CF_Three
CH₂CF_Three        CH (i-Pr) S (O)₂Me
CH₂CF_Three        CH (i-Pr) S (O)₂Et
CH₂CF_Three        CH (i-Pr) S (O)₂CF_Three
CH₂CF_Three        CH (i-Pr) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (n-Bu) SMe
CH₂CF_Three        CH (n-Bu) SEt
CH₂CF_Three        CH (n-Bu) SCF_Three
CH₂CF_Three        CH (n-Bu) SCH₂CF_Three
CH₂CF_Three        CH (n-Bu) S (O) Me
CH₂CF_Three        CH (n-Bu) S (O) Et
CH₂CF_Three        CH (n-Bu) S (O) CF_Three
CH₂CF_Three        CH (n-Bu) S (O) CH₂CF_Three
CH₂CF_Three        CH (n-Bu) S (O)₂Me
CH₂CF_Three        CH (n-Bu) S (O)₂Et
CH₂CF_Three        CH (n-Bu) S (O)₂CF_Three
CH₂CF_Three        CH (n-Bu) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (i-Bu) SMe
CH₂CF_Three        CH (i-Bu) SEt
CH₂CF_Three        CH (i-Bu) SCF_Three
CH₂CF_Three        CH (i-Bu) SCH₂CF_Three
CH₂CF_Three        CH (i-Bu) S (O) Me
CH₂CF_Three        CH (i-Bu) S (O) Et
CH₂CF_Three        CH (i-Bu) S (O) CF_Three
CH₂CF_Three        CH (i-Bu) S (O) CH₂CF_Three
CH₂CF_Three        CH (i-Bu) S (O)₂Me
CH₂CF_Three        CH (i-Bu) S (O)₂Et
CH₂CF_Three        CH (i-Bu) S (O)₂CF_Three
CH₂CF_Three        CH (i-Bu) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (s-Bu) SMe
CH₂CF_Three        CH (s-Bu) SEt
CH₂CF_Three        CH (s-Bu) SCF_Three
CH₂CF_Three        CH (s-Bu) SCH₂CF_Three
CH₂CF_Three        CH (s-Bu) S (O) Me
CH₂CF_Three        CH (s-Bu) S (O) Et
CH₂CF_Three        CH (s-Bu) S (O) CF_Three
CH₂CF_Three        CH (s-Bu) S (O) CH₂CF_Three
CH₂CF_Three        CH (s-Bu) S (O)₂Me
CH₂CF_Three        CH (s-Bu) S (O)₂Et
CH₂CF_Three        CH (s-Bu) S (O)₂CF_Three
CH₂CF_Three        CH (s-Bu) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (t-Bu) SMe
CH₂CF_Three        CH (t-Bu) SEt
CH₂CF_Three        CH (t-Bu) SCF_Three
CH₂CF_Three        CH (t-Bu) SCH₂CF_Three
CH₂CF_Three        CH (t-Bu) S (O) Me
CH₂CF_Three        CH (t-Bu) S (O) Et
CH₂CF_Three        CH (t-Bu) S (O) CF_Three
CH₂CF_Three        CH (t-Bu) S (O) CH₂CF_Three
CH₂CF_Three        CH (t-Bu) S (O)₂Me
CH₂CF_Three        CH (t-Bu) S (O)₂Et
CH₂CF_Three        CH (t-Bu) S (O)₂CF_Three
CH₂CF_Three        CH (t-Bu) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (CF_ThreeSMe
CH₂CF_Three        CH (CF_Three) SEt
CH₂CF_Three        CH (CF_Three) SCF_Three
CH₂CF_Three        CH (CF_Three) SCH₂CF_Three
CH₂CF_Three        CH (CF_Three) S (O) Me
CH₂CF_Three        CH (CF_Three) S (O) Et
CH₂CF_Three        CH (CF_Three) S (O) CF_Three
CH₂CF_Three        CH (CF_Three) S (O) CH₂CF_Three
CH₂CF_Three        CH (CF_Three) S (O)₂Me
CH₂CF_Three        CH (CF_Three) S (O)₂Et
CH₂CF_Three        CH (CF_Three) S (O)₂CF_Three
CH₂CF_Three        CH (CF_Three) S (O)₂CH₂CF_Three
CH₂CF_Three        CH₂CH₂SMe
CH₂CF_Three        CH₂CH₂SEt
CH₂CF_Three        CH₂CH₂SCF_Three
CH₂CF_Three        CH₂CH₂SCH₂CF_Three
CH₂CF_Three        CH₂CH₂S (O) Me
CH₂CF_Three        CH₂CH₂S (O) Et
CH₂CF_Three        CH₂CH₂S (O) CF_Three
CH₂CF_Three        CH₂CH₂S (O) CH₂CF_Three
CH₂CF_Three        CH₂CH₂S (O)₂Me
CH₂CF_Three        CH₂CH₂S (O)₂Et
CH₂CF_Three        CH₂CH₂S (O)₂CF_Three
CH₂CF_Three        CH₂CH₂S (O)₂CH₂CF_Three
CH₂CF_Three        CH (Me) CH₂SMe
CH₂CF_Three        CH (Me) CH₂SEt
CH₂CF_Three        CH (Me) CH₂SCF_Three
CH₂CF_Three        CH (Me) CH₂SCH₂CF_Three
CH₂CF_Three        CH (Me) CH₂S (O) Me
CH₂CF_Three        CH (Me) CH₂S (O) Et
CH₂CF_Three        CH (Me) CH₂S (O) CF_Three
CH₂CF_Three        CH (Me) CH₂S (O) CH₂CF_Three
CH₂CF_Three        CH (Me) CH₂S (O)₂Me
CH₂CF_Three        CH (Me) CH₂S (O)₂Et
CH₂CF_Three        CH (Me) CH₂S (O)₂CF_Three
CH₂CF_Three        CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂CF_Three        CH (Et) CH₂SMe
CH₂CF_Three        CH (Et) CH₂SEt
CH₂CF_Three        CH (Et) CH₂SCF_Three
CH₂CF_Three        CH (Et) CH₂SCH₂CF_Three
CH₂CF_Three        CH (Et) CH₂S (O) Me
CH₂CF_Three        CH (Et) CH₂S (O) Et
CH₂CF_Three        CH (Et) CH₂S (O) CF_Three
CH₂CF_Three        CH (Et) CH₂S (O) CH₂CF_Three
CH₂CF_Three        CH (Et) CH₂S (O)₂Me
CH₂CF_Three        CH (Et) CH₂S (O)₂Et
CH₂CF_Three        CH (Et) CH₂S (O)₂CF_Three
CH₂CF_Three        CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂CF_Three        C (Me)₂CH₂SMe
CH₂CF_Three        C (Me)₂CH₂SEt
CH₂CF_Three        C (Me)₂CH₂SCF_Three
CH₂CF_Three        C (Me)₂CH₂SCH₂CF_Three
CH₂CF_Three        C (Me)₂CH₂S (O) Me
CH₂CF_Three        C (Me)₂CH₂S (O) Et
CH₂CF_Three        C (Me)₂CH₂S (O) CF_Three
CH₂CF_Three        C (Me)₂CH₂S (O) CH₂CF_Three
CH₂CF_Three        C (Me)₂CH₂S (O)₂Me
CH₂CF_Three        C (Me)₂CH₂S (O)₂Et
CH₂CF_Three        C (Me)₂CH₂S (O)₂CF_Three
CH₂CF_Three        C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂CF_Three        CH₂CH (Me) SMe
CH₂CF_Three        CH₂CH (Me) SEt
CH₂CF_Three        CH₂CH (Me) SCF_Three
CH₂CF_Three        CH₂CH (Me) SCH₂CF_Three
CH₂CF_Three        CH₂CH (Me) S (O) Me
CH₂CF_Three        CH₂CH (Me) S (O) Et
CH₂CF_Three        CH₂CH (Me) S (O) CF_Three
CH₂CF_Three        CH₂CH (Me) S (O) CH₂CF_Three
CH₂CF_Three        CH₂CH (Me) S (O)₂Me
CH₂CF_Three        CH₂CH (Me) S (O)₂Et
CH₂CF_Three        CH₂CH (Me) S (O)₂CF_Three
CH₂CF_Three        CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂CF_Three        CH₂CH (Et) SMe
CH₂CF_Three        CH₂CH (Et) SEt
CH₂CF_Three        CH₂CH (Et) SCF_Three
CH₂CF_Three        CH₂CH (Et) SCH₂CF_Three
CH₂CF_Three        CH₂CH (Et) S (O) Me
CH₂CF_Three        CH₂CH (Et) S (O) Et
CH₂CF_Three        CH₂CH (Et) S (O) CF_Three
CH₂CF_Three        CH₂CH (Et) S (O) CH₂CF_Three
CH₂CF_Three        CH₂CH (Et) S (O)₂Me
CH₂CF_Three        CH₂CH (Et) S (O)₂Et
CH₂CF_Three        CH₂CH (Et) S (O)₂CF_Three
CH₂CF_Three        CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂CF_Three        CH (Me) CH (Me) SMe
CH₂CF_Three        CH (Me) CH (Me) SEt
CH₂CF_Three        CH (Me) CH (Me) SCF_Three
CH₂CF_Three        CH (Me) CH (Me) SCH₂CF_Three
CH₂CF_Three        CH (Me) CH (Me) S (O) Me
CH₂CF_Three        CH (Me) CH (Me) S (O) Et
CH₂CF_Three        CH (Me) CH (Me) S (O) CF_Three
CH₂CF_Three        CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂CF_Three        CH (Me) CH (Me) S (O)₂Me
CH₂CF_Three        CH (Me) CH (Me) S (O)₂Et
CH₂CF_Three        CH (Me) CH (Me) S (O)₂CF_Three
CH₂CF_Three        CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂CN CH₂SMe
CH₂CN CH₂SEt
CH₂CN CH₂SCF_Three
CH₂CN CH₂SCH₂CF_Three
CH₂CN CH₂S (O) Me
CH₂CN CH₂S (O) Et
CH₂CN CH₂S (O) CF_Three
CH₂CN CH₂S (O) CH₂CF_Three
CH₂CN CH₂S (O)₂Me
CH₂CN CH₂S (O)₂Et
CH₂CN CH₂S (O)₂CF_Three
CH₂CN CH₂S (O)₂CH₂CF_Three
CH₂CN CH (Me) SMe
CH₂CN CH (Me) SEt
CH₂CN CH (Me) SCF_Three
CH₂CN CH (Me) SCH₂CF_Three
CH₂CN CH (Me) S (O) Me
CH₂CN CH (Me) S (O) Et
CH₂CN CH (Me) S (O) CF_Three
CH₂CN CH (Me) S (O) CH₂CF_Three
CH₂CN CH (Me) S (O)₂Me
CH₂CN CH (Me) S (O)₂Et
CH₂CN CH (Me) S (O)₂CF_Three
CH₂CN CH (Me) S (O)₂CH₂CF_Three
CH₂CN CH (Et) SMe
CH₂CN CH (Et) SEt
CH₂CN CH (Et) SCF_Three
CH₂CN CH (Et) SCH₂CF_Three
CH₂CN CH (Et) S (O) Me
CH₂CN CH (Et) S (O) Et
CH₂CN CH (Et) S (O) CF_Three
CH₂CN CH (Et) S (O) CH₂CF_Three
CH₂CN CH (Et) S (O)₂Me
CH₂CN CH (Et) S (O)₂Et
CH₂CN CH (Et) S (O)₂CF_Three
CH₂CN CH (Et) S (O)₂CH₂CF_Three
CH₂CN CH (n-Pr) SMe
CH₂CN CH (n-Pr) SEt
CH₂CN CH (n-Pr) SCF_Three
CH₂CN CH (n-Pr) SCH₂CF_Three
CH₂CN CH (n-Pr) S (O) Me
CH₂CN CH (n-Pr) S (O) Et
CH₂CN CH (n-Pr) S (O) CF_Three
CH₂CN CH (n-Pr) S (O) CH₂CF_Three
CH₂CN CH (n-Pr) S (O)₂Me
CH₂CN CH (n-Pr) S (O)₂Et
CH₂CN CH (n-Pr) S (O)₂CF_Three
CH₂CN CH (n-Pr) S (O)₂CH₂CF_Three
CH₂CN CH (i-Pr) SMe
CH₂CN CH (i-Pr) SEt
CH₂CN CH (i-Pr) SCF_Three
CH₂CN CH (i-Pr) SCH₂CF_Three
CH₂CN CH (i-Pr) S (O) Me
CH₂CN CH (i-Pr) S (O) Et
CH₂CN CH (i-Pr) S (O) CF_Three
CH₂CN CH (i-Pr) S (O) CH₂CF_Three
CH₂CN CH (i-Pr) S (O)₂Me
CH₂CN CH (i-Pr) S (O)₂Et
CH₂CN CH (i-Pr) S (O)₂CF_Three
CH₂CN CH (i-Pr) S (O)₂CH₂CF_Three
CH₂CN CH (n-Bu) SMe
CH₂CN CH (n-Bu) SEt
CH₂CN CH (n-Bu) SCF_Three
CH₂CN CH (n-Bu) SCH₂CF_Three
CH₂CN CH (n-Bu) S (O) Me
CH₂CN CH (n-Bu) S (O) Et
CH₂CN CH (n-Bu) S (O) CF_Three
CH₂CN CH (n-Bu) S (O) CH₂CF_Three
CH₂CN CH (n-Bu) S (O)₂Me
CH₂CN CH (n-Bu) S (O)₂Et
CH₂CN CH (n-Bu) S (O)₂CF_Three
CH₂CN CH (n-Bu) S (O)₂CH₂CF_Three
CH₂CN CH (i-Bu) SMe
CH₂CN CH (i-Bu) SEt
CH₂CN CH (i-Bu) SCF_Three
CH₂CN CH (i-Bu) SCH₂CF_Three
CH₂CN CH (i-Bu) S (O) Me
CH₂CN CH (i-Bu) S (O) Et
CH₂CN CH (i-Bu) S (O) CF_Three
CH₂CN CH (i-Bu) S (O) CH₂CF_Three
CH₂CN CH (i-Bu) S (O)₂Me
CH₂CN CH (i-Bu) S (O)₂Et
CH₂CN CH (i-Bu) S (O)₂CF_Three
CH₂CN CH (i-Bu) S (O)₂CH₂CF_Three
CH₂CN CH (s-Bu) SMe
CH₂CN CH (s-Bu) SEt
CH₂CN CH (s-Bu) SCF_Three
CH₂CN CH (s-Bu) SCH₂CF_Three
CH₂CN CH (s-Bu) S (O) Me
CH₂CN CH (s-Bu) S (O) Et
CH₂CN CH (s-Bu) S (O) CF_Three
CH₂CN CH (s-Bu) S (O) CH₂CF_Three
CH₂CN CH (s-Bu) S (O)₂Me
CH₂CN CH (s-Bu) S (O)₂Et
CH₂CN CH (s-Bu) S (O)₂CF_Three
CH₂CN CH (s-Bu) S (O)₂CH₂CF_Three
CH₂CN CH (t-Bu) SMe
CH₂CN CH (t-Bu) SEt
CH₂CN CH (t-Bu) SCF_Three
CH₂CN CH (t-Bu) SCH₂CF_Three
CH₂CN CH (t-Bu) S (O) Me
CH₂CN CH (t-Bu) S (O) Et
CH₂CN CH (t-Bu) S (O) CF_Three
CH₂CN CH (t-Bu) S (O) CH₂CF_Three
CH₂CN CH (t-Bu) S (O)₂Me
CH₂CN CH (t-Bu) S (O)₂Et
CH₂CN CH (t-Bu) S (O)₂CF_Three
CH₂CN CH (t-Bu) S (O)₂CH₂CF_Three
CH₂CN CH (CF_ThreeSMe
CH₂CN CH (CF_Three) SEt
CH₂CN CH (CF_Three) SCF_Three
CH₂CN CH (CF_Three) SCH₂CF_Three
CH₂CN CH (CF_Three) S (O) Me
CH₂CN CH (CF_Three) S (O) Et
CH₂CN CH (CF_Three) S (O) CF_Three
CH₂CN CH (CF_Three) S (O) CH₂CF_Three
CH₂CN CH (CF_Three) S (O)₂Me
CH₂CN CH (CF_Three) S (O)₂Et
CH₂CN CH (CF_Three) S (O)₂CF_Three
CH₂CN CH (CF_Three) S (O)₂CH₂CF_Three
CH₂CN CH₂CH₂SMe
CH₂CN CH₂CH₂SEt
CH₂CN CH₂CH₂SCF_Three
CH₂CN CH₂CH₂SCH₂CF_Three
CH₂CN CH₂CH₂S (O) Me
CH₂CN CH₂CH₂S (O) Et
CH₂CN CH₂CH₂S (O) CF_Three
CH₂CN CH₂CH₂S (O) CH₂CF_Three
CH₂CN CH₂CH₂S (O)₂Me
CH₂CN CH₂CH₂S (O)₂Et
CH₂CN CH₂CH₂S (O)₂CF_Three
CH₂CN CH₂CH₂S (O)₂CH₂CF_Three
CH₂CN CH (Me) CH₂SMe
CH₂CN CH (Me) CH₂SEt
CH₂CN CH (Me) CH₂SCF_Three
CH₂CN CH (Me) CH₂SCH₂CF_Three
CH₂CN CH (Me) CH₂S (O) Me
CH₂CN CH (Me) CH₂S (O) Et
CH₂CN CH (Me) CH₂S (O) CF_Three
CH₂CN CH (Me) CH₂S (O) CH₂CF_Three
CH₂CN CH (Me) CH₂S (O)₂Me
CH₂CN CH (Me) CH₂S (O)₂Et
CH₂CN CH (Me) CH₂S (O)₂CF_Three
CH₂CN CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂CN CH (Et) CH₂SMe
CH₂CN CH (Et) CH₂SEt
CH₂CN CH (Et) CH₂SCF_Three
CH₂CN CH (Et) CH₂SCH₂CF_Three
CH₂CN CH (Et) CH₂S (O) Me
CH₂CN CH (Et) CH₂S (O) Et
CH₂CN CH (Et) CH₂S (O) CF_Three
CH₂CN CH (Et) CH₂S (O) CH₂CF_Three
CH₂CN CH (Et) CH₂S (O)₂Me
CH₂CN CH (Et) CH₂S (O)₂Et
CH₂CN CH (Et) CH₂S (O)₂CF_Three
CH₂CN CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂CN C (Me)₂CH₂SMe
CH₂CN C (Me)₂CH₂SEt
CH₂CN C (Me)₂CH₂SCF_Three
CH₂CN C (Me)₂CH₂SCH₂CF_Three
CH₂CN C (Me)₂CH₂S (O) Me
CH₂CN C (Me)₂CH₂S (O) Et
CH₂CN C (Me)₂CH₂S (O) CF_Three
CH₂CN C (Me)₂CH₂S (O) CH₂CF_Three
CH₂CN C (Me)₂CH₂S (O)₂Me
CH₂CN C (Me)₂CH₂S (O)₂Et
CH₂CN C (Me)₂CH₂S (O)₂CF_Three
CH₂CN C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂CN CH₂CH (Me) SMe
CH₂CN CH₂CH (Me) SEt
CH₂CN CH₂CH (Me) SCF_Three
CH₂CN CH₂CH (Me) SCH₂CF_Three
CH₂CN CH₂CH (Me) S (O) Me
CH₂CN CH₂CH (Me) S (O) Et
CH₂CN CH₂CH (Me) S (O) CF_Three
CH₂CN CH₂CH (Me) S (O) CH₂CF_Three
CH₂CN CH₂CH (Me) S (O)₂Me
CH₂CN CH₂CH (Me) S (O)₂Et
CH₂CN CH₂CH (Me) S (O)₂CF_Three
CH₂CN CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂CN CH₂CH (Et) SMe
CH₂CN CH₂CH (Et) SEt
CH₂CN CH₂CH (Et) SCF_Three
CH₂CN CH₂CH (Et) SCH₂CF_Three
CH₂CN CH₂CH (Et) S (O) Me
CH₂CN CH₂CH (Et) S (O) Et
CH₂CN CH₂CH (Et) S (O) CF_Three
CH₂CN CH₂CH (Et) S (O) CH₂CF_Three
CH₂CN CH₂CH (Et) S (O)₂Me
CH₂CN CH₂CH (Et) S (O)₂Et
CH₂CN CH₂CH (Et) S (O)₂CF_Three
CH₂CN CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂CN CH (Me) CH (Me) SMe
CH₂CN CH (Me) CH (Me) SEt
CH₂CN CH (Me) CH (Me) SCF_Three
CH₂CN CH (Me) CH (Me) SCH₂CF_Three
CH₂CN CH (Me) CH (Me) S (O) Me
CH₂CN CH (Me) CH (Me) S (O) Et
CH₂CN CH (Me) CH (Me) S (O) CF_Three
CH₂CN CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂CN CH (Me) CH (Me) S (O)₂Me
CH₂CN CH (Me) CH (Me) S (O)₂Et
CH₂CN CH (Me) CH (Me) S (O)₂CF_Three
CH₂CN CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH₂SMe
CH₂CH = CH₂     CH₂SEt
CH₂CH = CH₂     CH₂SCF_Three
CH₂CH = CH₂     CH₂SCH₂CF_Three
CH₂CH = CH₂     CH₂S (O) Me
CH₂CH = CH₂     CH₂S (O) Et
CH₂CH = CH₂     CH₂S (O) CF_Three
CH₂CH = CH₂     CH₂S (O) CH₂CF_Three
CH₂CH = CH₂     CH₂S (O)₂Me
CH₂CH = CH₂     CH₂S (O)₂Et
CH₂CH = CH₂     CH₂S (O)₂CF_Three
CH₂CH = CH₂     CH₂S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (Me) SMe
CH₂CH = CH₂     CH (Me) SEt
CH₂CH = CH₂     CH (Me) SCF_Three
CH₂CH = CH₂     CH (Me) SCH₂CF_Three
CH₂CH = CH₂     CH (Me) S (O) Me
CH₂CH = CH₂     CH (Me) S (O) Et
CH₂CH = CH₂     CH (Me) S (O) CF_Three
CH₂CH = CH₂     CH (Me) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (Me) S (O)₂Me
CH₂CH = CH₂     CH (Me) S (O)₂Et
CH₂CH = CH₂     CH (Me) S (O)₂CF_Three
CH₂CH = CH₂     CH (Me) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (Et) SMe
CH₂CH = CH₂     CH (Et) SEt
CH₂CH = CH₂     CH (Et) SCF_Three
CH₂CH = CH₂     CH (Et) SCH₂CF_Three
CH₂CH = CH₂     CH (Et) S (O) Me
CH₂CH = CH₂     CH (Et) S (O) Et
CH₂CH = CH₂     CH (Et) S (O) CF_Three
CH₂CH = CH₂     CH (Et) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (Et) S (O)₂Me
CH₂CH = CH₂     CH (Et) S (O)₂Et
CH₂CH = CH₂     CH (Et) S (O)₂CF_Three
CH₂CH = CH₂     CH (Et) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (n-Pr) SMe
CH₂CH = CH₂     CH (n-Pr) SEt
CH₂CH = CH₂     CH (n-Pr) SCF_Three
CH₂CH = CH₂     CH (n-Pr) SCH₂CF_Three
CH₂CH = CH₂     CH (n-Pr) S (O) Me
CH₂CH = CH₂     CH (n-Pr) S (O) Et
CH₂CH = CH₂     CH (n-Pr) S (O) CF_Three
CH₂CH = CH₂     CH (n-Pr) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (n-Pr) S (O)₂Me
CH₂CH = CH₂     CH (n-Pr) S (O)₂Et
CH₂CH = CH₂     CH (n-Pr) S (O)₂CF_Three
CH₂CH = CH₂     CH (n-Pr) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (i-Pr) SMe
CH₂CH = CH₂     CH (i-Pr) SEt
CH₂CH = CH₂     CH (i-Pr) SCF_Three
CH₂CH = CH₂     CH (i-Pr) SCH₂CF_Three
CH₂CH = CH₂     CH (i-Pr) S (O) Me
CH₂CH = CH₂     CH (i-Pr) S (O) Et
CH₂CH = CH₂     CH (i-Pr) S (O) CF_Three
CH₂CH = CH₂     CH (i-Pr) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (i-Pr) S (O)₂Me
CH₂CH = CH₂     CH (i-Pr) S (O)₂Et
CH₂CH = CH₂     CH (i-Pr) S (O)₂CF_Three
CH₂CH = CH₂     CH (i-Pr) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (n-Bu) SMe
CH₂CH = CH₂     CH (n-Bu) SEt
CH₂CH = CH₂     CH (n-Bu) SCF_Three
CH₂CH = CH₂     CH (n-Bu) SCH₂CF_Three
CH₂CH = CH₂     CH (n-Bu) S (O) Me
CH₂CH = CH₂     CH (n-Bu) S (O) Et
CH₂CH = CH₂     CH (n-Bu) S (O) CF_Three
CH₂CH = CH₂     CH (n-Bu) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (n-Bu) S (O)₂Me
CH₂CH = CH₂     CH (n-Bu) S (O)₂Et
CH₂CH = CH₂     CH (n-Bu) S (O)₂CF_Three
CH₂CH = CH₂     CH (n-Bu) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (i-Bu) SMe
CH₂CH = CH₂     CH (i-Bu) SEt
CH₂CH = CH₂     CH (i-Bu) SCF_Three
CH₂CH = CH₂     CH (i-Bu) SCH₂CF_Three
CH₂CH = CH₂     CH (i-Bu) S (O) Me
CH₂CH = CH₂     CH (i-Bu) S (O) Et
CH₂CH = CH₂     CH (i-Bu) S (O) CF_Three
CH₂CH = CH₂     CH (i-Bu) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (i-Bu) S (O)₂Me
CH₂CH = CH₂     CH (i-Bu) S (O)₂Et
CH₂CH = CH₂     CH (i-Bu) S (O)₂CF_Three
CH₂CH = CH₂     CH (i-Bu) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (s-Bu) SMe
CH₂CH = CH₂     CH (s-Bu) SEt
CH₂CH = CH₂     CH (s-Bu) SCF_Three
CH₂CH = CH₂     CH (s-Bu) SCH₂CF_Three
CH₂CH = CH₂     CH (s-Bu) S (O) Me
CH₂CH = CH₂     CH (s-Bu) S (O) Et
CH₂CH = CH₂     CH (s-Bu) S (O) CF_Three
CH₂CH = CH₂     CH (s-Bu) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (s-Bu) S (O)₂Me
CH₂CH = CH₂     CH (s-Bu) S (O)₂Et
CH₂CH = CH₂     CH (s-Bu) S (O)₂CF_Three
CH₂CH = CH₂     CH (s-Bu) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (t-Bu) SMe
CH₂CH = CH₂     CH (t-Bu) SEt
CH₂CH = CH₂     CH (t-Bu) SCF_Three
CH₂CH = CH₂     CH (t-Bu) SCH₂CF_Three
CH₂CH = CH₂     CH (t-Bu) S (O) Me
CH₂CH = CH₂     CH (t-Bu) S (O) Et
CH₂CH = CH₂     CH (t-Bu) S (O) CF_Three
CH₂CH = CH₂     CH (t-Bu) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (t-Bu) S (O)₂Me
CH₂CH = CH₂     CH (t-Bu) S (O)₂Et
CH₂CH = CH₂     CH (t-Bu) S (O)₂CF_Three
CH₂CH = CH₂     CH (t-Bu) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (CF_ThreeSMe
CH₂CH = CH₂     CH (CF_Three) SEt
CH₂CH = CH₂     CH (CF_Three) SCF_Three
CH₂CH = CH₂     CH (CF_Three) SCH₂CF_Three
CH₂CH = CH₂     CH (CF_Three) S (O) Me
CH₂CH = CH₂     CH (CF_Three) S (O) Et
CH₂CH = CH₂     CH (CF_Three) S (O) CF_Three
CH₂CH = CH₂     CH (CF_Three) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (CF_Three) S (O)₂Me
CH₂CH = CH₂     CH (CF_Three) S (O)₂Et
CH₂CH = CH₂     CH (CF_Three) S (O)₂CF_Three
CH₂CH = CH₂     CH (CF_Three) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH₂CH₂SMe
CH₂CH = CH₂     CH₂CH₂SEt
CH₂CH = CH₂     CH₂CH₂SCF_Three
CH₂CH = CH₂     CH₂CH₂SCH₂CF_Three
CH₂CH = CH₂     CH₂CH₂S (O) Me
CH₂CH = CH₂     CH₂CH₂S (O) Et
CH₂CH = CH₂     CH₂CH₂S (O) CF_Three
CH₂CH = CH₂     CH₂CH₂S (O) CH₂CF_Three
CH₂CH = CH₂     CH₂CH₂S (O)₂Me
CH₂CH = CH₂     CH₂CH₂S (O)₂Et
CH₂CH = CH₂     CH₂CH₂S (O)₂CF_Three
CH₂CH = CH₂     CH₂CH₂S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (Me) CH₂SMe
CH₂CH = CH₂     CH (Me) CH₂SEt
CH₂CH = CH₂     CH (Me) CH₂SCF_Three
CH₂CH = CH₂     CH (Me) CH₂SCH₂CF_Three
CH₂CH = CH₂     CH (Me) CH₂S (O) Me
CH₂CH = CH₂     CH (Me) CH₂S (O) Et
CH₂CH = CH₂     CH (Me) CH₂S (O) CF_Three
CH₂CH = CH₂     CH (Me) CH₂S (O) CH₂CF_Three
CH₂CH = CH₂     CH (Me) CH₂S (O)₂Me
CH₂CH = CH₂     CH (Me) CH₂S (O)₂Et
CH₂CH = CH₂     CH (Me) CH₂S (O)₂CF_Three
CH₂CH = CH₂     CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (Et) CH₂SMe
CH₂CH = CH₂     CH (Et) CH₂SEt
CH₂CH = CH₂     CH (Et) CH₂SCF_Three
CH₂CH = CH₂     CH (Et) CH₂SCH₂CF_Three
CH₂CH = CH₂     CH (Et) CH₂S (O) Me
CH₂CH = CH₂     CH (Et) CH₂S (O) Et
CH₂CH = CH₂     CH (Et) CH₂S (O) CF_Three
CH₂CH = CH₂     CH (Et) CH₂S (O) CH₂CF_Three
CH₂CH = CH₂     CH (Et) CH₂S (O)₂Me
CH₂CH = CH₂    CH (Et) CH₂S (O)₂Et
CH₂CH = CH₂     CH (Et) CH₂S (O)₂CF_Three
CH₂CH = CH₂     CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂CH = CH₂     C (Me)₂CH₂SMe
CH₂CH = CH₂     C (Me)₂CH₂SEt
CH₂CH = CH₂     C (Me)₂CH₂SCF_Three
CH₂CH = CH₂     C (Me)₂CH₂SCH₂CF_Three
CH₂CH = CH₂     C (Me)₂CH₂S (O) Me
CH₂CH = CH₂     C (Me)₂CH₂S (O) Et
CH₂CH = CH₂     C (Me)₂CH₂S (O) CF_Three
CH₂CH = CH₂     C (Me)₂CH₂S (O) CH₂CF_Three
CH₂CH = CH₂     C (Me)₂CH₂S (O)₂Me
CH₂CH = CH₂     C (Me)₂CH₂S (O)₂Et
CH₂CH = CH₂     C (Me)₂CH₂S (O)₂CF_Three
CH₂CH = CH₂     C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH₂CH (Me) SMe
CH₂CH = CH₂     CH₂CH (Me) SEt
CH₂CH = CH₂     CH₂CH (Me) SCF_Three
CH₂CH = CH₂     CH₂CH (Me) SCH₂CF_Three
CH₂CH = CH₂     CH₂CH (Me) S (O) Me
CH₂CH = CH₂     CH₂CH (Me) S (O) Et
CH₂CH = CH₂     CH₂CH (Me) S (O) CF_Three
CH₂CH = CH₂     CH₂CH (Me) S (O) CH₂CF_Three
CH₂CH = CH₂     CH₂CH (Me) S (O)₂Me
CH₂CH = CH₂     CH₂CH (Me) S (O)₂Et
CH₂CH = CH₂     CH₂CH (Me) S (O)₂CF_Three
CH₂CH = CH₂     CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH₂CH (Et) SMe
CH₂CH = CH₂     CH₂CH (Et) SEt
CH₂CH = CH₂     CH₂CH (Et) SCF_Three
CH₂CH = CH₂     CH₂CH (Et) SCH₂CF_Three
CH₂CH = CH₂     CH₂CH (Et) S (O) Me
CH₂CH = CH₂     CH₂CH (Et) S (O) Et
CH₂CH = CH₂     CH₂CH (Et) S (O) CF_Three
CH₂CH = CH₂     CH₂CH (Et) S (O) CH₂CF_Three
CH₂CH = CH₂     CH₂CH (Et) S (O)₂Me
CH₂CH = CH₂     CH₂CH (Et) S (O)₂Et
CH₂CH = CH₂     CH₂CH (Et) S (O)₂CF_Three
CH₂CH = CH₂     CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂CH = CH₂     CH (Me) CH (Me) SMe
CH₂CH = CH₂     CH (Me) CH (Me) SEt
CH₂CH = CH₂     CH (Me) CH (Me) SCF_Three
CH₂CH = CH₂     CH (Me) CH (Me) SCH₂CF_Three
CH₂CH = CH₂     CH (Me) CH (Me) S (O) Me
CH₂CH = CH₂     CH (Me) CH (Me) S (O) Et
CH₂CH = CH₂     CH (Me) CH (Me) S (O) CF_Three
CH₂CH = CH₂     CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂CH = CH₂     CH (Me) CH (Me) S (O)₂Me
CH₂CH = CH₂     CH (Me) CH (Me) S (O)₂Et
CH₂CH = CH₂     CH (Me) CH (Me) S (O)₂CF_Three
CH₂CH = CH₂     CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH₂SMe
CH₂CH (OMe)₂   CH₂SEt
CH₂CH (OMe)₂   CH₂SCF_Three
CH₂CH (OMe)₂   CH₂SCH₂CF_Three
CH₂CH (OMe)₂   CH₂S (O) Me
CH₂CH (OMe)₂   CH₂S (O) Et
CH₂CH (OMe)₂   CH₂S (O) CF_Three
CH₂CH (OMe)₂   CH₂S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH₂S (O)₂Me
CH₂CH (OMe)₂   CH₂S (O)₂Et
CH₂CH (OMe)₂   CH₂S (O)₂CF_Three
CH₂CH (OMe)₂   CH₂S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (Me) SMe
CH₂CH (OMe)₂   CH (Me) SEt
CH₂CH (OMe)₂   CH (Me) SCF_Three
CH₂CH (OMe)₂   CH (Me) SCH₂CF_Three
CH₂CH (OMe)₂   CH (Me) S (O) Me
CH₂CH (OMe)₂   CH (Me) S (O) Et
CH₂CH (OMe)₂   CH (Me) S (O) CF_Three
CH₂CH (OMe)₂   CH (Me) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (Me) S (O)₂Me
CH₂CH (OMe)₂   CH (Me) S (O)₂Et
CH₂CH (OMe)₂   CH (Me) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (Me) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (Et) SMe
CH₂CH (OMe)₂   CH (Et) SEt
CH₂CH (OMe)₂   CH (Et) SCF_Three
CH₂CH (OMe)₂   CH (Et) SCH₂CF_Three
CH₂CH (OMe)₂   CH (Et) S (O) Me
CH₂CH (OMe)₂   CH (Et) S (O) Et
CH₂CH (OMe)₂   CH (Et) S (O) CF_Three
CH₂CH (OMe)₂   CH (Et) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (Et) S (O)₂Me
CH₂CH (OMe)₂   CH (Et) S (O)₂Et
CH₂CH (OMe)₂   CH (Et) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (Et) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (n-Pr) SMe
CH₂CH (OMe)₂   CH (n-Pr) SEt
CH₂CH (OMe)₂   CH (n-Pr) SCF_Three
CH₂CH (OMe)₂   CH (n-Pr) SCH₂CF_Three
CH₂CH (OMe)₂   CH (n-Pr) S (O) Me
CH₂CH (OMe)₂   CH (n-Pr) S (O) Et
CH₂CH (OMe)₂   CH (n-Pr) S (O) CF_Three
CH₂CH (OMe)₂   CH (n-Pr) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (n-Pr) S (O)₂Me
CH₂CH (OMe)₂   CH (n-Pr) S (O)₂Et
CH₂CH (OMe)₂   CH (n-Pr) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (n-Pr) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (i-Pr) SMe
CH₂CH (OMe)₂   CH (i-Pr) SEt
CH₂CH (OMe)₂   CH (i-Pr) SCF_Three
CH₂CH (OMe)₂   CH (i-Pr) SCH₂CF_Three
CH₂CH (OMe)₂   CH (i-Pr) S (O) Me
CH₂CH (OMe)₂   CH (i-Pr) S (O) Et
CH₂CH (OMe)₂   CH (i-Pr) S (O) CF_Three
CH₂CH (OMe)₂   CH (i-Pr) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (i-Pr) S (O)₂Me
CH₂CH (OMe)₂   CH (i-Pr) S (O)₂Et
CH₂CH (OMe)₂   CH (i-Pr) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (i-Pr) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (n-Bu) SMe
CH₂CH (OMe)₂   CH (n-Bu) SEt
CH₂CH (OMe)₂   CH (n-Bu) SCF_Three
CH₂CH (OMe)₂   CH (n-Bu) SCH₂CF_Three
CH₂CH (OMe)₂   CH (n-Bu) S (O) Me
CH₂CH (OMe)₂   CH (n-Bu) S (O) Et
CH₂CH (OMe)₂   CH (n-Bu) S (O) CF_Three
CH₂CH (OMe)₂   CH (n-Bu) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (n-Bu) S (O)₂Me
CH₂CH (OMe)₂   CH (n-Bu) S (O)₂Et
CH₂CH (OMe)₂   CH (n-Bu) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (n-Bu) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (i-Bu) SMe
CH₂CH (OMe)₂   CH (i-Bu) SEt
CH₂CH (OMe)₂   CH (i-Bu) SCF_Three
CH₂CH (OMe)₂   CH (i-Bu) SCH₂CF_Three
CH₂CH (OMe)₂   CH (i-Bu) S (O) Me
CH₂CH (OMe)₂   CH (i-Bu) S (O) Et
CH₂CH (OMe)₂   CH (i-Bu) S (O) CF_Three
CH₂CH (OMe)₂   CH (i-Bu) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (i-Bu) S (O)₂Me
CH₂CH (OMe)₂   CH (i-Bu) S (O)₂Et
CH₂CH (OMe)₂   CH (i-Bu) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (i-Bu) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (s-Bu) SMe
CH₂CH (OMe)₂   CH (s-Bu) SEt
CH₂CH (OMe)₂   CH (s-Bu) SCF_Three
CH₂CH (OMe)₂   CH (s-Bu) SCH₂CF_Three
CH₂CH (OMe)₂   CH (s-Bu) S (O) Me
CH₂CH (OMe)₂   CH (s-Bu) S (O) Et
CH₂CH (OMe)₂   CH (s-Bu) S (O) CF_Three
CH₂CH (OMe)₂   CH (s-Bu) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (s-Bu) S (O)₂Me
CH₂CH (OMe)₂   CH (s-Bu) S (O)₂Et
CH₂CH (OMe)₂   CH (s-Bu) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (s-Bu) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (t-Bu) SMe
CH₂CH (OMe)₂   CH (t-Bu) SEt
CH₂CH (OMe)₂   CH (t-Bu) SCF_Three
CH₂CH (OMe)₂   CH (t-Bu) SCH₂CF_Three
CH₂CH (OMe)₂   CH (t-Bu) S (O) Me
CH₂CH (OMe)₂   CH (t-Bu) S (O) Et
CH₂CH (OMe)₂   CH (t-Bu) S (O) CF_Three
CH₂CH (OMe)₂   CH (t-Bu) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (t-Bu) S (O)₂Me
CH₂CH (OMe)₂   CH (t-Bu) S (O)₂Et
CH₂CH (OMe)₂   CH (t-Bu) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (t-Bu) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (CF_ThreeSMe
CH₂CH (OMe)₂   CH (CF_Three) SEt
CH₂CH (OMe)₂   CH (CF_Three) SCF_Three
CH₂CH (OMe)₂   CH (CF_Three) SCH₂CF_Three
CH₂CH (OMe)₂   CH (CF_Three) S (O) Me
CH₂CH (OMe)₂   CH (CF_Three) S (O) Et
CH₂CH (OMe)₂   CH (CF_Three) S (O) CF_Three
CH₂CH (OMe)₂   CH (CF_Three) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (CF_Three) S (O)₂Me
CH₂CH (OMe)₂   CH (CF_Three) S (O)₂Et
CH₂CH (OMe)₂   CH (CF_Three) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (CF_Three) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH₂CH₂SMe
CH₂CH (OMe)₂   CH₂CH₂SEt
CH₂CH (OMe)₂   CH₂CH₂SCF_Three
CH₂CH (OMe)₂   CH₂CH₂SCH₂CF_Three
CH₂CH (OMe)₂   CH₂CH₂S (O) Me
CH₂CH (OMe)₂   CH₂CH₂S (O) Et
CH₂CH (OMe)₂   CH₂CH₂S (O) CF_Three
CH₂CH (OMe)₂   CH₂CH₂S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH₂CH₂S (O)₂Me
CH₂CH (OMe)₂   CH₂CH₂S (O)₂Et
CH₂CH (OMe)₂   CH₂CH₂S (O)₂CF_Three
CH₂CH (OMe)₂   CH₂CH₂S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH₂SMe
CH₂CH (OMe)₂   CH (Me) CH₂SEt
CH₂CH (OMe)₂   CH (Me) CH₂SCF_Three
CH₂CH (OMe)₂   CH (Me) CH₂SCH₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH₂S (O) Me
CH₂CH (OMe)₂   CH (Me) CH₂S (O) Et
CH₂CH (OMe)₂   CH (Me) CH₂S (O) CF_Three
CH₂CH (OMe)₂   CH (Me) CH₂S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH₂S (O)₂Me
CH₂CH (OMe)₂   CH (Me) CH₂S (O)₂Et
CH₂CH (OMe)₂   CH (Me) CH₂S (O)₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (Et) CH₂SMe
CH₂CH (OMe)₂   CH (Et) CH₂SEt
CH₂CH (OMe)₂   CH (Et) CH₂SCF_Three
CH₂CH (OMe)₂   CH (Et) CH₂SCH₂CF_Three
CH₂CH (OMe)₂   CH (Et) CH₂S (O) Me
CH₂CH (OMe)₂   CH (Et) CH₂S (O) Et
CH₂CH (OMe)₂   CH (Et) CH₂S (O) CF_Three
CH₂CH (OMe)₂   CH (Et) CH₂S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (Et) CH₂S (O)₂Me
CH₂CH (OMe)₂   CH (Et) CH₂S (O)₂Et
CH₂CH (OMe)₂   CH (Et) CH₂S (O)₂CF_Three
CH₂CH (OMe)₂   CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   C (Me)₂CH₂SMe
CH₂CH (OMe)₂   C (Me)₂CH₂SEt
CH₂CH (OMe)₂   C (Me)₂CH₂SCF_Three
CH₂CH (OMe)₂   C (Me)₂CH₂SCH₂CF_Three
CH₂CH (OMe)₂   C (Me)₂CH₂S (O) Me
CH₂CH (OMe)₂   C (Me)₂CH₂S (O) Et
CH₂CH (OMe)₂   C (Me)₂CH₂S (O) CF_Three
CH₂CH (OMe)₂   C (Me)₂CH₂S (O) CH₂CF_Three
CH₂CH (OMe)₂   C (Me)₂CH₂S (O)₂Me
CH₂CH (OMe)₂   C (Me)₂CH₂S (O)₂Et
CH₂CH (OMe)₂   C (Me)₂CH₂S (O)₂CF_Three
CH₂CH (OMe)₂   C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Me) SMe
CH₂CH (OMe)₂   CH₂CH (Me) SEt
CH₂CH (OMe)₂   CH₂CH (Me) SCF_Three
CH₂CH (OMe)₂   CH₂CH (Me) SCH₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Me) S (O) Me
CH₂CH (OMe)₂   CH₂CH (Me) S (O) Et
CH₂CH (OMe)₂   CH₂CH (Me) S (O) CF_Three
CH₂CH (OMe)₂   CH₂CH (Me) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Me) S (O)₂Me
CH₂CH (OMe)₂   CH₂CH (Me) S (O)₂Et
CH₂CH (OMe)₂   CH₂CH (Me) S (O)₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Et) SMe
CH₂CH (OMe)₂   CH₂CH (Et) SEt
CH₂CH (OMe)₂   CH₂CH (Et) SCF_Three
CH₂CH (OMe)₂   CH₂CH (Et) SCH₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Et) S (O) Me
CH₂CH (OMe)₂   CH₂CH (Et) S (O) Et
CH₂CH (OMe)₂   CH₂CH (Et) S (O) CF_Three
CH₂CH (OMe)₂   CH₂CH (Et) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Et) S (O)₂Me
CH₂CH (OMe)₂   CH₂CH (Et) S (O)₂Et
CH₂CH (OMe)₂   CH₂CH (Et) S (O)₂CF_Three
CH₂CH (OMe)₂   CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH (Me) SMe
CH₂CH (OMe)₂   CH (Me) CH (Me) SEt
CH₂CH (OMe)₂   CH (Me) CH (Me) SCF_Three
CH₂CH (OMe)₂   CH (Me) CH (Me) SCH₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O) Me
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O) Et
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O) CF_Three
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O)₂Me
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O)₂Et
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O)₂CF_Three
CH₂CH (OMe)₂   CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH (Me) OEt CH₂SMe
CH (Me) OEt CH₂SEt
CH (Me) OEt CH₂SCF_Three
CH (Me) OEt CH₂SCH₂CF_Three
CH (Me) OEt CH₂S (O) Me
CH (Me) OEt CH₂S (O) Et
CH (Me) OEt CH₂S (O) CF_Three
CH (Me) OEt CH₂S (O) CH₂CF_Three
CH (Me) OEt CH₂S (O)₂Me
CH (Me) OEt CH₂S (O)₂Et
CH (Me) OEt CH₂S (O)₂CF_Three
CH (Me) OEt CH₂S (O)₂CH₂CF_Three
CH (Me) OEt CH (Me) SMe
CH (Me) OEt CH (Me) SEt
CH (Me) OEt CH (Me) SCF_Three
CH (Me) OEt CH (Me) SCH₂CF_Three
CH (Me) OEt CH (Me) S (O) Me
CH (Me) OEt CH (Me) S (O) Et
CH (Me) OEt CH (Me) S (O) CF_Three
CH (Me) OEt CH (Me) S (O) CH₂CF_Three
CH (Me) OEt CH (Me) S (O)₂Me
CH (Me) OEt CH (Me) S (O)₂Et
CH (Me) OEt CH (Me) S (O)₂CF_Three
CH (Me) OEt CH (Me) S (O)₂CH₂CF_Three
CH (Me) OEt CH (Et) SMe
CH (Me) OEt CH (Et) SEt
CH (Me) OEt CH (Et) SCF_Three
CH (Me) OEt CH (Et) SCH₂CF_Three
CH (Me) OEt CH (Et) S (O) Me
CH (Me) OEt CH (Et) S (O) Et
CH (Me) OEt CH (Et) S (O) CF_Three
CH (Me) OEt CH (Et) S (O) CH₂CF_Three
CH (Me) OEt CH (Et) S (O)₂Me
CH (Me) OEt CH (Et) S (O)₂Et
CH (Me) OEt CH (Et) S (O)₂CF_Three
CH (Me) OEt CH (Et) S (O)₂CH₂CF_Three
CH (Me) OEt CH (n-Pr) SMe
CH (Me) OEt CH (n-Pr) SEt
CH (Me) OEt CH (n-Pr) SCF_Three
CH (Me) OEt CH (n-Pr) SCH₂CF_Three
CH (Me) OEt CH (n-Pr) S (O) Me
CH (Me) OEt CH (n-Pr) S (O) Et
CH (Me) OEt CH (n-Pr) S (O) CF_Three
CH (Me) OEt CH (n-Pr) S (O) CH₂CF_Three
CH (Me) OEt CH (n-Pr) S (O)₂Me
CH (Me) OEt CH (n-Pr) S (O)₂Et
CH (Me) OEt CH (n-Pr) S (O)₂CF_Three
CH (Me) OEt CH (n-Pr) S (O)₂CH₂CF_Three
CH (Me) OEt CH (i-Pr) SMe
CH (Me) OEt CH (i-Pr) SEt
CH (Me) OEt CH (i-Pr) SCF_Three
CH (Me) OEt CH (i-Pr) SCH₂CF_Three
CH (Me) OEt CH (i-Pr) S (O) Me
CH (Me) OEt CH (i-Pr) S (O) Et
CH (Me) OEt CH (i-Pr) S (O) CF_Three
CH (Me) OEt CH (i-Pr) S (O) CH₂CF_Three
CH (Me) OEt CH (i-Pr) S (O)₂Me
CH (Me) OEt CH (i-Pr) S (O)₂Et
CH (Me) OEt CH (i-Pr) S (O)₂CF_Three
CH (Me) OEt CH (i-Pr) S (O)₂CH₂CF_Three
CH (Me) OEt CH (n-Bu) SMe
CH (Me) OEt CH (n-Bu) SEt
CH (Me) OEt CH (n-Bu) SCF_Three
CH (Me) OEt CH (n-Bu) SCH₂CF_Three
CH (Me) OEt CH (n-Bu) S (O) Me
CH (Me) OEt CH (n-Bu) S (O) Et
CH (Me) OEt CH (n-Bu) S (O) CF_Three
CH (Me) OEt CH (n-Bu) S (O) CH₂CF_Three
CH (Me) OEt CH (n-Bu) S (O)₂Me
CH (Me) OEt CH (n-Bu) S (O)₂Et
CH (Me) OEt CH (n-Bu) S (O)₂CF_Three
CH (Me) OEt CH (n-Bu) S (O)₂CH₂CF_Three
CH (Me) OEt CH (i-Bu) SMe
CH (Me) OEt CH (i-Bu) SEt
CH (Me) OEt CH (i-Bu) SCF_Three
CH (Me) OEt CH (i-Bu) SCH₂CF_Three
CH (Me) OEt CH (i-Bu) S (O) Me
CH (Me) OEt CH (i-Bu) S (O) Et
CH (Me) OEt CH (i-Bu) S (O) CF_Three
CH (Me) OEt CH (i-Bu) S (O) CH₂CF_Three
CH (Me) OEt CH (i-Bu) S (O)₂Me
CH (Me) OEt CH (i-Bu) S (O)₂Et
CH (Me) OEt CH (i-Bu) S (O)₂CF_Three
CH (Me) OEt CH (i-Bu) S (O)₂CH₂CF_Three
CH (Me) OEt CH (s-Bu) SMe
CH (Me) OEt CH (s-Bu) SEt
CH (Me) OEt CH (s-Bu) SCF_Three
CH (Me) OEt CH (s-Bu) SCH₂CF_Three
CH (Me) OEt CH (s-Bu) S (O) Me
CH (Me) OEt CH (s-Bu) S (O) Et
CH (Me) OEt CH (s-Bu) S (O) CF_Three
CH (Me) OEt CH (s-Bu) S (O) CH₂CF_Three
CH (Me) OEt CH (s-Bu) S (O)₂Me
CH (Me) OEt CH (s-Bu) S (O)₂Et
CH (Me) OEt CH (s-Bu) S (O)₂CF_Three
CH (Me) OEt CH (s-Bu) S (O)₂CH₂CF_Three
CH (Me) OEt CH (t-Bu) SMe
CH (Me) OEt CH (t-Bu) SEt
CH (Me) OEt CH (t-Bu) SCF_Three
CH (Me) OEt CH (t-Bu) SCH₂CF_Three
CH (Me) OEt CH (t-Bu) S (O) Me
CH (Me) OEt CH (t-Bu) S (O) Et
CH (Me) OEt CH (t-Bu) S (O) CF_Three
CH (Me) OEt CH (t-Bu) S (O) CH₂CF_Three
CH (Me) OEt CH (t-Bu) S (O)₂Me
CH (Me) OEt CH (t-Bu) S (O)₂Et
CH (Me) OEt CH (t-Bu) S (O)₂CF_Three
CH (Me) OEt CH (t-Bu) S (O)₂CH₂CF_Three
CH (Me) OEt CH (CF_ThreeSMe
CH (Me) OEt CH (CF_Three) SEt
CH (Me) OEt CH (CF_Three) SCF_Three
CH (Me) OEt CH (CF_Three) SCH₂CF_Three
CH (Me) OEt CH (CF_Three) S (O) Me
CH (Me) OEt CH (CF_Three) S (O) Et
CH (Me) OEt CH (CF_Three) S (O) CF_Three
CH (Me) OEt CH (CF_Three) S (O) CH₂CF_Three
CH (Me) OEt CH (CF_Three) S (O)₂Me
CH (Me) OEt CH (CF_Three) S (O)₂Et
CH (Me) OEt CH (CF_Three) S (O)₂CF_Three
CH (Me) OEt CH (CF_Three) S (O)₂CH₂CF_Three
CH (Me) OEt CH₂CH₂SMe
CH (Me) OEt CH₂CH₂SEt
CH (Me) OEt CH₂CH₂SCF_Three
CH (Me) OEt CH₂CH₂SCH₂CF_Three
CH (Me) OEt CH₂CH₂S (O) Me
CH (Me) OEt CH₂CH₂S (O) Et
CH (Me) OEt CH₂CH₂S (O) CF_Three
CH (Me) OEt CH₂CH₂S (O) CH₂CF_Three
CH (Me) OEt CH₂CH₂S (O)₂Me
CH (Me) OEt CH₂CH₂S (O)₂Et
CH (Me) OEt CH₂CH₂S (O)₂CF_Three
CH (Me) OEt CH₂CH₂S (O)₂CH₂CF_Three
CH (Me) OEt CH (Me) CH₂SMe
CH (Me) OEt CH (Me) CH₂SEt
CH (Me) OEt CH (Me) CH₂SCF_Three
CH (Me) OEt CH (Me) CH₂SCH₂CF_Three
CH (Me) OEt CH (Me) CH₂S (O) Me
CH (Me) OEt CH (Me) CH₂S (O) Et
CH (Me) OEt CH (Me) CH₂S (O) CF_Three
CH (Me) OEt CH (Me) CH₂S (O) CH₂CF_Three
CH (Me) OEt CH (Me) CH₂S (O)₂Me
CH (Me) OEt CH (Me) CH₂S (O)₂Et
CH (Me) OEt CH (Me) CH₂S (O)₂CF_Three
CH (Me) OEt CH (Me) CH₂S (O)₂CH₂CF_Three
CH (Me) OEt CH (Et) CH₂SMe
CH (Me) OEt CH (Et) CH₂SEt
CH (Me) OEt CH (Et) CH₂SCF_Three
CH (Me) OEt CH (Et) CH₂SCH₂CF_Three
CH (Me) OEt CH (Et) CH₂S (O) Me
CH (Me) OEt CH (Et) CH₂S (O) Et
CH (Me) OEt CH (Et) CH₂S (O) CF_Three
CH (Me) OEt CH (Et) CH₂S (O) CH₂CF_Three
CH (Me) OEt CH (Et) CH₂S (O)₂Me
CH (Me) OEt CH (Et) CH₂S (O)₂Et
CH (Me) OEt CH (Et) CH₂S (O)₂CF_Three
CH (Me) OEt CH (Et) CH₂S (O)₂CH₂CF_Three
CH (Me) OEt C (Me)₂CH₂SMe
CH (Me) OEt C (Me)₂CH₂SEt
CH (Me) OEt C (Me)₂CH₂SCF_Three
CH (Me) OEt C (Me)₂CH₂SCH₂CF_Three
CH (Me) OEt C (Me)₂CH₂S (O) Me
CH (Me) OEt C (Me)₂CH₂S (O) Et
CH (Me) OEt C (Me)₂CH₂S (O) CF_Three
CH (Me) OEt C (Me)₂CH₂S (O) CH₂CF_Three
CH (Me) OEt C (Me)₂CH₂S (O)₂Me
CH (Me) OEt C (Me)₂CH₂S (O)₂Et
CH (Me) OEt C (Me)₂CH₂S (O)₂CF_Three
CH (Me) OEt C (Me)₂CH₂S (O)₂CH₂CF_Three
CH (Me) OEt CH₂CH (Me) SMe
CH (Me) OEt CH₂CH (Me) SEt
CH (Me) OEt CH₂CH (Me) SCF_Three
CH (Me) OEt CH₂CH (Me) SCH₂CF_Three
CH (Me) OEt CH₂CH (Me) S (O) Me
CH (Me) OEt CH₂CH (Me) S (O) Et
CH (Me) OEt CH₂CH (Me) S (O) CF_Three
CH (Me) OEt CH₂CH (Me) S (O) CH₂CF_Three
CH (Me) OEt CH₂CH (Me) S (O)₂Me
CH (Me) OEt CH₂CH (Me) S (O)₂Et
CH (Me) OEt CH₂CH (Me) S (O)₂CF_Three
CH (Me) OEt CH₂CH (Me) S (O)₂CH₂CF_Three
CH (Me) OEt CH₂CH (Et) SMe
CH (Me) OEt CH₂CH (Et) SEt
CH (Me) OEt CH₂CH (Et) SCF_Three
CH (Me) OEt CH₂CH (Et) SCH₂CF_Three
CH (Me) OEt CH₂CH (Et) S (O) Me
CH (Me) OEt CH₂CH (Et) S (O) Et
CH (Me) OEt CH₂CH (Et) S (O) CF_Three
CH (Me) OEt CH₂CH (Et) S (O) CH₂CF_Three
CH (Me) OEt CH₂CH (Et) S (O)₂Me
CH (Me) OEt CH₂CH (Et) S (O)₂Et
CH (Me) OEt CH₂CH (Et) S (O)₂CF_Three
CH (Me) OEt CH₂CH (Et) S (O)₂CH₂CF_Three
CH (Me) OEt CH (Me) CH (Me) SMe
CH (Me) OEt CH (Me) CH (Me) SEt
CH (Me) OEt CH (Me) CH (Me) SCF_Three
CH (Me) OEt CH (Me) CH (Me) SCH₂CF_Three
CH (Me) OEt CH (Me) CH (Me) S (O) Me
CH (Me) OEt CH (Me) CH (Me) S (O) Et
CH (Me) OEt CH (Me) CH (Me) S (O) CF_Three
CH (Me) OEt CH (Me) CH (Me) S (O) CH₂CF_Three
CH (Me) OEt CH (Me) CH (Me) S (O)₂Me
CH (Me) OEt CH (Me) CH (Me) S (O)₂Et
CH (Me) OEt CH (Me) CH (Me) S (O)₂CF_Three
CH (Me) OEt CH (Me) CH (Me) S (O)₂CH₂CF_Three
S (O)₂Me CH₂SMe
S (O)₂Me CH₂SEt
S (O)₂Me CH₂SCF_Three
S (O)₂Me CH₂SCH₂CF_Three
S (O)₂Me CH₂S (O) Me
S (O)₂Me CH₂S (O) Et
S (O)₂Me CH₂S (O) CF_Three
S (O)₂Me CH₂S (O) CH₂CF_Three
S (O)₂Me CH₂S (O)₂Me
S (O)₂Me CH₂S (O)₂Et
S (O)₂Me CH₂S (O)₂CF_Three
S (O)₂Me CH₂S (O)₂CH₂CF_Three
S (O)₂Me CH (Me) SMe
S (O)₂Me CH (Me) SEt
S (O)₂Me CH (Me) SCF_Three
S (O)₂Me CH (Me) SCH₂CF_Three
S (O)₂Me CH (Me) S (O) Me
S (O)₂Me CH (Me) S (O) Et
S (O)₂Me CH (Me) S (O) CF_Three
S (O)₂Me CH (Me) S (O) CH₂CF_Three
S (O)₂Me CH (Me) S (O)₂Me
S (O)₂Me CH (Me) S (O)₂Et
S (O)₂Me CH (Me) S (O)₂CF_Three
S (O)₂Me CH (Me) S (O)₂CH₂CF_Three
S (O)₂Me CH (Et) SMe
S (O)₂Me CH (Et) SEt
S (O)₂Me CH (Et) SCF_Three
S (O)₂Me CH (Et) SCH₂CF_Three
S (O)₂Me CH (Et) S (O) Me
S (O)₂Me CH (Et) S (O) Et
S (O)₂Me CH (Et) S (O) CF_Three
S (O)₂Me CH (Et) S (O) CH₂CF_Three
S (O)₂Me CH (Et) S (O)₂Me
S (O)₂Me CH (Et) S (O)₂Et
S (O)₂Me CH (Et) S (O)₂CF_Three
S (O)₂Me CH (Et) S (O)₂CH₂CF_Three
S (O)₂Me CH (n-Pr) SMe
S (O)₂Me CH (n-Pr) SEt
S (O)₂Me CH (n-Pr) SCF_Three
S (O)₂Me CH (n-Pr) SCH₂CF_Three
S (O)₂Me CH (n-Pr) S (O) Me
S (O)₂Me CH (n-Pr) S (O) Et
S (O)₂Me CH (n-Pr) S (O) CF_Three
S (O)₂Me CH (n-Pr) S (O) CH₂CF_Three
S (O)₂Me CH (n-Pr) S (O)₂Me
S (O)₂Me CH (n-Pr) S (O)₂Et
S (O)₂Me CH (n-Pr) S (O)₂CF_Three
S (O)₂Me CH (n-Pr) S (O)₂CH₂CF_Three
S (O)₂Me CH (i-Pr) SMe
S (O)₂Me CH (i-Pr) SEt
S (O)₂Me CH (i-Pr) SCF_Three
S (O)₂Me CH (i-Pr) SCH₂CF_Three
S (O)₂Me CH (i-Pr) S (O) Me
S (O)₂Me CH (i-Pr) S (O) Et
S (O)₂Me CH (i-Pr) S (O) CF_Three
S (O)₂Me CH (i-Pr) S (O) CH₂CF_Three
S (O)₂Me CH (i-Pr) S (O)₂Me
S (O)₂Me CH (i-Pr) S (O)₂Et
S (O)₂Me CH (i-Pr) S (O)₂CF_Three
S (O)₂Me CH (i-Pr) S (O)₂CH₂CF_Three
S (O)₂Me CH (n-Bu) SMe
S (O)₂Me CH (n-Bu) SEt
S (O)₂Me CH (n-Bu) SCF_Three
S (O)₂Me CH (n-Bu) SCH₂CF_Three
S (O)₂Me CH (n-Bu) S (O) Me
S (O)₂Me CH (n-Bu) S (O) Et
S (O)₂Me CH (n-Bu) S (O) CF_Three
S (O)₂Me CH (n-Bu) S (O) CH₂CF_Three
S (O)₂Me CH (n-Bu) S (O)₂Me
S (O)₂Me CH (n-Bu) S (O)₂Et
S (O)₂Me CH (n-Bu) S (O)₂CF_Three
S (O)₂Me CH (n-Bu) S (O)₂CH₂CF_Three
S (O)₂Me CH (i-Bu) SMe
S (O)₂Me CH (i-Bu) SEt
S (O)₂Me CH (i-Bu) SCF_Three
S (O)₂Me CH (i-Bu) SCH₂CF_Three
S (O)₂Me CH (i-Bu) S (O) Me
S (O)₂Me CH (i-Bu) S (O) Et
S (O)₂Me CH (i-Bu) S (O) CF_Three
S (O)₂Me CH (i-Bu) S (O) CH₂CF_Three
S (O)₂Me CH (i-Bu) S (O)₂Me
S (O)₂Me CH (i-Bu) S (O)₂Et
S (O)₂Me CH (i-Bu) S (O)₂CF_Three
S (O)₂Me CH (i-Bu) S (O)₂CH₂CF_Three
S (O)₂Me CH (s-Bu) SMe
S (O)₂Me CH (s-Bu) SEt
S (O)₂Me CH (s-Bu) SCF_Three
S (O)₂Me CH (s-Bu) SCH₂CF_Three
S (O)₂Me CH (s-Bu) S (O) Me
S (O)₂Me CH (s-Bu) S (O) Et
S (O)₂Me CH (s-Bu) S (O) CF_Three
S (O)₂Me CH (s-Bu) S (O) CH₂CF_Three
S (O)₂Me CH (s-Bu) S (O)₂Me
S (O)₂Me CH (s-Bu) S (O)₂Et
S (O)₂Me CH (s-Bu) S (O)₂CF_Three
S (O)₂Me CH (s-Bu) S (O)₂CH₂CF_Three
S (O)₂Me CH (t-Bu) SMe
S (O)₂Me CH (t-Bu) SEt
S (O)₂Me CH (t-Bu) SCF_Three
S (O)₂Me CH (t-Bu) SCH₂CF_Three
S (O)₂Me CH (t-Bu) S (O) Me
S (O)₂Me CH (t-Bu) S (O) Et
S (O)₂Me CH (t-Bu) S (O) CF_Three
S (O)₂Me CH (t-Bu) S (O) CH₂CF_Three
S (O)₂Me CH (t-Bu) S (O)₂Me
S (O)₂Me CH (t-Bu) S (O)₂Et
S (O)₂Me CH (t-Bu) S (O)₂CF_Three
S (O)₂Me CH (t-Bu) S (O)₂CH₂CF_Three
S (O)₂Me CH (CF_ThreeSMe
S (O)₂Me CH (CF_Three) SEt
S (O)₂Me CH (CF_Three) SCF_Three
S (O)₂Me CH (CF_Three) SCH₂CF_Three
S (O)₂Me CH (CF_Three) S (O) Me
S (O)₂Me CH (CF_Three) S (O) Et
S (O)₂Me CH (CF_Three) S (O) CF_Three
S (O)₂Me CH (CF_Three) S (O) CH₂CF_Three
S (O)₂Me CH (CF_Three) S (O)₂Me
S (O)₂Me CH (CF_Three) S (O)₂Et
S (O)₂Me CH (CF_Three) S (O)₂CF_Three
S (O)₂Me CH (CF_Three) S (O)₂CH₂CF_Three
S (O)₂Me CH₂CH₂SMe
S (O)₂Me CH₂CH₂SEt
S (O)₂Me CH₂CH₂SCF_Three
S (O)₂Me CH₂CH₂SCH₂CF_Three
S (O)₂Me CH₂CH₂S (O) Me
S (O)₂Me CH₂CH₂S (O) Et
S (O)₂Me CH₂CH₂S (O) CF_Three
S (O)₂Me CH₂CH₂S (O) CH₂CF_Three
S (O)₂Me CH₂CH₂S (O)₂Me
S (O)₂Me CH₂CH₂S (O)₂Et
S (O)₂Me CH₂CH₂S (O)₂CF_Three
S (O)₂Me CH₂CH₂S (O)₂CH₂CF_Three
S (O)₂Me CH (Me) CH₂SMe
S (O)₂Me CH (Me) CH₂SEt
S (O)₂Me CH (Me) CH₂SCF_Three
S (O)₂Me CH (Me) CH₂SCH₂CF_Three
S (O)₂Me CH (Me) CH₂S (O) Me
S (O)₂Me CH (Me) CH₂S (O) Et
S (O)₂Me CH (Me) CH₂S (O) CF_Three
S (O)₂Me CH (Me) CH₂S (O) CH₂CF_Three
S (O)₂Me CH (Me) CH₂S (O)₂Me
S (O)₂Me CH (Me) CH₂S (O)₂Et
S (O)₂Me CH (Me) CH₂S (O)₂CF_Three
S (O)₂Me CH (Me) CH₂S (O)₂CH₂CF_Three
S (O)₂Me CH (Et) CH₂SMe
S (O)₂Me CH (Et) CH₂SEt
S (O)₂Me CH (Et) CH₂SCF_Three
S (O)₂Me CH (Et) CH₂SCH₂CF_Three
S (O)₂Me CH (Et) CH₂S (O) Me
S (O)₂Me CH (Et) CH₂S (O) Et
S (O)₂Me CH (Et) CH₂S (O) CF_Three
S (O)₂Me CH (Et) CH₂S (O) CH₂CF_Three
S (O)₂Me CH (Et) CH₂S (O)₂Me
S (O)₂Me CH (Et) CH₂S (O)₂Et
S (O)₂Me CH (Et) CH₂S (O)₂CF_Three
S (O)₂Me CH (Et) CH₂S (O)₂CH₂CF_Three
S (O)₂Me C (Me)₂CH₂SMe
S (O)₂Me C (Me)₂CH₂SEt
S (O)₂Me C (Me)₂CH₂SCF_Three
S (O)₂Me C (Me)₂CH₂SCH₂CF_Three
S (O)₂Me C (Me)₂CH₂S (O) Me
S (O)₂Me C (Me)₂CH₂S (O) Et
S (O)₂Me C (Me)₂CH₂S (O) CF_Three
S (O)₂Me C (Me)₂CH₂S (O) CH₂CF_Three
S (O)₂Me C (Me)₂CH₂S (O)₂Me
S (O)₂Me C (Me)₂CH₂S (O)₂Et
S (O)₂Me C (Me)₂CH₂S (O)₂CF_Three
S (O)₂Me C (Me)₂CH₂S (O)₂CH₂CF_Three
S (O)₂Me CH₂CH (Me) SMe
S (O)₂Me CH₂CH (Me) SEt
S (O)₂Me CH₂CH (Me) SCF_Three
S (O)₂Me CH₂CH (Me) SCH₂CF_Three
S (O)₂Me CH₂CH (Me) S (O) Me
S (O)₂Me CH₂CH (Me) S (O) Et
S (O)₂Me CH₂CH (Me) S (O) CF_Three
S (O)₂Me CH₂CH (Me) S (O) CH₂CF_Three
S (O)₂Me CH₂CH (Me) S (O)₂Me
S (O)₂Me CH₂CH (Me) S (O)₂Et
S (O)₂Me CH₂CH (Me) S (O)₂CF_Three
S (O)₂Me CH₂CH (Me) S (O)₂CH₂CF_Three
S (O)₂Me CH₂CH (Et) SMe
S (O)₂Me CH₂CH (Et) SEt
S (O)₂Me CH₂CH (Et) SCF_Three
S (O)₂Me CH₂CH (Et) SCH₂CF_Three
S (O)₂Me CH₂CH (Et) S (O) Me
S (O)₂Me CH₂CH (Et) S (O) Et
S (O)₂Me CH₂CH (Et) S (O) CF_Three
S (O)₂Me CH₂CH (Et) S (O) CH₂CF_Three
S (O)₂Me CH₂CH (Et) S (O)₂Me
S (O)₂Me CH₂CH (Et) S (O)₂Et
S (O)₂Me CH₂CH (Et) S (O)₂CF_Three
S (O)₂Me CH₂CH (Et) S (O)₂CH₂CF_Three
S (O)₂Me CH (Me) CH (Me) SMe
S (O)₂Me CH (Me) CH (Me) SEt
S (O)₂Me CH (Me) CH (Me) SCF_Three
S (O)₂Me CH (Me) CH (Me) SCH₂CF_Three
S (O)₂Me CH (Me) CH (Me) S (O) Me
S (O)₂Me CH (Me) CH (Me) S (O) Et
S (O)₂Me CH (Me) CH (Me) S (O) CF_Three
S (O)₂Me CH (Me) CH (Me) S (O) CH₂CF_Three
S (O)₂Me CH (Me) CH (Me) S (O)₂Me
S (O)₂Me CH (Me) CH (Me) S (O)₂Et
S (O)₂Me CH (Me) CH (Me) S (O)₂CF_Three
S (O)₂Me CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-32a CH₂SMe
D2-32a CH₂SEt
D2-32a CH₂SCF_Three
D2-32a CH₂SCH₂CF_Three
D2-32a CH₂S (O) Me
D2-32a CH₂S (O) Et
D2-32a CH₂S (O) CF_Three
D2-32a CH₂S (O) CH₂CF_Three
D2-32a CH₂S (O)₂Me
D2-32a CH₂S (O)₂Et
D2-32a CH₂S (O)₂CF_Three
D2-32a CH₂S (O)₂CH₂CF_Three
D2-32a CH (Me) SMe
D2-32a CH (Me) SEt
D2-32a CH (Me) SCF_Three
D2-32a CH (Me) SCH₂CF_Three
D2-32a CH (Me) S (O) Me
D2-32a CH (Me) S (O) Et
D2-32a CH (Me) S (O) CF_Three
D2-32a CH (Me) S (O) CH₂CF_Three
D2-32a CH (Me) S (O)₂Me
D2-32a CH (Me) S (O)₂Et
D2-32a CH (Me) S (O)₂CF_Three
D2-32a CH (Me) S (O)₂CH₂CF_Three
D2-32a CH (Et) SMe
D2-32a CH (Et) SEt
D2-32a CH (Et) SCF_Three
D2-32a CH (Et) SCH₂CF_Three
D2-32a CH (Et) S (O) Me
D2-32a CH (Et) S (O) Et
D2-32a CH (Et) S (O) CF_Three
D2-32a CH (Et) S (O) CH₂CF_Three
D2-32a CH (Et) S (O)₂Me
D2-32a CH (Et) S (O)₂Et
D2-32a CH (Et) S (O)₂CF_Three
D2-32a CH (Et) S (O)₂CH₂CF_Three
D2-32a CH (n-Pr) SMe
D2-32a CH (n-Pr) SEt
D2-32a CH (n-Pr) SCF_Three
D2-32a CH (n-Pr) SCH₂CF_Three
D2-32a CH (n-Pr) S (O) Me
D2-32a CH (n-Pr) S (O) Et
D2-32a CH (n-Pr) S (O) CF_Three
D2-32a CH (n-Pr) S (O) CH₂CF_Three
D2-32a CH (n-Pr) S (O)₂Me
D2-32a CH (n-Pr) S (O)₂Et
D2-32a CH (n-Pr) S (O)₂CF_Three
D2-32a CH (n-Pr) S (O)₂CH₂CF_Three
D2-32a CH (i-Pr) SMe
D2-32a CH (i-Pr) SEt
D2-32a CH (i-Pr) SCF_Three
D2-32a CH (i-Pr) SCH₂CF_Three
D2-32a CH (i-Pr) S (O) Me
D2-32a CH (i-Pr) S (O) Et
D2-32a CH (i-Pr) S (O) CF_Three
D2-32a CH (i-Pr) S (O) CH₂CF_Three
D2-32a CH (i-Pr) S (O)₂Me
D2-32a CH (i-Pr) S (O)₂Et
D2-32a CH (i-Pr) S (O)₂CF_Three
D2-32a CH (i-Pr) S (O)₂CH₂CF_Three
D2-32a CH (n-Bu) SMe
D2-32a CH (n-Bu) SEt
D2-32a CH (n-Bu) SCF_Three
D2-32a CH (n-Bu) SCH₂CF_Three
D2-32a CH (n-Bu) S (O) Me
D2-32a CH (n-Bu) S (O) Et
D2-32a CH (n-Bu) S (O) CF_Three
D2-32a CH (n-Bu) S (O) CH₂CF_Three
D2-32a CH (n-Bu) S (O)₂Me
D2-32a CH (n-Bu) S (O)₂Et
D2-32a CH (n-Bu) S (O)₂CF_Three
D2-32a CH (n-Bu) S (O)₂CH₂CF_Three
D2-32a CH (i-Bu) SMe
D2-32a CH (i-Bu) SEt
D2-32a CH (i-Bu) SCF_Three
D2-32a CH (i-Bu) SCH₂CF_Three
D2-32a CH (i-Bu) S (O) Me
D2-32a CH (i-Bu) S (O) Et
D2-32a CH (i-Bu) S (O) CF_Three
D2-32a CH (i-Bu) S (O) CH₂CF_Three
D2-32a CH (i-Bu) S (O)₂Me
D2-32a CH (i-Bu) S (O)₂Et
D2-32a CH (i-Bu) S (O)₂CF_Three
D2-32a CH (i-Bu) S (O)₂CH₂CF_Three
D2-32a CH (s-Bu) SMe
D2-32a CH (s-Bu) SEt
D2-32a CH (s-Bu) SCF_Three
D2-32a CH (s-Bu) SCH₂CF_Three
D2-32a CH (s-Bu) S (O) Me
D2-32a CH (s-Bu) S (O) Et
D2-32a CH (s-Bu) S (O) CF_Three
D2-32a CH (s-Bu) S (O) CH₂CF_Three
D2-32a CH (s-Bu) S (O)₂Me
D2-32a CH (s-Bu) S (O)₂Et
D2-32a CH (s-Bu) S (O)₂CF_Three
D2-32a CH (s-Bu) S (O)₂CH₂CF_Three
D2-32a CH (t-Bu) SMe
D2-32a CH (t-Bu) SEt
D2-32a CH (t-Bu) SCF_Three
D2-32a CH (t-Bu) SCH₂CF_Three
D2-32a CH (t-Bu) S (O) Me
D2-32a CH (t-Bu) S (O) Et
D2-32a CH (t-Bu) S (O) CF_Three
D2-32a CH (t-Bu) S (O) CH₂CF_Three
D2-32a CH (t-Bu) S (O)₂Me
D2-32a CH (t-Bu) S (O)₂Et
D2-32a CH (t-Bu) S (O)₂CF_Three
D2-32a CH (t-Bu) S (O)₂CH₂CF_Three
D2-32a CH (CF_ThreeSMe
D2-32a CH (CF_Three) SEt
D2-32a CH (CF_Three) SCF_Three
D2-32a CH (CF_Three) SCH₂CF_Three
D2-32a CH (CF_Three) S (O) Me
D2-32a CH (CF_Three) S (O) Et
D2-32a CH (CF_Three) S (O) CF_Three
D2-32a CH (CF_Three) S (O) CH₂CF_Three
D2-32a CH (CF_Three) S (O)₂Me
D2-32a CH (CF_Three) S (O)₂Et
D2-32a CH (CF_Three) S (O)₂CF_Three
D2-32a CH (CF_Three) S (O)₂CH₂CF_Three
D2-32a CH₂CH₂SMe
D2-32a CH₂CH₂SEt
D2-32a CH₂CH₂SCF_Three
D2-32a CH₂CH₂SCH₂CF_Three
D2-32a CH₂CH₂S (O) Me
D2-32a CH₂CH₂S (O) Et
D2-32a CH₂CH₂S (O) CF_Three
D2-32a CH₂CH₂S (O) CH₂CF_Three
D2-32a CH₂CH₂S (O)₂Me
D2-32a CH₂CH₂S (O)₂Et
D2-32a CH₂CH₂S (O)₂CF_Three
D2-32a CH₂CH₂S (O)₂CH₂CF_Three
D2-32a CH (Me) CH₂SMe
D2-32a CH (Me) CH₂SEt
D2-32a CH (Me) CH₂SCF_Three
D2-32a CH (Me) CH₂SCH₂CF_Three
D2-32a CH (Me) CH₂S (O) Me
D2-32a CH (Me) CH₂S (O) Et
D2-32a CH (Me) CH₂S (O) CF_Three
D2-32a CH (Me) CH₂S (O) CH₂CF_Three
D2-32a CH (Me) CH₂S (O)₂Me
D2-32a CH (Me) CH₂S (O)₂Et
D2-32a CH (Me) CH₂S (O)₂CF_Three
D2-32a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-32a CH (Et) CH₂SMe
D2-32a CH (Et) CH₂SEt
D2-32a CH (Et) CH₂SCF_Three
D2-32a CH (Et) CH₂SCH₂CF_Three
D2-32a CH (Et) CH₂S (O) Me
D2-32a CH (Et) CH₂S (O) Et
D2-32a CH (Et) CH₂S (O) CF_Three
D2-32a CH (Et) CH₂S (O) CH₂CF_Three
D2-32a CH (Et) CH₂S (O)₂Me
D2-32a CH (Et) CH₂S (O)₂Et
D2-32a CH (Et) CH₂S (O)₂CF_Three
D2-32a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-32a C (Me)₂CH₂SMe
D2-32a C (Me)₂CH₂SEt
D2-32a C (Me)₂CH₂SCF_Three
D2-32a C (Me)₂CH₂SCH₂CF_Three
D2-32a C (Me)₂CH₂S (O) Me
D2-32a C (Me)₂CH₂S (O) Et
D2-32a C (Me)₂CH₂S (O) CF_Three
D2-32a C (Me)₂CH₂S (O) CH₂CF_Three
D2-32a C (Me)₂CH₂S (O)₂Me
D2-32a C (Me)₂CH₂S (O)₂Et
D2-32a C (Me)₂CH₂S (O)₂CF_Three
D2-32a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-32a CH₂CH (Me) SMe
D2-32a CH₂CH (Me) SEt
D2-32a CH₂CH (Me) SCF_Three
D2-32a CH₂CH (Me) SCH₂CF_Three
D2-32a CH₂CH (Me) S (O) Me
D2-32a CH₂CH (Me) S (O) Et
D2-32a CH₂CH (Me) S (O) CF_Three
D2-32a CH₂CH (Me) S (O) CH₂CF_Three
D2-32a CH₂CH (Me) S (O)₂Me
D2-32a CH₂CH (Me) S (O)₂Et
D2-32a CH₂CH (Me) S (O)₂CF_Three
D2-32a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-32a CH₂CH (Et) SMe
D2-32a CH₂CH (Et) SEt
D2-32a CH₂CH (Et) SCF_Three
D2-32a CH₂CH (Et) SCH₂CF_Three
D2-32a CH₂CH (Et) S (O) Me
D2-32a CH₂CH (Et) S (O) Et
D2-32a CH₂CH (Et) S (O) CF_Three
D2-32a CH₂CH (Et) S (O) CH₂CF_Three
D2-32a CH₂CH (Et) S (O)₂Me
D2-32a CH₂CH (Et) S (O)₂Et
D2-32a CH₂CH (Et) S (O)₂CF_Three
D2-32a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-32a CH (Me) CH (Me) SMe
D2-32a CH (Me) CH (Me) SEt
D2-32a CH (Me) CH (Me) SCF_Three
D2-32a CH (Me) CH (Me) SCH₂CF_Three
D2-32a CH (Me) CH (Me) S (O) Me
D2-32a CH (Me) CH (Me) S (O) Et
D2-32a CH (Me) CH (Me) S (O) CF_Three
D2-32a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-32a CH (Me) CH (Me) S (O)₂Me
D2-32a CH (Me) CH (Me) S (O)₂Et
D2-32a CH (Me) CH (Me) S (O)₂CF_Three
D2-32a CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-33a CH₂SMe
D2-33a CH₂SEt
D2-33a CH₂SCF_Three
D2-33a CH₂SCH₂CF_Three
D2-33a CH₂S (O) Me
D2-33a CH₂S (O) Et
D2-33a CH₂S (O) CF_Three
D2-33a CH₂S (O) CH₂CF_Three
D2-33a CH₂S (O)₂Me
D2-33a CH₂S (O)₂Et
D2-33a CH₂S (O)₂CF_Three
D2-33a CH₂S (O)₂CH₂CF_Three
D2-33a CH (Me) SMe
D2-33a CH (Me) SEt
D2-33a CH (Me) SCF_Three
D2-33a CH (Me) SCH₂CF_Three
D2-33a CH (Me) S (O) Me
D2-33a CH (Me) S (O) Et
D2-33a CH (Me) S (O) CF_Three
D2-33a CH (Me) S (O) CH₂CF_Three
D2-33a CH (Me) S (O)₂Me
D2-33a CH (Me) S (O)₂Et
D2-33a CH (Me) S (O)₂CF_Three
D2-33a CH (Me) S (O)₂CH₂CF_Three
D2-33a CH (Et) SMe
D2-33a CH (Et) SEt
D2-33a CH (Et) SCF_Three
D2-33a CH (Et) SCH₂CF_Three
D2-33a CH (Et) S (O) Me
D2-33a CH (Et) S (O) Et
D2-33a CH (Et) S (O) CF_Three
D2-33a CH (Et) S (O) CH₂CF_Three
D2-33a CH (Et) S (O)₂Me
D2-33a CH (Et) S (O)₂Et
D2-33a CH (Et) S (O)₂CF_Three
D2-33a CH (Et) S (O)₂CH₂CF_Three
D2-33a CH (n-Pr) SMe
D2-33a CH (n-Pr) SEt
D2-33a CH (n-Pr) SCF_Three
D2-33a CH (n-Pr) SCH₂CF_Three
D2-33a CH (n-Pr) S (O) Me
D2-33a CH (n-Pr) S (O) Et
D2-33a CH (n-Pr) S (O) CF_Three
D2-33a CH (n-Pr) S (O) CH₂CF_Three
D2-33a CH (n-Pr) S (O)₂Me
D2-33a CH (n-Pr) S (O)₂Et
D2-33a CH (n-Pr) S (O)₂CF_Three
D2-33a CH (n-Pr) S (O)₂CH₂CF_Three
D2-33a CH (i-Pr) SMe
D2-33a CH (i-Pr) SEt
D2-33a CH (i-Pr) SCF_Three
D2-33a CH (i-Pr) SCH₂CF_Three
D2-33a CH (i-Pr) S (O) Me
D2-33a CH (i-Pr) S (O) Et
D2-33a CH (i-Pr) S (O) CF_Three
D2-33a CH (i-Pr) S (O) CH₂CF_Three
D2-33a CH (i-Pr) S (O)₂Me
D2-33a CH (i-Pr) S (O)₂Et
D2-33a CH (i-Pr) S (O)₂CF_Three
D2-33a CH (i-Pr) S (O)₂CH₂CF_Three
D2-33a CH (n-Bu) SMe
D2-33a CH (n-Bu) SEt
D2-33a CH (n-Bu) SCF_Three
D2-33a CH (n-Bu) SCH₂CF_Three
D2-33a CH (n-Bu) S (O) Me
D2-33a CH (n-Bu) S (O) Et
D2-33a CH (n-Bu) S (O) CF_Three
D2-33a CH (n-Bu) S (O) CH₂CF_Three
D2-33a CH (n-Bu) S (O)₂Me
D2-33a CH (n-Bu) S (O)₂Et
D2-33a CH (n-Bu) S (O)₂CF_Three
D2-33a CH (n-Bu) S (O)₂CH₂CF_Three
D2-33a CH (i-Bu) SMe
D2-33a CH (i-Bu) SEt
D2-33a CH (i-Bu) SCF_Three
D2-33a CH (i-Bu) SCH₂CF_Three
D2-33a CH (i-Bu) S (O) Me
D2-33a CH (i-Bu) S (O) Et
D2-33a CH (i-Bu) S (O) CF_Three
D2-33a CH (i-Bu) S (O) CH₂CF_Three
D2-33a CH (i-Bu) S (O)₂Me
D2-33a CH (i-Bu) S (O)₂Et
D2-33a CH (i-Bu) S (O)₂CF_Three
D2-33a CH (i-Bu) S (O)₂CH₂CF_Three
D2-33a CH (s-Bu) SMe
D2-33a CH (s-Bu) SEt
D2-33a CH (s-Bu) SCF_Three
D2-33a CH (s-Bu) SCH₂CF_Three
D2-33a CH (s-Bu) S (O) Me
D2-33a CH (s-Bu) S (O) Et
D2-33a CH (s-Bu) S (O) CF_Three
D2-33a CH (s-Bu) S (O) CH₂CF_Three
D2-33a CH (s-Bu) S (O)₂Me
D2-33a CH (s-Bu) S (O)₂Et
D2-33a CH (s-Bu) S (O)₂CF_Three
D2-33a CH (s-Bu) S (O)₂CH₂CF_Three
D2-33a CH (t-Bu) SMe
D2-33a CH (t-Bu) SEt
D2-33a CH (t-Bu) SCF_Three
D2-33a CH (t-Bu) SCH₂CF_Three
D2-33a CH (t-Bu) S (O) Me
D2-33a CH (t-Bu) S (O) Et
D2-33a CH (t-Bu) S (O) CF_Three
D2-33a CH (t-Bu) S (O) CH₂CF_Three
D2-33a CH (t-Bu) S (O)₂Me
D2-33a CH (t-Bu) S (O)₂Et
D2-33a CH (t-Bu) S (O)₂CF_Three
D2-33a CH (t-Bu) S (O)₂CH₂CF_Three
D2-33a CH (CF_ThreeSMe
D2-33a CH (CF_Three) SEt
D2-33a CH (CF_Three) SCF_Three
D2-33a CH (CF_Three) SCH₂CF_Three
D2-33a CH (CF_Three) S (O) Me
D2-33a CH (CF_Three) S (O) Et
D2-33a CH (CF_Three) S (O) CF_Three
D2-33a CH (CF_Three) S (O) CH₂CF_Three
D2-33a CH (CF_Three) S (O)₂Me
D2-33a CH (CF_Three) S (O)₂Et
D2-33a CH (CF_Three) S (O)₂CF_Three
D2-33a CH (CF_Three) S (O)₂CH₂CF_Three
D2-33a CH₂CH₂SMe
D2-33a CH₂CH₂SEt
D2-33a CH₂CH₂SCF_Three
D2-33a CH₂CH₂SCH₂CF_Three
D2-33a CH₂CH₂S (O) Me
D2-33a CH₂CH₂S (O) Et
D2-33a CH₂CH₂S (O) CF_Three
D2-33a CH₂CH₂S (O) CH₂CF_Three
D2-33a CH₂CH₂S (O)₂Me
D2-33a CH₂CH₂S (O)₂Et
D2-33a CH₂CH₂S (O)₂CF_Three
D2-33a CH₂CH₂S (O)₂CH₂CF_Three
D2-33a CH (Me) CH₂SMe
D2-33a CH (Me) CH₂SEt
D2-33a CH (Me) CH₂SCF_Three
D2-33a CH (Me) CH₂SCH₂CF_Three
D2-33a CH (Me) CH₂S (O) Me
D2-33a CH (Me) CH₂S (O) Et
D2-33a CH (Me) CH₂S (O) CF_Three
D2-33a CH (Me) CH₂S (O) CH₂CF_Three
D2-33a CH (Me) CH₂S (O)₂Me
D2-33a CH (Me) CH₂S (O)₂Et
D2-33a CH (Me) CH₂S (O)₂CF_Three
D2-33a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-33a CH (Et) CH₂SMe
D2-33a CH (Et) CH₂SEt
D2-33a CH (Et) CH₂SCF_Three
D2-33a CH (Et) CH₂SCH₂CF_Three
D2-33a CH (Et) CH₂S (O) Me
D2-33a CH (Et) CH₂S (O) Et
D2-33a CH (Et) CH₂S (O) CF_Three
D2-33a CH (Et) CH₂S (O) CH₂CF_Three
D2-33a CH (Et) CH₂S (O)₂Me
D2-33a CH (Et) CH₂S (O)₂Et
D2-33a CH (Et) CH₂S (O)₂CF_Three
D2-33a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-33a C (Me)₂CH₂SMe
D2-33a C (Me)₂CH₂SEt
D2-33a C (Me)₂CH₂SCF_Three
D2-33a C (Me)₂CH₂SCH₂CF_Three
D2-33a C (Me)₂CH₂S (O) Me
D2-33a C (Me)₂CH₂S (O) Et
D2-33a C (Me)₂CH₂S (O) CF_Three
D2-33a C (Me)₂CH₂S (O) CH₂CF_Three
D2-33a C (Me)₂CH₂S (O)₂Me
D2-33a C (Me)₂CH₂S (O)₂Et
D2-33a C (Me)₂CH₂S (O)₂CF_Three
D2-33a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-33a CH₂CH (Me) SMe
D2-33a CH₂CH (Me) SEt
D2-33a CH₂CH (Me) SCF_Three
D2-33a CH₂CH (Me) SCH₂CF_Three
D2-33a CH₂CH (Me) S (O) Me
D2-33a CH₂CH (Me) S (O) Et
D2-33a CH₂CH (Me) S (O) CF_Three
D2-33a CH₂CH (Me) S (O) CH₂CF_Three
D2-33a CH₂CH (Me) S (O)₂Me
D2-33a CH₂CH (Me) S (O)₂Et
D2-33a CH₂CH (Me) S (O)₂CF_Three
D2-33a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-33a CH₂CH (Et) SMe
D2-33a CH₂CH (Et) SEt
D2-33a CH₂CH (Et) SCF_Three
D2-33a CH₂CH (Et) SCH₂CF_Three
D2-33a CH₂CH (Et) S (O) Me
D2-33a CH₂CH (Et) S (O) Et
D2-33a CH₂CH (Et) S (O) CF_Three
D2-33a CH₂CH (Et) S (O) CH₂CF_Three
D2-33a CH₂CH (Et) S (O)₂Me
D2-33a CH₂CH (Et) S (O)₂Et
D2-33a CH₂CH (Et) S (O)₂CF_Three
D2-33a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-33a CH (Me) CH (Me) SMe
D2-33a CH (Me) CH (Me) SEt
D2-33a CH (Me) CH (Me) SCF_Three
D2-33a CH (Me) CH (Me) SCH₂CF_Three
D2-33a CH (Me) CH (Me) S (O) Me
D2-33a CH (Me) CH (Me) S (O) Et
D2-33a CH (Me) CH (Me) S (O) CF_Three
D2-33a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-33a CH (Me) CH (Me) S (O)₂Me
D2-33a CH (Me) CH (Me) S (O)₂Et
D2-33a CH (Me) CH (Me) S (O)₂CF_Three
D2-33a CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-34a CH₂SMe
D2-34a CH₂SEt
D2-34a CH₂SCF_Three
D2-34a CH₂SCH₂CF_Three
D2-34a CH₂S (O) Me
D2-34a CH₂S (O) Et
D2-34a CH₂S (O) CF_Three
D2-34a CH₂S (O) CH₂CF_Three
D2-34a CH₂S (O)₂Me
D2-34a CH₂S (O)₂Et
D2-34a CH₂S (O)₂CF_Three
D2-34a CH₂S (O)₂CH₂CF_Three
D2-34a CH (Me) SMe
D2-34a CH (Me) SEt
D2-34a CH (Me) SCF_Three
D2-34a CH (Me) SCH₂CF_Three
D2-34a CH (Me) S (O) Me
D2-34a CH (Me) S (O) Et
D2-34a CH (Me) S (O) CF_Three
D2-34a CH (Me) S (O) CH₂CF_Three
D2-34a CH (Me) S (O)₂Me
D2-34a CH (Me) S (O)₂Et
D2-34a CH (Me) S (O)₂CF_Three
D2-34a CH (Me) S (O)₂CH₂CF_Three
D2-34a CH (Et) SMe
D2-34a CH (Et) SEt
D2-34a CH (Et) SCF_Three
D2-34a CH (Et) SCH₂CF_Three
D2-34a CH (Et) S (O) Me
D2-34a CH (Et) S (O) Et
D2-34a CH (Et) S (O) CF_Three
D2-34a CH (Et) S (O) CH₂CF_Three
D2-34a CH (Et) S (O)₂Me
D2-34a CH (Et) S (O)₂Et
D2-34a CH (Et) S (O)₂CF_Three
D2-34a CH (Et) S (O)₂CH₂CF_Three
D2-34a CH (n-Pr) SMe
D2-34a CH (n-Pr) SEt
D2-34a CH (n-Pr) SCF_Three
D2-34a CH (n-Pr) SCH₂CF_Three
D2-34a CH (n-Pr) S (O) Me
D2-34a CH (n-Pr) S (O) Et
D2-34a CH (n-Pr) S (O) CF_Three
D2-34a CH (n-Pr) S (O) CH₂CF_Three
D2-34a CH (n-Pr) S (O)₂Me
D2-34a CH (n-Pr) S (O)₂Et
D2-34a CH (n-Pr) S (O)₂CF_Three
D2-34a CH (n-Pr) S (O)₂CH₂CF_Three
D2-34a CH (i-Pr) SMe
D2-34a CH (i-Pr) SEt
D2-34a CH (i-Pr) SCF_Three
D2-34a CH (i-Pr) SCH₂CF_Three
D2-34a CH (i-Pr) S (O) Me
D2-34a CH (i-Pr) S (O) Et
D2-34a CH (i-Pr) S (O) CF_Three
D2-34a CH (i-Pr) S (O) CH₂CF_Three
D2-34a CH (i-Pr) S (O)₂Me
D2-34a CH (i-Pr) S (O)₂Et
D2-34a CH (i-Pr) S (O)₂CF_Three
D2-34a CH (i-Pr) S (O)₂CH₂CF_Three
D2-34a CH (n-Bu) SMe
D2-34a CH (n-Bu) SEt
D2-34a CH (n-Bu) SCF_Three
D2-34a CH (n-Bu) SCH₂CF_Three
D2-34a CH (n-Bu) S (O) Me
D2-34a CH (n-Bu) S (O) Et
D2-34a CH (n-Bu) S (O) CF_Three
D2-34a CH (n-Bu) S (O) CH₂CF_Three
D2-34a CH (n-Bu) S (O)₂Me
D2-34a CH (n-Bu) S (O)₂Et
D2-34a CH (n-Bu) S (O)₂CF_Three
D2-34a CH (n-Bu) S (O)₂CH₂CF_Three
D2-34a CH (i-Bu) SMe
D2-34a CH (i-Bu) SEt
D2-34a CH (i-Bu) SCF_Three
D2-34a CH (i-Bu) SCH₂CF_Three
D2-34a CH (i-Bu) S (O) Me
D2-34a CH (i-Bu) S (O) Et
D2-34a CH (i-Bu) S (O) CF_Three
D2-34a CH (i-Bu) S (O) CH₂CF_Three
D2-34a CH (i-Bu) S (O)₂Me
D2-34a CH (i-Bu) S (O)₂Et
D2-34a CH (i-Bu) S (O)₂CF_Three
D2-34a CH (i-Bu) S (O)₂CH₂CF_Three
D2-34a CH (s-Bu) SMe
D2-34a CH (s-Bu) SEt
D2-34a CH (s-Bu) SCF_Three
D2-34a CH (s-Bu) SCH₂CF_Three
D2-34a CH (s-Bu) S (O) Me
D2-34a CH (s-Bu) S (O) Et
D2-34a CH (s-Bu) S (O) CF_Three
D2-34a CH (s-Bu) S (O) CH₂CF_Three
D2-34a CH (s-Bu) S (O)₂Me
D2-34a CH (s-Bu) S (O)₂Et
D2-34a CH (s-Bu) S (O)₂CF_Three
D2-34a CH (s-Bu) S (O)₂CH₂CF_Three
D2-34a CH (t-Bu) SMe
D2-34a CH (t-Bu) SEt
D2-34a CH (t-Bu) SCF_Three
D2-34a CH (t-Bu) SCH₂CF_Three
D2-34a CH (t-Bu) S (O) Me
D2-34a CH (t-Bu) S (O) Et
D2-34a CH (t-Bu) S (O) CF_Three
D2-34a CH (t-Bu) S (O) CH₂CF_Three
D2-34a CH (t-Bu) S (O)₂Me
D2-34a CH (t-Bu) S (O)₂Et
D2-34a CH (t-Bu) S (O)₂CF_Three
D2-34a CH (t-Bu) S (O)₂CH₂CF_Three
D2-34a CH (CF_ThreeSMe
D2-34a CH (CF_Three) SEt
D2-34a CH (CF_Three) SCF_Three
D2-34a CH (CF_Three) SCH₂CF_Three
D2-34a CH (CF_Three) S (O) Me
D2-34a CH (CF_Three) S (O) Et
D2-34a CH (CF_Three) S (O) CF_Three
D2-34a CH (CF_Three) S (O) CH₂CF_Three
D2-34a CH (CF_Three) S (O)₂Me
D2-34a CH (CF_Three) S (O)₂Et
D2-34a CH (CF_Three) S (O)₂CF_Three
D2-34a CH (CF_Three) S (O)₂CH₂CF_Three
D2-34a CH₂CH₂SMe
D2-34a CH₂CH₂SEt
D2-34a CH₂CH₂SCF_Three
D2-34a CH₂CH₂SCH₂CF_Three
D2-34a CH₂CH₂S (O) Me
D2-34a CH₂CH₂S (O) Et
D2-34a CH₂CH₂S (O) CF_Three
D2-34a CH₂CH₂S (O) CH₂CF_Three
D2-34a CH₂CH₂S (O)₂Me
D2-34a CH₂CH₂S (O)₂Et
D2-34a CH₂CH₂S (O)₂CF_Three
D2-34a CH₂CH₂S (O)₂CH₂CF_Three
D2-34a CH (Me) CH₂SMe
D2-34a CH (Me) CH₂SEt
D2-34a CH (Me) CH₂SCF_Three
D2-34a CH (Me) CH₂SCH₂CF_Three
D2-34a CH (Me) CH₂S (O) Me
D2-34a CH (Me) CH₂S (O) Et
D2-34a CH (Me) CH₂S (O) CF_Three
D2-34a CH (Me) CH₂S (O) CH₂CF_Three
D2-34a CH (Me) CH₂S (O)₂Me
D2-34a CH (Me) CH₂S (O)₂Et
D2-34a CH (Me) CH₂S (O)₂CF_Three
D2-34a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-34a CH (Et) CH₂SMe
D2-34a CH (Et) CH₂SEt
D2-34a CH (Et) CH₂SCF_Three
D2-34a CH (Et) CH₂SCH₂CF_Three
D2-34a CH (Et) CH₂S (O) Me
D2-34a CH (Et) CH₂S (O) Et
D2-34a CH (Et) CH₂S (O) CF_Three
D2-34a CH (Et) CH₂S (O) CH₂CF_Three
D2-34a CH (Et) CH₂S (O)₂Me
D2-34a CH (Et) CH₂S (O)₂Et
D2-34a CH (Et) CH₂S (O)₂CF_Three
D2-34a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-34a C (Me)₂CH₂SMe
D2-34a C (Me)₂CH₂SEt
D2-34a C (Me)₂CH₂SCF_Three
D2-34a C (Me)₂CH₂SCH₂CF_Three
D2-34a C (Me)₂CH₂S (O) Me
D2-34a C (Me)₂CH₂S (O) Et
D2-34a C (Me)₂CH₂S (O) CF_Three
D2-34a C (Me)₂CH₂S (O) CH₂CF_Three
D2-34a C (Me)₂CH₂S (O)₂Me
D2-34a C (Me)₂CH₂S (O)₂Et
D2-34a C (Me)₂CH₂S (O)₂CF_Three
D2-34a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-34a CH₂CH (Me) SMe
D2-34a CH₂CH (Me) SEt
D2-34a CH₂CH (Me) SCF_Three
D2-34a CH₂CH (Me) SCH₂CF_Three
D2-34a CH₂CH (Me) S (O) Me
D2-34a CH₂CH (Me) S (O) Et
D2-34a CH₂CH (Me) S (O) CF_Three
D2-34a CH₂CH (Me) S (O) CH₂CF_Three
D2-34a CH₂CH (Me) S (O)₂Me
D2-34a CH₂CH (Me) S (O)₂Et
D2-34a CH₂CH (Me) S (O)₂CF_Three
D2-34a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-34a CH₂CH (Et) SMe
D2-34a CH₂CH (Et) SEt
D2-34a CH₂CH (Et) SCF_Three
D2-34a CH₂CH (Et) SCH₂CF_Three
D2-34a CH₂CH (Et) S (O) Me
D2-34a CH₂CH (Et) S (O) Et
D2-34a CH₂CH (Et) S (O) CF_Three
D2-34a CH₂CH (Et) S (O) CH₂CF_Three
D2-34a CH₂CH (Et) S (O)₂Me
D2-34a CH₂CH (Et) S (O)₂Et
D2-34a CH₂CH (Et) S (O)₂CF_Three
D2-34a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-34a CH (Me) CH (Me) SMe
D2-34a CH (Me) CH (Me) SEt
D2-34a CH (Me) CH (Me) SCF_Three
D2-34a CH (Me) CH (Me) SCH₂CF_Three
D2-34a CH (Me) CH (Me) S (O) Me
D2-34a CH (Me) CH (Me) S (O) Et
D2-34a CH (Me) CH (Me) S (O) CF_Three
D2-34a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-34a CH (Me) CH (Me) S (O)₂Me
D2-34a CH (Me) CH (Me) S (O)₂Et
D2-34a CH (Me) CH (Me) S (O)₂CF_Three
D2-34a CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-36a CH₂SMe
D2-36a CH₂SEt
D2-36a CH₂SCF_Three
D2-36a CH₂SCH₂CF_Three
D2-36a CH₂S (O) Me
D2-36a CH₂S (O) Et
D2-36a CH₂S (O) CF_Three
D2-36a CH₂S (O) CH₂CF_Three
D2-36a CH₂S (O)₂Me
D2-36a CH₂S (O)₂Et
D2-36a CH₂S (O)₂CF_Three
D2-36a CH₂S (O)₂CH₂CF_Three
D2-36a CH (Me) SMe
D2-36a CH (Me) SEt
D2-36a CH (Me) SCF_Three
D2-36a CH (Me) SCH₂CF_Three
D2-36a CH (Me) S (O) Me
D2-36a CH (Me) S (O) Et
D2-36a CH (Me) S (O) CF_Three
D2-36a CH (Me) S (O) CH₂CF_Three
D2-36a CH (Me) S (O)₂Me
D2-36a CH (Me) S (O)₂Et
D2-36a CH (Me) S (O)₂CF_Three
D2-36a CH (Me) S (O)₂CH₂CF_Three
D2-36a CH (Et) SMe
D2-36a CH (Et) SEt
D2-36a CH (Et) SCF_Three
D2-36a CH (Et) SCH₂CF_Three
D2-36a CH (Et) S (O) Me
D2-36a CH (Et) S (O) Et
D2-36a CH (Et) S (O) CF_Three
D2-36a CH (Et) S (O) CH₂CF_Three
D2-36a CH (Et) S (O)₂Me
D2-36a CH (Et) S (O)₂Et
D2-36a CH (Et) S (O)₂CF_Three
D2-36a CH (Et) S (O)₂CH₂CF_Three
D2-36a CH (n-Pr) SMe
D2-36a CH (n-Pr) SEt
D2-36a CH (n-Pr) SCF_Three
D2-36a CH (n-Pr) SCH₂CF_Three
D2-36a CH (n-Pr) S (O) Me
D2-36a CH (n-Pr) S (O) Et
D2-36a CH (n-Pr) S (O) CF_Three
D2-36a CH (n-Pr) S (O) CH₂CF_Three
D2-36a CH (n-Pr) S (O)₂Me
D2-36a CH (n-Pr) S (O)₂Et
D2-36a CH (n-Pr) S (O)₂CF_Three
D2-36a CH (n-Pr) S (O)₂CH₂CF_Three
D2-36a CH (i-Pr) SMe
D2-36a CH (i-Pr) SEt
D2-36a CH (i-Pr) SCF_Three
D2-36a CH (i-Pr) SCH₂CF_Three
D2-36a CH (i-Pr) S (O) Me
D2-36a CH (i-Pr) S (O) Et
D2-36a CH (i-Pr) S (O) CF_Three
D2-36a CH (i-Pr) S (O) CH₂CF_Three
D2-36a CH (i-Pr) S (O)₂Me
D2-36a CH (i-Pr) S (O)₂Et
D2-36a CH (i-Pr) S (O)₂CF_Three
D2-36a CH (i-Pr) S (O)₂CH₂CF_Three
D2-36a CH (n-Bu) SMe
D2-36a CH (n-Bu) SEt
D2-36a CH (n-Bu) SCF_Three
D2-36a CH (n-Bu) SCH₂CF_Three
D2-36a CH (n-Bu) S (O) Me
D2-36a CH (n-Bu) S (O) Et
D2-36a CH (n-Bu) S (O) CF_Three
D2-36a CH (n-Bu) S (O) CH₂CF_Three
D2-36a CH (n-Bu) S (O)₂Me
D2-36a CH (n-Bu) S (O)₂Et
D2-36a CH (n-Bu) S (O)₂CF_Three
D2-36a CH (n-Bu) S (O)₂CH₂CF_Three
D2-36a CH (i-Bu) SMe
D2-36a CH (i-Bu) SEt
D2-36a CH (i-Bu) SCF_Three
D2-36a CH (i-Bu) SCH₂CF_Three
D2-36a CH (i-Bu) S (O) Me
D2-36a CH (i-Bu) S (O) Et
D2-36a CH (i-Bu) S (O) CF_Three
D2-36a CH (i-Bu) S (O) CH₂CF_Three
D2-36a CH (i-Bu) S (O)₂Me
D2-36a CH (i-Bu) S (O)₂Et
D2-36a CH (i-Bu) S (O)₂CF_Three
D2-36a CH (i-Bu) S (O)₂CH₂CF_Three
D2-36a CH (s-Bu) SMe
D2-36a CH (s-Bu) SEt
D2-36a CH (s-Bu) SCF_Three
D2-36a CH (s-Bu) SCH₂CF_Three
D2-36a CH (s-Bu) S (O) Me
D2-36a CH (s-Bu) S (O) Et
D2-36a CH (s-Bu) S (O) CF_Three
D2-36a CH (s-Bu) S (O) CH₂CF_Three
D2-36a CH (s-Bu) S (O)₂Me
D2-36a CH (s-Bu) S (O)₂Et
D2-36a CH (s-Bu) S (O)₂CF_Three
D2-36a CH (s-Bu) S (O)₂CH₂CF_Three
D2-36a CH (t-Bu) SMe
D2-36a CH (t-Bu) SEt
D2-36a CH (t-Bu) SCF_Three
D2-36a CH (t-Bu) SCH₂CF_Three
D2-36a CH (t-Bu) S (O) Me
D2-36a CH (t-Bu) S (O) Et
D2-36a CH (t-Bu) S (O) CF_Three
D2-36a CH (t-Bu) S (O) CH₂CF_Three
D2-36a CH (t-Bu) S (O)₂Me
D2-36a CH (t-Bu) S (O)₂Et
D2-36a CH (t-Bu) S (O)₂CF_Three
D2-36a CH (t-Bu) S (O)₂CH₂CF_Three
D2-36a CH (CF_ThreeSMe
D2-36a CH (CF_Three) SEt
D2-36a CH (CF_Three) SCF_Three
D2-36a CH (CF_Three) SCH₂CF_Three
D2-36a CH (CF_Three) S (O) Me
D2-36a CH (CF_Three) S (O) Et
D2-36a CH (CF_Three) S (O) CF_Three
D2-36a CH (CF_Three) S (O) CH₂CF_Three
D2-36a CH (CF_Three) S (O)₂Me
D2-36a CH (CF_Three) S (O)₂Et
D2-36a CH (CF_Three) S (O)₂CF_Three
D2-36a CH (CF_Three) S (O)₂CH₂CF_Three
D2-36a CH₂CH₂SMe
D2-36a CH₂CH₂SEt
D2-36a CH₂CH₂SCF_Three
D2-36a CH₂CH₂SCH₂CF_Three
D2-36a CH₂CH₂S (O) Me
D2-36a CH₂CH₂S (O) Et
D2-36a CH₂CH₂S (O) CF_Three
D2-36a CH₂CH₂S (O) CH₂CF_Three
D2-36a CH₂CH₂S (O)₂Me
D2-36a CH₂CH₂S (O)₂Et
D2-36a CH₂CH₂S (O)₂CF_Three
D2-36a CH₂CH₂S (O)₂CH₂CF_Three
D2-36a CH (Me) CH₂SMe
D2-36a CH (Me) CH₂SEt
D2-36a CH (Me) CH₂SCF_Three
D2-36a CH (Me) CH₂SCH₂CF_Three
D2-36a CH (Me) CH₂S (O) Me
D2-36a CH (Me) CH₂S (O) Et
D2-36a CH (Me) CH₂S (O) CF_Three
D2-36a CH (Me) CH₂S (O) CH₂CF_Three
D2-36a CH (Me) CH₂S (O)₂Me
D2-36a CH (Me) CH₂S (O)₂Et
D2-36a CH (Me) CH₂S (O)₂CF_Three
D2-36a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-36a CH (Et) CH₂SMe
D2-36a CH (Et) CH₂SEt
D2-36a CH (Et) CH₂SCF_Three
D2-36a CH (Et) CH₂SCH₂CF_Three
D2-36a CH (Et) CH₂S (O) Me
D2-36a CH (Et) CH₂S (O) Et
D2-36a CH (Et) CH₂S (O) CF_Three
D2-36a CH (Et) CH₂S (O) CH₂CF_Three
D2-36a CH (Et) CH₂S (O)₂Me
D2-36a CH (Et) CH₂S (O)₂Et
D2-36a CH (Et) CH₂S (O)₂CF_Three
D2-36a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-36a C (Me)₂CH₂SMe
D2-36a C (Me)₂CH₂SEt
D2-36a C (Me)₂CH₂SCF_Three
D2-36a C (Me)₂CH₂SCH₂CF_Three
D2-36a C (Me)₂CH₂S (O) Me
D2-36a C (Me)₂CH₂S (O) Et
D2-36a C (Me)₂CH₂S (O) CF_Three
D2-36a C (Me)₂CH₂S (O) CH₂CF_Three
D2-36a C (Me)₂CH₂S (O)₂Me
D2-36a C (Me)₂CH₂S (O)₂Et
D2-36a C (Me)₂CH₂S (O)₂CF_Three
D2-36a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-36a CH₂CH (Me) SMe
D2-36a CH₂CH (Me) SEt
D2-36a CH₂CH (Me) SCF_Three
D2-36a CH₂CH (Me) SCH₂CF_Three
D2-36a CH₂CH (Me) S (O) Me
D2-36a CH₂CH (Me) S (O) Et
D2-36a CH₂CH (Me) S (O) CF_Three
D2-36a CH₂CH (Me) S (O) CH₂CF_Three
D2-36a CH₂CH (Me) S (O)₂Me
D2-36a CH₂CH (Me) S (O)₂Et
D2-36a CH₂CH (Me) S (O)₂CF_Three
D2-36a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-36a CH₂CH (Et) SMe
D2-36a CH₂CH (Et) SEt
D2-36a CH₂CH (Et) SCF_Three
D2-36a CH₂CH (Et) SCH₂CF_Three
D2-36a CH₂CH (Et) S (O) Me
D2-36a CH₂CH (Et) S (O) Et
D2-36a CH₂CH (Et) S (O) CF_Three
D2-36a CH₂CH (Et) S (O) CH₂CF_Three
D2-36a CH₂CH (Et) S (O)₂Me
D2-36a CH₂CH (Et) S (O)₂Et
D2-36a CH₂CH (Et) S (O)₂CF_Three
D2-36a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-36a CH (Me) CH (Me) SMe
D2-36a CH (Me) CH (Me) SEt
D2-36a CH (Me) CH (Me) SCF_Three
D2-36a CH (Me) CH (Me) SCH₂CF_Three
D2-36a CH (Me) CH (Me) S (O) Me
D2-36a CH (Me) CH (Me) S (O) Et
D2-36a CH (Me) CH (Me) S (O) CF_Three
D2-36a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-36a CH (Me) CH (Me) S (O)₂Me
D2-36a CH (Me) CH (Me) S (O)₂Et
D2-36a CH (Me) CH (Me) S (O)₂CF_Three
D2-36a CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-37a CH₂SMe
D2-37a CH₂SEt
D2-37a CH₂SCF_Three
D2-37a CH₂SCH₂CF_Three
D2-37a CH₂S (O) Me
D2-37a CH₂S (O) Et
D2-37a CH₂S (O) CF_Three
D2-37a CH₂S (O) CH₂CF_Three
D2-37a CH₂S (O)₂Me
D2-37a CH₂S (O)₂Et
D2-37a CH₂S (O)₂CF_Three
D2-37a CH₂S (O)₂CH₂CF_Three
D2-37a CH (Me) SMe
D2-37a CH (Me) SEt
D2-37a CH (Me) SCF_Three
D2-37a CH (Me) SCH₂CF_Three
D2-37a CH (Me) S (O) Me
D2-37a CH (Me) S (O) Et
D2-37a CH (Me) S (O) CF_Three
D2-37a CH (Me) S (O) CH₂CF_Three
D2-37a CH (Me) S (O)₂Me
D2-37a CH (Me) S (O)₂Et
D2-37a CH (Me) S (O)₂CF_Three
D2-37a CH (Me) S (O)₂CH₂CF_Three
D2-37a CH (Et) SMe
D2-37a CH (Et) SEt
D2-37a CH (Et) SCF_Three
D2-37a CH (Et) SCH₂CF_Three
D2-37a CH (Et) S (O) Me
D2-37a CH (Et) S (O) Et
D2-37a CH (Et) S (O) CF_Three
D2-37a CH (Et) S (O) CH₂CF_Three
D2-37a CH (Et) S (O)₂Me
D2-37a CH (Et) S (O)₂Et
D2-37a CH (Et) S (O)₂CF_Three
D2-37a CH (Et) S (O)₂CH₂CF_Three
D2-37a CH (n-Pr) SMe
D2-37a CH (n-Pr) SEt
D2-37a CH (n-Pr) SCF_Three
D2-37a CH (n-Pr) SCH₂CF_Three
D2-37a CH (n-Pr) S (O) Me
D2-37a CH (n-Pr) S (O) Et
D2-37a CH (n-Pr) S (O) CF_Three
D2-37a CH (n-Pr) S (O) CH₂CF_Three
D2-37a CH (n-Pr) S (O)₂Me
D2-37a CH (n-Pr) S (O)₂Et
D2-37a CH (n-Pr) S (O)₂CF_Three
D2-37a CH (n-Pr) S (O)₂CH₂CF_Three
D2-37a CH (i-Pr) SMe
D2-37a CH (i-Pr) SEt
D2-37a CH (i-Pr) SCF_Three
D2-37a CH (i-Pr) SCH₂CF_Three
D2-37a CH (i-Pr) S (O) Me
D2-37a CH (i-Pr) S (O) Et
D2-37a CH (i-Pr) S (O) CF_Three
D2-37a CH (i-Pr) S (O) CH₂CF_Three
D2-37a CH (i-Pr) S (O)₂Me
D2-37a CH (i-Pr) S (O)₂Et
D2-37a CH (i-Pr) S (O)₂CF_Three
D2-37a CH (i-Pr) S (O)₂CH₂CF_Three
D2-37a CH (n-Bu) SMe
D2-37a CH (n-Bu) SEt
D2-37a CH (n-Bu) SCF_Three
D2-37a CH (n-Bu) SCH₂CF_Three
D2-37a CH (n-Bu) S (O) Me
D2-37a CH (n-Bu) S (O) Et
D2-37a CH (n-Bu) S (O) CF_Three
D2-37a CH (n-Bu) S (O) CH₂CF_Three
D2-37a CH (n-Bu) S (O)₂Me
D2-37a CH (n-Bu) S (O)₂Et
D2-37a CH (n-Bu) S (O)₂CF_Three
D2-37a CH (n-Bu) S (O)₂CH₂CF_Three
D2-37a CH (i-Bu) SMe
D2-37a CH (i-Bu) SEt
D2-37a CH (i-Bu) SCF_Three
D2-37a CH (i-Bu) SCH₂CF_Three
D2-37a CH (i-Bu) S (O) Me
D2-37a CH (i-Bu) S (O) Et
D2-37a CH (i-Bu) S (O) CF_Three
D2-37a CH (i-Bu) S (O) CH₂CF_Three
D2-37a CH (i-Bu) S (O)₂Me
D2-37a CH (i-Bu) S (O)₂Et
D2-37a CH (i-Bu) S (O)₂CF_Three
D2-37a CH (i-Bu) S (O)₂CH₂CF_Three
D2-37a CH (s-Bu) SMe
D2-37a CH (s-Bu) SEt
D2-37a CH (s-Bu) SCF_Three
D2-37a CH (s-Bu) SCH₂CF_Three
D2-37a CH (s-Bu) S (O) Me
D2-37a CH (s-Bu) S (O) Et
D2-37a CH (s-Bu) S (O) CF_Three
D2-37a CH (s-Bu) S (O) CH₂CF_Three
D2-37a CH (s-Bu) S (O)₂Me
D2-37a CH (s-Bu) S (O)₂Et
D2-37a CH (s-Bu) S (O)₂CF_Three
D2-37a CH (s-Bu) S (O)₂CH₂CF_Three
D2-37a CH (t-Bu) SMe
D2-37a CH (t-Bu) SEt
D2-37a CH (t-Bu) SCF_Three
D2-37a CH (t-Bu) SCH₂CF_Three
D2-37a CH (t-Bu) S (O) Me
D2-37a CH (t-Bu) S (O) Et
D2-37a CH (t-Bu) S (O) CF_Three
D2-37a CH (t-Bu) S (O) CH₂CF_Three
D2-37a CH (t-Bu) S (O)₂Me
D2-37a CH (t-Bu) S (O)₂Et
D2-37a CH (t-Bu) S (O)₂CF_Three
D2-37a CH (t-Bu) S (O)₂CH₂CF_Three
D2-37a CH (CF_ThreeSMe
D2-37a CH (CF_Three) SEt
D2-37a CH (CF_Three) SCF_Three
D2-37a CH (CF_Three) SCH₂CF_Three
D2-37a CH (CF_Three) S (O) Me
D2-37a CH (CF_Three) S (O) Et
D2-37a CH (CF_Three) S (O) CF_Three
D2-37a CH (CF_Three) S (O) CH₂CF_Three
D2-37a CH (CF_Three) S (O)₂Me
D2-37a CH (CF_Three) S (O)₂Et
D2-37a CH (CF_Three) S (O)₂CF_Three
D2-37a CH (CF_Three) S (O)₂CH₂CF_Three
D2-37a CH₂CH₂SMe
D2-37a CH₂CH₂SEt
D2-37a CH₂CH₂SCF_Three
D2-37a CH₂CH₂SCH₂CF_Three
D2-37a CH₂CH₂S (O) Me
D2-37a CH₂CH₂S (O) Et
D2-37a CH₂CH₂S (O) CF_Three
D2-37a CH₂CH₂S (O) CH₂CF_Three
D2-37a CH₂CH₂S (O)₂Me
D2-37a CH₂CH₂S (O)₂Et
D2-37a CH₂CH₂S (O)₂CF_Three
D2-37a CH₂CH₂S (O)₂CH₂CF_Three
D2-37a CH (Me) CH₂SMe
D2-37a CH (Me) CH₂SEt
D2-37a CH (Me) CH₂SCF_Three
D2-37a CH (Me) CH₂SCH₂CF_Three
D2-37a CH (Me) CH₂S (O) Me
D2-37a CH (Me) CH₂S (O) Et
D2-37a CH (Me) CH₂S (O) CF_Three
D2-37a CH (Me) CH₂S (O) CH₂CF_Three
D2-37a CH (Me) CH₂S (O)₂Me
D2-37a CH (Me) CH₂S (O)₂Et
D2-37a CH (Me) CH₂S (O)₂CF_Three
D2-37a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-37a CH (Et) CH₂SMe
D2-37a CH (Et) CH₂SEt
D2-37a CH (Et) CH₂SCF_Three
D2-37a CH (Et) CH₂SCH₂CF_Three
D2-37a CH (Et) CH₂S (O) Me
D2-37a CH (Et) CH₂S (O) Et
D2-37a CH (Et) CH₂S (O) CF_Three
D2-37a CH (Et) CH₂S (O) CH₂CF_Three
D2-37a CH (Et) CH₂S (O)₂Me
D2-37a CH (Et) CH₂S (O)₂Et
D2-37a CH (Et) CH₂S (O)₂CF_Three
D2-37a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-37a C (Me)₂CH₂SMe
D2-37a C (Me)₂CH₂SEt
D2-37a C (Me)₂CH₂SCF_Three
D2-37a C (Me)₂CH₂SCH₂CF_Three
D2-37a C (Me)₂CH₂S (O) Me
D2-37a C (Me)₂CH₂S (O) Et
D2-37a C (Me)₂CH₂S (O) CF_Three
D2-37a C (Me)₂CH₂S (O) CH₂CF_Three
D2-37a C (Me)₂CH₂S (O)₂Me
D2-37a C (Me)₂CH₂S (O)₂Et
D2-37a C (Me)₂CH₂S (O)₂CF_Three
D2-37a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-37a CH₂CH (Me) SMe
D2-37a CH₂CH (Me) SEt
D2-37a CH₂CH (Me) SCF_Three
D2-37a CH₂CH (Me) SCH₂CF_Three
D2-37a CH₂CH (Me) S (O) Me
D2-37a CH₂CH (Me) S (O) Et
D2-37a CH₂CH (Me) S (O) CF_Three
D2-37a CH₂CH (Me) S (O) CH₂CF_Three
D2-37a CH₂CH (Me) S (O)₂Me
D2-37a CH₂CH (Me) S (O)₂Et
D2-37a CH₂CH (Me) S (O)₂CF_Three
D2-37a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-37a CH₂CH (Et) SMe
D2-37a CH₂CH (Et) SEt
D2-37a CH₂CH (Et) SCF_Three
D2-37a CH₂CH (Et) SCH₂CF_Three
D2-37a CH₂CH (Et) S (O) Me
D2-37a CH₂CH (Et) S (O) Et
D2-37a CH₂CH (Et) S (O) CF_Three
D2-37a CH₂CH (Et) S (O) CH₂CF_Three
D2-37a CH₂CH (Et) S (O)₂Me
D2-37a CH₂CH (Et) S (O)₂Et
D2-37a CH₂CH (Et) S (O)₂CF_Three
D2-37a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-37a CH (Me) CH (Me) SMe
D2-37a CH (Me) CH (Me) SEt
D2-37a CH (Me) CH (Me) SCF_Three
D2-37a CH (Me) CH (Me) SCH₂CF_Three
D2-37a CH (Me) CH (Me) S (O) Me
D2-37a CH (Me) CH (Me) S (O) Et
D2-37a CH (Me) CH (Me) S (O) CF_Three
D2-37a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-37a CH (Me) CH (Me) S (O)₂Me
D2-37a CH (Me) CH (Me) S (O)₂Et
D2-37a CH (Me) CH (Me) S (O)₂CF_Three
D2-37a CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-38a CH₂SMe
D2-38a CH₂SEt
D2-38a CH₂SCF_Three
D2-38a CH₂SCH₂CF_Three
D2-38a CH₂S (O) Me
D2-38a CH₂S (O) Et
D2-38a CH₂S (O) CF_Three
D2-38a CH₂S (O) CH₂CF_Three
D2-38a CH₂S (O)₂Me
D2-38a CH₂S (O)₂Et
D2-38a CH₂S (O)₂CF_Three
D2-38a CH₂S (O)₂CH₂CF_Three
D2-38a CH (Me) SMe
D2-38a CH (Me) SEt
D2-38a CH (Me) SCF_Three
D2-38a CH (Me) SCH₂CF_Three
D2-38a CH (Me) S (O) Me
D2-38a CH (Me) S (O) Et
D2-38a CH (Me) S (O) CF_Three
D2-38a CH (Me) S (O) CH₂CF_Three
D2-38a CH (Me) S (O)₂Me
D2-38a CH (Me) S (O)₂Et
D2-38a CH (Me) S (O)₂CF_Three
D2-38a CH (Me) S (O)₂CH₂CF_Three
D2-38a CH (Et) SMe
D2-38a CH (Et) SEt
D2-38a CH (Et) SCF_Three
D2-38a CH (Et) SCH₂CF_Three
D2-38a CH (Et) S (O) Me
D2-38a CH (Et) S (O) Et
D2-38a CH (Et) S (O) CF_Three
D2-38a CH (Et) S (O) CH₂CF_Three
D2-38a CH (Et) S (O)₂Me
D2-38a CH (Et) S (O)₂Et
D2-38a CH (Et) S (O)₂CF_Three
D2-38a CH (Et) S (O)₂CH₂CF_Three
D2-38a CH (n-Pr) SMe
D2-38a CH (n-Pr) SEt
D2-38a CH (n-Pr) SCF_Three
D2-38a CH (n-Pr) SCH₂CF_Three
D2-38a CH (n-Pr) S (O) Me
D2-38a CH (n-Pr) S (O) Et
D2-38a CH (n-Pr) S (O) CF_Three
D2-38a CH (n-Pr) S (O) CH₂CF_Three
D2-38a CH (n-Pr) S (O)₂Me
D2-38a CH (n-Pr) S (O)₂Et
D2-38a CH (n-Pr) S (O)₂CF_Three
D2-38a CH (n-Pr) S (O)₂CH₂CF_Three
D2-38a CH (i-Pr) SMe
D2-38a CH (i-Pr) SEt
D2-38a CH (i-Pr) SCF_Three
D2-38a CH (i-Pr) SCH₂CF_Three
D2-38a CH (i-Pr) S (O) Me
D2-38a CH (i-Pr) S (O) Et
D2-38a CH (i-Pr) S (O) CF_Three
D2-38a CH (i-Pr) S (O) CH₂CF_Three
D2-38a CH (i-Pr) S (O)₂Me
D2-38a CH (i-Pr) S (O)₂Et
D2-38a CH (i-Pr) S (O)₂CF_Three
D2-38a CH (i-Pr) S (O)₂CH₂CF_Three
D2-38a CH (n-Bu) SMe
D2-38a CH (n-Bu) SEt
D2-38a CH (n-Bu) SCF_Three
D2-38a CH (n-Bu) SCH₂CF_Three
D2-38a CH (n-Bu) S (O) Me
D2-38a CH (n-Bu) S (O) Et
D2-38a CH (n-Bu) S (O) CF_Three
D2-38a CH (n-Bu) S (O) CH₂CF_Three
D2-38a CH (n-Bu) S (O)₂Me
D2-38a CH (n-Bu) S (O)₂Et
D2-38a CH (n-Bu) S (O)₂CF_Three
D2-38a CH (n-Bu) S (O)₂CH₂CF_Three
D2-38a CH (i-Bu) SMe
D2-38a CH (i-Bu) SEt
D2-38a CH (i-Bu) SCF_Three
D2-38a CH (i-Bu) SCH₂CF_Three
D2-38a CH (i-Bu) S (O) Me
D2-38a CH (i-Bu) S (O) Et
D2-38a CH (i-Bu) S (O) CF_Three
D2-38a CH (i-Bu) S (O) CH₂CF_Three
D2-38a CH (i-Bu) S (O)₂Me
D2-38a CH (i-Bu) S (O)₂Et
D2-38a CH (i-Bu) S (O)₂CF_Three
D2-38a CH (i-Bu) S (O)₂CH₂CF_Three
D2-38a CH (s-Bu) SMe
D2-38a CH (s-Bu) SEt
D2-38a CH (s-Bu) SCF_Three
D2-38a CH (s-Bu) SCH₂CF_Three
D2-38a CH (s-Bu) S (O) Me
D2-38a CH (s-Bu) S (O) Et
D2-38a CH (s-Bu) S (O) CF_Three
D2-38a CH (s-Bu) S (O) CH₂CF_Three
D2-38a CH (s-Bu) S (O)₂Me
D2-38a CH (s-Bu) S (O)₂Et
D2-38a CH (s-Bu) S (O)₂CF_Three
D2-38a CH (s-Bu) S (O)₂CH₂CF_Three
D2-38a CH (t-Bu) SMe
D2-38a CH (t-Bu) SEt
D2-38a CH (t-Bu) SCF_Three
D2-38a CH (t-Bu) SCH₂CF_Three
D2-38a CH (t-Bu) S (O) Me
D2-38a CH (t-Bu) S (O) Et
D2-38a CH (t-Bu) S (O) CF_Three
D2-38a CH (t-Bu) S (O) CH₂CF_Three
D2-38a CH (t-Bu) S (O)₂Me
D2-38a CH (t-Bu) S (O)₂Et
D2-38a CH (t-Bu) S (O)₂CF_Three
D2-38a CH (t-Bu) S (O)₂CH₂CF_Three
D2-38a CH (CF_ThreeSMe
D2-38a CH (CF_Three) SEt
D2-38a CH (CF_Three) SCF_Three
D2-38a CH (CF_Three) SCH₂CF_Three
D2-38a CH (CF_Three) S (O) Me
D2-38a CH (CF_Three) S (O) Et
D2-38a CH (CF_Three) S (O) CF_Three
D2-38a CH (CF_Three) S (O) CH₂CF_Three
D2-38a CH (CF_Three) S (O)₂Me
D2-38a CH (CF_Three) S (O)₂Et
D2-38a CH (CF_Three) S (O)₂CF_Three
D2-38a CH (CF_Three) S (O)₂CH₂CF_Three
D2-38a CH₂CH₂SMe
D2-38a CH₂CH₂SEt
D2-38a CH₂CH₂SCF_Three
D2-38a CH₂CH₂SCH₂CF_Three
D2-38a CH₂CH₂S (O) Me
D2-38a CH₂CH₂S (O) Et
D2-38a CH₂CH₂S (O) CF_Three
D2-38a CH₂CH₂S (O) CH₂CF_Three
D2-38a CH₂CH₂S (O)₂Me
D2-38a CH₂CH₂S (O)₂Et
D2-38a CH₂CH₂S (O)₂CF_Three
D2-38a CH₂CH₂S (O)₂CH₂CF_Three
D2-38a CH (Me) CH₂SMe
D2-38a CH (Me) CH₂SEt
D2-38a CH (Me) CH₂SCF_Three
D2-38a CH (Me) CH₂SCH₂CF_Three
D2-38a CH (Me) CH₂S (O) Me
D2-38a CH (Me) CH₂S (O) Et
D2-38a CH (Me) CH₂S (O) CF_Three
D2-38a CH (Me) CH₂S (O) CH₂CF_Three
D2-38a CH (Me) CH₂S (O)₂Me
D2-38a CH (Me) CH₂S (O)₂Et
D2-38a CH (Me) CH₂S (O)₂CF_Three
D2-38a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-38a CH (Et) CH₂SMe
D2-38a CH (Et) CH₂SEt
D2-38a CH (Et) CH₂SCF_Three
D2-38a CH (Et) CH₂SCH₂CF_Three
D2-38a CH (Et) CH₂S (O) Me
D2-38a CH (Et) CH₂S (O) Et
D2-38a CH (Et) CH₂S (O) CF_Three
D2-38a CH (Et) CH₂S (O) CH₂CF_Three
D2-38a CH (Et) CH₂S (O)₂Me
D2-38a CH (Et) CH₂S (O)₂Et
D2-38a CH (Et) CH₂S (O)₂CF_Three
D2-38a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-38a C (Me)₂CH₂SMe
D2-38a C (Me)₂CH₂SEt
D2-38a C (Me)₂CH₂SCF_Three
D2-38a C (Me)₂CH₂SCH₂CF_Three
D2-38a C (Me)₂CH₂S (O) Me
D2-38a C (Me)₂CH₂S (O) Et
D2-38a C (Me)₂CH₂S (O) CF_Three
D2-38a C (Me)₂CH₂S (O) CH₂CF_Three
D2-38a C (Me)₂CH₂S (O)₂Me
D2-38a C (Me)₂CH₂S (O)₂Et
D2-38a C (Me)₂CH₂S (O)₂CF_Three
D2-38a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-38a CH₂CH (Me) SMe
D2-38a CH₂CH (Me) SEt
D2-38a CH₂CH (Me) SCF_Three
D2-38a CH₂CH (Me) SCH₂CF_Three
D2-38a CH₂CH (Me) S (O) Me
D2-38a CH₂CH (Me) S (O) Et
D2-38a CH₂CH (Me) S (O) CF_Three
D2-38a CH₂CH (Me) S (O) CH₂CF_Three
D2-38a CH₂CH (Me) S (O)₂Me
D2-38a CH₂CH (Me) S (O)₂Et
D2-38a CH₂CH (Me) S (O)₂CF_Three
D2-38a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-38a CH₂CH (Et) SMe
D2-38a CH₂CH (Et) SEt
D2-38a CH₂CH (Et) SCF_Three
D2-38a CH₂CH (Et) SCH₂CF_Three
D2-38a CH₂CH (Et) S (O) Me
D2-38a CH₂CH (Et) S (O) Et
D2-38a CH₂CH (Et) S (O) CF_Three
D2-38a CH₂CH (Et) S (O) CH₂CF_Three
D2-38a CH₂CH (Et) S (O)₂Me
D2-38a CH₂CH (Et) S (O)₂Et
D2-38a CH₂CH (Et) S (O)₂CF_Three
D2-38a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-38a CH (Me) CH (Me) SMe
D2-38a CH (Me) CH (Me) SEt
D2-38a CH (Me) CH (Me) SCF_Three
D2-38a CH (Me) CH (Me) SCH₂CF_Three
D2-38a CH (Me) CH (Me) S (O) Me
D2-38a CH (Me) CH (Me) S (O) Et
D2-38a CH (Me) CH (Me) S (O) CF_Three
D2-38a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-38a CH (Me) CH (Me) S (O)₂Me
D2-38a CH (Me) CH (Me) S (O)₂Et
D2-38a CH (Me) CH (Me) S (O)₂CF_Three
D2-38a CH (Me) CH (Me) S (O)₂CH₂CF_Three
D2-92a CH₂SMe
D2-92a CH₂SEt
D2-92a CH₂SCF_Three
D2-92a CH₂SCH₂CF_Three
D2-92a CH₂S (O) Me
D2-92a CH₂S (O) Et
D2-92a CH₂S (O) CF_Three
D2-92a CH₂S (O) CH₂CF_Three
D2-92a CH₂S (O)₂Me
D2-92a CH₂S (O)₂Et
D2-92a CH₂S (O)₂CF_Three
D2-92a CH₂S (O)₂CH₂CF_Three
D2-92a CH (Me) SMe
D2-92a CH (Me) SEt
D2-92a CH (Me) SCF_Three
D2-92a CH (Me) SCH₂CF_Three
D2-92a CH (Me) S (O) Me
D2-92a CH (Me) S (O) Et
D2-92a CH (Me) S (O) CF_Three
D2-92a CH (Me) S (O) CH₂CF_Three
D2-92a CH (Me) S (O)₂Me
D2-92a CH (Me) S (O)₂Et
D2-92a CH (Me) S (O)₂CF_Three
D2-92a CH (Me) S (O)₂CH₂CF_Three
D2-92a CH (Et) SMe
D2-92a CH (Et) SEt
D2-92a CH (Et) SCF_Three
D2-92a CH (Et) SCH₂CF_Three
D2-92a CH (Et) S (O) Me
D2-92a CH (Et) S (O) Et
D2-92a CH (Et) S (O) CF_Three
D2-92a CH (Et) S (O) CH₂CF_Three
D2-92a CH (Et) S (O)₂Me
D2-92a CH (Et) S (O)₂Et
D2-92a CH (Et) S (O)₂CF_Three
D2-92a CH (Et) S (O)₂CH₂CF_Three
D2-92a CH (n-Pr) SMe
D2-92a CH (n-Pr) SEt
D2-92a CH (n-Pr) SCF_Three
D2-92a CH (n-Pr) SCH₂CF_Three
D2-92a CH (n-Pr) S (O) Me
D2-92a CH (n-Pr) S (O) Et
D2-92a CH (n-Pr) S (O) CF_Three
D2-92a CH (n-Pr) S (O) CH₂CF_Three
D2-92a CH (n-Pr) S (O)₂Me
D2-92a CH (n-Pr) S (O)₂Et
D2-92a CH (n-Pr) S (O)₂CF_Three
D2-92a CH (n-Pr) S (O)₂CH₂CF_Three
D2-92a CH (i-Pr) SMe
D2-92a CH (i-Pr) SEt
D2-92a CH (i-Pr) SCF_Three
D2-92a CH (i-Pr) SCH₂CF_Three
D2-92a CH (i-Pr) S (O) Me
D2-92a CH (i-Pr) S (O) Et
D2-92a CH (i-Pr) S (O) CF_Three
D2-92a CH (i-Pr) S (O) CH₂CF_Three
D2-92a CH (i-Pr) S (O)₂Me
D2-92a CH (i-Pr) S (O)₂Et
D2-92a CH (i-Pr) S (O)₂CF_Three
D2-92a CH (i-Pr) S (O)₂CH₂CF_Three
D2-92a CH (n-Bu) SMe
D2-92a CH (n-Bu) SEt
D2-92a CH (n-Bu) SCF_Three
D2-92a CH (n-Bu) SCH₂CF_Three
D2-92a CH (n-Bu) S (O) Me
D2-92a CH (n-Bu) S (O) Et
D2-92a CH (n-Bu) S (O) CF_Three
D2-92a CH (n-Bu) S (O) CH₂CF_Three
D2-92a CH (n-Bu) S (O)₂Me
D2-92a CH (n-Bu) S (O)₂Et
D2-92a CH (n-Bu) S (O)₂CF_Three
D2-92a CH (n-Bu) S (O)₂CH₂CF_Three
D2-92a CH (i-Bu) SMe
D2-92a CH (i-Bu) SEt
D2-92a CH (i-Bu) SCF_Three
D2-92a CH (i-Bu) SCH₂CF_Three
D2-92a CH (i-Bu) S (O) Me
D2-92a CH (i-Bu) S (O) Et
D2-92a CH (i-Bu) S (O) CF_Three
D2-92a CH (i-Bu) S (O) CH₂CF_Three
D2-92a CH (i-Bu) S (O)₂Me
D2-92a CH (i-Bu) S (O)₂Et
D2-92a CH (i-Bu) S (O)₂CF_Three
D2-92a CH (i-Bu) S (O)₂CH₂CF_Three
D2-92a CH (s-Bu) SMe
D2-92a CH (s-Bu) SEt
D2-92a CH (s-Bu) SCF_Three
D2-92a CH (s-Bu) SCH₂CF_Three
D2-92a CH (s-Bu) S (O) Me
D2-92a CH (s-Bu) S (O) Et
D2-92a CH (s-Bu) S (O) CF_Three
D2-92a CH (s-Bu) S (O) CH₂CF_Three
D2-92a CH (s-Bu) S (O)₂Me
D2-92a CH (s-Bu) S (O)₂Et
D2-92a CH (s-Bu) S (O)₂CF_Three
D2-92a CH (s-Bu) S (O)₂CH₂CF_Three
D2-92a CH (t-Bu) SMe
D2-92a CH (t-Bu) SEt
D2-92a CH (t-Bu) SCF_Three
D2-92a CH (t-Bu) SCH₂CF_Three
D2-92a CH (t-Bu) S (O) Me
D2-92a CH (t-Bu) S (O) Et
D2-92a CH (t-Bu) S (O) CF_Three
D2-92a CH (t-Bu) S (O) CH₂CF_Three
D2-92a CH (t-Bu) S (O)₂Me
D2-92a CH (t-Bu) S (O)₂Et
D2-92a CH (t-Bu) S (O)₂CF_Three
D2-92a CH (t-Bu) S (O)₂CH₂CF_Three
D2-92a CH (CF_ThreeSMe
D2-92a CH (CF_Three) SEt
D2-92a CH (CF_Three) SCF_Three
D2-92a CH (CF_Three) SCH₂CF_Three
D2-92a CH (CF_Three) S (O) Me
D2-92a CH (CF_Three) S (O) Et
D2-92a CH (CF_Three) S (O) CF_Three
D2-92a CH (CF_Three) S (O) CH₂CF_Three
D2-92a CH (CF_Three) S (O)₂Me
D2-92a CH (CF_Three) S (O)₂Et
D2-92a CH (CF_Three) S (O)₂CF_Three
D2-92a CH (CF_Three) S (O)₂CH₂CF_Three
D2-92a CH₂CH₂SMe
D2-92a CH₂CH₂SEt
D2-92a CH₂CH₂SCF_Three
D2-92a CH₂CH₂SCH₂CF_Three
D2-92a CH₂CH₂S (O) Me
D2-92a CH₂CH₂S (O) Et
D2-92a CH₂CH₂S (O) CF_Three
D2-92a CH₂CH₂S (O) CH₂CF_Three
D2-92a CH₂CH₂S (O)₂Me
D2-92a CH₂CH₂S (O)₂Et
D2-92a CH₂CH₂S (O)₂CF_Three
D2-92a CH₂CH₂S (O)₂CH₂CF_Three
D2-92a CH (Me) CH₂SMe
D2-92a CH (Me) CH₂SEt
D2-92a CH (Me) CH₂SCF_Three
D2-92a CH (Me) CH₂SCH₂CF_Three
D2-92a CH (Me) CH₂S (O) Me
D2-92a CH (Me) CH₂S (O) Et
D2-92a CH (Me) CH₂S (O) CF_Three
D2-92a CH (Me) CH₂S (O) CH₂CF_Three
D2-92a CH (Me) CH₂S (O)₂Me
D2-92a CH (Me) CH₂S (O)₂Et
D2-92a CH (Me) CH₂S (O)₂CF_Three
D2-92a CH (Me) CH₂S (O)₂CH₂CF_Three
D2-92a CH (Et) CH₂SMe
D2-92a CH (Et) CH₂SEt
D2-92a CH (Et) CH₂SCF_Three
D2-92a CH (Et) CH₂SCH₂CF_Three
D2-92a CH (Et) CH₂S (O) Me
D2-92a CH (Et) CH₂S (O) Et
D2-92a CH (Et) CH₂S (O) CF_Three
D2-92a CH (Et) CH₂S (O) CH₂CF_Three
D2-92a CH (Et) CH₂S (O)₂Me
D2-92a CH (Et) CH₂S (O)₂Et
D2-92a CH (Et) CH₂S (O)₂CF_Three
D2-92a CH (Et) CH₂S (O)₂CH₂CF_Three
D2-92a C (Me)₂CH₂SMe
D2-92a C (Me)₂CH₂SEt
D2-92a C (Me)₂CH₂SCF_Three
D2-92a C (Me)₂CH₂SCH₂CF_Three
D2-92a C (Me)₂CH₂S (O) Me
D2-92a C (Me)₂CH₂S (O) Et
D2-92a C (Me)₂CH₂S (O) CF_Three
D2-92a C (Me)₂CH₂S (O) CH₂CF_Three
D2-92a C (Me)₂CH₂S (O)₂Me
D2-92a C (Me)₂CH₂S (O)₂Et
D2-92a C (Me)₂CH₂S (O)₂CF_Three
D2-92a C (Me)₂CH₂S (O)₂CH₂CF_Three
D2-92a CH₂CH (Me) SMe
D2-92a CH₂CH (Me) SEt
D2-92a CH₂CH (Me) SCF_Three
D2-92a CH₂CH (Me) SCH₂CF_Three
D2-92a CH₂CH (Me) S (O) Me
D2-92a CH₂CH (Me) S (O) Et
D2-92a CH₂CH (Me) S (O) CF_Three
D2-92a CH₂CH (Me) S (O) CH₂CF_Three
D2-92a CH₂CH (Me) S (O)₂Me
D2-92a CH₂CH (Me) S (O)₂Et
D2-92a CH₂CH (Me) S (O)₂CF_Three
D2-92a CH₂CH (Me) S (O)₂CH₂CF_Three
D2-92a CH₂CH (Et) SMe
D2-92a CH₂CH (Et) SEt
D2-92a CH₂CH (Et) SCF_Three
D2-92a CH₂CH (Et) SCH₂CF_Three
D2-92a CH₂CH (Et) S (O) Me
D2-92a CH₂CH (Et) S (O) Et
D2-92a CH₂CH (Et) S (O) CF_Three
D2-92a CH₂CH (Et) S (O) CH₂CF_Three
D2-92a CH₂CH (Et) S (O)₂Me
D2-92a CH₂CH (Et) S (O)₂Et
D2-92a CH₂CH (Et) S (O)₂CF_Three
D2-92a CH₂CH (Et) S (O)₂CH₂CF_Three
D2-92a CH (Me) CH (Me) SMe
D2-92a CH (Me) CH (Me) SEt
D2-92a CH (Me) CH (Me) SCF_Three
D2-92a CH (Me) CH (Me) SCH₂CF_Three
D2-92a CH (Me) CH (Me) S (O) Me
D2-92a CH (Me) CH (Me) S (O) Et
D2-92a CH (Me) CH (Me) S (O) CF_Three
D2-92a CH (Me) CH (Me) S (O) CH₂CF_Three
D2-92a CH (Me) CH (Me) S (O)₂Me
D2-92a CH (Me) CH (Me) S (O)₂Et
D2-92a CH (Me) CH (Me) S (O)₂CF_Three
D2-92a CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH (Me) SMe CH₂SMe
CH (Me) SMe CH₂SEt
CH (Me) SMe CH₂SCF_Three
CH (Me) SMe CH₂SCH₂CF_Three
CH (Me) SMe CH₂S (O) Me
CH (Me) SMe CH₂S (O) Et
CH (Me) SMe CH₂S (O) CF_Three
CH (Me) SMe CH₂S (O) CH₂CF_Three
CH (Me) SMe CH₂S (O)₂Me
CH (Me) SMe CH₂S (O)₂Et
CH (Me) SMe CH₂S (O)₂CF_Three
CH (Me) SMe CH₂S (O)₂CH₂CF_Three
CH (Me) SMe CH (Me) SMe
CH (Me) SMe CH (Me) SEt
CH (Me) SMe CH (Me) SCF_Three
CH (Me) SMe CH (Me) SCH₂CF_Three
CH (Me) SMe CH (Me) S (O) Me
CH (Me) SMe CH (Me) S (O) Et
CH (Me) SMe CH (Me) S (O) CF_Three
CH (Me) SMe CH (Me) S (O) CH₂CF_Three
CH (Me) SMe CH (Me) S (O)₂Me
CH (Me) SMe CH (Me) S (O)₂Et
CH (Me) SMe CH (Me) S (O)₂CF_Three
CH (Me) SMe CH (Me) S (O)₂CH₂CF_Three
CH (Me) SMe CH (Et) SMe
CH (Me) SMe CH (Et) SEt
CH (Me) SMe CH (Et) SCF_Three
CH (Me) SMe CH (Et) SCH₂CF_Three
CH (Me) SMe CH (Et) S (O) Me
CH (Me) SMe CH (Et) S (O) Et
CH (Me) SMe CH (Et) S (O) CF_Three
CH (Me) SMe CH (Et) S (O) CH₂CF_Three
CH (Me) SMe CH (Et) S (O)₂Me
CH (Me) SMe CH (Et) S (O)₂Et
CH (Me) SMe CH (Et) S (O)₂CF_Three
CH (Me) SMe CH (Et) S (O)₂CH₂CF_Three
CH (Me) SMe CH (n-Pr) SMe
CH (Me) SMe CH (n-Pr) SEt
CH (Me) SMe CH (n-Pr) SCF_Three
CH (Me) SMe CH (n-Pr) SCH₂CF_Three
CH (Me) SMe CH (n-Pr) S (O) Me
CH (Me) SMe CH (n-Pr) S (O) Et
CH (Me) SMe CH (n-Pr) S (O) CF_Three
CH (Me) SMe CH (n-Pr) S (O) CH₂CF_Three
CH (Me) SMe CH (n-Pr) S (O)₂Me
CH (Me) SMe CH (n-Pr) S (O)₂Et
CH (Me) SMe CH (n-Pr) S (O)₂CF_Three
CH (Me) SMe CH (n-Pr) S (O)₂CH₂CF_Three
CH (Me) SMe CH (i-Pr) SMe
CH (Me) SMe CH (i-Pr) SEt
CH (Me) SMe CH (i-Pr) SCF_Three
CH (Me) SMe CH (i-Pr) SCH₂CF_Three
CH (Me) SMe CH (i-Pr) S (O) Me
CH (Me) SMe CH (i-Pr) S (O) Et
CH (Me) SMe CH (i-Pr) S (O) CF_Three
CH (Me) SMe CH (i-Pr) S (O) CH₂CF_Three
CH (Me) SMe CH (i-Pr) S (O)₂Me
CH (Me) SMe CH (i-Pr) S (O)₂Et
CH (Me) SMe CH (i-Pr) S (O)₂CF_Three
CH (Me) SMe CH (i-Pr) S (O)₂CH₂CF_Three
CH (Me) SMe CH (n-Bu) SMe
CH (Me) SMe CH (n-Bu) SEt
CH (Me) SMe CH (n-Bu) SCF_Three
CH (Me) SMe CH (n-Bu) SCH₂CF_Three
CH (Me) SMe CH (n-Bu) S (O) Me
CH (Me) SMe CH (n-Bu) S (O) Et
CH (Me) SMe CH (n-Bu) S (O) CF_Three
CH (Me) SMe CH (n-Bu) S (O) CH₂CF_Three
CH (Me) SMe CH (n-Bu) S (O)₂Me
CH (Me) SMe CH (n-Bu) S (O)₂Et
CH (Me) SMe CH (n-Bu) S (O)₂CF_Three
CH (Me) SMe CH (n-Bu) S (O)₂CH₂CF_Three
CH (Me) SMe CH (i-Bu) SMe
CH (Me) SMe CH (i-Bu) SEt
CH (Me) SMe CH (i-Bu) SCF_Three
CH (Me) SMe CH (i-Bu) SCH₂CF_Three
CH (Me) SMe CH (i-Bu) S (O) Me
CH (Me) SMe CH (i-Bu) S (O) Et
CH (Me) SMe CH (i-Bu) S (O) CF_Three
CH (Me) SMe CH (i-Bu) S (O) CH₂CF_Three
CH (Me) SMe CH (i-Bu) S (O)₂Me
CH (Me) SMe CH (i-Bu) S (O)₂Et
CH (Me) SMe CH (i-Bu) S (O)₂CF_Three
CH (Me) SMe CH (i-Bu) S (O)₂CH₂CF_Three
CH (Me) SMe CH (s-Bu) SMe
CH (Me) SMe CH (s-Bu) SEt
CH (Me) SMe CH (s-Bu) SCF_Three
CH (Me) SMe CH (s-Bu) SCH₂CF_Three
CH (Me) SMe CH (s-Bu) S (O) Me
CH (Me) SMe CH (s-Bu) S (O) Et
CH (Me) SMe CH (s-Bu) S (O) CF_Three
CH (Me) SMe CH (s-Bu) S (O) CH₂CF_Three
CH (Me) SMe CH (s-Bu) S (O)₂Me
CH (Me) SMe CH (s-Bu) S (O)₂Et
CH (Me) SMe CH (s-Bu) S (O)₂CF_Three
CH (Me) SMe CH (s-Bu) S (O)₂CH₂CF_Three
CH (Me) SMe CH (t-Bu) SMe
CH (Me) SMe CH (t-Bu) SEt
CH (Me) SMe CH (t-Bu) SCF_Three
CH (Me) SMe CH (t-Bu) SCH₂CF_Three
CH (Me) SMe CH (t-Bu) S (O) Me
CH (Me) SMe CH (t-Bu) S (O) Et
CH (Me) SMe CH (t-Bu) S (O) CF_Three
CH (Me) SMe CH (t-Bu) S (O) CH₂CF_Three
CH (Me) SMe CH (t-Bu) S (O)₂Me
CH (Me) SMe CH (t-Bu) S (O)₂Et
CH (Me) SMe CH (t-Bu) S (O)₂CF_Three
CH (Me) SMe CH (t-Bu) S (O)₂CH₂CF_Three
CH (Me) SMe CH (CF_ThreeSMe
CH (Me) SMe CH (CF_Three) SEt
CH (Me) SMe CH (CF_Three) SCF_Three
CH (Me) SMe CH (CF_Three) SCH₂CF_Three
CH (Me) SMe CH (CF_Three) S (O) Me
CH (Me) SMe CH (CF_Three) S (O) Et
CH (Me) SMe CH (CF_Three) S (O) CF_Three
CH (Me) SMe CH (CF_Three) S (O) CH₂CF_Three
CH (Me) SMe CH (CF_Three) S (O)₂Me
CH (Me) SMe CH (CF_Three) S (O)₂Et
CH (Me) SMe CH (CF_Three) S (O)₂CF_Three
CH (Me) SMe CH (CF_Three) S (O)₂CH₂CF_Three
CH (Me) SMe CH₂CH₂SMe
CH (Me) SMe CH₂CH₂SEt
CH (Me) SMe CH₂CH₂SCF_Three
CH (Me) SMe CH₂CH₂SCH₂CF_Three
CH (Me) SMe CH₂CH₂S (O) Me
CH (Me) SMe CH₂CH₂S (O) Et
CH (Me) SMe CH₂CH₂S (O) CF_Three
CH (Me) SMe CH₂CH₂S (O) CH₂CF_Three
CH (Me) SMe CH₂CH₂S (O)₂Me
CH (Me) SMe CH₂CH₂S (O)₂Et
CH (Me) SMe CH₂CH₂S (O)₂CF_Three
CH (Me) SMe CH₂CH₂S (O)₂CH₂CF_Three
CH (Me) SMe CH (Me) CH₂SMe
CH (Me) SMe CH (Me) CH₂SEt
CH (Me) SMe CH (Me) CH₂SCF_Three
CH (Me) SMe CH (Me) CH₂SCH₂CF_Three
CH (Me) SMe CH (Me) CH₂S (O) Me
CH (Me) SMe CH (Me) CH₂S (O) Et
CH (Me) SMe CH (Me) CH₂S (O) CF_Three
CH (Me) SMe CH (Me) CH₂S (O) CH₂CF_Three
CH (Me) SMe CH (Me) CH₂S (O)₂Me
CH (Me) SMe CH (Me) CH₂S (O)₂Et
CH (Me) SMe CH (Me) CH₂S (O)₂CF_Three
CH (Me) SMe CH (Me) CH₂S (O)₂CH₂CF_Three
CH (Me) SMe CH (Et) CH₂SMe
CH (Me) SMe CH (Et) CH₂SEt
CH (Me) SMe CH (Et) CH₂SCF_Three
CH (Me) SMe CH (Et) CH₂SCH₂CF_Three
CH (Me) SMe CH (Et) CH₂S (O) Me
CH (Me) SMe CH (Et) CH₂S (O) Et
CH (Me) SMe CH (Et) CH₂S (O) CF_Three
CH (Me) SMe CH (Et) CH₂S (O) CH₂CF_Three
CH (Me) SMe CH (Et) CH₂S (O)₂Me
CH (Me) SMe CH (Et) CH₂S (O)₂Et
CH (Me) SMe CH (Et) CH₂S (O)₂CF_Three
CH (Me) SMe CH (Et) CH₂S (O)₂CH₂CF_Three
CH (Me) SMe C (Me)₂CH₂SMe
CH (Me) SMe C (Me)₂CH₂SEt
CH (Me) SMe C (Me)₂CH₂SCF_Three
CH (Me) SMe C (Me)₂CH₂SCH₂CF_Three
CH (Me) SMe C (Me)₂CH₂S (O) Me
CH (Me) SMe C (Me)₂CH₂S (O) Et
CH (Me) SMe C (Me)₂CH₂S (O) CF_Three
CH (Me) SMe C (Me)₂CH₂S (O) CH₂CF_Three
CH (Me) SMe C (Me)₂CH₂S (O)₂Me
CH (Me) SMe C (Me)₂CH₂S (O)₂Et
CH (Me) SMe C (Me)₂CH₂S (O)₂CF_Three
CH (Me) SMe C (Me)₂CH₂S (O)₂CH₂CF_Three
CH (Me) SMe CH₂CH (Me) SMe
CH (Me) SMe CH₂CH (Me) SEt
CH (Me) SMe CH₂CH (Me) SCF_Three
CH (Me) SMe CH₂CH (Me) SCH₂CF_Three
CH (Me) SMe CH₂CH (Me) S (O) Me
CH (Me) SMe CH₂CH (Me) S (O) Et
CH (Me) SMe CH₂CH (Me) S (O) CF_Three
CH (Me) SMe CH₂CH (Me) S (O) CH₂CF_Three
CH (Me) SMe CH₂CH (Me) S (O)₂Me
CH (Me) SMe CH₂CH (Me) S (O)₂Et
CH (Me) SMe CH₂CH (Me) S (O)₂CF_Three
CH (Me) SMe CH₂CH (Me) S (O)₂CH₂CF_Three
CH (Me) SMe CH₂CH (Et) SMe
CH (Me) SMe CH₂CH (Et) SEt
CH (Me) SMe CH₂CH (Et) SCF_Three
CH (Me) SMe CH₂CH (Et) SCH₂CF_Three
CH (Me) SMe CH₂CH (Et) S (O) Me
CH (Me) SMe CH₂CH (Et) S (O) Et
CH (Me) SMe CH₂CH (Et) S (O) CF_Three
CH (Me) SMe CH₂CH (Et) S (O) CH₂CF_Three
CH (Me) SMe CH₂CH (Et) S (O)₂Me
CH (Me) SMe CH₂CH (Et) S (O)₂Et
CH (Me) SMe CH₂CH (Et) S (O)₂CF_Three
CH (Me) SMe CH₂CH (Et) S (O)₂CH₂CF_Three
CH (Me) SMe CH (Me) CH (Me) SMe
CH (Me) SMe CH (Me) CH (Me) SEt
CH (Me) SMe CH (Me) CH (Me) SCF_Three
CH (Me) SMe CH (Me) CH (Me) SCH₂CF_Three
CH (Me) SMe CH (Me) CH (Me) S (O) Me
CH (Me) SMe CH (Me) CH (Me) S (O) Et
CH (Me) SMe CH (Me) CH (Me) S (O) CF_Three
CH (Me) SMe CH (Me) CH (Me) S (O) CH₂CF_Three
CH (Me) SMe CH (Me) CH (Me) S (O)₂Me
CH (Me) SMe CH (Me) CH (Me) S (O)₂Et
CH (Me) SMe CH (Me) CH (Me) S (O)₂CF_Three
CH (Me) SMe CH (Me) CH (Me) S (O)₂CH₂CF_Three
C (O) Me CH₂SMe
C (O) Me CH₂SEt
C (O) Me CH₂SCF_Three
C (O) Me CH₂SCH₂CF_Three
C (O) Me CH₂S (O) Me
C (O) Me CH₂S (O) Et
C (O) Me CH₂S (O) CF_Three
C (O) Me CH₂S (O) CH₂CF_Three
C (O) Me CH₂S (O)₂Me
C (O) Me CH₂S (O)₂Et
C (O) Me CH₂S (O)₂CF_Three
C (O) Me CH₂S (O)₂CH₂CF_Three
C (O) Me CH (Me) SMe
C (O) Me CH (Me) SEt
C (O) Me CH (Me) SCF_Three
C (O) Me CH (Me) SCH₂CF_Three
C (O) Me CH (Me) S (O) Me
C (O) Me CH (Me) S (O) Et
C (O) Me CH (Me) S (O) CF_Three
C (O) Me CH (Me) S (O) CH₂CF_Three
C (O) Me CH (Me) S (O)₂Me
C (O) Me CH (Me) S (O)₂Et
C (O) Me CH (Me) S (O)₂CF_Three
C (O) Me CH (Me) S (O)₂CH₂CF_Three
C (O) Me CH (Et) SMe
C (O) Me CH (Et) SEt
C (O) Me CH (Et) SCF_Three
C (O) Me CH (Et) SCH₂CF_Three
C (O) Me CH (Et) S (O) Me
C (O) Me CH (Et) S (O) Et
C (O) Me CH (Et) S (O) CF_Three
C (O) Me CH (Et) S (O) CH₂CF_Three
C (O) Me CH (Et) S (O)₂Me
C (O) Me CH (Et) S (O)₂Et
C (O) Me CH (Et) S (O)₂CF_Three
C (O) Me CH (Et) S (O)₂CH₂CF_Three
C (O) Me CH (n-Pr) SMe
C (O) Me CH (n-Pr) SEt
C (O) Me CH (n-Pr) SCF_Three
C (O) Me CH (n-Pr) SCH₂CF_Three
C (O) Me CH (n-Pr) S (O) Me
C (O) Me CH (n-Pr) S (O) Et
C (O) Me CH (n-Pr) S (O) CF_Three
C (O) Me CH (n-Pr) S (O) CH₂CF_Three
C (O) Me CH (n-Pr) S (O)₂Me
C (O) Me CH (n-Pr) S (O)₂Et
C (O) Me CH (n-Pr) S (O)₂CF_Three
C (O) Me CH (n-Pr) S (O)₂CH₂CF_Three
C (O) Me CH (i-Pr) SMe
C (O) Me CH (i-Pr) SEt
C (O) Me CH (i-Pr) SCF_Three
C (O) Me CH (i-Pr) SCH₂CF_Three
C (O) Me CH (i-Pr) S (O) Me
C (O) Me CH (i-Pr) S (O) Et
C (O) Me CH (i-Pr) S (O) CF_Three
C (O) Me CH (i-Pr) S (O) CH₂CF_Three
C (O) Me CH (i-Pr) S (O)₂Me
C (O) Me CH (i-Pr) S (O)₂Et
C (O) Me CH (i-Pr) S (O)₂CF_Three
C (O) Me CH (i-Pr) S (O)₂CH₂CF_Three
C (O) Me CH (n-Bu) SMe
C (O) Me CH (n-Bu) SEt
C (O) Me CH (n-Bu) SCF_Three
C (O) Me CH (n-Bu) SCH₂CF_Three
C (O) Me CH (n-Bu) S (O) Me
C (O) Me CH (n-Bu) S (O) Et
C (O) Me CH (n-Bu) S (O) CF_Three
C (O) Me CH (n-Bu) S (O) CH₂CF_Three
C (O) Me CH (n-Bu) S (O)₂Me
C (O) Me CH (n-Bu) S (O)₂Et
C (O) Me CH (n-Bu) S (O)₂CF_Three
C (O) Me CH (n-Bu) S (O)₂CH₂CF_Three
C (O) Me CH (i-Bu) SMe
C (O) Me CH (i-Bu) SEt
C (O) Me CH (i-Bu) SCF_Three
C (O) Me CH (i-Bu) SCH₂CF_Three
C (O) Me CH (i-Bu) S (O) Me
C (O) Me CH (i-Bu) S (O) Et
C (O) Me CH (i-Bu) S (O) CF_Three
C (O) Me CH (i-Bu) S (O) CH₂CF_Three
C (O) Me CH (i-Bu) S (O)₂Me
C (O) Me CH (i-Bu) S (O)₂Et
C (O) Me CH (i-Bu) S (O)₂CF_Three
C (O) Me CH (i-Bu) S (O)₂CH₂CF_Three
C (O) Me CH (s-Bu) SMe
C (O) Me CH (s-Bu) SEt
C (O) Me CH (s-Bu) SCF_Three
C (O) Me CH (s-Bu) SCH₂CF_Three
C (O) Me CH (s-Bu) S (O) Me
C (O) Me CH (s-Bu) S (O) Et
C (O) Me CH (s-Bu) S (O) CF_Three
C (O) Me CH (s-Bu) S (O) CH₂CF_Three
C (O) Me CH (s-Bu) S (O)₂Me
C (O) Me CH (s-Bu) S (O)₂Et
C (O) Me CH (s-Bu) S (O)₂CF_Three
C (O) Me CH (s-Bu) S (O)₂CH₂CF_Three
C (O) Me CH (t-Bu) SMe
C (O) Me CH (t-Bu) SEt
C (O) Me CH (t-Bu) SCF_Three
C (O) Me CH (t-Bu) SCH₂CF_Three
C (O) Me CH (t-Bu) S (O) Me
C (O) Me CH (t-Bu) S (O) Et
C (O) Me CH (t-Bu) S (O) CF_Three
C (O) Me CH (t-Bu) S (O) CH₂CF_Three
C (O) Me CH (t-Bu) S (O)₂Me
C (O) Me CH (t-Bu) S (O)₂Et
C (O) Me CH (t-Bu) S (O)₂CF_Three
C (O) Me CH (t-Bu) S (O)₂CH₂CF_Three
C (O) Me CH (CF_ThreeSMe
C (O) Me CH (CF_Three) SEt
C (O) Me CH (CF_Three) SCF_Three
C (O) Me CH (CF_Three) SCH₂CF_Three
C (O) Me CH (CF_Three) S (O) Me
C (O) Me CH (CF_Three) S (O) Et
C (O) Me CH (CF_Three) S (O) CF_Three
C (O) Me CH (CF_Three) S (O) CH₂CF_Three
C (O) Me CH (CF_Three) S (O)₂Me
C (O) Me CH (CF_Three) S (O)₂Et
C (O) Me CH (CF_Three) S (O)₂CF_Three
C (O) Me CH (CF_Three) S (O)₂CH₂CF_Three
C (O) Me CH₂CH₂SMe
C (O) Me CH₂CH₂SEt
C (O) Me CH₂CH₂SCF_Three
C (O) Me CH₂CH₂SCH₂CF_Three
C (O) Me CH₂CH₂S (O) Me
C (O) Me CH₂CH₂S (O) Et
C (O) Me CH₂CH₂S (O) CF_Three
C (O) Me CH₂CH₂S (O) CH₂CF_Three
C (O) Me CH₂CH₂S (O)₂Me
C (O) Me CH₂CH₂S (O)₂Et
C (O) Me CH₂CH₂S (O)₂CF_Three
C (O) Me CH₂CH₂S (O)₂CH₂CF_Three
C (O) Me CH (Me) CH₂SMe
C (O) Me CH (Me) CH₂SEt
C (O) Me CH (Me) CH₂SCF_Three
C (O) Me CH (Me) CH₂SCH₂CF_Three
C (O) Me CH (Me) CH₂S (O) Me
C (O) Me CH (Me) CH₂S (O) Et
C (O) Me CH (Me) CH₂S (O) CF_Three
C (O) Me CH (Me) CH₂S (O) CH₂CF_Three
C (O) Me CH (Me) CH₂S (O)₂Me
C (O) Me CH (Me) CH₂S (O)₂Et
C (O) Me CH (Me) CH₂S (O)₂CF_Three
C (O) Me CH (Me) CH₂S (O)₂CH₂CF_Three
C (O) Me CH (Et) CH₂SMe
C (O) Me CH (Et) CH₂SEt
C (O) Me CH (Et) CH₂SCF_Three
C (O) Me CH (Et) CH₂SCH₂CF_Three
C (O) Me CH (Et) CH₂S (O) Me
C (O) Me CH (Et) CH₂S (O) Et
C (O) Me CH (Et) CH₂S (O) CF_Three
C (O) Me CH (Et) CH₂S (O) CH₂CF_Three
C (O) Me CH (Et) CH₂S (O)₂Me
C (O) Me CH (Et) CH₂S (O)₂Et
C (O) Me CH (Et) CH₂S (O)₂CF_Three
C (O) Me CH (Et) CH₂S (O)₂CH₂CF_Three
C (O) Me C (Me)₂CH₂SMe
C (O) Me C (Me)₂CH₂SEt
C (O) Me C (Me)₂CH₂SCF_Three
C (O) Me C (Me)₂CH₂SCH₂CF_Three
C (O) Me C (Me)₂CH₂S (O) Me
C (O) Me C (Me)₂CH₂S (O) Et
C (O) Me C (Me)₂CH₂S (O) CF_Three
C (O) Me C (Me)₂CH₂S (O) CH₂CF_Three
C (O) Me C (Me)₂CH₂S (O)₂Me
C (O) Me C (Me)₂CH₂S (O)₂Et
C (O) Me C (Me)₂CH₂S (O)₂CF_Three
C (O) Me C (Me)₂CH₂S (O)₂CH₂CF_Three
C (O) Me CH₂CH (Me) SMe
C (O) Me CH₂CH (Me) SEt
C (O) Me CH₂CH (Me) SCF_Three
C (O) Me CH₂CH (Me) SCH₂CF_Three
C (O) Me CH₂CH (Me) S (O) Me
C (O) Me CH₂CH (Me) S (O) Et
C (O) Me CH₂CH (Me) S (O) CF_Three
C (O) Me CH₂CH (Me) S (O) CH₂CF_Three
C (O) Me CH₂CH (Me) S (O)₂Me
C (O) Me CH₂CH (Me) S (O)₂Et
C (O) Me CH₂CH (Me) S (O)₂CF_Three
C (O) Me CH₂CH (Me) S (O)₂CH₂CF_Three
C (O) Me CH₂CH (Et) SMe
C (O) Me CH₂CH (Et) SEt
C (O) Me CH₂CH (Et) SCF_Three
C (O) Me CH₂CH (Et) SCH₂CF_Three
C (O) Me CH₂CH (Et) S (O) Me
C (O) Me CH₂CH (Et) S (O) Et
C (O) Me CH₂CH (Et) S (O) CF_Three
C (O) Me CH₂CH (Et) S (O) CH₂CF_Three
C (O) Me CH₂CH (Et) S (O)₂Me
C (O) Me CH₂CH (Et) S (O)₂Et
C (O) Me CH₂CH (Et) S (O)₂CF_Three
C (O) Me CH₂CH (Et) S (O)₂CH₂CF_Three
C (O) Me CH (Me) CH (Me) SMe
C (O) Me CH (Me) CH (Me) SEt
C (O) Me CH (Me) CH (Me) SCF_Three
C (O) Me CH (Me) CH (Me) SCH₂CF_Three
C (O) Me CH (Me) CH (Me) S (O) Me
C (O) Me CH (Me) CH (Me) S (O) Et
C (O) Me CH (Me) CH (Me) S (O) CF_Three
C (O) Me CH (Me) CH (Me) S (O) CH₂CF_Three
C (O) Me CH (Me) CH (Me) S (O)₂Me
C (O) Me CH (Me) CH (Me) S (O)₂Et
C (O) Me CH (Me) CH (Me) S (O)₂CF_Three
C (O) Me CH (Me) CH (Me) S (O)₂CH₂CF_Three
C (O) OMe CH₂SMe
C (O) OMe CH₂SEt
C (O) OMe CH₂SCF_Three
C (O) OMe CH₂SCH₂CF_Three
C (O) OMe CH₂S (O) Me
C (O) OMe CH₂S (O) Et
C (O) OMe CH₂S (O) CF_Three
C (O) OMe CH₂S (O) CH₂CF_Three
C (O) OMe CH₂S (O)₂Me
C (O) OMe CH₂S (O)₂Et
C (O) OMe CH₂S (O)₂CF_Three
C (O) OMe CH₂S (O)₂CH₂CF_Three
C (O) OMe CH (Me) SMe
C (O) OMe CH (Me) SEt
C (O) OMe CH (Me) SCF_Three
C (O) OMe CH (Me) SCH₂CF_Three
C (O) OMe CH (Me) S (O) Me
C (O) OMe CH (Me) S (O) Et
C (O) OMe CH (Me) S (O) CF_Three
C (O) OMe CH (Me) S (O) CH₂CF_Three
C (O) OMe CH (Me) S (O)₂Me
C (O) OMe CH (Me) S (O)₂Et
C (O) OMe CH (Me) S (O)₂CF_Three
C (O) OMe CH (Me) S (O)₂CH₂CF_Three
C (O) OMe CH (Et) SMe
C (O) OMe CH (Et) SEt
C (O) OMe CH (Et) SCF_Three
C (O) OMe CH (Et) SCH₂CF_Three
C (O) OMe CH (Et) S (O) Me
C (O) OMe CH (Et) S (O) Et
C (O) OMe CH (Et) S (O) CF_Three
C (O) OMe CH (Et) S (O) CH₂CF_Three
C (O) OMe CH (Et) S (O)₂Me
C (O) OMe CH (Et) S (O)₂Et
C (O) OMe CH (Et) S (O)₂CF_Three
C (O) OMe CH (Et) S (O)₂CH₂CF_Three
C (O) OMe CH (n-Pr) SMe
C (O) OMe CH (n-Pr) SEt
C (O) OMe CH (n-Pr) SCF_Three
C (O) OMe CH (n-Pr) SCH₂CF_Three
C (O) OMe CH (n-Pr) S (O) Me
C (O) OMe CH (n-Pr) S (O) Et
C (O) OMe CH (n-Pr) S (O) CF_Three
C (O) OMe CH (n-Pr) S (O) CH₂CF_Three
C (O) OMe CH (n-Pr) S (O)₂Me
C (O) OMe CH (n-Pr) S (O)₂Et
C (O) OMe CH (n-Pr) S (O)₂CF_Three
C (O) OMe CH (n-Pr) S (O)₂CH₂CF_Three
C (O) OMe CH (i-Pr) SMe
C (O) OMe CH (i-Pr) SEt
C (O) OMe CH (i-Pr) SCF_Three
C (O) OMe CH (i-Pr) SCH₂CF_Three
C (O) OMe CH (i-Pr) S (O) Me
C (O) OMe CH (i-Pr) S (O) Et
C (O) OMe CH (i-Pr) S (O) CF_Three
C (O) OMe CH (i-Pr) S (O) CH₂CF_Three
C (O) OMe CH (i-Pr) S (O)₂Me
C (O) OMe CH (i-Pr) S (O)₂Et
C (O) OMe CH (i-Pr) S (O)₂CF_Three
C (O) OMe CH (i-Pr) S (O)₂CH₂CF_Three
C (O) OMe CH (n-Bu) SMe
C (O) OMe CH (n-Bu) SEt
C (O) OMe CH (n-Bu) SCF_Three
C (O) OMe CH (n-Bu) SCH₂CF_Three
C (O) OMe CH (n-Bu) S (O) Me
C (O) OMe CH (n-Bu) S (O) Et
C (O) OMe CH (n-Bu) S (O) CF_Three
C (O) OMe CH (n-Bu) S (O) CH₂CF_Three
C (O) OMe CH (n-Bu) S (O)₂Me
C (O) OMe CH (n-Bu) S (O)₂Et
C (O) OMe CH (n-Bu) S (O)₂CF_Three
C (O) OMe CH (n-Bu) S (O)₂CH₂CF_Three
C (O) OMe CH (i-Bu) SMe
C (O) OMe CH (i-Bu) SEt
C (O) OMe CH (i-Bu) SCF_Three
C (O) OMe CH (i-Bu) SCH₂CF_Three
C (O) OMe CH (i-Bu) S (O) Me
C (O) OMe CH (i-Bu) S (O) Et
C (O) OMe CH (i-Bu) S (O) CF_Three
C (O) OMe CH (i-Bu) S (O) CH₂CF_Three
C (O) OMe CH (i-Bu) S (O)₂Me
C (O) OMe CH (i-Bu) S (O)₂Et
C (O) OMe CH (i-Bu) S (O)₂CF_Three
C (O) OMe CH (i-Bu) S (O)₂CH₂CF_Three
C (O) OMe CH (s-Bu) SMe
C (O) OMe CH (s-Bu) SEt
C (O) OMe CH (s-Bu) SCF_Three
C (O) OMe CH (s-Bu) SCH₂CF_Three
C (O) OMe CH (s-Bu) S (O) Me
C (O) OMe CH (s-Bu) S (O) Et
C (O) OMe CH (s-Bu) S (O) CF_Three
C (O) OMe CH (s-Bu) S (O) CH₂CF_Three
C (O) OMe CH (s-Bu) S (O)₂Me
C (O) OMe CH (s-Bu) S (O)₂Et
C (O) OMe CH (s-Bu) S (O)₂CF_Three
C (O) OMe CH (s-Bu) S (O)₂CH₂CF_Three
C (O) OMe CH (t-Bu) SMe
C (O) OMe CH (t-Bu) SEt
C (O) OMe CH (t-Bu) SCF_Three
C (O) OMe CH (t-Bu) SCH₂CF_Three
C (O) OMe CH (t-Bu) S (O) Me
C (O) OMe CH (t-Bu) S (O) Et
C (O) OMe CH (t-Bu) S (O) CF_Three
C (O) OMe CH (t-Bu) S (O) CH₂CF_Three
C (O) OMe CH (t-Bu) S (O)₂Me
C (O) OMe CH (t-Bu) S (O)₂Et
C (O) OMe CH (t-Bu) S (O)₂CF_Three
C (O) OMe CH (t-Bu) S (O)₂CH₂CF_Three
C (O) OMe CH (CF_ThreeSMe
C (O) OMe CH (CF_Three) SEt
C (O) OMe CH (CF_Three) SCF_Three
C (O) OMe CH (CF_Three) SCH₂CF_Three
C (O) OMe CH (CF_Three) S (O) Me
C (O) OMe CH (CF_Three) S (O) Et
C (O) OMe CH (CF_Three) S (O) CF_Three
C (O) OMe CH (CF_Three) S (O) CH₂CF_Three
C (O) OMe CH (CF_Three) S (O)₂Me
C (O) OMe CH (CF_Three) S (O)₂Et
C (O) OMe CH (CF_Three) S (O)₂CF_Three
C (O) OMe CH (CF_Three) S (O)₂CH₂CF_Three
C (O) OMe CH₂CH₂SMe
C (O) OMe CH₂CH₂SEt
C (O) OMe CH₂CH₂SCF_Three
C (O) OMe CH₂CH₂SCH₂CF_Three
C (O) OMe CH₂CH₂S (O) Me
C (O) OMe CH₂CH₂S (O) Et
C (O) OMe CH₂CH₂S (O) CF_Three
C (O) OMe CH₂CH₂S (O) CH₂CF_Three
C (O) OMe CH₂CH₂S (O)₂Me
C (O) OMe CH₂CH₂S (O)₂Et
C (O) OMe CH₂CH₂S (O)₂CF_Three
C (O) OMe CH₂CH₂S (O)₂CH₂CF_Three
C (O) OMe CH (Me) CH₂SMe
C (O) OMe CH (Me) CH₂SEt
C (O) OMe CH (Me) CH₂SCF_Three
C (O) OMe CH (Me) CH₂SCH₂CF_Three
C (O) OMe CH (Me) CH₂S (O) Me
C (O) OMe CH (Me) CH₂S (O) Et
C (O) OMe CH (Me) CH₂S (O) CF_Three
C (O) OMe CH (Me) CH₂S (O) CH₂CF_Three
C (O) OMe CH (Me) CH₂S (O)₂Me
C (O) OMe CH (Me) CH₂S (O)₂Et
C (O) OMe CH (Me) CH₂S (O)₂CF_Three
C (O) OMe CH (Me) CH₂S (O)₂CH₂CF_Three
C (O) OMe CH (Et) CH₂SMe
C (O) OMe CH (Et) CH₂SEt
C (O) OMe CH (Et) CH₂SCF_Three
C (O) OMe CH (Et) CH₂SCH₂CF_Three
C (O) OMe CH (Et) CH₂S (O) Me
C (O) OMe CH (Et) CH₂S (O) Et
C (O) OMe CH (Et) CH₂S (O) CF_Three
C (O) OMe CH (Et) CH₂S (O) CH₂CF_Three
C (O) OMe CH (Et) CH₂S (O)₂Me
C (O) OMe CH (Et) CH₂S (O)₂Et
C (O) OMe CH (Et) CH₂S (O)₂CF_Three
C (O) OMe CH (Et) CH₂S (O)₂CH₂CF_Three
C (O) OMe C (Me)₂CH₂SMe
C (O) OMe C (Me)₂CH₂SEt
C (O) OMe C (Me)₂CH₂SCF_Three
C (O) OMe C (Me)₂CH₂SCH₂CF_Three
C (O) OMe C (Me)₂CH₂S (O) Me
C (O) OMe C (Me)₂CH₂S (O) Et
C (O) OMe C (Me)₂CH₂S (O) CF_Three
C (O) OMe C (Me)₂CH₂S (O) CH₂CF_Three
C (O) OMe C (Me)₂CH₂S (O)₂Me
C (O) OMe C (Me)₂CH₂S (O)₂Et
C (O) OMe C (Me)₂CH₂S (O)₂CF_Three
C (O) OMe C (Me)₂CH₂S (O)₂CH₂CF_Three
C (O) OMe CH₂CH (Me) SMe
C (O) OMe CH₂CH (Me) SEt
C (O) OMe CH₂CH (Me) SCF_Three
C (O) OMe CH₂CH (Me) SCH₂CF_Three
C (O) OMe CH₂CH (Me) S (O) Me
C (O) OMe CH₂CH (Me) S (O) Et
C (O) OMe CH₂CH (Me) S (O) CF_Three
C (O) OMe CH₂CH (Me) S (O) CH₂CF_Three
C (O) OMe CH₂CH (Me) S (O)₂Me
C (O) OMe CH₂CH (Me) S (O)₂Et
C (O) OMe CH₂CH (Me) S (O)₂CF_Three
C (O) OMe CH₂CH (Me) S (O)₂CH₂CF_Three
C (O) OMe CH₂CH (Et) SMe
C (O) OMe CH₂CH (Et) SEt
C (O) OMe CH₂CH (Et) SCF_Three
C (O) OMe CH₂CH (Et) SCH₂CF_Three
C (O) OMe CH₂CH (Et) S (O) Me
C (O) OMe CH₂CH (Et) S (O) Et
C (O) OMe CH₂CH (Et) S (O) CF_Three
C (O) OMe CH₂CH (Et) S (O) CH₂CF_Three
C (O) OMe CH₂CH (Et) S (O)₂Me
C (O) OMe CH₂CH (Et) S (O)₂Et
C (O) OMe CH₂CH (Et) S (O)₂CF_Three
C (O) OMe CH₂CH (Et) S (O)₂CH₂CF_Three
C (O) OMe CH (Me) CH (Me) SMe
C (O) OMe CH (Me) CH (Me) SEt
C (O) OMe CH (Me) CH (Me) SCF_Three
C (O) OMe CH (Me) CH (Me) SCH₂CF_Three
C (O) OMe CH (Me) CH (Me) S (O) Me
C (O) OMe CH (Me) CH (Me) S (O) Et
C (O) OMe CH (Me) CH (Me) S (O) CF_Three
C (O) OMe CH (Me) CH (Me) S (O) CH₂CF_Three
C (O) OMe CH (Me) CH (Me) S (O)₂Me
C (O) OMe CH (Me) CH (Me) S (O)₂Et
C (O) OMe CH (Me) CH (Me) S (O)₂CF_Three
C (O) OMe CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂OMe CH₂SMe
CH₂OMe CH₂SEt
CH₂OMe CH₂SCF_Three
CH₂OMe CH₂SCH₂CF_Three
CH₂OMe CH₂S (O) Me
CH₂OMe CH₂S (O) Et
CH₂OMe CH₂S (O) CF_Three
CH₂OMe CH₂S (O) CH₂CF_Three
CH₂OMe CH₂S (O)₂Me
CH₂OMe CH₂S (O)₂Et
CH₂OMe CH₂S (O)₂CF_Three
CH₂OMe CH₂S (O)₂CH₂CF_Three
CH₂OMe CH (Me) SMe
CH₂OMe CH (Me) SEt
CH₂OMe CH (Me) SCF_Three
CH₂OMe CH (Me) SCH₂CF_Three
CH₂OMe CH (Me) S (O) Me
CH₂OMe CH (Me) S (O) Et
CH₂OMe CH (Me) S (O) CF_Three
CH₂OMe CH (Me) S (O) CH₂CF_Three
CH₂OMe CH (Me) S (O)₂Me
CH₂OMe CH (Me) S (O)₂Et
CH₂OMe CH (Me) S (O)₂CF_Three
CH₂OMe CH (Me) S (O)₂CH₂CF_Three
CH₂OMe CH (Et) SMe
CH₂OMe CH (Et) SEt
CH₂OMe CH (Et) SCF_Three
CH₂OMe CH (Et) SCH₂CF_Three
CH₂OMe CH (Et) S (O) Me
CH₂OMe CH (Et) S (O) Et
CH₂OMe CH (Et) S (O) CF_Three
CH₂OMe CH (Et) S (O) CH₂CF_Three
CH₂OMe CH (Et) S (O)₂Me
CH₂OMe CH (Et) S (O)₂Et
CH₂OMe CH (Et) S (O)₂CF_Three
CH₂OMe CH (Et) S (O)₂CH₂CF_Three
CH₂OMe CH (n-Pr) SMe
CH₂OMe CH (n-Pr) SEt
CH₂OMe CH (n-Pr) SCF_Three
CH₂OMe CH (n-Pr) SCH₂CF_Three
CH₂OMe CH (n-Pr) S (O) Me
CH₂OMe CH (n-Pr) S (O) Et
CH₂OMe CH (n-Pr) S (O) CF_Three
CH₂OMe CH (n-Pr) S (O) CH₂CF_Three
CH₂OMe CH (n-Pr) S (O)₂Me
CH₂OMe CH (n-Pr) S (O)₂Et
CH₂OMe CH (n-Pr) S (O)₂CF_Three
CH₂OMe CH (n-Pr) S (O)₂CH₂CF_Three
CH₂OMe CH (i-Pr) SMe
CH₂OMe CH (i-Pr) SEt
CH₂OMe CH (i-Pr) SCF_Three
CH₂OMe CH (i-Pr) SCH₂CF_Three
CH₂OMe CH (i-Pr) S (O) Me
CH₂OMe CH (i-Pr) S (O) Et
CH₂OMe CH (i-Pr) S (O) CF_Three
CH₂OMe CH (i-Pr) S (O) CH₂CF_Three
CH₂OMe CH (i-Pr) S (O)₂Me
CH₂OMe CH (i-Pr) S (O)₂Et
CH₂OMe CH (i-Pr) S (O)₂CF_Three
CH₂OMe CH (i-Pr) S (O)₂CH₂CF_Three
CH₂OMe CH (n-Bu) SMe
CH₂OMe CH (n-Bu) SEt
CH₂OMe CH (n-Bu) SCF_Three
CH₂OMe CH (n-Bu) SCH₂CF_Three
CH₂OMe CH (n-Bu) S (O) Me
CH₂OMe CH (n-Bu) S (O) Et
CH₂OMe CH (n-Bu) S (O) CF_Three
CH₂OMe CH (n-Bu) S (O) CH₂CF_Three
CH₂OMe CH (n-Bu) S (O)₂Me
CH₂OMe CH (n-Bu) S (O)₂Et
CH₂OMe CH (n-Bu) S (O)₂CF_Three
CH₂OMe CH (n-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (i-Bu) SMe
CH₂OMe CH (i-Bu) SEt
CH₂OMe CH (i-Bu) SCF_Three
CH₂OMe CH (i-Bu) SCH₂CF_Three
CH₂OMe CH (i-Bu) S (O) Me
CH₂OMe CH (i-Bu) S (O) Et
CH₂OMe CH (i-Bu) S (O) CF_Three
CH₂OMe CH (i-Bu) S (O) CH₂CF_Three
CH₂OMe CH (i-Bu) S (O)₂Me
CH₂OMe CH (i-Bu) S (O)₂Et
CH₂OMe CH (i-Bu) S (O)₂CF_Three
CH₂OMe CH (i-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (s-Bu) SMe
CH₂OMe CH (s-Bu) SEt
CH₂OMe CH (s-Bu) SCF_Three
CH₂OMe CH (s-Bu) SCH₂CF_Three
CH₂OMe CH (s-Bu) S (O) Me
CH₂OMe CH (s-Bu) S (O) Et
CH₂OMe CH (s-Bu) S (O) CF_Three
CH₂OMe CH (s-Bu) S (O) CH₂CF_Three
CH₂OMe CH (s-Bu) S (O)₂Me
CH₂OMe CH (s-Bu) S (O)₂Et
CH₂OMe CH (s-Bu) S (O)₂CF_Three
CH₂OMe CH (s-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (t-Bu) SMe
CH₂OMe CH (t-Bu) SEt
CH₂OMe CH (t-Bu) SCF_Three
CH₂OMe CH (t-Bu) SCH₂CF_Three
CH₂OMe CH (t-Bu) S (O) Me
CH₂OMe CH (t-Bu) S (O) Et
CH₂OMe CH (t-Bu) S (O) CF_Three
CH₂OMe CH (t-Bu) S (O) CH₂CF_Three
CH₂OMe CH (t-Bu) S (O)₂Me
CH₂OMe CH (t-Bu) S (O)₂Et
CH₂OMe CH (t-Bu) S (O)₂CF_Three
CH₂OMe CH (t-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (CF_ThreeSMe
CH₂OMe CH (CF_Three) SEt
CH₂OMe CH (CF_Three) SCF_Three
CH₂OMe CH (CF_Three) SCH₂CF_Three
CH₂OMe CH (CF_Three) S (O) Me
CH₂OMe CH (CF_Three) S (O) Et
CH₂OMe CH (CF_Three) S (O) CF_Three
CH₂OMe CH (CF_Three) S (O) CH₂CF_Three
CH₂OMe CH (CF_Three) S (O)₂Me
CH₂OMe CH (CF_Three) S (O)₂Et
CH₂OMe CH (CF_Three) S (O)₂CF_Three
CH₂OMe CH (CF_Three) S (O)₂CH₂CF_Three
CH₂OMe CH₂CH₂SMe
CH₂OMe CH₂CH₂SEt
CH₂OMe CH₂CH₂SCF_Three
CH₂OMe CH₂CH₂SCH₂CF_Three
CH₂OMe CH₂CH₂S (O) Me
CH₂OMe CH₂CH₂S (O) Et
CH₂OMe CH₂CH₂S (O) CF_Three
CH₂OMe CH₂CH₂S (O) CH₂CF_Three
CH₂OMe CH₂CH₂S (O)₂Me
CH₂OMe CH₂CH₂S (O)₂Et
CH₂OMe CH₂CH₂S (O)₂CF_Three
CH₂OMe CH₂CH₂S (O)₂CH₂CF_Three
CH₂OMe CH (Me) CH₂SMe
CH₂OMe CH (Me) CH₂SEt
CH₂OMe CH (Me) CH₂SCF_Three
CH₂OMe CH (Me) CH₂SCH₂CF_Three
CH₂OMe CH (Me) CH₂S (O) Me
CH₂OMe CH (Me) CH₂S (O) Et
CH₂OMe CH (Me) CH₂S (O) CF_Three
CH₂OMe CH (Me) CH₂S (O) CH₂CF_Three
CH₂OMe CH (Me) CH₂S (O)₂Me
CH₂OMe CH (Me) CH₂S (O)₂Et
CH₂OMe CH (Me) CH₂S (O)₂CF_Three
CH₂OMe CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂OMe CH (Et) CH₂SMe
CH₂OMe CH (Et) CH₂SEt
CH₂OMe CH (Et) CH₂SCF_Three
CH₂OMe CH (Et) CH₂SCH₂CF_Three
CH₂OMe CH (Et) CH₂S (O) Me
CH₂OMe CH (Et) CH₂S (O) Et
CH₂OMe CH (Et) CH₂S (O) CF_Three
CH₂OMe CH (Et) CH₂S (O) CH₂CF_Three
CH₂OMe CH (Et) CH₂S (O)₂Me
CH₂OMe CH (Et) CH₂S (O)₂Et
CH₂OMe CH (Et) CH₂S (O)₂CF_Three
CH₂OMe CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂OMe C (Me)₂CH₂SMe
CH₂OMe C (Me)₂CH₂SEt
CH₂OMe C (Me)₂CH₂SCF_Three
CH₂OMe C (Me)₂CH₂SCH₂CF_Three
CH₂OMe C (Me)₂CH₂S (O) Me
CH₂OMe C (Me)₂CH₂S (O) Et
CH₂OMe C (Me)₂CH₂S (O) CF_Three
CH₂OMe C (Me)₂CH₂S (O) CH₂CF_Three
CH₂OMe C (Me)₂CH₂S (O)₂Me
CH₂OMe C (Me)₂CH₂S (O)₂Et
CH₂OMe C (Me)₂CH₂S (O)₂CF_Three
CH₂OMe C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂OMe CH₂CH (Me) SMe
CH₂OMe CH₂CH (Me) SEt
CH₂OMe CH₂CH (Me) SCF_Three
CH₂OMe CH₂CH (Me) SCH₂CF_Three
CH₂OMe CH₂CH (Me) S (O) Me
CH₂OMe CH₂CH (Me) S (O) Et
CH₂OMe CH₂CH (Me) S (O) CF_Three
CH₂OMe CH₂CH (Me) S (O) CH₂CF_Three
CH₂OMe CH₂CH (Me) S (O)₂Me
CH₂OMe CH₂CH (Me) S (O)₂Et
CH₂OMe CH₂CH (Me) S (O)₂CF_Three
CH₂OMe CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂OMe CH₂CH (Et) SMe
CH₂OMe CH₂CH (Et) SEt
CH₂OMe CH₂CH (Et) SCF_Three
CH₂OMe CH₂CH (Et) SCH₂CF_Three
CH₂OMe CH₂CH (Et) S (O) Me
CH₂OMe CH₂CH (Et) S (O) Et
CH₂OMe CH₂CH (Et) S (O) CF_Three
CH₂OMe CH₂CH (Et) S (O) CH₂CF_Three
CH₂OMe CH₂CH (Et) S (O)₂Me
CH₂OMe CH₂CH (Et) S (O)₂Et
CH₂OMe CH₂CH (Et) S (O)₂CF_Three
CH₂OMe CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂OMe CH (Me) CH (Me) SMe
CH₂OMe CH (Me) CH (Me) SEt
CH₂OMe CH (Me) CH (Me) SCF_Three
CH₂OMe CH (Me) CH (Me) SCH₂CF_Three
CH₂OMe CH (Me) CH (Me) S (O) Me
CH₂OMe CH (Me) CH (Me) S (O) Et
CH₂OMe CH (Me) CH (Me) S (O) CF_Three
CH₂OMe CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂OMe CH (Me) CH (Me) S (O)₂Me
CH₂OMe CH (Me) CH (Me) S (O)₂Et
CH₂OMe CH (Me) CH (Me) S (O)₂CF_Three
CH₂OMe CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂SMe CH₂SMe
CH₂SEt CH₂SMe
CH₂S (O) Me CH₂SMe
CH₂S (O) Et CH₂SMe
CH₂S (O)₂Me CH₂SMe
CH₂S (O)₂Et CH₂SMe
CH (Me) SMe CH₂SMe
CH (Me) SEt CH₂SMe
CH (Me) S (O) Me CH₂SMe
CH (Me) S (O) Et CH₂SMe
CH (Me) S (O)₂Me CH₂SMe
CH (Me) S (O)₂Et CH₂SMe
CH (Et) SMe CH₂SMe
CH (Et) SEt CH₂SMe
CH (Et) S (O) Me CH₂SMe
CH (Et) S (O) Et CH₂SMe
CH (Et) S (O)₂Me CH₂SMe
CH (Et) S (O)₂Et CH₂SMe
CH (n-Pr) SMe CH₂SMe
CH (n-Pr) SEt CH₂SMe
CH (n-Pr) S (O) Me CH₂SMe
CH (n-Pr) S (O) Et CH₂SMe
CH (n-Pr) S (O)₂Me CH₂SMe
CH (n-Pr) S (O)₂Et CH₂SMe
CH (i-Pr) SMe CH₂SMe
CH (i-Pr) SEt CH₂SMe
CH (i-Pr) S (O) Me CH₂SMe
CH (i-Pr) S (O) Et CH₂SMe
CH (i-Pr) S (O)₂Me CH₂SMe
CH (i-Pr) S (O)₂Et CH₂SMe
CH (n-Bu) SMe CH₂SMe
CH (n-Bu) SEt CH₂SMe
CH (n-Bu) S (O) Me CH₂SMe
CH (n-Bu) S (O) Et CH₂SMe
CH (n-Bu) S (O)₂Me CH₂SMe
CH (n-Bu) S (O)₂Et CH₂SMe
CH (i-Bu) SMe CH₂SMe
CH (i-Bu) SEt CH₂SMe
CH (i-Bu) S (O) Me CH₂SMe
CH (i-Bu) S (O) Et CH₂SMe
CH (i-Bu) S (O)₂Me CH₂SMe
CH (i-Bu) S (O)₂Et CH₂SMe
CH (s-Bu) SMe CH₂SMe
CH (s-Bu) SEt CH₂SMe
CH (s-Bu) S (O) Me CH₂SMe
CH (s-Bu) S (O) Et CH₂SMe
CH (s-Bu) S (O)₂Me CH₂SMe
CH (s-Bu) S (O)₂Et CH₂SMe
CH (t-Bu) SMe CH₂SMe
CH (t-Bu) SEt CH₂SMe
CH (t-Bu) S (O) Me CH₂SMe
CH (t-Bu) S (O) Et CH₂SMe
CH (t-Bu) S (O)₂Me CH₂SMe
CH (t-Bu) S (O)₂Et CH₂SMe
CH₂CH₂SMe CH₂SMe
CH₂CH₂SEt CH₂SMe
CH₂CH₂S (O)₂Me CH₂SMe
CH₂CH₂S (O)₂Et CH₂SMe
CH (Me) CH₂SMe CH₂SMe
CH (Me) CH₂SEt CH₂SMe
CH (Me) CH₂S (O) Me CH₂SMe
CH (Me) CH₂S (O) Et CH₂SMe
CH (Me) CH₂S (O)₂Me CH₂SMe
CH (Me) CH₂S (O)₂Et CH₂SMe
CH (Et) CH₂SMe CH₂SMe
CH (Et) CH₂SEt CH₂SMe
CH (Et) CH₂S (O) Me CH₂SMe
CH (Et) CH₂S (O) Et CH₂SMe
CH (Et) CH₂S (O)₂Me CH₂SMe
CH (Et) CH₂S (O)₂Et CH₂SMe
C (Me)₂CH₂SMe CH₂SMe
C (Me)₂CH₂SEt CH₂SMe
C (Me)₂CH₂S (O) Me CH₂SMe
C (Me)₂CH₂S (O) Et CH₂SMe
C (Me)₂CH₂S (O)₂Me CH₂SMe
C (Me)₂CH₂S (O)₂Et CH₂SMe
CH₂CH (Me) SMe CH₂SMe
CH₂CH (Me) SEt CH₂SMe
CH₂CH (Me) S (O) Me CH₂SMe
CH₂CH (Me) S (O) Et CH₂SMe
CH₂CH (Me) S (O)₂Me CH₂SMe
CH₂CH (Me) S (O)₂Et CH₂SMe
CH₂CH (Et) SMe CH₂SMe
CH₂CH (Et) SEt CH₂SMe
CH₂CH (Et) S (O) Me CH₂SMe
CH₂CH (Et) S (O) Et CH₂SMe
CH₂CH (Et) S (O)₂Me CH₂SMe
CH₂CH (Et) S (O)₂Et CH₂SMe
CH (Me) CH (Me) SMe CH₂SMe
CH (Me) CH (Me) SEt CH₂SMe
CH (Me) CH (Me) S (O) Me CH₂SMe
CH (Me) CH (Me) S (O) Et CH₂SMe
CH (Me) CH (Me) S (O)₂Me CH₂SMe
CH (Me) CH (Me) S (O)₂Et CH₂SMe
CH₂SMe CH₂S (O) Me
CH₂SEt CH₂S (O) Me
CH₂S (O) Me CH₂S (O) Me
CH₂S (O) Et CH₂S (O) Me
CH₂S (O)₂Me CH₂S (O) Me
CH₂S (O)₂Et CH₂S (O) Me
CH (Me) SMe CH₂S (O) Me
CH (Me) SEt CH₂S (O) Me
CH (Me) S (O) Me CH₂S (O) Me
CH (Me) S (O) Et CH₂S (O) Me
CH (Me) S (O)₂Me CH₂S (O) Me
CH (Me) S (O)₂Et CH₂S (O) Me
CH (Et) SMe CH₂S (O) Me
CH (Et) SEt CH₂S (O) Me
CH (Et) S (O) Me CH₂S (O) Me
CH (Et) S (O) Et CH₂S (O) Me
CH (Et) S (O)₂Me CH₂S (O) Me
CH (Et) S (O)₂Et CH₂S (O) Me
CH (n-Pr) SMe CH₂S (O) Me
CH (n-Pr) SEt CH₂S (O) Me
CH (n-Pr) S (O) Me CH₂S (O) Me
CH (n-Pr) S (O) Et CH₂S (O) Me
CH (n-Pr) S (O)₂Me CH₂S (O) Me
CH (n-Pr) S (O)₂Et CH₂S (O) Me
CH (i-Pr) SMe CH₂S (O) Me
CH (i-Pr) SEt CH₂S (O) Me
CH (i-Pr) S (O) Me CH₂S (O) Me
CH (i-Pr) S (O) Et CH₂S (O) Me
CH (i-Pr) S (O)₂Me CH₂S (O) Me
CH (i-Pr) S (O)₂Et CH₂S (O) Me
CH (n-Bu) SMe CH₂S (O) Me
CH (n-Bu) SEt CH₂S (O) Me
CH (n-Bu) S (O) Me CH₂S (O) Me
CH (n-Bu) S (O) Et CH₂S (O) Me
CH (n-Bu) S (O)₂Me CH₂S (O) Me
CH (n-Bu) S (O)₂Et CH₂S (O) Me
CH (i-Bu) SMe CH₂S (O) Me
CH (i-Bu) SEt CH₂S (O) Me
CH (i-Bu) S (O) Me CH₂S (O) Me
CH (i-Bu) S (O) Et CH₂S (O) Me
CH (i-Bu) S (O)₂Me CH₂S (O) Me
CH (i-Bu) S (O)₂Et CH₂S (O) Me
CH (s-Bu) SMe CH₂S (O) Me
CH (s-Bu) SEt CH₂S (O) Me
CH (s-Bu) S (O) Me CH₂S (O) Me
CH (s-Bu) S (O) Et CH₂S (O) Me
CH (s-Bu) S (O)₂Me CH₂S (O) Me
CH (s-Bu) S (O)₂Et CH₂S (O) Me
CH (t-Bu) SMe CH₂S (O) Me
CH (t-Bu) SEt CH₂S (O) Me
CH (t-Bu) S (O) Me CH₂S (O) Me
CH (t-Bu) S (O) Et CH₂S (O) Me
CH (t-Bu) S (O)₂Me CH₂S (O) Me
CH (t-Bu) S (O)₂Et CH₂S (O) Me
CH₂CH₂SMe CH₂S (O) Me
CH₂CH₂SEt CH₂S (O) Me
CH₂CH₂S (O)₂Me CH₂S (O) Me
CH₂CH₂S (O)₂Et CH₂S (O) Me
CH (Me) CH₂SMe CH₂S (O) Me
CH (Me) CH₂SEt CH₂S (O) Me
CH (Me) CH₂S (O) Me CH₂S (O) Me
CH (Me) CH₂S (O) Et CH₂S (O) Me
CH (Me) CH₂S (O)₂Me CH₂S (O) Me
CH (Me) CH₂S (O)₂Et CH₂S (O) Me
CH (Et) CH₂SMe CH₂S (O) Me
CH (Et) CH₂SEt CH₂S (O) Me
CH (Et) CH₂S (O) Me CH₂S (O) Me
CH (Et) CH₂S (O) Et CH₂S (O) Me
CH (Et) CH₂S (O)₂Me CH₂S (O) Me
CH (Et) CH₂S (O)₂Et CH₂S (O) Me
C (Me)₂CH₂SMe CH₂S (O) Me
C (Me)₂CH₂SEt CH₂S (O) Me
C (Me)₂CH₂S (O) Me CH₂S (O) Me
C (Me)₂CH₂S (O) Et CH₂S (O) Me
C (Me)₂CH₂S (O)₂Me CH₂S (O) Me
C (Me)₂CH₂S (O)₂Et CH₂S (O) Me
CH₂CH (Me) SMe CH₂S (O) Me
CH₂CH (Me) SEt CH₂S (O) Me
CH₂CH (Me) S (O) Me CH₂S (O) Me
CH₂CH (Me) S (O) Et CH₂S (O) Me
CH₂CH (Me) S (O)₂Me CH₂S (O) Me
CH₂CH (Me) S (O)₂Et CH₂S (O) Me
CH₂CH (Et) SMe CH₂S (O) Me
CH₂CH (Et) SEt CH₂S (O) Me
CH₂CH (Et) S (O) Me CH₂S (O) Me
CH₂CH (Et) S (O) Et CH₂S (O) Me
CH₂CH (Et) S (O)₂Me CH₂S (O) Me
CH₂CH (Et) S (O)₂Et CH₂S (O) Me
CH (Me) CH (Me) SMe CH₂S (O) Me
CH (Me) CH (Me) SEt CH₂S (O) Me
CH (Me) CH (Me) S (O) Me CH₂S (O) Me
CH (Me) CH (Me) S (O) Et CH₂S (O) Me
CH (Me) CH (Me) S (O)₂Me CH₂S (O) Me
CH (Me) CH (Me) S (O)₂Et CH₂S (O) Me
CH₂SMe CH₂S (O)₂Me
CH₂SEt CH₂S (O)₂Me
CH₂S (O) Me CH₂S (O)₂Me
CH₂S (O) Et CH₂S (O)₂Me
CH₂S (O)₂Me CH₂S (O)₂Me
CH₂S (O)₂Et CH₂S (O)₂Me
CH (Me) SMe CH₂S (O)₂Me
CH (Me) SEt CH₂S (O)₂Me
CH (Me) S (O) Me CH₂S (O)₂Me
CH (Me) S (O) Et CH₂S (O)₂Me
CH (Me) S (O)₂Me CH₂S (O)₂Me
CH (Me) S (O)₂Et CH₂S (O)₂Me
CH (Et) SMe CH₂S (O)₂Me
CH (Et) SEt CH₂S (O)₂Me
CH (Et) S (O) Me CH₂S (O)₂Me
CH (Et) S (O) Et CH₂S (O)₂Me
CH (Et) S (O)₂Me CH₂S (O)₂Me
CH (Et) S (O)₂Et CH₂S (O)₂Me
CH (n-Pr) SMe CH₂S (O)₂Me
CH (n-Pr) SEt CH₂S (O)₂Me
CH (n-Pr) S (O) Me CH₂S (O)₂Me
CH (n-Pr) S (O) Et CH₂S (O)₂Me
CH (n-Pr) S (O)₂Me CH₂S (O)₂Me
CH (n-Pr) S (O)₂Et CH₂S (O)₂Me
CH (i-Pr) SMe CH₂S (O)₂Me
CH (i-Pr) SEt CH₂S (O)₂Me
CH (i-Pr) S (O) Me CH₂S (O)₂Me
CH (i-Pr) S (O) Et CH₂S (O)₂Me
CH (i-Pr) S (O)₂Me CH₂S (O)₂Me
CH (i-Pr) S (O)₂Et CH₂S (O)₂Me
CH (n-Bu) SMe CH₂S (O)₂Me
CH (n-Bu) SEt CH₂S (O)₂Me
CH (n-Bu) S (O) Me CH₂S (O)₂Me
CH (n-Bu) S (O) Et CH₂S (O)₂Me
CH (n-Bu) S (O)₂Me CH₂S (O)₂Me
CH (n-Bu) S (O)₂Et CH₂S (O)₂Me
CH (i-Bu) SMe CH₂S (O)₂Me
CH (i-Bu) SEt CH₂S (O)₂Me
CH (i-Bu) S (O) Me CH₂S (O)₂Me
CH (i-Bu) S (O) Et CH₂S (O)₂Me
CH (i-Bu) S (O)₂Me CH₂S (O)₂Me
CH (i-Bu) S (O)₂Et CH₂S (O)₂Me
CH (s-Bu) SMe CH₂S (O)₂Me
CH (s-Bu) SEt CH₂S (O)₂Me
CH (s-Bu) S (O) Me CH₂S (O)₂Me
CH (s-Bu) S (O) Et CH₂S (O)₂Me
CH (s-Bu) S (O)₂Me CH₂S (O)₂Me
CH (s-Bu) S (O)₂Et CH₂S (O)₂Me
CH (t-Bu) SMe CH₂S (O)₂Me
CH (t-Bu) SEt CH₂S (O)₂Me
CH (t-Bu) S (O) Me CH₂S (O)₂Me
CH (t-Bu) S (O) Et CH₂S (O)₂Me
CH (t-Bu) S (O)₂Me CH₂S (O)₂Me
CH (t-Bu) S (O)₂Et CH₂S (O)₂Me
CH₂CH₂SMe CH₂S (O)₂Me
CH₂CH₂SEt CH₂S (O)₂Me
CH₂CH₂S (O)₂Me CH₂S (O)₂Me
CH₂CH₂S (O)₂Et CH₂S (O)₂Me
CH (Me) CH₂SMe CH₂S (O)₂Me
CH (Me) CH₂SEt CH₂S (O)₂Me
CH (Me) CH₂S (O) Me CH₂S (O)₂Me
CH (Me) CH₂S (O) Et CH₂S (O)₂Me
CH (Me) CH₂S (O)₂Me CH₂S (O)₂Me
CH (Me) CH₂S (O)₂Et CH₂S (O)₂Me
CH (Et) CH₂SMe CH₂S (O)₂Me
CH (Et) CH₂SEt CH₂S (O)₂Me
CH (Et) CH₂S (O) Me CH₂S (O)₂Me
CH (Et) CH₂S (O) Et CH₂S (O)₂Me
CH (Et) CH₂S (O)₂Me CH₂S (O)₂Me
CH (Et) CH₂S (O)₂Et CH₂S (O)₂Me
C (Me)₂CH₂SMe CH₂S (O)₂Me
C (Me)₂CH₂SEt CH₂S (O)₂Me
C (Me)₂CH₂S (O) Me CH₂S (O)₂Me
C (Me)₂CH₂S (O) Et CH₂S (O)₂Me
C (Me)₂CH₂S (O)₂Me CH₂S (O)₂Me
C (Me)₂CH₂S (O)₂Et CH₂S (O)₂Me
CH₂CH (Me) SMe CH₂S (O)₂Me
CH₂CH (Me) SEt CH₂S (O)₂Me
CH₂CH (Me) S (O) Me CH₂S (O)₂Me
CH₂CH (Me) S (O) Et CH₂S (O)₂Me
CH₂CH (Me) S (O)₂Me CH₂S (O)₂Me
CH₂CH (Me) S (O)₂Et CH₂S (O)₂Me
CH₂CH (Et) SMe CH₂S (O)₂Me
CH₂CH (Et) SEt CH₂S (O)₂Me
CH₂CH (Et) S (O) Me CH₂S (O)₂Me
CH₂CH (Et) S (O) Et CH₂S (O)₂Me
CH₂CH (Et) S (O)₂Me CH₂S (O)₂Me
CH₂CH (Et) S (O)₂Et CH₂S (O)₂Me
CH (Me) CH (Me) SMe CH₂S (O)₂Me
CH (Me) CH (Me) SEt CH₂S (O)₂Me
CH (Me) CH (Me) S (O) Me CH₂S (O)₂Me
CH (Me) CH (Me) S (O) Et CH₂S (O)₂Me
CH (Me) CH (Me) S (O)₂Me CH₂S (O)₂Me
CH (Me) CH (Me) S (O)₂Et CH₂S (O)₂Me
CH₂SMe SMe
CH₂SEt SMe
CH₂S (O) Me SMe
CH₂S (O) Et SMe
CH₂S (O)₂Me SMe
CH₂S (O)₂Et SMe
CH (Me) SMe SMe
CH (Me) SEt SMe
CH (Me) S (O) Me SMe
CH (Me) S (O) Et SMe
CH (Me) S (O)₂Me SMe
CH (Me) S (O)₂Et SMe
CH (Et) SMe SMe
CH (Et) SEt SMe
CH (Et) S (O) Me SMe
CH (Et) S (O) Et SMe
CH (Et) S (O)₂Me SMe
CH (Et) S (O)₂Et SMe
CH (n-Pr) SMe SMe
CH (n-Pr) SEt SMe
CH (n-Pr) S (O) Me SMe
CH (n-Pr) S (O) Et SMe
CH (n-Pr) S (O)₂Me SMe
CH (n-Pr) S (O)₂Et SMe
CH (i-Pr) SMe SMe
CH (i-Pr) SEt SMe
CH (i-Pr) S (O) Me SMe
CH (i-Pr) S (O) Et SMe
CH (i-Pr) S (O)₂Me SMe
CH (i-Pr) S (O)₂Et SMe
CH (n-Bu) SMe SMe
CH (n-Bu) SEt SMe
CH (n-Bu) S (O) Me SMe
CH (n-Bu) S (O) Et SMe
CH (n-Bu) S (O)₂Me SMe
CH (n-Bu) S (O)₂Et SMe
CH (i-Bu) SMe SMe
CH (i-Bu) SEt SMe
CH (i-Bu) S (O) Me SMe
CH (i-Bu) S (O) Et SMe
CH (i-Bu) S (O)₂Me SMe
CH (i-Bu) S (O)₂Et SMe
CH (s-Bu) SMe SMe
CH (s-Bu) SEt SMe
CH (s-Bu) S (O) Me SMe
CH (s-Bu) S (O) Et SMe
CH (s-Bu) S (O)₂Me SMe
CH (s-Bu) S (O)₂Et SMe
CH (t-Bu) SMe SMe
CH (t-Bu) SEt SMe
CH (t-Bu) S (O) Me SMe
CH (t-Bu) S (O) Et SMe
CH (t-Bu) S (O)₂Me SMe
CH (t-Bu) S (O)₂Et SMe
CH₂CH₂SMeSMe
CH₂CH₂SEtSMe
CH₂CH₂S (O)₂Me SMe
CH₂CH₂S (O)₂Et SMe
CH (Me) CH₂SMe SMe
CH (Me) CH₂SEt SMe
CH (Me) CH₂S (O) Me SMe
CH (Me) CH₂S (O) Et SMe
CH (Me) CH₂S (O)₂Me SMe
CH (Me) CH₂S (O)₂Et SMe
CH (Et) CH₂SMe SMe
CH (Et) CH₂SEt SMe
CH (Et) CH₂S (O) Me SMe
CH (Et) CH₂S (O) Et SMe
CH (Et) CH₂S (O)₂Me SMe
CH (Et) CH₂S (O)₂Et SMe
C (Me)₂CH₂SMe SMe
C (Me)₂CH₂SEt SMe
C (Me)₂CH₂S (O) Me SMe
C (Me)₂CH₂S (O) Et SMe
C (Me)₂CH₂S (O)₂Me SMe
C (Me)₂CH₂S (O)₂Et SMe
CH₂CH (Me) SMe SMe
CH₂CH (Me) SEt SMe
CH₂CH (Me) S (O) Me SMe
CH₂CH (Me) S (O) Et SMe
CH₂CH (Me) S (O)₂Me SMe
CH₂CH (Me) S (O)₂Et SMe
CH₂CH (Et) SMe SMe
CH₂CH (Et) SEt SMe
CH₂CH (Et) S (O) Me SMe
CH₂CH (Et) S (O) Et SMe
CH₂CH (Et) S (O)₂Me SMe
CH₂CH (Et) S (O)₂Et SMe
CH (Me) CH (Me) SMe SMe
CH (Me) CH (Me) SEt SMe
CH (Me) CH (Me) S (O) Me SMe
CH (Me) CH (Me) S (O) Et SMe
CH (Me) CH (Me) S (O)₂Me SMe
CH (Me) CH (Me) S (O)₂Et SMe
CH₂SMe S (O) Me
CH₂SEt S (O) Me
CH₂S (O) Me S (O) Me
CH₂S (O) Et S (O) Me
CH₂S (O)₂Me S (O) Me
CH₂S (O)₂Et S (O) Me
CH (Me) SMe S (O) Me
CH (Me) SEt S (O) Me
CH (Me) S (O) Me S (O) Me
CH (Me) S (O) Et S (O) Me
CH (Me) S (O)₂Me S (O) Me
CH (Me) S (O)₂Et S (O) Me
CH (Et) SMe S (O) Me
CH (Et) SEt S (O) Me
CH (Et) S (O) Me S (O) Me
CH (Et) S (O) Et S (O) Me
CH (Et) S (O)₂Me S (O) Me
CH (Et) S (O)₂Et S (O) Me
CH (n-Pr) SMe S (O) Me
CH (n-Pr) SEt S (O) Me
CH (n-Pr) S (O) Me S (O) Me
CH (n-Pr) S (O) Et S (O) Me
CH (n-Pr) S (O)₂Me S (O) Me
CH (n-Pr) S (O)₂Et S (O) Me
CH (i-Pr) SMe S (O) Me
CH (i-Pr) SEt S (O) Me
CH (i-Pr) S (O) Me S (O) Me
CH (i-Pr) S (O) Et S (O) Me
CH (i-Pr) S (O)₂Me S (O) Me
CH (i-Pr) S (O)₂Et S (O) Me
CH (n-Bu) SMe S (O) Me
CH (n-Bu) SEt S (O) Me
CH (n-Bu) S (O) Me S (O) Me
CH (n-Bu) S (O) Et S (O) Me
CH (n-Bu) S (O)₂Me S (O) Me
CH (n-Bu) S (O)₂Et S (O) Me
CH (i-Bu) SMe S (O) Me
CH (i-Bu) SEt S (O) Me
CH (i-Bu) S (O) Me S (O) Me
CH (i-Bu) S (O) Et S (O) Me
CH (i-Bu) S (O)₂Me S (O) Me
CH (i-Bu) S (O)₂Et S (O) Me
CH (s-Bu) SMe S (O) Me
CH (s-Bu) SEt S (O) Me
CH (s-Bu) S (O) Me S (O) Me
CH (s-Bu) S (O) Et S (O) Me
CH (s-Bu) S (O)₂Me S (O) Me
CH (s-Bu) S (O)₂Et S (O) Me
CH (t-Bu) SMe S (O) Me
CH (t-Bu) SEt S (O) Me
CH (t-Bu) S (O) Me S (O) Me
CH (t-Bu) S (O) Et S (O) Me
CH (t-Bu) S (O)₂Me S (O) Me
CH (t-Bu) S (O)₂Et S (O) Me
CH₂CH₂SMeS (O) Me
CH₂CH₂SEtS (O) Me
CH₂CH₂S (O)₂Me S (O) Me
CH₂CH₂S (O)₂Et S (O) Me
CH (Me) CH₂SMe S (O) Me
CH (Me) CH₂SEt S (O) Me
CH (Me) CH₂S (O) Me S (O) Me
CH (Me) CH₂S (O) Et S (O) Me
CH (Me) CH₂S (O)₂Me S (O) Me
CH (Me) CH₂S (O)₂Et S (O) Me
CH (Et) CH₂SMe S (O) Me
CH (Et) CH₂SEt S (O) Me
CH (Et) CH₂S (O) Me S (O) Me
CH (Et) CH₂S (O) Et S (O) Me
CH (Et) CH₂S (O)₂Me S (O) Me
CH (Et) CH₂S (O)₂Et S (O) Me
C (Me)₂CH₂SMe S (O) Me
C (Me)₂CH₂SEt S (O) Me
C (Me)₂CH₂S (O) Me S (O) Me
C (Me)₂CH₂S (O) Et S (O) Me
C (Me)₂CH₂S (O)₂Me S (O) Me
C (Me)₂CH₂S (O)₂Et S (O) Me
CH₂CH (Me) SMe S (O) Me
CH₂CH (Me) SEt S (O) Me
CH₂CH (Me) S (O) Me S (O) Me
CH₂CH (Me) S (O) Et S (O) Me
CH₂CH (Me) S (O)₂Me S (O) Me
CH₂CH (Me) S (O)₂Et S (O) Me
CH₂CH (Et) SMe S (O) Me
CH₂CH (Et) SEt S (O) Me
CH₂CH (Et) S (O) Me S (O) Me
CH₂CH (Et) S (O) Et S (O) Me
CH₂CH (Et) S (O)₂Me S (O) Me
CH₂CH (Et) S (O)₂Et S (O) Me
CH (Me) CH (Me) SMe S (O) Me
CH (Me) CH (Me) SEt S (O) Me
CH (Me) CH (Me) S (O) Me S (O) Me
CH (Me) CH (Me) S (O) Et S (O) Me
CH (Me) CH (Me) S (O)₂Me S (O) Me
CH (Me) CH (Me) S (O)₂Et S (O) Me
CH₂SMe S (O)₂Me
CH₂SEt S (O)₂Me
CH₂S (O) Me S (O)₂Me
CH₂S (O) Et S (O)₂Me
CH₂S (O)₂Me S (O)₂Me
CH₂S (O)₂Et S (O)₂Me
CH (Me) SMe S (O)₂Me
CH (Me) SEt S (O)₂Me
CH (Me) S (O) Me S (O)₂Me
CH (Me) S (O) Et S (O)₂Me
CH (Me) S (O)₂Me S (O)₂Me
CH (Me) S (O)₂Et S (O)₂Me
CH (Et) SMe S (O)₂Me
CH (Et) SEt S (O)₂Me
CH (Et) S (O) Me S (O)₂Me
CH (Et) S (O) Et S (O)₂Me
CH (Et) S (O)₂Me S (O)₂Me
CH (Et) S (O)₂Et S (O)₂Me
CH (n-Pr) SMe S (O)₂Me
CH (n-Pr) SEt S (O)₂Me
CH (n-Pr) S (O) Me S (O)₂Me
CH (n-Pr) S (O) Et S (O)₂Me
CH (n-Pr) S (O)₂Me S (O)₂Me
CH (n-Pr) S (O)₂Et S (O)₂Me
CH (i-Pr) SMe S (O)₂Me
CH (i-Pr) SEt S (O)₂Me
CH (i-Pr) S (O) Me S (O)₂Me
CH (i-Pr) S (O) Et S (O)₂Me
CH (i-Pr) S (O)₂Me S (O)₂Me
CH (i-Pr) S (O)₂Et S (O)₂Me
CH (n-Bu) SMe S (O)₂Me
CH (n-Bu) SEt S (O)₂Me
CH (n-Bu) S (O) Me S (O)₂Me
CH (n-Bu) S (O) Et S (O)₂Me
CH (n-Bu) S (O)₂Me S (O)₂Me
CH (n-Bu) S (O)₂Et S (O)₂Me
CH (i-Bu) SMe S (O)₂Me
CH (i-Bu) SEt S (O)₂Me
CH (i-Bu) S (O) Me S (O)₂Me
CH (i-Bu) S (O) Et S (O)₂Me
CH (i-Bu) S (O)₂Me S (O)₂Me
CH (i-Bu) S (O)₂Et S (O)₂Me
CH (s-Bu) SMe S (O)₂Me
CH (s-Bu) SEt S (O)₂Me
CH (s-Bu) S (O) Me S (O)₂Me
CH (s-Bu) S (O) Et S (O)₂Me
CH (s-Bu) S (O)₂Me S (O)₂Me
CH (s-Bu) S (O)₂Et S (O)₂Me
CH (t-Bu) SMe S (O)₂Me
CH (t-Bu) SEt S (O)₂Me
CH (t-Bu) S (O) Me S (O)₂Me
CH (t-Bu) S (O) Et S (O)₂Me
CH (t-Bu) S (O)₂Me S (O)₂Me
CH (t-Bu) S (O)₂Et S (O)₂Me
CH₂CH₂SMeS (O)₂Me
CH₂CH₂SEtS (O)₂Me
CH₂CH₂S (O)₂Me S (O)₂Me
CH₂CH₂S (O)₂Et S (O)₂Me
CH (Me) CH₂SMe S (O)₂Me
CH (Me) CH₂SEt S (O)₂Me
CH (Me) CH₂S (O) Me S (O)₂Me
CH (Me) CH₂S (O) Et S (O)₂Me
CH (Me) CH₂S (O)₂Me S (O)₂Me
CH (Me) CH₂S (O)₂Et S (O)₂Me
CH (Et) CH₂SMe S (O)₂Me
CH (Et) CH₂SEt S (O)₂Me
CH (Et) CH₂S (O) Me S (O)₂Me
CH (Et) CH₂S (O) Et S (O)₂Me
CH (Et) CH₂S (O)₂Me S (O)₂Me
CH (Et) CH₂S (O)₂Et S (O)₂Me
C (Me)₂CH₂SMe S (O)₂Me
C (Me)₂CH₂SEt S (O)₂Me
C (Me)₂CH₂S (O) Me S (O)₂Me
C (Me)₂CH₂S (O) Et S (O)₂Me
C (Me)₂CH₂S (O)₂Me S (O)₂Me
C (Me)₂CH₂S (O)₂Et S (O)₂Me
CH₂CH (Me) SMe S (O)₂Me
CH₂CH (Me) SEt S (O)₂Me
CH₂CH (Me) S (O) Me S (O)₂Me
CH₂CH (Me) S (O) Et S (O)₂Me
CH₂CH (Me) S (O)₂Me S (O)₂Me
CH₂CH (Me) S (O)₂Et S (O)₂Me
CH₂CH (Et) SMe S (O)₂Me
CH₂CH (Et) SEt S (O)₂Me
CH₂CH (Et) S (O) Me S (O)₂Me
CH₂CH (Et) S (O) Et S (O)₂Me
CH₂CH (Et) S (O)₂Me S (O)₂Me
CH₂CH (Et) S (O)₂Et S (O)₂Me
CH (Me) CH (Me) SMe S (O)₂Me
CH (Me) CH (Me) SEt S (O)₂Me
CH (Me) CH (Me) S (O) Me S (O)₂Me
CH (Me) CH (Me) S (O) Et S (O)₂Me
CH (Me) CH (Me) S (O)₂Me S (O)₂Me
CH (Me) CH (Me) S (O)₂Et S (O)₂Me
CH₂SMe H
CH₂SEt H
CH₂S (O) Me H
CH₂S (O) Et H
CH₂S (O)₂Me H
CH₂S (O)₂Et H
CH (Me) SMe H
CH (Me) SEt H
CH (Me) S (O) Me H
CH (Me) S (O) Et H
CH (Me) S (O)₂Me H
CH (Me) S (O)₂Et H
CH (Et) SMe H
CH (Et) SEt H
CH (Et) S (O) Me H
CH (Et) S (O) Et H
CH (Et) S (O)₂Me H
CH (Et) S (O)₂Et H
CH (n-Pr) SMe H
CH (n-Pr) SEt H
CH (n-Pr) S (O) Me H
CH (n-Pr) S (O) Et H
CH (n-Pr) S (O)₂Me H
CH (n-Pr) S (O)₂Et H
CH (i-Pr) SMe H
CH (i-Pr) SEt H
CH (i-Pr) S (O) Me H
CH (i-Pr) S (O) Et H
CH (i-Pr) S (O)₂Me H
CH (i-Pr) S (O)₂Et H
CH (n-Bu) SMe H
CH (n-Bu) SEt H
CH (n-Bu) S (O) Me H
CH (n-Bu) S (O) Et H
CH (n-Bu) S (O)₂Me H
CH (n-Bu) S (O)₂Et H
CH (i-Bu) SMe H
CH (i-Bu) SEt H
CH (i-Bu) S (O) Me H
CH (i-Bu) S (O) Et H
CH (i-Bu) S (O)₂Me H
CH (i-Bu) S (O)₂Et H
CH (s-Bu) SMe H
CH (s-Bu) SEt H
CH (s-Bu) S (O) Me H
CH (s-Bu) S (O) Et H
CH (s-Bu) S (O)₂Me H
CH (s-Bu) S (O)₂Et H
CH (t-Bu) SMe H
CH (t-Bu) SEt H
CH (t-Bu) S (O) Me H
CH (t-Bu) S (O) Et H
CH (t-Bu) S (O)₂Me H
CH (t-Bu) S (O)₂Et H
CH₂CH₂SMe H
CH₂CH₂SEt H
CH₂CH₂S (O)₂Me H
CH₂CH₂S (O)₂Et H
CH (Me) CH₂SMe H
CH (Me) CH₂SEt H
CH (Me) CH₂S (O) Me H
CH (Me) CH₂S (O) Et H
CH (Me) CH₂S (O)₂Me H
CH (Me) CH₂S (O)₂Et H
CH (Et) CH₂SMe H
CH (Et) CH₂SEt H
CH (Et) CH₂S (O) Me H
CH (Et) CH₂S (O) Et H
CH (Et) CH₂S (O)₂Me H
CH (Et) CH₂S (O)₂Et H
C (Me)₂CH₂SMe H
C (Me)₂CH₂SEt H
C (Me)₂CH₂S (O) Me H
C (Me)₂CH₂S (O) Et H
C (Me)₂CH₂S (O)₂Me H
C (Me)₂CH₂S (O)₂Et H
CH₂CH (Me) SMe H
CH₂CH (Me) SEt H
CH₂CH (Me) S (O) Me H
CH₂CH (Me) S (O) Et H
CH₂CH (Me) S (O)₂Me H
CH₂CH (Me) S (O)₂Et H
CH₂CH (Et) SMe H
CH₂CH (Et) SEt H
CH₂CH (Et) S (O) Me H
CH₂CH (Et) S (O) Et H
CH₂CH (Et) S (O)₂Me H
CH₂CH (Et) S (O)₂Et H
CH (Me) CH (Me) SMe H
CH (Me) CH (Me) SEt H
CH (Me) CH (Me) S (O) Me H
CH (Me) CH (Me) S (O) Et H
CH (Me) CH (Me) S (O)₂Me H
CH (Me) CH (Me) S (O)₂Et H
CH₂SMe Me
CH₂SEt Me
CH₂S (O) Me Me
CH₂S (O) Et Me
CH₂S (O)₂Me Me
CH₂S (O)₂Et Me
CH (Me) SMe Me
CH (Me) SEt Me
CH (Me) S (O) Me Me
CH (Me) S (O) Et Me
CH (Me) S (O)₂Me Me
CH (Me) S (O)₂Et Me
CH (Et) SMe Me
CH (Et) SEt Me
CH (Et) S (O) Me Me
CH (Et) S (O) Et Me
CH (Et) S (O)₂Me Me
CH (Et) S (O)₂Et Me
CH (n-Pr) SMe Me
CH (n-Pr) SEt Me
CH (n-Pr) S (O) Me Me
CH (n-Pr) S (O) Et Me
CH (n-Pr) S (O)₂Me Me
CH (n-Pr) S (O)₂Et Me
CH (i-Pr) SMe Me
CH (i-Pr) SEt Me
CH (i-Pr) S (O) Me Me
CH (i-Pr) S (O) Et Me
CH (i-Pr) S (O)₂Me Me
CH (i-Pr) S (O)₂Et Me
CH (n-Bu) SMe Me
CH (n-Bu) SEt Me
CH (n-Bu) S (O) Me Me
CH (n-Bu) S (O) Et Me
CH (n-Bu) S (O)₂Me Me
CH (n-Bu) S (O)₂Et Me
CH (i-Bu) SMe Me
CH (i-Bu) SEt Me
CH (i-Bu) S (O) Me Me
CH (i-Bu) S (O) Et Me
CH (i-Bu) S (O)₂Me Me
CH (i-Bu) S (O)₂Et Me
CH (s-Bu) SMe Me
CH (s-Bu) SEt Me
CH (s-Bu) S (O) Me Me
CH (s-Bu) S (O) Et Me
CH (s-Bu) S (O)₂Me Me
CH (s-Bu) S (O)₂Et Me
CH (t-Bu) SMe Me
CH (t-Bu) SEt Me
CH (t-Bu) S (O) Me Me
CH (t-Bu) S (O) Et Me
CH (t-Bu) S (O)₂Me Me
CH (t-Bu) S (O)₂Et Me
CH₂CH₂SMe Me
CH₂CH₂SEt Me
CH₂CH₂S (O)₂Me Me
CH₂CH₂S (O)₂Et Me
CH (Me) CH₂SMe Me
CH (Me) CH₂SEt Me
CH (Me) CH₂S (O) Me Me
CH (Me) CH₂S (O) Et Me
CH (Me) CH₂S (O)₂Me Me
CH (Me) CH₂S (O)₂Et Me
CH (Et) CH₂SMe Me
CH (Et) CH₂SEt Me
CH (Et) CH₂S (O) Me Me
CH (Et) CH₂S (O) Et Me
CH (Et) CH₂S (O)₂Me Me
CH (Et) CH₂S (O)₂Et Me
C (Me)₂CH₂SMe Me
C (Me)₂CH₂SEt Me
C (Me)₂CH₂S (O) Me Me
C (Me)₂CH₂S (O) Et Me
C (Me)₂CH₂S (O)₂Me Me
C (Me)₂CH₂S (O)₂Et Me
CH₂CH (Me) SMe Me
CH₂CH (Me) SEt Me
CH₂CH (Me) S (O) Me Me
CH₂CH (Me) S (O) Et Me
CH₂CH (Me) S (O)₂Me Me
CH₂CH (Me) S (O)₂Et Me
CH₂CH (Et) SMe Me
CH₂CH (Et) SEt Me
CH₂CH (Et) S (O) Me Me
CH₂CH (Et) S (O) Et Me
CH₂CH (Et) S (O)₂Me Me
CH₂CH (Et) S (O)₂Et Me
CH (Me) CH (Me) SMe Me
CH (Me) CH (Me) SEt Me
CH (Me) CH (Me) S (O) Me Me
CH (Me) CH (Me) S (O) Et Me
CH (Me) CH (Me) S (O)₂Me Me
CH (Me) CH (Me) S (O)₂Et Me
CH₂SMe CF_Three
CH₂SEt CF_Three
CH₂S (O) Me CF_Three
CH₂S (O) Et CF_Three
CH₂S (O)₂Me CF_Three
CH₂S (O)₂Et CF_Three
CH (Me) SMe CF_Three
CH (Me) SEt CF_Three
CH (Me) S (O) Me CF_Three
CH (Me) S (O) Et CF_Three
CH (Me) S (O)₂Me CF_Three
CH (Me) S (O)₂Et CF_Three
CH (Et) SMe CF_Three
CH (Et) SEt CF_Three
CH (Et) S (O) Me CF_Three
CH (Et) S (O) Et CF_Three
CH (Et) S (O)₂Me CF_Three
CH (Et) S (O)₂Et CF_Three
CH (n-Pr) SMe CF_Three
CH (n-Pr) SEt CF_Three
CH (n-Pr) S (O) Me CF_Three
CH (n-Pr) S (O) Et CF_Three
CH (n-Pr) S (O)₂Me CF_Three
CH (n-Pr) S (O)₂Et CF_Three
CH (i-Pr) SMe CF_Three
CH (i-Pr) SEt CF_Three
CH (i-Pr) S (O) Me CF_Three
CH (i-Pr) S (O) Et CF_Three
CH (i-Pr) S (O)₂Me CF_Three
CH (i-Pr) S (O)₂Et CF_Three
CH (n-Bu) SMe CF_Three
CH (n-Bu) SEt CF_Three
CH (n-Bu) S (O) Me CF_Three
CH (n-Bu) S (O) Et CF_Three
CH (n-Bu) S (O)₂Me CF_Three
CH (n-Bu) S (O)₂Et CF_Three
CH (i-Bu) SMe CF_Three
CH (i-Bu) SEt CF_Three
CH (i-Bu) S (O) Me CF_Three
CH (i-Bu) S (O) Et CF_Three
CH (i-Bu) S (O)₂Me CF_Three
CH (i-Bu) S (O)₂Et CF_Three
CH (s-Bu) SMe CF_Three
CH (s-Bu) SEt CF_Three
CH (s-Bu) S (O) Me CF_Three
CH (s-Bu) S (O) Et CF_Three
CH (s-Bu) S (O)₂Me CF_Three
CH (s-Bu) S (O)₂Et CF_Three
CH (t-Bu) SMe CF_Three
CH (t-Bu) SEt CF_Three
CH (t-Bu) S (O) Me CF_Three
CH (t-Bu) S (O) Et CF_Three
CH (t-Bu) S (O)₂Me CF_Three
CH (t-Bu) S (O)₂Et CF_Three
CH₂CH₂SMe CF_Three
CH₂CH₂SEt CF_Three
CH₂CH₂S (O)₂Me CF_Three
CH₂CH₂S (O)₂Et CF_Three
CH (Me) CH₂SMe CF_Three
CH (Me) CH₂SEt CF_Three
CH (Me) CH₂S (O) Me CF_Three
CH (Me) CH₂S (O) Et CF_Three
CH (Me) CH₂S (O)₂Me CF_Three
CH (Me) CH₂S (O)₂Et CF_Three
CH (Et) CH₂SMe CF_Three
CH (Et) CH₂SEt CF_Three
CH (Et) CH₂S (O) Me CF_Three
CH (Et) CH₂S (O) Et CF_Three
CH (Et) CH₂S (O)₂Me CF_Three
CH (Et) CH₂S (O)₂Et CF_Three
C (Me)₂CH₂SMe CF_Three
C (Me)₂CH₂SEt CF_Three
C (Me)₂CH₂S (O) Me CF_Three
C (Me)₂CH₂S (O) Et CF_Three
C (Me)₂CH₂S (O)₂Me CF_Three
C (Me)₂CH₂S (O)₂Et CF_Three
CH₂CH (Me) SMe CF_Three
CH₂CH (Me) SEt CF_Three
CH₂CH (Me) S (O) Me CF_Three
CH₂CH (Me) S (O) Et CF_Three
CH₂CH (Me) S (O)₂Me CF_Three
CH₂CH (Me) S (O)₂Et CF_Three
CH₂CH (Et) SMe CF_Three
CH₂CH (Et) SEt CF_Three
CH₂CH (Et) S (O) Me CF_Three
CH₂CH (Et) S (O) Et CF_Three
CH₂CH (Et) S (O)₂Me CF_Three
CH₂CH (Et) S (O)₂Et CF_Three
CH (Me) CH (Me) SMe CF_Three
CH (Me) CH (Me) SEt CF_Three
CH (Me) CH (Me) S (O) Me CF_Three
CH (Me) CH (Me) S (O) Et CF_Three
CH (Me) CH (Me) S (O)₂Me CF_Three
CH (Me) CH (Me) S (O)₂Et CF_Three
CH₂SMe CN
CH₂SEt CN
CH₂S (O) Me CN
CH₂S (O) Et CN
CH₂S (O)₂Me CN
CH₂S (O)₂Et CN
CH (Me) SMe CN
CH (Me) SEt CN
CH (Me) S (O) Me CN
CH (Me) S (O) Et CN
CH (Me) S (O)₂Me CN
CH (Me) S (O)₂Et CN
CH (Et) SMe CN
CH (Et) SEt CN
CH (Et) S (O) Me CN
CH (Et) S (O) Et CN
CH (Et) S (O)₂Me CN
CH (Et) S (O)₂Et CN
CH (n-Pr) SMe CN
CH (n-Pr) SEt CN
CH (n-Pr) S (O) Me CN
CH (n-Pr) S (O) Et CN
CH (n-Pr) S (O)₂Me CN
CH (n-Pr) S (O)₂Et CN
CH (i-Pr) SMe CN
CH (i-Pr) SEt CN
CH (i-Pr) S (O) Me CN
CH (i-Pr) S (O) Et CN
CH (i-Pr) S (O)₂Me CN
CH (i-Pr) S (O)₂Et CN
CH (n-Bu) SMe CN
CH (n-Bu) SEt CN
CH (n-Bu) S (O) Me CN
CH (n-Bu) S (O) Et CN
CH (n-Bu) S (O)₂Me CN
CH (n-Bu) S (O)₂Et CN
CH (i-Bu) SMe CN
CH (i-Bu) SEt CN
CH (i-Bu) S (O) Me CN
CH (i-Bu) S (O) Et CN
CH (i-Bu) S (O)₂Me CN
CH (i-Bu) S (O)₂Et CN
CH (s-Bu) SMe CN
CH (s-Bu) SEt CN
CH (s-Bu) S (O) Me CN
CH (s-Bu) S (O) Et CN
CH (s-Bu) S (O)₂Me CN
CH (s-Bu) S (O)₂Et CN
CH (t-Bu) SMe CN
CH (t-Bu) SEt CN
CH (t-Bu) S (O) Me CN
CH (t-Bu) S (O) Et CN
CH (t-Bu) S (O)₂Me CN
CH (t-Bu) S (O)₂Et CN
CH₂CH₂SMe CN
CH₂CH₂SEt CN
CH₂CH₂S (O)₂Me CN
CH₂CH₂S (O)₂Et CN
CH (Me) CH₂SMe CN
CH (Me) CH₂SEt CN
CH (Me) CH₂S (O) Me CN
CH (Me) CH₂S (O) Et CN
CH (Me) CH₂S (O)₂Me CN
CH (Me) CH₂S (O)₂Et CN
CH (Et) CH₂SMe CN
CH (Et) CH₂SEt CN
CH (Et) CH₂S (O) Me CN
CH (Et) CH₂S (O) Et CN
CH (Et) CH₂S (O)₂Me CN
CH (Et) CH₂S (O)₂Et CN
C (Me)₂CH₂SMe CN
C (Me)₂CH₂SEt CN
C (Me)₂CH₂S (O) Me CN
C (Me)₂CH₂S (O) Et CN
C (Me)₂CH₂S (O)₂Me CN
C (Me)₂CH₂S (O)₂Et CN
CH₂CH (Me) SMe CN
CH₂CH (Me) SEt CN
CH₂CH (Me) S (O) Me CN
CH₂CH (Me) S (O) Et CN
CH₂CH (Me) S (O)₂Me CN
CH₂CH (Me) S (O)₂Et CN
CH₂CH (Et) SMe CN
CH₂CH (Et) SEt CN
CH₂CH (Et) S (O) Me CN
CH₂CH (Et) S (O) Et CN
CH₂CH (Et) S (O)₂Me CN
CH₂CH (Et) S (O)₂Et CN
CH (Me) CH (Me) SMe CN
CH (Me) CH (Me) SEt CN
CH (Me) CH (Me) S (O) Me CN
CH (Me) CH (Me) S (O) Et CN
CH (Me) CH (Me) S (O)₂Me CN
CH (Me) CH (Me) S (O)₂Et CN
CH₂SMe Cl
CH₂SEt Cl
CH₂S (O) Me Cl
CH₂S (O) Et Cl
CH₂S (O)₂Me Cl
CH₂S (O)₂Et Cl
CH (Me) SMe Cl
CH (Me) SEt Cl
CH (Me) S (O) Me Cl
CH (Me) S (O) Et Cl
CH (Me) S (O)₂Me Cl
CH (Me) S (O)₂Et Cl
CH (Et) SMe Cl
CH (Et) SEt Cl
CH (Et) S (O) Me Cl
CH (Et) S (O) Et Cl
CH (Et) S (O)₂Me Cl
CH (Et) S (O)₂Et Cl
CH (n-Pr) SMe Cl
CH (n-Pr) SEt Cl
CH (n-Pr) S (O) Me Cl
CH (n-Pr) S (O) Et Cl
CH (n-Pr) S (O)₂Me Cl
CH (n-Pr) S (O)₂Et Cl
CH (i-Pr) SMe Cl
CH (i-Pr) SEt Cl
CH (i-Pr) S (O) Me Cl
CH (i-Pr) S (O) Et Cl
CH (i-Pr) S (O)₂Me Cl
CH (i-Pr) S (O)₂Et Cl
CH (n-Bu) SMe Cl
CH (n-Bu) SEt Cl
CH (n-Bu) S (O) Me Cl
CH (n-Bu) S (O) Et Cl
CH (n-Bu) S (O)₂Me Cl
CH (n-Bu) S (O)₂Et Cl
CH (i-Bu) SMe Cl
CH (i-Bu) SEt Cl
CH (i-Bu) S (O) Me Cl
CH (i-Bu) S (O) Et Cl
CH (i-Bu) S (O)₂Me Cl
CH (i-Bu) S (O)₂Et Cl
CH (s-Bu) SMe Cl
CH (s-Bu) SEt Cl
CH (s-Bu) S (O) Me Cl
CH (s-Bu) S (O) Et Cl
CH (s-Bu) S (O)₂Me Cl
CH (s-Bu) S (O)₂Et Cl
CH (t-Bu) SMe Cl
CH (t-Bu) SEt Cl
CH (t-Bu) S (O) Me Cl
CH (t-Bu) S (O) Et Cl
CH (t-Bu) S (O)₂Me Cl
CH (t-Bu) S (O)₂Et Cl
CH₂CH₂SMe Cl
CH₂CH₂SEt Cl
CH₂CH₂S (O)₂Me Cl
CH₂CH₂S (O)₂Et Cl
CH (Me) CH₂SMe Cl
CH (Me) CH₂SEt Cl
CH (Me) CH₂S (O) Me Cl
CH (Me) CH₂S (O) Et Cl
CH (Me) CH₂S (O)₂Me Cl
CH (Me) CH₂S (O)₂Et Cl
CH (Et) CH₂SMe Cl
CH (Et) CH₂SEt Cl
CH (Et) CH₂S (O) Me Cl
CH (Et) CH₂S (O) Et Cl
CH (Et) CH₂S (O)₂Me Cl
CH (Et) CH₂S (O)₂Et Cl
C (Me)₂CH₂SMe Cl
C (Me)₂CH₂SEt Cl
C (Me)₂CH₂S (O) Me Cl
C (Me)₂CH₂S (O) Et Cl
C (Me)₂CH₂S (O)₂Me Cl
C (Me)₂CH₂S (O)₂Et Cl
CH₂CH (Me) SMe Cl
CH₂CH (Me) SEt Cl
CH₂CH (Me) S (O) Me Cl
CH₂CH (Me) S (O) Et Cl
CH₂CH (Me) S (O)₂Me Cl
CH₂CH (Me) S (O)₂Et Cl
CH₂CH (Et) SMe Cl
CH₂CH (Et) SEt Cl
CH₂CH (Et) S (O) Me Cl
CH₂CH (Et) S (O) Et Cl
CH₂CH (Et) S (O)₂Me Cl
CH₂CH (Et) S (O)₂Et Cl
CH (Me) CH (Me) SMe Cl
CH (Me) CH (Me) SEt Cl
CH (Me) CH (Me) S (O) Me Cl
CH (Me) CH (Me) S (O) Et Cl
CH (Me) CH (Me) S (O)₂Me Cl
CH (Me) CH (Me) S (O)₂Et Cl
CH₂SMe C (O) OMe
CH₂SEt C (O) OMe
CH₂S (O) Me C (O) OMe
CH₂S (O) Et C (O) OMe
CH₂S (O)₂Me C (O) OMe
CH₂S (O)₂Et C (O) OMe
CH (Me) SMe C (O) OMe
CH (Me) SEt C (O) OMe
CH (Me) S (O) Me C (O) OMe
CH (Me) S (O) Et C (O) OMe
CH (Me) S (O)₂Me C (O) OMe
CH (Me) S (O)₂Et C (O) OMe
CH (Et) SMe C (O) OMe
CH (Et) SEt C (O) OMe
CH (Et) S (O) Me C (O) OMe
CH (Et) S (O) Et C (O) OMe
CH (Et) S (O)₂Me C (O) OMe
CH (Et) S (O)₂Et C (O) OMe
CH (n-Pr) SMe C (O) OMe
CH (n-Pr) SEt C (O) OMe
CH (n-Pr) S (O) Me C (O) OMe
CH (n-Pr) S (O) Et C (O) OMe
CH (n-Pr) S (O)₂Me C (O) OMe
CH (n-Pr) S (O)₂Et C (O) OMe
CH (i-Pr) SMe C (O) OMe
CH (i-Pr) SEt C (O) OMe
CH (i-Pr) S (O) Me C (O) OMe
CH (i-Pr) S (O) Et C (O) OMe
CH (i-Pr) S (O)₂Me C (O) OMe
CH (i-Pr) S (O)₂Et C (O) OMe
CH (n-Bu) SMe C (O) OMe
CH (n-Bu) SEt C (O) OMe
CH (n-Bu) S (O) Me C (O) OMe
CH (n-Bu) S (O) Et C (O) OMe
CH (n-Bu) S (O)₂Me C (O) OMe
CH (n-Bu) S (O)₂Et C (O) OMe
CH (i-Bu) SMe C (O) OMe
CH (i-Bu) SEt C (O) OMe
CH (i-Bu) S (O) Me C (O) OMe
CH (i-Bu) S (O) Et C (O) OMe
CH (i-Bu) S (O)₂Me C (O) OMe
CH (i-Bu) S (O)₂Et C (O) OMe
CH (s-Bu) SMe C (O) OMe
CH (s-Bu) SEt C (O) OMe
CH (s-Bu) S (O) Me C (O) OMe
CH (s-Bu) S (O) Et C (O) OMe
CH (s-Bu) S (O)₂Me C (O) OMe
CH (s-Bu) S (O)₂Et C (O) OMe
CH (t-Bu) SMe C (O) OMe
CH (t-Bu) SEt C (O) OMe
CH (t-Bu) S (O) Me C (O) OMe
CH (t-Bu) S (O) Et C (O) OMe
CH (t-Bu) S (O)₂Me C (O) OMe
CH (t-Bu) S (O)₂Et C (O) OMe
CH₂CH₂SMe C (O) OMe
CH₂CH₂SEt C (O) OMe
CH₂CH₂S (O)₂Me C (O) OMe
CH₂CH₂S (O)₂Et C (O) OMe
CH (Me) CH₂SMe C (O) OMe
CH (Me) CH₂SEt C (O) OMe
CH (Me) CH₂S (O) Me C (O) OMe
CH (Me) CH₂S (O) Et C (O) OMe
CH (Me) CH₂S (O)₂Me C (O) OMe
CH (Me) CH₂S (O)₂Et C (O) OMe
CH (Et) CH₂SMe C (O) OMe
CH (Et) CH₂SEt C (O) OMe
CH (Et) CH₂S (O) Me C (O) OMe
CH (Et) CH₂S (O) Et C (O) OMe
CH (Et) CH₂S (O)₂Me C (O) OMe
CH (Et) CH₂S (O)₂Et C (O) OMe
C (Me)₂CH₂SMe C (O) OMe
C (Me)₂CH₂SEt C (O) OMe
C (Me)₂CH₂S (O) Me C (O) OMe
C (Me)₂CH₂S (O) Et C (O) OMe
C (Me)₂CH₂S (O)₂Me C (O) OMe
C (Me)₂CH₂S (O)₂Et C (O) OMe
CH₂CH (Me) SMe C (O) OMe
CH₂CH (Me) SEt C (O) OMe
CH₂CH (Me) S (O) Me C (O) OMe
CH₂CH (Me) S (O) Et C (O) OMe
CH₂CH (Me) S (O)₂Me C (O) OMe
CH₂CH (Me) S (O)₂Et C (O) OMe
CH₂CH (Et) SMe C (O) OMe
CH₂CH (Et) SEt C (O) OMe
CH₂CH (Et) S (O) Me C (O) OMe
CH₂CH (Et) S (O) Et C (O) OMe
CH₂CH (Et) S (O)₂Me C (O) OMe
CH₂CH (Et) S (O)₂Et C (O) OMe
CH (Me) CH (Me) SMe C (O) OMe
CH (Me) CH (Me) SEt C (O) OMe
CH (Me) CH (Me) S (O) Me C (O) OMe
CH (Me) CH (Me) S (O) Et C (O) OMe
CH (Me) CH (Me) S (O)₂Me C (O) OMe
CH (Me) CH (Me) S (O)₂Et C (O) OMe
CH₂OMe CH₂SMe
CH₂OMe CH₂SEt
CH₂OMe CH₂SCF_Three
CH₂OMe CH₂SCH₂CF_Three
CH₂OMe CH₂S (O) Me
CH₂OMe CH₂S (O) Et
CH₂OMe CH₂S (O) CF_Three
CH₂OMe CH₂S (O) CH₂CF_Three
CH₂OMe CH₂S (O)₂Me
CH₂OMe CH₂S (O)₂Et
CH₂OMe CH₂S (O)₂CF_Three
CH₂OMe CH₂S (O)₂CH₂CF_Three
CH₂OMe CH (Me) SMe
CH₂OMe CH (Me) SEt
CH₂OMe CH (Me) SCF_Three
CH₂OMe CH (Me) SCH₂CF_Three
CH₂OMe CH (Me) S (O) Me
CH₂OMe CH (Me) S (O) Et
CH₂OMe CH (Me) S (O) CF_Three
CH₂OMe CH (Me) S (O) CH₂CF_Three
CH₂OMe CH (Me) S (O)₂Me
CH₂OMe CH (Me) S (O)₂Et
CH₂OMe CH (Me) S (O)₂CF_Three
CH₂OMe CH (Me) S (O)₂CH₂CF_Three
CH₂OMe CH (Et) SMe
CH₂OMe CH (Et) SEt
CH₂OMe CH (Et) SCF_Three
CH₂OMe CH (Et) SCH₂CF_Three
CH₂OMe CH (Et) S (O) Me
CH₂OMe CH (Et) S (O) Et
CH₂OMe CH (Et) S (O) CF_Three
CH₂OMe CH (Et) S (O) CH₂CF_Three
CH₂OMe CH (Et) S (O)₂Me
CH₂OMe CH (Et) S (O)₂Et
CH₂OMe CH (Et) S (O)₂CF_Three
CH₂OMe CH (Et) S (O)₂CH₂CF_Three
CH₂OMe CH (n-Pr) SMe
CH₂OMe CH (n-Pr) SEt
CH₂OMe CH (n-Pr) SCF_Three
CH₂OMe CH (n-Pr) SCH₂CF_Three
CH₂OMe CH (n-Pr) S (O) Me
CH₂OMe CH (n-Pr) S (O) Et
CH₂OMe CH (n-Pr) S (O) CF_Three
CH₂OMe CH (n-Pr) S (O) CH₂CF_Three
CH₂OMe CH (n-Pr) S (O)₂Me
CH₂OMe CH (n-Pr) S (O)₂Et
CH₂OMe CH (n-Pr) S (O)₂CF_Three
CH₂OMe CH (n-Pr) S (O)₂CH₂CF_Three
CH₂OMe CH (i-Pr) SMe
CH₂OMe CH (i-Pr) SEt
CH₂OMe CH (i-Pr) SCF_Three
CH₂OMe CH (i-Pr) SCH₂CF_Three
CH₂OMe CH (i-Pr) S (O) Me
CH₂OMe CH (i-Pr) S (O) Et
CH₂OMe CH (i-Pr) S (O) CF_Three
CH₂OMe CH (i-Pr) S (O) CH₂CF_Three
CH₂OMe CH (i-Pr) S (O)₂Me
CH₂OMe CH (i-Pr) S (O)₂Et
CH₂OMe CH (i-Pr) S (O)₂CF_Three
CH₂OMe CH (i-Pr) S (O)₂CH₂CF_Three
CH₂OMe CH (n-Bu) SMe
CH₂OMe CH (n-Bu) SEt
CH₂OMe CH (n-Bu) SCF_Three
CH₂OMe CH (n-Bu) SCH₂CF_Three
CH₂OMe CH (n-Bu) S (O) Me
CH₂OMe CH (n-Bu) S (O) Et
CH₂OMe CH (n-Bu) S (O) CF_Three
CH₂OMe CH (n-Bu) S (O) CH₂CF_Three
CH₂OMe CH (n-Bu) S (O)₂Me
CH₂OMe CH (n-Bu) S (O)₂Et
CH₂OMe CH (n-Bu) S (O)₂CF_Three
CH₂OMe CH (n-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (i-Bu) SMe
CH₂OMe CH (i-Bu) SEt
CH₂OMe CH (i-Bu) SCF_Three
CH₂OMe CH (i-Bu) SCH₂CF_Three
CH₂OMe CH (i-Bu) S (O) Me
CH₂OMe CH (i-Bu) S (O) Et
CH₂OMe CH (i-Bu) S (O) CF_Three
CH₂OMe CH (i-Bu) S (O) CH₂CF_Three
CH₂OMe CH (i-Bu) S (O)₂Me
CH₂OMe CH (i-Bu) S (O)₂Et
CH₂OMe CH (i-Bu) S (O)₂CF_Three
CH₂OMe CH (i-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (s-Bu) SMe
CH₂OMe CH (s-Bu) SEt
CH₂OMe CH (s-Bu) SCF_Three
CH₂OMe CH (s-Bu) SCH₂CF_Three
CH₂OMe CH (s-Bu) S (O) Me
CH₂OMe CH (s-Bu) S (O) Et
CH₂OMe CH (s-Bu) S (O) CF_Three
CH₂OMe CH (s-Bu) S (O) CH₂CF_Three
CH₂OMe CH (s-Bu) S (O)₂Me
CH₂OMe CH (s-Bu) S (O)₂Et
CH₂OMe CH (s-Bu) S (O)₂CF_Three
CH₂OMe CH (s-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (t-Bu) SMe
CH₂OMe CH (t-Bu) SEt
CH₂OMe CH (t-Bu) SCF_Three
CH₂OMe CH (t-Bu) SCH₂CF_Three
CH₂OMe CH (t-Bu) S (O) Me
CH₂OMe CH (t-Bu) S (O) Et
CH₂OMe CH (t-Bu) S (O) CF_Three
CH₂OMe CH (t-Bu) S (O) CH₂CF_Three
CH₂OMe CH (t-Bu) S (O)₂Me
CH₂OMe CH (t-Bu) S (O)₂Et
CH₂OMe CH (t-Bu) S (O)₂CF_Three
CH₂OMe CH (t-Bu) S (O)₂CH₂CF_Three
CH₂OMe CH (CF_ThreeSMe
CH₂OMe CH (CF_Three) SEt
CH₂OMe CH (CF_Three) SCF_Three
CH₂OMe CH (CF_Three) SCH₂CF_Three
CH₂OMe CH (CF_Three) S (O) Me
CH₂OMe CH (CF_Three) S (O) Et
CH₂OMe CH (CF_Three) S (O) CF_Three
CH₂OMe CH (CF_Three) S (O) CH₂CF_Three
CH₂OMe CH (CF_Three) S (O)₂Me
CH₂OMe CH (CF_Three) S (O)₂Et
CH₂OMe CH (CF_Three) S (O)₂CF_Three
CH₂OMe CH (CF_Three) S (O)₂CH₂CF_Three
CH₂OMe CH₂CH₂SMe
CH₂OMe CH₂CH₂SEt
CH₂OMe CH₂CH₂SCF_Three
CH₂OMe CH₂CH₂SCH₂CF_Three
CH₂OMe CH₂CH₂S (O) Me
CH₂OMe CH₂CH₂S (O) Et
CH₂OMe CH₂CH₂S (O) CF_Three
CH₂OMe CH₂CH₂S (O) CH₂CF_Three
CH₂OMe CH₂CH₂S (O)₂Me
CH₂OMe CH₂CH₂S (O)₂Et
CH₂OMe CH₂CH₂S (O)₂CF_Three
CH₂OMe CH₂CH₂S (O)₂CH₂CF_Three
CH₂OMe CH (Me) CH₂SMe
CH₂OMe CH (Me) CH₂SEt
CH₂OMe CH (Me) CH₂SCF_Three
CH₂OMe CH (Me) CH₂SCH₂CF_Three
CH₂OMe CH (Me) CH₂S (O) Me
CH₂OMe CH (Me) CH₂S (O) Et
CH₂OMe CH (Me) CH₂S (O) CF_Three
CH₂OMe CH (Me) CH₂S (O) CH₂CF_Three
CH₂OMe CH (Me) CH₂S (O)₂Me
CH₂OMe CH (Me) CH₂S (O)₂Et
CH₂OMe CH (Me) CH₂S (O)₂CF_Three
CH₂OMe CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂OMe CH (Et) CH₂SMe
CH₂OMe CH (Et) CH₂SEt
CH₂OMe CH (Et) CH₂SCF_Three
CH₂OMe CH (Et) CH₂SCH₂CF_Three
CH₂OMe CH (Et) CH₂S (O) Me
CH₂OMe CH (Et) CH₂S (O) Et
CH₂OMe CH (Et) CH₂S (O) CF_Three
CH₂OMe CH (Et) CH₂S (O) CH₂CF_Three
CH₂OMe CH (Et) CH₂S (O)₂Me
CH₂OMe CH (Et) CH₂S (O)₂Et
CH₂OMe CH (Et) CH₂S (O)₂CF_Three
CH₂OMe CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂OMe C (Me)₂CH₂SMe
CH₂OMe C (Me)₂CH₂SEt
CH₂OMe C (Me)₂CH₂SCF_Three
CH₂OMe C (Me)₂CH₂SCH₂CF_Three
CH₂OMe C (Me)₂CH₂S (O) Me
CH₂OMe C (Me)₂CH₂S (O) Et
CH₂OMe C (Me)₂CH₂S (O) CF_Three
CH₂OMe C (Me)₂CH₂S (O) CH₂CF_Three
CH₂OMe C (Me)₂CH₂S (O)₂Me
CH₂OMe C (Me)₂CH₂S (O)₂Et
CH₂OMe C (Me)₂CH₂S (O)₂CF_Three
CH₂OMe C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂OMe CH₂CH (Me) SMe
CH₂OMe CH₂CH (Me) SEt
CH₂OMe CH₂CH (Me) SCF_Three
CH₂OMe CH₂CH (Me) SCH₂CF_Three
CH₂OMe CH₂CH (Me) S (O) Me
CH₂OMe CH₂CH (Me) S (O) Et
CH₂OMe CH₂CH (Me) S (O) CF_Three
CH₂OMe CH₂CH (Me) S (O) CH₂CF_Three
CH₂OMe CH₂CH (Me) S (O)₂Me
CH₂OMe CH₂CH (Me) S (O)₂Et
CH₂OMe CH₂CH (Me) S (O)₂CF_Three
CH₂OMe CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂OMe CH₂CH (Et) SMe
CH₂OMe CH₂CH (Et) SEt
CH₂OMe CH₂CH (Et) SCF_Three
CH₂OMe CH₂CH (Et) SCH₂CF_Three
CH₂OMe CH₂CH (Et) S (O) Me
CH₂OMe CH₂CH (Et) S (O) Et
CH₂OMe CH₂CH (Et) S (O) CF_Three
CH₂OMe CH₂CH (Et) S (O) CH₂CF_Three
CH₂OMe CH₂CH (Et) S (O)₂Me
CH₂OMe CH₂CH (Et) S (O)₂Et
CH₂OMe CH₂CH (Et) S (O)₂CF_Three
CH₂OMe CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂OMe CH (Me) CH (Me) SMe
CH₂OMe CH (Me) CH (Me) SEt
CH₂OMe CH (Me) CH (Me) SCF_Three
CH₂OMe CH (Me) CH (Me) SCH₂CF_Three
CH₂OMe CH (Me) CH (Me) S (O) Me
CH₂OMe CH (Me) CH (Me) S (O) Et
CH₂OMe CH (Me) CH (Me) S (O) CF_Three
CH₂OMe CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂OMe CH (Me) CH (Me) S (O)₂Me
CH₂OMe CH (Me) CH (Me) S (O)₂Et
CH₂OMe CH (Me) CH (Me) S (O)₂CF_Three
CH₂OMe CH (Me) CH (Me) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH₂SMe
CH₂C (= NOMe) Me CH₂SEt
CH₂C (= NOMe) Me CH₂SCF_Three
CH₂C (= NOMe) Me CH₂SCH₂CF_Three
CH₂C (= NOMe) Me CH₂S (O) Me
CH₂C (= NOMe) Me CH₂S (O) Et
CH₂C (= NOMe) Me CH₂S (O) CF_Three
CH₂C (= NOMe) Me CH₂S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH₂S (O)₂Me
CH₂C (= NOMe) Me CH₂S (O)₂Et
CH₂C (= NOMe) Me CH₂S (O)₂CF_Three
CH₂C (= NOMe) Me CH₂S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (Me) SMe
CH₂C (= NOMe) Me CH (Me) SEt
CH₂C (= NOMe) Me CH (Me) SCF_Three
CH₂C (= NOMe) Me CH (Me) SCH₂CF_Three
CH₂C (= NOMe) Me CH (Me) S (O) Me
CH₂C (= NOMe) Me CH (Me) S (O) Et
CH₂C (= NOMe) Me CH (Me) S (O) CF_Three
CH₂C (= NOMe) Me CH (Me) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (Me) S (O)₂Me
CH₂C (= NOMe) Me CH (Me) S (O)₂Et
CH₂C (= NOMe) Me CH (Me) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (Me) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (Et) SMe
CH₂C (= NOMe) Me CH (Et) SEt
CH₂C (= NOMe) Me CH (Et) SCF_Three
CH₂C (= NOMe) Me CH (Et) SCH₂CF_Three
CH₂C (= NOMe) Me CH (Et) S (O) Me
CH₂C (= NOMe) Me CH (Et) S (O) Et
CH₂C (= NOMe) Me CH (Et) S (O) CF_Three
CH₂C (= NOMe) Me CH (Et) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (Et) S (O)₂Me
CH₂C (= NOMe) Me CH (Et) S (O)₂Et
CH₂C (= NOMe) Me CH (Et) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (Et) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (n-Pr) SMe
CH₂C (= NOMe) Me CH (n-Pr) SEt
CH₂C (= NOMe) Me CH (n-Pr) SCF_Three
CH₂C (= NOMe) Me CH (n-Pr) SCH₂CF_Three
CH₂C (= NOMe) Me CH (n-Pr) S (O) Me
CH₂C (= NOMe) Me CH (n-Pr) S (O) Et
CH₂C (= NOMe) Me CH (n-Pr) S (O) CF_Three
CH₂C (= NOMe) Me CH (n-Pr) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (n-Pr) S (O)₂Me
CH₂C (= NOMe) Me CH (n-Pr) S (O)₂Et
CH₂C (= NOMe) Me CH (n-Pr) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (n-Pr) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (i-Pr) SMe
CH₂C (= NOMe) Me CH (i-Pr) SEt
CH₂C (= NOMe) Me CH (i-Pr) SCF_Three
CH₂C (= NOMe) Me CH (i-Pr) SCH₂CF_Three
CH₂C (= NOMe) Me CH (i-Pr) S (O) Me
CH₂C (= NOMe) Me CH (i-Pr) S (O) Et
CH₂C (= NOMe) Me CH (i-Pr) S (O) CF_Three
CH₂C (= NOMe) Me CH (i-Pr) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (i-Pr) S (O)₂Me
CH₂C (= NOMe) Me CH (i-Pr) S (O)₂Et
CH₂C (= NOMe) Me CH (i-Pr) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (i-Pr) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (n-Bu) SMe
CH₂C (= NOMe) Me CH (n-Bu) SEt
CH₂C (= NOMe) Me CH (n-Bu) SCF_Three
CH₂C (= NOMe) Me CH (n-Bu) SCH₂CF_Three
CH₂C (= NOMe) Me CH (n-Bu) S (O) Me
CH₂C (= NOMe) Me CH (n-Bu) S (O) Et
CH₂C (= NOMe) Me CH (n-Bu) S (O) CF_Three
CH₂C (= NOMe) Me CH (n-Bu) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (n-Bu) S (O)₂Me
CH₂C (= NOMe) Me CH (n-Bu) S (O)₂Et
CH₂C (= NOMe) Me CH (n-Bu) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (n-Bu) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (i-Bu) SMe
CH₂C (= NOMe) Me CH (i-Bu) SEt
CH₂C (= NOMe) Me CH (i-Bu) SCF_Three
CH₂C (= NOMe) Me CH (i-Bu) SCH₂CF_Three
CH₂C (= NOMe) Me CH (i-Bu) S (O) Me
CH₂C (= NOMe) Me CH (i-Bu) S (O) Et
CH₂C (= NOMe) Me CH (i-Bu) S (O) CF_Three
CH₂C (= NOMe) Me CH (i-Bu) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (i-Bu) S (O)₂Me
CH₂C (= NOMe) Me CH (i-Bu) S (O)₂Et
CH₂C (= NOMe) Me CH (i-Bu) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (i-Bu) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (s-Bu) SMe
CH₂C (= NOMe) Me CH (s-Bu) SEt
CH₂C (= NOMe) Me CH (s-Bu) SCF_Three
CH₂C (= NOMe) Me CH (s-Bu) SCH₂CF_Three
CH₂C (= NOMe) Me CH (s-Bu) S (O) Me
CH₂C (= NOMe) Me CH (s-Bu) S (O) Et
CH₂C (= NOMe) Me CH (s-Bu) S (O) CF_Three
CH₂C (= NOMe) Me CH (s-Bu) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (s-Bu) S (O)₂Me
CH₂C (= NOMe) Me CH (s-Bu) S (O)₂Et
CH₂C (= NOMe) Me CH (s-Bu) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (s-Bu) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (t-Bu) SMe
CH₂C (= NOMe) Me CH (t-Bu) SEt
CH₂C (= NOMe) Me CH (t-Bu) SCF_Three
CH₂C (= NOMe) Me CH (t-Bu) SCH₂CF_Three
CH₂C (= NOMe) Me CH (t-Bu) S (O) Me
CH₂C (= NOMe) Me CH (t-Bu) S (O) Et
CH₂C (= NOMe) Me CH (t-Bu) S (O) CF_Three
CH₂C (= NOMe) Me CH (t-Bu) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (t-Bu) S (O)₂Me
CH₂C (= NOMe) Me CH (t-Bu) S (O)₂Et
CH₂C (= NOMe) Me CH (t-Bu) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (t-Bu) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (CF_ThreeSMe
CH₂C (= NOMe) Me CH (CF_Three) SEt
CH₂C (= NOMe) Me CH (CF_Three) SCF_Three
CH₂C (= NOMe) Me CH (CF_Three) SCH₂CF_Three
CH₂C (= NOMe) Me CH (CF_Three) S (O) Me
CH₂C (= NOMe) Me CH (CF_Three) S (O) Et
CH₂C (= NOMe) Me CH (CF_Three) S (O) CF_Three
CH₂C (= NOMe) Me CH (CF_Three) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (CF_Three) S (O)₂Me
CH₂C (= NOMe) Me CH (CF_Three) S (O)₂Et
CH₂C (= NOMe) Me CH (CF_Three) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (CF_Three) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH₂CH₂SMe
CH₂C (= NOMe) Me CH₂CH₂SEt
CH₂C (= NOMe) Me CH₂CH₂SCF_Three
CH₂C (= NOMe) Me CH₂CH₂SCH₂CF_Three
CH₂C (= NOMe) Me CH₂CH₂S (O) Me
CH₂C (= NOMe) Me CH₂CH₂S (O) Et
CH₂C (= NOMe) Me CH₂CH₂S (O) CF_Three
CH₂C (= NOMe) Me CH₂CH₂S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH₂CH₂S (O)₂Me
CH₂C (= NOMe) Me CH₂CH₂S (O)₂Et
CH₂C (= NOMe) Me CH₂CH₂S (O)₂CF_Three
CH₂C (= NOMe) Me CH₂CH₂S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH₂SMe
CH₂C (= NOMe) Me CH (Me) CH₂SEt
CH₂C (= NOMe) Me CH (Me) CH₂SCF_Three
CH₂C (= NOMe) Me CH (Me) CH₂SCH₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH₂S (O) Me
CH₂C (= NOMe) Me CH (Me) CH₂S (O) Et
CH₂C (= NOMe) Me CH (Me) CH₂S (O) CF_Three
CH₂C (= NOMe) Me CH (Me) CH₂S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH₂S (O)₂Me
CH₂C (= NOMe) Me CH (Me) CH₂S (O)₂Et
CH₂C (= NOMe) Me CH (Me) CH₂S (O)₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH₂S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (Et) CH₂SMe
CH₂C (= NOMe) Me CH (Et) CH₂SEt
CH₂C (= NOMe) Me CH (Et) CH₂SCF_Three
CH₂C (= NOMe) Me CH (Et) CH₂SCH₂CF_Three
CH₂C (= NOMe) Me CH (Et) CH₂S (O) Me
CH₂C (= NOMe) Me CH (Et) CH₂S (O) Et
CH₂C (= NOMe) Me CH (Et) CH₂S (O) CF_Three
CH₂C (= NOMe) Me CH (Et) CH₂S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (Et) CH₂S (O)₂Me
CH₂C (= NOMe) Me CH (Et) CH₂S (O)₂Et
CH₂C (= NOMe) Me CH (Et) CH₂S (O)₂CF_Three
CH₂C (= NOMe) Me CH (Et) CH₂S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me C (Me)₂CH₂SMe
CH₂C (= NOMe) Me C (Me)₂CH₂SEt
CH₂C (= NOMe) Me C (Me)₂CH₂SCF_Three
CH₂C (= NOMe) Me C (Me)₂CH₂SCH₂CF_Three
CH₂C (= NOMe) Me C (Me)₂CH₂S (O) Me
CH₂C (= NOMe) Me C (Me)₂CH₂S (O) Et
CH₂C (= NOMe) Me C (Me)₂CH₂S (O) CF_Three
CH₂C (= NOMe) Me C (Me)₂CH₂S (O) CH₂CF_Three
CH₂C (= NOMe) Me C (Me)₂CH₂S (O)₂Me
CH₂C (= NOMe) Me C (Me)₂CH₂S (O)₂Et
CH₂C (= NOMe) Me C (Me)₂CH₂S (O)₂CF_Three
CH₂C (= NOMe) Me C (Me)₂CH₂S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Me) SMe
CH₂C (= NOMe) Me CH₂CH (Me) SEt
CH₂C (= NOMe) Me CH₂CH (Me) SCF_Three
CH₂C (= NOMe) Me CH₂CH (Me) SCH₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Me) S (O) Me
CH₂C (= NOMe) Me CH₂CH (Me) S (O) Et
CH₂C (= NOMe) Me CH₂CH (Me) S (O) CF_Three
CH₂C (= NOMe) Me CH₂CH (Me) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Me) S (O)₂Me
CH₂C (= NOMe) Me CH₂CH (Me) S (O)₂Et
CH₂C (= NOMe) Me CH₂CH (Me) S (O)₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Me) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Et) SMe
CH₂C (= NOMe) Me CH₂CH (Et) SEt
CH₂C (= NOMe) Me CH₂CH (Et) SCF_Three
CH₂C (= NOMe) Me CH₂CH (Et) SCH₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Et) S (O) Me
CH₂C (= NOMe) Me CH₂CH (Et) S (O) Et
CH₂C (= NOMe) Me CH₂CH (Et) S (O) CF_Three
CH₂C (= NOMe) Me CH₂CH (Et) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Et) S (O)₂Me
CH₂C (= NOMe) Me CH₂CH (Et) S (O)₂Et
CH₂C (= NOMe) Me CH₂CH (Et) S (O)₂CF_Three
CH₂C (= NOMe) Me CH₂CH (Et) S (O)₂CH₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH (Me) SMe
CH₂C (= NOMe) Me CH (Me) CH (Me) SEt
CH₂C (= NOMe) Me CH (Me) CH (Me) SCF_Three
CH₂C (= NOMe) Me CH (Me) CH (Me) SCH₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O) Me
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O) Et
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O) CF_Three
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O) CH₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O)₂Me
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O)₂Et
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O)₂CF_Three
CH₂C (= NOMe) Me CH (Me) CH (Me) S (O)₂CH₂CF_Three
――――――――――――――――――
  The compounds of the present invention are stored in warehouses, so-called agricultural pests that harm agricultural and horticultural crops and trees, so-called livestock pests that parasitize livestock and poultry, so-called sanitary pests that cause various adverse effects in the human living environment such as houses. It is possible to effectively control insects such as so-called stored grain pests that harm cereals and the like, and pests such as mites, crustaceans, molluscs, and nematodes that occur and harm in similar situations at low concentrations.

本発明化合物を用いて防除しうる昆虫類、ダニ類、甲殻類、軟体動物及び線虫類には具体的に、例えば、
チャノコカクモンハマキ(Adoxophyes honmai)、リンゴコカクモンハマキ(Adoxophyes orana faciata)、リンゴモンハマキ(Archips breviplicanus)、ミダレカクモンハマキ(Archips fuscocupreanus)、ナシヒメシンクイ(Grapholita molesta)、チャハマキ(Homona magnanima)、マメシンクイガ(Leguminivora glycinivorella)、マメヒメサヤムシガ(Matsumuraeses phaseoli)、トビハマキ(Pandemis heparana)、ナシチビガ(Bucculatrix pyrivorella)、モモハモグリガ(Lyonetia clerkella)、ギンモンハモグリガ(Lyonetia prunifoliella malinella)、チャノホソガ(Caloptilia theivora)、キンモンホソガ(Phyllonorycter ringoniella)、ミカンハモグリガ(Phyllocnistis citrella)、ネギコガ(Acrolepiopsis sapporensis)、ヤマノイモコガ(Acrolepiopsis suzukiella)、コナガ(Plutella xylostella)、カキノヘタムシガ(Stathmopoda masinissa)、イモキバガ(Helcystogramma triannulella)、ワタアカミムシ(Pectinophora gossypiella)、モモシンクイガ(Carposina sasakii)、コドリンガ(Cydla pomonella)、ニカメイガ(Chilo suppressalis)、コブノメイガ(Cnaphalocrocis medinalis)、モモノゴマダラノメイガ(Conogethes punctiferalis)、ワタヘリクロノメイガ(Diaphania indica)、シロイチモジマダラメイガ(Etiella zinckenella)、クワノメイガ(Glyphodes pyloalis)、ハイマダラノメイガ(Hellula undalis)、アワノメイガ(Ostrinia furnacalis)、アズキノメイガ(Ostrinia scapulalis)、ヨーロピアンコーンボーラー(Ostrinia nubilalis)、シバツトガ(Parapediasia teterrella)、イチモンジセセリ(Parnara guttata)、オオモンシロチョウ(Pieris brassicae)、モンシロチョウ(Pieris rapae crucivora)、ヨモギエダシャク(Ascotis selenaria)、ソイビーンルーパー(Pseudoplusia includens)、チャドクガ(Euproctis pseudoconspersa)、マイマイガ(Lymantria dispar)、ヒメシロモンドクガ(Orgyia thyellina)、アメリカシロヒトリ(Hyphantria cunea)、クワゴマダラヒトリ(Lemyra imparilis)、アケビコノハ(Adris tyrannus)、ナカジロシタバ(Aedia leucomelas)、タマナヤガ(Agrotis ipsilon)、カブラヤガ(Agrotis segetum)、タマナギンウワバ(Autographa nigrisigna)、ミツモンキンウワバ(Ctenoplusia agnata)、オオタバコガ(Helicoverpa armigera)、タバコガ(Helicoverpa assulta)、コットンボールワーム(Helicoverpa zea)、タバコバッドワーム(Heliothis virescens)、ヨトウガ(Mamestra brassicae)、アワヨトウ(Mythimna separata)、フタオビコヤガ(Naranga aenescens)、サザンアーミーワーム(Spodoptera eridania)、シロイチモジヨトウ(Spodoptera exigua)、フォールアーミーワーム(Spodoptera frugiperda)、コットンリーフワーム(Spodoptera littoralis)、ハスモンヨトウ(Spodoptera litura)、スジキリヨトウ(Spodoptera depravata)、イラクサギンウワバ(Trichoplusia ni)、グレープベリーモス(Endopiza viteana)、トマトホーンワーム(Manduca quinquemaculata)、タバコホーンワーム(Manduca sexta)等の鱗翅目昆虫、
ヒラズハナアザミウマ(Frankliniella intonsa)、ミカンキイロアザミウマ(Frankliniella occidentalis)、クロトンアザミウマ(Heliothrips haemorrhoidalis)、チャノキイロアザミウマ(Scirtothrips dorsalis)、ミナミキイロアザミウマ(Thrips palmi)、ネギアザミウマ(Thrips tabaci)、カキクダアザミウマ(Ponticulothrips diospyrosi)等の総翅目昆虫、
ブチヒゲカメムシ(Dolycoris baccarum)、ナガメ(Eurydema rugosum)、トゲシラホシカメムシ(Eysarcoris aeneus)、オオトゲシラホシカメムシ(Eysarcoris lewisi)、シラホシカメムシ(Eysarcoris ventralis)、ツヤアオカメムシ(Glaucias subpunctatus)、クサギカメムシ(Halyomorpha halys)、アオクサカメムシ(Nezara antennata)、ミナミアオカメムシ(Nezara viridula)、イチモンジカメムシ(Piezodorus hybneri)、チャバネアオカメムシ(Plautia crossota)、イネクロカメムシ(Scotinophora lurida)、ホソハリカメムシ(Cletus punctiger)、クモヘリカメムシ(Leptocorisa chinensis)、ホソヘリカメムシ(Riptortus clavatus)、アカヒメヘリカメムシ(Rhopalus msculatus)、カンシャコバネナガカメムシ(Cavelerius saccharivorus)、コバネヒョウタンナガカメムシ(Togo hemipterus)、アカホシカメムシ(Dysdercus cingulatus)、ツツジグンバイ(Stephanitis pyrioides)、クロトビカスミカメ(Halticus insularis)、ターニッシュドプラントバグ(Lygus lineolaris)、ナガムギカスミカメ(Stenodema sibiricum)、アカスジカスミカメ(Stenotus rubrovittatus)、イネホソミドリカスミカメ(Trigonotylus caelestialium)、フタテンヒメヨコバイ(Arboridia apicalis)、ミドリナガヨコバイ(Balclutha saltuella)、フタテンオオヨコバイ(Epiacanthus stramineus)、ポテトリーフホッパー(Empoasca fabae)、カキノヒメヨコバイ(Empoasca nipponica)、チャノミドリヒメヨコバイ(Empoasca onukii)、マメノミドリヒメヨコバイ(Empoasca sakaii)、ヒメフタテンヨコバイ(Macrosteles striifrons)、ツマグロヨコバイ(Nephotettix cinctinceps)、コットンフリーホッパー(Psuedatomoscelis seriatus)、ヒメトビウンカ(Laodelphax striatella)、トビイロウンカ(Nilaparvata lugens)、セジロウンカ(Sogatella furcifera)、ミカンキジラミ(Diaphorina citri)、ナシキジラミ(Psylla pyrisuga)、ミカントゲコナジラミ(Aleurocanthus spiniferus)、シルバーリーフコナジラミ(Bemisia argentifolii)、タバココナジラミ(Bemisia tabaci)、ミカンコナジラミ(Dialeurodes citri)、オンシツコナジラミ(Trialeurodes vaporariorum)、ブドウネアブラムシ(Viteus vitifolii)、ワタアブラムシ(Aphis gossypii)、ユキヤナギアブラムシ(Aphis spiraecola)、モモアカアブラムシ(Myzus persicae)、コミカンアブラムシ(Toxoptera aurantii)、オオワラジカイガラムシ(Drosicha corpulenta)、イセリアカイガラムシ(Icerya purchasi)、ナスコナカイガラムシ(Phenacoccus solani)、ミカンコナカイガラムシ(Planococcus citri)、フジコナカイガラムシ(Planococcus kuraunhiae)、クワコナカイガラムシ(Pseudococcus comstocki)、ツノロウムシ(Ceroplastes ceriferus)、ルビーロウムシ(Ceroplastes rubens)、アカマルカイガラムシ(Aonidiella aurantii)、ナシマルカイガラムシ(Comstockaspis perniciosa)、ティースケール(Fiorinia theae)、チャノマルカイガラムシ(Pseudaonidia paeoniae)、クワシロカイガラムシ(Pseudaulacaspis pentagona)、ウメシロカイガラムシ(Pseudaulacaspis prunicola)、マサキナガカイガラムシ(Unaspis euonymi)、ヤノネカイガラムシ(Unaspis yanonensis)、トコジラミ(Cimex lectularius)等の半翅目昆虫、
ドウガネブイブイ(Anomala cuprea)、ヒメコガネ(Anomala rufocuprea)、コアオハナムグリ(Gametis jucunda)、ナガチャコガネ(Heptophylla picea)、マメコガネ(Popillia japonica)、コロラドポテトビートル(Lepinotarsa decemlineata)、マルクビクシコメツキ(Melanotus fortnumi)、カンシャクシコメツキ(Melanotus tamsuyensis)、タバコシバンムシ(Lasioderma serricorne)、ヒメヒラタケシキスイ(Epuraea domina)、インゲンテントウ(Epilachna varivestis)、ニジュウヤホシテントウ(Epilachna vigintioctopunctata)、チャイロコメノゴミムシダマシ(Tenebrio molitor)、コクヌストモドキ(Tribolium castaneum)、ゴマダラカミキリ(Anoplophora malasiaca)、マツノマダラカミキリ(Monochamus alternatus)、キボシカミキリ(Psacothea hilaris)、ブドウトラカミキリ(Xylotrechus pyrrhoderus)、アズキゾウムシ(Callosobruchus chinensis)、ウリハムシ(Aulacophora femoralis)、テンサイトビハムシ(Chaetocnema concinna)、サザンコーンルートワーム(Diabrotica undecimpunctata)、ウエスタンコーンルートワーム(Diabrotica virgifera)、ノーザンコーンルートワーム(Diabrotica barberi)、イネドロオイムシ(Oulema oryzae)、キスジノミハムシ(Phyllotreta striolata)、ナスナガスネトビハムシ(Psylliodes angusticollis)、モモチョッキリゾウムシ(Rhynchites heros)、アリモドキゾウムシ(Cylas formicarius)、ワタミゾウムシ(Anthonomus grandis)、イネゾウムシ(Echinocnemus squameus)、イモゾウムシ(Euscepes postfasciatus)、アルファルファタコゾウムシ(Hypera postica)、イネミズゾウムシ(Lissohoptrus oryzophilus)、キンケクチブトゾウムシ(Otiorhynchus sulcatus)、グラナリーウィービル(Sitophilus granarius)、コクゾウムシ(Sitophilus zeamais)、シバオサゾウムシ(Sphenophorus venatus vestitus)、アオバアリガタハネカクシ(Paederus fuscipes)等の鞘翅目昆虫、
ダイズサヤタマバエ(Asphondylia yushimai)、ムギアカタマバエ(Sitodiplosis mosellana)、ウリミバエ(Bactrocera cucurbitae)、ミカンコミバエ(Bactrocera dorsalis)、チチュウカイミバエ(Ceratitis capitata)、イネヒメハモグリバエ(Hydrellia griseola)、オウトウショウジョウバエ(Drosophila suzukii)、イネハモグリバエ(Agromyza oryzae)、ナモグリバエ(Chromatomyia horticola)、ナスハモグリバエ(Liriomyza bryoniae)、ネギハモグリバエ(Liriomyza chinensis)、トマトハモグリバエ(Liriomyza sativae)、マメハモグリバエ(Liriomyza trifolii)、タネバエ(Delia platura)、テンサイモグリハナバエ(Pegomya cunicularia)、アップルマゴット(Rhagoletis pomonella)、ヘシアンフライ(Mayetiola destructor)、イエバエ(Musca domestica)、サシバエ(Stomoxys calcitrans)、ヒツジシラミバエ(Melophagus ovinus)、ウシバエ(Hypoderma bovis)、キスジウシバエ(Hypoderma lineatum)、ヒツジバエ(Oestrus ovis)、ツェツェバエ(Glossina palpalis, Glossina morsitans)、キアシオオブユ(Prosimulium yezoensis)、ウシアブ(Tabanus trigonus)、オオチョウバエ(Telmatoscopus albipunctatus)、トクナガヌカカ(Leptoconops nipponensis)、アカイエカ(Culex pipiens pallens)、ネッタイシマカ(Aedes aegypti)、ヒトスジシマカ(Aedes albopicutus)、シナハマダラカ(Anopheles hyracanus sinesis)等の双翅目昆虫、
クリハバチ(Apethymus kuri)、カブラハバチ(Athalia rosae)、チュウレンジハバチ(Arge pagana)、マツノキハバチ(Neodiprion sertifer)、クリタマバチ(Dryocosmus kuriphilus)、グンタイアリ(Eciton burchelli, Eciton schmitti)、クロオオアリ(Camponotus japonicus)、オオスズメバチ(Vespa mandarina)、ブルドックアント(Myrmecia spp.)、ファイヤーアント類(Solenopsis spp.)、ファラオアント(Monomorium pharaonis)等の膜翅目昆虫、
エンマコオロギ(Teleogryllus emma)、ケラ(Gryllotalpa orientalis)、トノサマバッタ(Locusta migratoria)、コバネイナゴ(Oxya yezoensis)、サバクワタリバッタ(Schistocerca gregaria)等の直翅目昆虫、
トゲナシシロトビムシ(Onychiurus folsomi)、シベリアシロトビムシ(Onychiurus sibiricus)、キボシマルトビムシ(Bourletiella hortensis)等の粘管目昆虫、
クロゴキブリ(Periplaneta fuliginosa)、ヤマトゴキブリ(Periplaneta japonica)、チャバネゴキブリ(Blattella germanica)等の網翅目昆虫、
イエシロアリ(Coptotermes formosanus)、ヤマトシロアリ(Reticulitermes speratus)、タイワンシロアリ(Odontotermes formosanus)等のシロアリ目昆虫、
ネコノミ(Ctenocephalidae felis)、イヌノミ（Ctenocephalides canis)、ニワトリノミ（Echidnophaga gallinacea)、ヒトノミ(Pulex irritans)、ケオプスネズミノミ(Xenopsylla cheopis)等の等翅目昆虫、
ニワトリオオハジラミ(Menacanthus stramineus)、ウシハジラミ(Bovicola bovis)等のハジラミ目昆虫、
ウシジラミ(Haematopinus eurysternus)、ブタジラミ(Haematopinus suis)、ウシホソジラミ(Linognathus vituli)、ケブカウシジラミ(Solenopotes capillatus)等のシラミ目昆虫、
シクラメンホコリダニ(Phytonemus pallidus)、チャノホコリダニ(Polyphagotarsonemus latus)、スジブトホコリダニ(Tarsonemus bilobatus)等のホコリダニ類、
ハクサイダニ(Penthaleus erythrocephalus)、ムギダニ(Penthaleus major)等のハシリダニ類、
イネハダニ(Oligonychus shinkajii)、ミカンハダニ(Panonychus citri)、クワオオハダニ(Panonychus mori)、リンゴハダニ(Panonychus ulmi)、カンザワハダニ(Tetranychus kanzawai)、ナミハダニ(Tetranychus urticae)等のハダニ類、
チャノナガサビダニ(Acaphylla theavagrans)、チューリップサビダニ(Aceria tulipae)、トマトサビダニ(Aculops lycopersici)、ミカンサビダニ(Aculops pelekassi)、リンゴサビダニ(Aculus schlechtendali)、ニセナシサビダニ(Eriophyes chibaensis)、シトラスラストマイト(Phyllocoptruta oleivora)等のフシダニ類、
ロビンネダニ(Rhizoglyphus robini)、ケナガコナダニ(Tyrophagus putrescentiae)、ホウレンソウケナガコナダニ(Tyrophagus similis)等のコナダニ類、
ミツバチヘギイタダニ(Varroa jacobsoni)等のハチダニ類、
オウシマダニ(Boophilus microplus)、クリイロコイタマダニ(Rhipicephalus sanguineus)、フタトゲチマダニ(Haemaphysalis longicornis)、キチマダニ(Haemophysalis flava)、ツリガネチマダニ(Haemophysalis campanulata)、ヤマトマダニ(Ixodes ovatus)、シュルツェマダニ(Ixodes persulcatus)、オオマダニ(Amblyomma spp.)、アミメマダニ(Dermacentor spp.)等のマダニ類、
イヌツメダニ(Cheyletiella yasguri)、ネコツメダニ(Cheyletiella blakei)等のツメダニ類、
イヌニキビダニ(Demodex canis)、ネコニキビダニ(Demodex cati)などのニキビダニ類、
ヒツジキュウセンダニ(Psoroptes ovis)等のキュウセンダニ類、
センコウヒゼンダニ(Sarcoptes scabiei)、ネコショウセンコウヒゼンダニ(Notoedres cati)、ニワトリヒゼンダニ(Knemidocoptes spp.)等のヒゼンダニ類、
オカダンゴムシ(Armadillidium vulgare)等の甲殻類、
スクミリンゴガイ(Pomacea canaliculata)、アフリカマイマイ(Achatina fulica)、ナメクジ(Meghimatium bilineatum)、チャコウラナメクジ(Limax Valentiana)、ウスカワマイマイ(Acusta despecta sieboldiana)、ミスジマイマイ(Euhadra peliomphala)等の腹足類、
ミナミネグサレセンチュウ(Prathylenchus coffeae)、キタネグサレセンチュウ(Prathylenchus penetrans)、クルミネグサレセンチュウ(Prathylenchus vulnus)、ジャガイモシストセンチュウ(Globodera rostochiensis)、ダイズシストセンチュウ(Heterodera glycines)、キタネコブセンチュウ(Meloidogyne hapla)、サツマイモネコブセンチュウ(Meloidogyne incognita)、イネシンガレセンチュウ(Aphelenchoides besseyi)、マツノザイセンチュウ(Bursaphelenchus xylophilus)等の線虫類、
等が挙げられるが、本発明はこれらのみに限定されるものではない。 Specific examples of insects, mites, crustaceans, molluscs and nematodes that can be controlled using the compounds of the present invention include:
Adoxophyes honmai, Adoxophyes orana faciata, Archips breviplicanus, Archips fuscocupreanus, Grapholita molesta, Chama magnan Leguminivora glycinivorella), Matsumuraeses phaseoli, Pandemis heparana, Bucculatrix pyrivorella, Lyonetia clerkella, Lyonetia prunifal ringoniella), mandarin leaf moth (Phyllocnistis citrella), green moth (Acrolepiopsis sapporensis), wild moth (Acrolepiopsis suzukiella), black moth (Plutella xylostella), oyster leaf moth (Stathmopoda masinissa), cystogram tria ora gossypiella), peach sinker moth (Carposina sasakii), codling moth (Cydla pomonella), green moth (Chilo suppressalis), corn borer (Cnaphalocrocis medinalis), peach moth (Conogethes punctiferalis), cotton moth (Dia) (Etiella zinckenella), Glyphodes pyloalis, Hellula undalis, Ostrinia furnacalis, Ostrinia scapulalis, European corn borer (Ostrinia nubilaliseter, Pesta pal) ), White-tailed butterfly (Pieris brassicae), white-tailed butterfly (Pieris rapae crucivora), mugwort (Ascotis selenaria), soy bean looper (Pseudoplusia includens), chadokuga (Euproctis pseudoconspersa), maimaiga (Lymantria disparia), thymeina ), White-spotted starfish (Hyphantria cunea), white-spotted starfish (Lemyra imparilis), Akebiko-no-ha (Adris tyrannus), red-footed butterfly (Aedia leucomelas), red-footed squirrel (Agrotis ipsilon), red-tailed squirrel (Agrotis segetum) Uwaba (Ctenoplusia agnata), Helicoverpa armigera, Tobacco moth (Helicoverpa assulta), Cotton ball worm (Helicoverpa zea), Tobacco bad worm (Heliothis virescens), Mamestra brassicae, Mythimna naa ), Southern army worm (Spodoptera eridania), Spodoptera exigua, Fall army worm (Spodoptera frugiperda), Cotton leaf worm (Spodoptera littoralis), Spodoptera litura, Spodoptera litura, Spodoptera era ), Leeb Berry Moss (Endopiza viteana), tomato horn worm (Manduca quinquemaculata), tobacco horn worm (Manduca sexta) lepidopteran insects such as,
Thrips thrips (Frankliniella intonsa), Citrus thrips (Frankliniella occidentalis), Croton thrips (Prithia thrips) The total insect of the
Spotted beetle (Dolycoris baccarum), sea turtle (Eurydema rugosum), bark beetle (Eysarcoris aeneus), horseshoe beetle (Eysarcoris lewisi), white-headed beetle (Eysarcoris ventralis), subtilus , Nezara antennata, Nezara viridula, Piezodorus hybneri, Plautia crossota, Scotinophora lurida, tiger C Stink bug (Leptocorisa chinensis), Hoso-heli beetle (Riptortus clavatus), Red-headed beetle (Rhopalus msculatus), Cavelerius saccharivorus, Toba hemipterus cus, Togo hemipterus (Stephanitis pyrioides), Kuroto Bikasumi turtle (Halticus insularis), Turned plant bug (Lygus lineolaris), Nagamu sika turtle (Stenodema sibiricum), Akasika sika turtle (Stenotus rubrovittatus), Rice moss turtle (Trigonotylus caelestialium), ical Arisbori dia Green leafhopper (Balclutha saltuella), butterfly leafhopper (Epiacanthus stramineus), potato leaf hopper (Empoasca fabae), oyster leafhopper (Empoasca nipponica), Chanomidorimempei (Empoasca onukii), omenosaka ), Leafhopper leafhopper (Macrosteles striifrons), leafhopper leafhopper (Nephotettix cinctinceps), cotton-free hopper (Psuedatomoscelis seriatus), leafhopper (Laodelphax striatella), leafhopper (Nilaparvata lugens) Psylla pyrisuga, Aleurocanthus spiniferus, Silver leaf whitefly (Bemisia argentifolii), Tobacco whitefly (Bemisia tabaci), Citrus whitefly (Dialeurodes citri), Onsitsuna whitefly (trialeurous grape rum, Trialeurodes vapor Cotton Aphid (Aphis gossypii), Snowy Aphid (Aphis spiraecola), Peach Aphid (Myzus persicae), Komikan Aphid (Toxoptera aurantii), Alaska Scale Aphid (Drosicha corpulenta), Iceria scale P solani), citrus scale insect (Planococcus citri), stag beetle scale (Planococcus kuraunhiae), stag beetle scale (Pseudococcus comstocki), horn beetle (Ceroplastes ceriferus), ruby rotum (Ceroplastes rubens), red scallop Nymphalidae (Comstockaspis perniciosa), tea scale (Fiorinia theae), chanomarine scale insect (Pseudaonidia paeoniae), stag beetle (Pseudaulacaspis pentagona), scallop scale (Pseudaulacaspis prunicola), euglena (Unaspis yanonensis), Hemiptera insects such as Cimex lectularius,
Douganebubui (Anomala cuprea), Japanese common squirrel (Anomala rufocuprea), Core ohanamuri (Gametis jucunda), Nagachakogane (Heptophylla picea), Japanese beetle (Popillia japonica), Colorado potato beetle (Lepinotarsa decemlineata) White-footed beetle (Melanotus tamsuyensis), Tobacco beetle (Lasioderma serricorne), Himetaketakekisui (Epuraea domina), Green beetle (Epilachna varivestis), Nijuya-hoshi-tento (Epilachna vigintioctopunctata), T. Tribolium castaneum, Anoplophora malasiaca, Monochamus alternatus, Psacothea hilaris, Xylotrechus pyrrhoderus, callosobruchus, Callosobruchus Western Root beetle (Chaetocnema concinna), Southern corn root worm (Diabrotica undecimpunctata), Western corn root worm (Diabrotica virgifera), Northern corn root worm (Diabrotica barberi), Inedro beetle (Oulema oryzae), Phyllotreta nastriatum, Phyllotreta striol Tobet beetle (Psylliodes angusticollis), peach weevil (Rhynchites heros), aphid weevil (Cylas formicarius), cotton weevil (Anthonomus grandis), weevil (Echinocnemus squameus), weevil (Euscepes postfasciatus) Rice weevil (Lissohoptrus oryzophilus), horned weevil (Otiorhynchus sulcatus), granary weevil (Sitophilus granarius), hornet weevil (Sitophilus zeamais), bark weevil (Sphenophorus venatus vestitus moth) erus fuscipes), etc.
Soybean flies (Asphondylia yushimai), mud wings (Sitodiplosis mosellana), fruit flies (Bactrocera cucurbitae), citrus fruit flies (Bactrocera dorsalis), citrus fruit flies (Ceratitis capitata), rice moth flies Leafhopper (Agromyza oryzae), Leafworm (Chromatomyia horticola), Eggplant leaffly (Liriomyza bryoniae), Leafhopper (Liriomyza chinensis), Tomato leaffly (Liriomyza sativae), Beanworm (Liriomyza trifoli), Liriomyza trifoli (Pegomya cunicularia), apple haggot (Rhagoletis pomonella), hessian fly (Mayetiola destructor), housefly (Musca domestica), barn fly (Stomoxys calcitrans), sheep flies (Melophagus ovinus), bullflies (Hypoderma bovisma), , Sheep flies (Oestrus ovis), tsetse flies (Glossina palpalis, Glossina morsitans), black-headed ayu (Prosimulium yezoensis), bullfly (Tabanus trigonus), giant fly (Telmatoscopus albipunctatus), nipponen sip (Leptocons) Diptera, such as Aedes aegypti), Aedes albopicutus, Anopheles hyracanus sinesis,
Bumblebee (Apethymus kuri), Bumblebee (Athalia rosae), Bumblebee (Arge pagana), Bumblebee (Neodiprion sertifer), Bumblebee (Dryocosmus kuriphilus), Gantai (Eciton burchelli, Eciton schmitus), Eciton burchelli, Eciton schmitus mandarina), bulldog ant (Myrmecia spp.), fire ant (Solenopsis spp.), pharaoh ant (Monomorium pharaonis), etc.
Straight-legged insects, such as Teleogryllus emma, Kera (Gryllotalpa orientalis), Tosama grasshopper (Locusta migratoria), Oxya yezoensis, Sabaquat grasshopper (Schistocerca gregaria),
Coleoptera insects such as the white-headed beetle (Onychiurus folsomi), the Siberian white-headed beetle (Onychiurus sibiricus), the Bourletiella hortensis,
Reticulate insects such as black cockroach (Periplaneta fuliginosa), cockroach (Periplaneta japonica), German cockroach (Blattella germanica),
Termite insects such as the termites (Coptotermes formosanus), Yamato termites (Reticulitermes speratus), Taiwan termites (Odontotermes formosanus),
Insect insects such as cat fleas (Ctenocephalidae felis), dog fleas (Ctenocephalides canis), chicken fleas (Echidnophaga gallinacea), human fleas (Pulex irritans), keops mouse fleas (Xenopsylla cheopis),
Insects such as chicken lice (Menacanthus stramineus) and bovine lice (Bovicola bovis),
Lice insects such as cattle lice (Haematopinus eurysternus), pig lice (Haematopinus suis), cattle white lice (Linognathus vituli), horned lice (Solenopotes capillatus),
Dust mites such as cyclamen dust mite (Phytonemus pallidus), chano dust mite (Polyphagotarsonemus latus), red mite dust mite (Tarsonemus bilobatus),
Spider mites (Penthaleus erythrocephalus), wheat mites (Penthaleus major), etc.
Spider mites such as rice spider mite (Oligonychus shinkajii), citrus spider mite (Panonychus citri), blue spider mite (Panonychus mori), apple spider mite (Panonychus ulmi), Kanzawa spider mite (Tetranychus kanzawai), spider mite (Tetranychus urticae), etc.
Chinese cabbage mite (Acaphylla theavagrans), tulip rust mite (Aceria tulipae), tomato rust mite (Aculops lycopersici), citrus red mite (Aculops pelekassi), apple rust mite (Aculus schlechtendali), black rust mite (Eriophyes chitrastrostrum) ), Etc.,
Acarids such as robin mite (Rhizoglyphus robini), mushroom mite (Tyrophagus putrescentiae), spinach mushroom mite (Tyrophagus similis),
Bee mites such as honeybee mite (Varroa jacobsoni),
Tick tick (Boophilus microplus), Rhipicephalus sanguineus, Tick tick (Haemaphysalis longicornis), Tick tick (Haemophysalis flava), Tick tick (Haemophysalis campanulata), Tick tick (Ixo tus tick) Amblyomma spp.), Ticks such as Dermacentor spp.
Claw mites (Cheyletiella yasguri), claw mites (Cheyletiella blakei),
Acne mites, such as Inodecarid mites (Demodex canis), Feline mites (Demodex cati),
Cucumber mites such as sheep cucumber mites (Psoroptes ovis),
Spider mites, such as Sarcoptes scabiei, Caterpillar spider mite (Notoedres cati), Chicken spider mite (Knemidocoptes spp.),
Crustaceans such as the armadillum (Armadillidium vulgare),
Gastropods such as Pomacea canaliculata, African mussel (Achatina fulica), Slug (Meghimatium bilineatum), Chaukoura slug (Limax Valentiana), Uskawamai (Acusta despecta sieboldiana), Mishamai mai (Euhadra peliomphala), etc.
Southern nematode nematode (Prathylenchus coffeae), Kitane-negususa nematode (Prathylenchus penetrans), Kurume rushes nematode (Prathylenchus vulnus), potato cyst nematode (Globodera rostochiensis), soybean cyst nematode (Heterodera lypter Nematodes such as root-knot nematode (Meloidogyne incognita), rice-spotted nematode (Aphelenchoides besseyi), pine wood nematode (Bursaphelenchus xylophilus),
However, the present invention is not limited to these examples.

また、本発明化合物を用いて防除しうる家畜、家禽、愛玩動物等の内部寄生虫としては具体的に、例えば、
ヘモンクス属(Haemonchus)、トリコストロンギルス属(Trichostrongylus)、オステルターギヤ属(Ostertagia)、ネマトディルス属(Nematodirus)、クーペリア属(Cooperia)、アスカリス属(Ascaris)、ブノストムーム属(Bunostomum)、エスファゴストムーム属(Oesophagostomum)、チャベルチア属(Chabertia)、トリキュリス属(Trichuris)、ストロンギルス属(Storongylus)、トリコネマ属(Trichonema)、ディクチオカウルス属(Dictyocaulus)、キャピラリア属(Capillaria)、ヘテラキス属(Heterakis)、トキソカラ属(Toxocara)、アスカリディア属(Ascaridia)、オキシウリス属(Oxyuris)、アンキロストーマ属(Ancylostoma)、ウンシナリア属(Uncinaria)、トキサスカリス属(Toxascaris)、パラスカリス属(Parascaris)などの線虫類、
ブツヘレリア属(Wuchereria)、ブルージア属(Brugia)、オンコセルカ属(Onchoceca)、ディロフィラリア属(Dirofilaria)、ロア糸状虫属(Loa)などのフィラリア科(Filariidae)線虫類、
ドラクンクルス属(Deacunculus)などの蛇状線虫科(Dracunculidae)線虫類、
犬条虫(Dipylidium caninum)、猫条虫(Taenia taeniaeformis)、有鉤条虫(Taenia solium)、無鉤条虫(Taenia saginata)、縮小条虫(Hymenolepis diminuta)、ベネデン条虫(Moniezia benedeni)、広節裂頭条虫(Diphyllobothrium latum)、マンソン裂頭条虫(Diphyllobothrium erinacei)、単包条虫(Echinococcus granulosus)、多包条虫(Echinococcus multilocularis)などの条虫類、
肝蛭(Fasciola hepatica,F.gigantica)、ウエステルマン肺吸虫(Paragonimus westermanii)、肥大吸虫(Fasciolopsic bruski)、膵吸虫(Eurytrema pancreaticum,E.coelomaticum)、肝吸虫(Clonorchis sinensis)、日本住血吸虫(Schistosoma japonicum)、ビルハルツ住血吸虫(Schistosoma haematobium)、マンソン住血吸虫(Schistosoma mansoni)などの吸虫類、
エイメリア・テネラ(Eimeria tenella)、エイメリア・アセルブリナ(Eimeria acervulina)、エイメリア・ブルネッチ(Eimeria brunetti)、エイメリア・マクシマ(Eimeria maxima)、エイメリア・ネカトリクス(Eimeria necatrix)、エイメリア・ボビス(Eimeria bovis)、エイメリア・オビノイダリス(Eimeria ovinoidalis)のようなエイメリア類(Eimeria spp.)、
クルーズトリパノソーマ(Trypanosomsa cruzi)、リーシュマニア類(Leishmania spp.)、マラリア原虫(Plasmodium spp.)、バベシア類(Babesis spp.)、トリコモナス類(Trichomonadidae spp.)、ヒストモナス類(Histomanas spp.)、ジアルディア類(Giardia spp.)、トキソプラズマ類(Toxoplasma spp.)、赤痢アメーバ(Entamoeba histolytica)、タイレリア類(Theileria spp.)、
等が挙げられるが、本発明はこれらのみに限定されるものではない。 In addition, specific examples of endoparasites such as livestock, poultry, and pet animals that can be controlled using the compounds of the present invention include, for example,
Haemonchus, Trichostrongylus, Ostertagia, Nematodirus, Cooperia, Ascaris, Bunostomum, Esphagostomum Genus (Oesophagostomum), Chabertia, Trichuris, Strongylus, Trichonema, Dictyocaulus, Capillaria, Heterakis ), Toxocara, Ascaridia, Oxyuris, Ancylostoma, Uncinaria, Toxacaris, Parascaris, and other nematodes ,
Filariidae nematodes such as Wuchereria, Blueia, Onchoceca, Dirofilaria, Loa
Dracunculidae nematodes such as the genus Deacunculus,
Dogworms (Dipylidium caninum), caterpillars (Taenia taeniaeformis), rodents (Taenia solium), striped tapeworms (Taenia saginata), contracted tapeworms (Hymenolepis diminuta), Beneden tapeworms (Moniezia benedeni), Tapeworms such as Diphyllobothrium latum, Manson cleftworm (Diphyllobothrium erinacei), Echinococcus granulosus, Echinococcus multilocularis,
Fasciola hepatica (F. gigantica), Westermann lung fluke (Paragonimus westermanii), hypertrophic fluke (Fasciolopsic bruski), pancreatic fluke (Eurytrema pancreaticum, E. coelomaticum), liver fluke (Clonorchis sinensis), Schistosoma Schistosoma japonicum), Schistosoma haematobium, Schistosoma mansoni, etc.,
Eimeria tenella, Eimeria acervulina, Eimeria brunetti, Eimeria maxima, Eimeria necatrix, Eimeria bovis, Eimeria bovis Eimeria spp., Such as Eimeria ovinoidalis,
Trypanosomsa cruzi, Leishmania spp., Plasmodium spp., Babesis spp., Trichomonadidae spp., Histomanas spp., Giardia (Giardia spp.), Toxoplasma spp., Entamoeba histolytica, Theileria spp.,
However, the present invention is not limited to these examples.

さらに、本発明化合物は、有機燐系化合物、カーバメート系化合物又はピレスロイド系化合物等の既存の殺虫剤に対して抵抗性の発達した有害生物に対しても有効である。 Furthermore, the compound of the present invention is also effective against pests that have developed resistance to existing insecticides such as organophosphorus compounds, carbamate compounds, and pyrethroid compounds.

すなわち、本発明化合物は、粘管目(トビムシ目)、網翅目(ゴキブリ目)、直翅目(バッタ目)、シロアリ目、総翅目(アザミウマ目)、半翅目(カメムシ目及びヨコバイ目)、鱗翅目(チョウ目)、鞘翅目(コウチュウ目)、膜翅目(ハチ目)、双翅目(ハエ目)、等翅目(ノミ目)及びシラミ目等の昆虫類、ダニ類、腹足類及び線虫類等に属する有害生物を低濃度で有効に防除することが出来る。一方、本発明化合物はホ乳類、魚類、甲殻類及び益虫(ミツバチ、マルハナバチ等の有用昆虫やツヤコバチ、アブラバチ、ヤドリバエ、ヒメハナカメムシ、カブリダニ等の天敵)に対してほとんど悪影響の無い極めて有用な特長を有している。 That is, the compound of the present invention is composed of the order of mucous eyes (Coleoptera), reticulates (Roaches), straight moths (Grasshoppers), termites, common moths (Thrips), hemimorphs (stink bugs and leafhoppers). Eyes), Lepidoptera (Lepidoptera), Coleoptera (Coleoptera), Hymenoptera (Hymenoptera), Diptera (Flyidae), Islamic (Flea), Liceid, and other insects, ticks In addition, pests belonging to gastropods and nematodes can be effectively controlled at low concentrations. On the other hand, the compounds of the present invention are extremely useful with little adverse effect on mammals, fish, crustaceans and beneficial insects (beneficial insects such as bees and bumblebees, natural enemies such as honeybees, wasps, mistletoe flies, mosquitoes, and mites). Has features.

本発明化合物を使用するにあたっては、通常適当な固体担体又は液体担体と混合し、更に所望により界面活性剤、浸透剤、展着剤、増粘剤、凍結防止剤、結合剤、固結防止剤、崩壊剤、消泡剤、防腐剤及び分解防止剤等を添加して、液剤（soluble concentrate）、乳剤（emulsifiable concentrate）、水和剤（wettable powder）、水溶剤（water soluble powder）、顆粒水和剤（water dispersible granule）、顆粒水溶剤（water soluble granule）、懸濁剤（suspension concentrate）、乳濁剤（concentrated emulsion）、サスポエマルジョン（suspoemulsion）、マイクロエマルジョン（microemulsion）、粉剤（dustable powder）、粒剤（granule）錠剤（tablet）及び乳化性ゲル剤（emulsifiable gel）等任意の剤型の製剤にて実用に供することができる。また、省力化及び安全性向上の観点から、上記任意の剤型の製剤を、水溶性カプセル及び水溶性フィルムの袋等の水溶性包装体に封入して供することもできる。 When using the compound of the present invention, it is usually mixed with a suitable solid carrier or liquid carrier, and if desired, a surfactant, penetrant, spreading agent, thickener, antifreezing agent, binder, anti-caking agent. , Disintegrating agents, antifoaming agents, preservatives and anti-decomposition agents, etc., and soluble concentrate, emulsion (emulsifiable concentrate), wettable powder, water-soluble solvent, granular water Water dispersible granule, water soluble granule, suspension concentrate, concentrated emulsion, suspoemulsion, microemulsion, dustable powder ), Granule tablets and emulsifiable gels, and can be put to practical use. In addition, from the viewpoint of labor saving and safety improvement, the preparations of the above arbitrary dosage forms can be provided by being enclosed in a water-soluble package such as a water-soluble capsule and a bag of a water-soluble film.

固体担体としては、例えば石英、方解石、海泡石、ドロマイト、チョーク、カオリナイト、パイロフィライト、セリサイト、ハロサイト、メタハロサイト、木節粘土、蛙目粘土、陶石、ジークライト、アロフェン、シラス、きら、タルク、ベントナイト、活性白土、酸性白土、軽石、アタパルジャイト、ゼオライト及び珪藻土等の天然鉱物質、例えば焼成クレー、パーライト、シラスバルーン、バーミキュライト、アタパルガスクレー及び焼成珪藻土等の天然鉱物質の焼成品、例えば炭酸マグネシウム、炭酸カルシウム、炭酸ナトリウム、炭酸水素ナトリウム、硫酸アンモニウム、硫酸ナトリウム、硫酸マグネシウム、リン酸水素二アンモニウム、リン酸二水素アンモニウム及び塩化カリウム等の無機塩類、例えばブドウ糖、果糖、しょ糖及び乳糖などの糖類、例えば澱粉、粉末セルロース及びデキストリン等の多糖類、例えば尿素、尿素誘導体、安息香酸及び安息香酸の塩等の有機物、例えば木粉、コルク粉、トウモロコシ穂軸、クルミ殻及びタバコ茎等の植物類、フライアッシュ、ホワイトカーボン（例えば、含水合成シリカ、無水合成シリカ及び含水合成シリケート等）ならびに肥料等が挙げられる。 Examples of the solid carrier include quartz, calcite, gypsum, dolomite, chalk, kaolinite, pyrophyllite, sericite, halosite, metahalosite, kibushi clay, glazed clay, porcelain stone, siegrite, allophane , Shirasu, Kira, Talc, Bentonite, Activated clay, Acid clay, Pumice, Attapulgite, Zeolite and diatomite Baked products, such as magnesium carbonate, calcium carbonate, sodium carbonate, sodium bicarbonate, ammonium sulfate, sodium sulfate, magnesium sulfate, diammonium hydrogen phosphate, ammonium dihydrogen phosphate and potassium chloride, such as glucose, fructose , Sucrose and Sugars such as lactose, polysaccharides such as starch, powdered cellulose and dextrin, organic substances such as urea, urea derivatives, benzoic acid and benzoic acid salts, such as wood flour, cork powder, corn cob, walnut shell and tobacco stem And the like, fly ash, white carbon (for example, hydrous synthetic silica, anhydrous synthetic silica, hydrous synthetic silicate, etc.) and fertilizer.

液体担体としては、例えばキシレン、アルキル（Ｃ₉又はＣ₁₀等）ベンゼン、フェニルキシリルエタン及びアルキル（Ｃ₁又はＣ₃等）ナフタレン等の芳香族炭化水素類、マシン油、ノルマルパラフィン、イソパラフィン及びナフテン等の脂肪族炭化水素類、ケロシン等の芳香族炭化水素と脂肪族炭化水素の混合物、エタノール、イソプロパノール、シクロヘキサノール、フェノキシエタノール及びベンジルアルコール等のアルコール、エチレングリコール、プロピレングリコール、ジエチレングリコール、ヘキシレングリコール、ポリエチレングリコール及びポリプロピレングリコール等の多価アルコール、プロピルセロソルブ、ブチルセロソルブ、フェニルセロソルブ、プロピレングリコールモノメチルエーテル、プロピレングリコールモノエチルエーテル、プロピレングリコールモノプロピルエーテル、プロピレングリコールモノブチルエーテル及びプロピレングリコールモノフェニルエーテル等のエーテル、アセトフェノン、シクロヘキサノン及びγ−ブチロラクトン等のケトン、脂肪酸メチルエステル、コハク酸ジアルキルエステル、グルタミン酸ジアルキルエステル、アジピン酸ジアルキルエステル及びフタル酸ジアルキルエステル等のエステル、Ｎ−アルキル（Ｃ₁、Ｃ₈又はＣ₁₂等）ピロリドン等の酸アミド、大豆油、アマニ油、ナタネ油、ヤシ油、綿実油及びヒマシ油等の油脂、ジメチルスルホキシドならびに水が挙げられる。 Examples of the liquid carrier include aromatic hydrocarbons such as xylene, alkyl (C ₉ or C ₁₀ ) benzene, phenylxylylethane and alkyl (C ₁ or C ₃ ) naphthalene, machine oil, normal paraffin, isoparaffin, and the like. Aliphatic hydrocarbons such as naphthene, mixtures of aromatic and aliphatic hydrocarbons such as kerosene, alcohols such as ethanol, isopropanol, cyclohexanol, phenoxyethanol and benzyl alcohol, ethylene glycol, propylene glycol, diethylene glycol, hexylene glycol , Polyhydric alcohols such as polyethylene glycol and polypropylene glycol, propyl cellosolve, butyl cellosolve, phenyl cellosolve, propylene glycol monomethyl ether, propylene glycol Ethers such as ethyl ether, propylene glycol monopropyl ether, propylene glycol monobutyl ether and propylene glycol monophenyl ether, ketones such as acetophenone, cyclohexanone and γ-butyrolactone, fatty acid methyl esters, dialkyl esters of succinic acid, dialkyl esters of glutamic acid, dialkyl adipates Esters such as esters and dialkyl phthalates, acid amides such as N-alkyl (C ₁ , C ₈ or C ₁₂ ) pyrrolidone, soybean oil, linseed oil, rapeseed oil, oils and fats such as coconut oil, cottonseed oil and castor oil, Examples include dimethyl sulfoxide as well as water.

これら固体及び液体担体は、単独で用いても２種以上を併用してもよい。 These solid and liquid carriers may be used alone or in combination of two or more.

界面活性剤としては、例えばポリオキシエチレンアルキルエーテル、ポリオキシエチレンアルキル（モノ又はジ）フェニルエーテル、ポリオキシエチレン（モノ、ジ又はトリ）スチリルフェニルエーテル、ポリオキシエチレンポリオキシプロピレンブロックコポリマー、ポリオキシエチレン脂肪酸（モノ又はジ）エステル、ソルビタン脂肪酸エステル、ポリオキシエチレンソルビタン脂肪酸エステル、ヒマシ油エチレンオキサイド付加物、アセチレングリコール、アセチレンアルコール、アセチレングリコールのエチレンオキサイド付加物、アセチレンアルコールのエチレンオキサイド付加物及びアルキルグリコシド等のノニオン性界面活性剤、アルキル硫酸エステル塩、アルキルベンゼンスルホン酸塩、リグニンスルホン酸塩、アルキルスルホコハク酸塩、ナフタレンスルホン酸塩、アルキルナフタレンスルホン酸塩、ナフタレンスルホン酸のホルマリン縮合物の塩、アルキルナフタレンスルホン酸のホルマリン縮合物の塩、ポリオキシエチレンアルキルエーテル硫酸又は燐酸エステル塩、ポリオキシエチレン（モノ又はジ）アルキルフェニルエーテル硫酸又は燐酸エステル塩、ポリオキシエチレン（モノ、ジ又はトリ）スチリルフェニルエーテル硫酸又は燐酸エステル塩、ポリカルボン酸塩（例えば、ポリアクリル酸塩、ポリマレイン酸塩及びマレイン酸とオレフィンとの共重合物等）及びポリスチレンスルホン酸塩等のアニオン性界面活性剤、アルキルアミン塩及びアルキル４級アンモニウム塩等のカチオン性界面活性剤、アミノ酸型及びベタイン型等の両性界面活性剤、シリコーン系界面活性剤ならびにフッ素系界面活性剤が挙げられる。 Examples of the surfactant include polyoxyethylene alkyl ether, polyoxyethylene alkyl (mono or di) phenyl ether, polyoxyethylene (mono, di or tri) styryl phenyl ether, polyoxyethylene polyoxypropylene block copolymer, polyoxyethylene Ethylene fatty acid (mono or di) ester, sorbitan fatty acid ester, polyoxyethylene sorbitan fatty acid ester, castor oil ethylene oxide adduct, acetylene glycol, acetylene alcohol, ethylene oxide adduct of acetylene glycol, ethylene oxide adduct of acetylene alcohol and alkyl Nonionic surfactants such as glycosides, alkyl sulfate esters, alkylbenzene sulfonates, lignin sulfonates, alkyls Succinate, naphthalenesulfonate, alkylnaphthalenesulfonate, salt of formalin condensate of naphthalenesulfonic acid, salt of formalin condensate of alkylnaphthalenesulfonic acid, polyoxyethylene alkyl ether sulfate or phosphate ester salt, polyoxyethylene (Mono or di) alkyl phenyl ether sulfate or phosphate ester salt, polyoxyethylene (mono, di or tri) styryl phenyl ether sulfate or phosphate ester salt, polycarboxylate (eg, polyacrylate, polymaleate and maleate) Copolymers of acid and olefins) and anionic surfactants such as polystyrene sulfonates, cationic surfactants such as alkylamine salts and alkyl quaternary ammonium salts, and amphoteric surfactants such as amino acid types and betaine types Agent Corn-based surfactants and fluorine-based surfactants.

これら界面活性剤の含有量は、特に限定されるものではないが、本発明の製剤１００重量部に対し、通常０．０５〜２０重量部の範囲が望ましい。また、これら界面活性剤は、単独で用いても２種以上を併用してもよい。 The content of these surfactants is not particularly limited, but is usually preferably in the range of 0.05 to 20 parts by weight with respect to 100 parts by weight of the preparation of the present invention. These surfactants may be used alone or in combination of two or more.

本発明化合物の施用薬量は適用場面、施用時期、施用方法、栽培作物等により差異は有るが、一般には有効成分量としてヘクタール（ha）当たり０.００５〜５０kg程度が適当である。 The application amount of the compound of the present invention varies depending on the application scene, application time, application method, cultivated crops, etc., but generally 0.005 to 50 kg per hectare (ha) is appropriate as the amount of active ingredient.

一方、家畜及び愛玩動物としての哺乳動物及び鳥類の外部又は内部寄生虫の防除に本発明化合物を使用するにあたっては、有効量の本発明化合物を製剤用添加物とともに経口投与、注射（筋肉内、皮下、静脈内、腹腔内）などの非経口投与；浸漬、スプレー、入浴、洗浄、滴下（pouring-on)及びスポッティング(spotting-on)並びにダスティング(dusting)などの経皮投与；経鼻投与により投与することができる。本発明化合物はまた、細片、プレート、バンド、カラー、イヤー・マーク(ear mark)、リム(limb)・バンド、標識装置などを用いた成形製品により投与することができる。投与にあたっては本発明化合物を投与経路に適した任意の剤型とすることができる。 On the other hand, when using the compound of the present invention for the control of the ectoparasites of mammals and birds as domestic animals and pets, an effective amount of the compound of the present invention is administered orally together with injections (intramuscular, Parenteral administration such as subcutaneous, intravenous, intraperitoneal); transdermal administration such as immersion, spraying, bathing, washing, pouring-on and spotting-on and dusting; nasal administration Can be administered. The compounds of the present invention can also be administered by molded products using strips, plates, bands, collars, ear marks, limb bands, labeling devices and the like. In administration, the compound of the present invention can be in any dosage form suitable for the administration route.

調製される任意の剤型としては、粉剤、粒剤、水和剤、ペレット、錠剤、大丸薬、カプセル剤、活性化合物を含む成形製品などの固体調製物；注射用液剤、経口用液剤、皮膚上又は体腔中に用いる液剤；滴下（Pour-on)剤、点下(Spot-on)剤、フロアブル剤、乳剤などの溶液調製物；軟膏剤、ゲルなどの半固体調製物などが挙げられる。 Arbitrary forms to be prepared include solid preparations such as powders, granules, wettable powders, pellets, tablets, large pills, capsules, molded products containing active compounds; injection solutions, oral solutions, skin Liquid preparations used above or in body cavities; solution preparations such as Pour-on agents, spot-on agents, flowable agents and emulsions; semi-solid preparations such as ointments and gels.

固体調製物は、主に経口投与あるいは水などで希釈して経皮投与にあるいは環境処理にて用いることができる。固体調製物は、活性化合物を必要ならば補助剤を加えて適当な賦形剤と共に混合し、そして所望の形状に変えることにより調製できる。適当な賦形剤としては、例えば炭酸塩、炭酸水素塩、リン酸塩、酸化アルミニウム、シリカ、粘土などの無機物質、糖、セルロース、粉砕された穀物、澱粉などの有機物質がある。 The solid preparation can be used mainly for oral administration or diluted with water for transdermal administration or environmental treatment. Solid preparations can be prepared by adding the active compound, if necessary, with adjuncts, mixing with appropriate excipients, and converting to the desired shape. Suitable excipients include, for example, inorganic substances such as carbonates, bicarbonates, phosphates, aluminum oxides, silicas, clays, and organic substances such as sugars, cellulose, crushed grains, and starches.

注射用液剤は、静脈内、筋肉内及び皮下に投与できる、注射用液剤は、活性化合物を適当な溶媒に溶解させ、そして必要ならば可溶化剤、酸、塩基、緩衝用塩、酸化防止剤及び保護剤などの添加剤を加えることにより調製できる。適当な溶媒としては、水、エタノール、ブタノール、ベンジルアルコール、グリセリン、プロピレングリコール、ポリエチレングリコール、Ｎ−メチルピロリドン並びにこれらの混合物、生理学的に許容しうる植物油、注射に適する合成油などがあげられる。可溶化剤としては、ポリビニルピロリドン、ポリオキシエチル化されたヒマシ油及びポリオキシエチル化されたソルビタンエステルなどがあげられる。保護剤には、ベンジルアルコール、トリクロロブタノール、ｐ−ヒドロキシ安息香酸エステル及びｎ−ブタノールなどがある。 Injection solutions can be administered intravenously, intramuscularly and subcutaneously. Injection solutions dissolve the active compound in a suitable solvent and, if necessary, solubilizers, acids, bases, buffer salts, antioxidants. And an additive such as a protective agent. Suitable solvents include water, ethanol, butanol, benzyl alcohol, glycerin, propylene glycol, polyethylene glycol, N-methylpyrrolidone and mixtures thereof, physiologically acceptable vegetable oils, synthetic oils suitable for injection, and the like. Examples of the solubilizer include polyvinylpyrrolidone, polyoxyethylated castor oil, polyoxyethylated sorbitan ester, and the like. Protecting agents include benzyl alcohol, trichlorobutanol, p-hydroxybenzoic acid ester and n-butanol.

経口液剤は直接又は希釈して投与することができる。注射用液剤と同様に調製することができる。 Oral solutions can be administered directly or diluted. It can be prepared in the same manner as an injectable solution.

フロアブル剤、乳剤、などは直接又は希釈して経皮的に、又は環境処理にて投与できる。 Flowables, emulsions, etc. can be administered directly or diluted transdermally or by environmental treatment.

皮膚上で用いる液剤は、滴下し、広げ、すり込み、噴霧し、散布するか、又は浸漬（浸漬、入浴又は洗浄）により塗布することにより投与できる。これらの液剤は注射用液剤と同様に調製できる。 Solutions used on the skin can be administered by dripping, spreading, rubbing, spraying, spraying or applying by dipping (immersion, bathing or washing). These solutions can be prepared in the same manner as injection solutions.

滴下(Pour-on)剤及び点下(Spot-on)剤は皮膚の限定された場所に滴下するか、又は噴霧し、これにより活性化合物を皮膚に浸漬させそして全身的に作用させることができる。滴下剤及び点下剤は、有効成分を適当な皮膚適合性溶媒又は溶媒混合物に溶解するか、懸濁させるか又は乳化することにより調製できる。必要ならば、界面活性剤、着色剤、吸収促進物質、酸化防止剤、光安定剤及び接着剤などの補助剤を加えてもよい。 Pour-on and spot-on agents can be dripped or sprayed onto a limited area of the skin, so that the active compound can be immersed in the skin and act systemically . Drops and drop preparations can be prepared by dissolving, suspending or emulsifying the active ingredient in suitable skin-compatible solvents or solvent mixtures. If necessary, auxiliary agents such as surfactants, colorants, absorption promoting substances, antioxidants, light stabilizers and adhesives may be added.

適当な溶媒としては、水、アルカノール、グリコール、ポリエチレングリコール、ポリプロピレングリコール、グリセリン、ベンジルアルコール、フェニルエタノール、フェノキシエタノール、酢酸エチル、酢酸ブチル、安息香酸ベンジル、ジプロピレングリコールモノメチルエーテル、ジエチレングリコールモノブチルエーテル、アセトン、メチルエチルケトン、芳香族及び／又は脂肪族炭化水素、植物又は合成油、ＤＭＦ、流動パラフィン、軽質流動パラフィン、シリコーン、ジメチルアセトアミド、Ｎ−メチルピロリドン又は２，２−ジメチル−４−オキシ−メチレン−１，３−ジオキソランが挙げられる。吸収促進物質には、ＤＭＳＯ、ミリスチン酸イソプロピル、ペラルゴン酸ジプロピレングリコール、シリコーン油、脂肪族エステル、トリグリセリド及び脂肪アルコールが挙げられる。酸化防止剤には、亜硫酸塩、メタ重亜硫酸塩、アスコルビン酸、ブチルヒドロキシトルエン、ブチルヒドロキシアニソール及びトコフェロールが挙げられる。 Suitable solvents include water, alkanol, glycol, polyethylene glycol, polypropylene glycol, glycerin, benzyl alcohol, phenylethanol, phenoxyethanol, ethyl acetate, butyl acetate, benzyl benzoate, dipropylene glycol monomethyl ether, diethylene glycol monobutyl ether, acetone, Methyl ethyl ketone, aromatic and / or aliphatic hydrocarbons, vegetable or synthetic oil, DMF, liquid paraffin, light liquid paraffin, silicone, dimethylacetamide, N-methylpyrrolidone or 2,2-dimethyl-4-oxy-methylene-1, 3-dioxolane is mentioned. Absorption enhancers include DMSO, isopropyl myristate, dipropylene glycol pelargonate, silicone oil, aliphatic esters, triglycerides and fatty alcohols. Antioxidants include sulfites, metabisulfites, ascorbic acid, butylhydroxytoluene, butylhydroxyanisole and tocopherol.

乳剤は、経口投与、経皮投与又は注射として投与できる。乳剤は、有効成分を疎水性相又は親水性相に溶解させ、このものを適当な乳化剤により、必要ならばさらに着色剤、吸収促進物質、保護剤、酸化防止剤、遮光剤及び増粘物質などの補助剤と共に他の相の溶媒と均質化することにより調製できる。 The emulsion can be administered orally, transdermally or as an injection. In the emulsion, the active ingredient is dissolved in a hydrophobic phase or a hydrophilic phase, and this is added with a suitable emulsifier, and if necessary, a colorant, an absorption promoting substance, a protective agent, an antioxidant, a light-shielding agent, a thickening substance, etc. Can be prepared by homogenizing with other phase solvents together with other auxiliary agents.

疎水性相（油）としては、パラフィン油、シリコーン油、ゴマ油、アーモンド油、ヒマシ油、合成トリグリセリド、ステアリン酸エチル、アジピン酸ジーｎ−ブチリル、ラウリル酸ヘキシル、ペラルゴン酸ジプロピレングリコール、分枝鎖状の短鎖長脂肪酸と鎖長Ｃ_１６〜Ｃ_１８の飽和脂肪酸とのエステル、ミリスチン酸イソプロピル、パルミチン酸イソプロピル、鎖長Ｃ_１２〜Ｃ_１８の飽和脂肪アルコールのカプリル／カプリン酸エステル、ステアリン酸イソプロピル、オレイン酸オレイル、オレイン酸デシル、オレイン酸エチル、乳酸エチル、ワックス状脂肪酸エステル、フタル酸ジブチル、アジピン酸ジイソプロピル、イソトリデシルアルコール、２−オクチルドデカノール、セチルステアリルアルコール、オレイルアルコールが挙げられる。 As hydrophobic phase (oil), paraffin oil, silicone oil, sesame oil, almond oil, castor oil, synthetic triglyceride, ethyl stearate, di-n-butyryl adipate, hexyl laurate, dipropylene glycol pelargonate, branched chain esters of saturated fatty acids shaped for short chain length fatty acids and chain length _C 16 _{-C 18,} isopropyl myristate, caprylic / capric acid esters of saturated fatty alcohols of isopropyl palmitate, chain length _C 12 _{-C 18,} isopropyl stearate Oleyl oleate, decyl oleate, ethyl oleate, ethyl lactate, waxy fatty acid ester, dibutyl phthalate, diisopropyl adipate, isotridecyl alcohol, 2-octyldodecanol, cetyl stearyl alcohol, oleyl alcohol It is below.

親水性相としては、水、プロピレングリコール、グリセリン、ソルビトールが挙げられる。 Examples of the hydrophilic phase include water, propylene glycol, glycerin, and sorbitol.

乳化剤としては、ポリオキシエチル化されたヒマシ油、ポリオキシエチル化されたモノオレフィン酸ソルビタン、モノステアリン酸ソルビタン、モノステアリン酸グリセリン、ステアリン酸ポリオキシエチル、アルキルフェノールポリグリコールエーテルなどの非イオン性界面活性剤；Ｎ−ラウリル−β−イミノジプロピオン酸二ナトリウム、レシチンなどの両性界面活性剤；ラウリル硫酸ナトリウム、脂肪アルコール硫酸エーテル、モノ／ジアルキルポリグリコールオルトリン酸エステルのモノエタノールアミン塩などの陰イオン性界面活性剤；塩化セチルトリメチルアンモニウムなどの陽イオン性界面活性剤などが挙げられる。 Emulsifiers include nonionic interfaces such as polyoxyethylated castor oil, polyoxyethylated sorbitan monoolefin acid, sorbitan monostearate, glyceryl monostearate, polyoxyethyl stearate, alkylphenol polyglycol ether, etc. Activators; amphoteric surfactants such as disodium N-lauryl-β-iminodipropionate and lecithin; anions such as sodium lauryl sulfate, fatty alcohol sulfate ether, monoethanolamine salt of mono / dialkyl polyglycol orthophosphate Surfactants; cationic surfactants such as cetyltrimethylammonium chloride.

他の補助剤として、カルボキシメチルセルロース、メチルセルロース、ポリアクリレート、アルギネート、ゼラチン、アラビアゴム、ポリビニルピロリドン、ポリビニルアルコール、メチルビニルエーテル、無水マレイン酸の共重合体、ポリエチレングリコール、ワックス、コロイド状シリカが挙げられる。 Other adjuvants include carboxymethyl cellulose, methyl cellulose, polyacrylate, alginate, gelatin, gum arabic, polyvinyl pyrrolidone, polyvinyl alcohol, methyl vinyl ether, a copolymer of maleic anhydride, polyethylene glycol, wax, colloidal silica.

半固体調製物は皮膚上に塗布するか、もしくは広げるか、又は体腔中に導入することにより投与できる。ゲルは注射用液剤について上記したように調製した溶液に、軟膏状の粘稠性を有する透明な物質を生じさせるに十分なシックナーを加えることにより調製できる。 Semi-solid preparations can be administered by application on the skin or spreading or introduction into body cavities. Gels can be prepared by adding sufficient thickener to a solution prepared as described above for an injectable solution to produce a clear material having an ointment-like consistency.

次に本発明化合物を用いる場合の製剤の配合例を示す。但し本発明の配合例は、これらのみに限定されるものではない。なお、以下の配合例において「部」は重量部を意味する。 Next, formulation examples of the preparation when using the compound of the present invention are shown. However, the formulation examples of the present invention are not limited to these. In the following formulation examples, “parts” means parts by weight.

〔水和剤〕
本発明化合物０.１〜８０部
固体担体５〜９８.９部
界面活性剤１〜１０部
その他０〜５部
その他として、例えば固結防止剤、分解防止剤等があげれらる。 [Wettable powder]
Compound of the present invention 0.1 to 80 parts Solid carrier 5 to 98.9 parts Surfactant 1 to 10 parts Others 0 to 5 parts Other examples include anti-caking agents and decomposition inhibitors.

〔乳剤〕
本発明化合物０.１〜３０部
液体担体４５〜９５部
界面活性剤４.９〜１５部
その他０〜１０部
その他として、例えば展着剤、分解防止剤等が挙げられる。 [Milk]
Compound of the present invention 0.1-30 parts Liquid carrier 45-95 parts Surfactant 4.9-15 parts Others 0-10 parts Others include, for example, spreading agents, decomposition inhibitors, and the like.

〔懸濁剤〕
本発明化合物０.１〜７０部
液体担体１５〜９８.８９部
界面活性剤１〜１２部
その他０.０１〜３０部
その他として、例えば凍結防止剤、増粘剤等が挙げられる。 [Suspension]
Compound of the present invention 0.1 to 70 parts Liquid carrier 15 to 98.89 parts Surfactant 1 to 12 parts Others 0.01 to 30 parts Others include, for example, antifreezing agents and thickeners.

〔顆粒水和剤〕
本発明化合物０.１〜９０部
固体担体０〜９８.９部
界面活性剤１〜２０部
その他０〜１０部
その他として、例えば結合剤、分解防止剤等が挙げられる。 [Granule wettable powder]
Compound of the present invention 0.1 to 90 parts Solid carrier 0 to 98.9 parts Surfactant 1 to 20 parts Others 0 to 10 parts Others include, for example, binders and decomposition inhibitors.

〔液剤〕
本発明化合物０.０１〜７０部
液体担体２０〜９９.９９部
その他０〜１０部
その他として、例えば凍結防止剤、展着剤等が挙げられる。 (Liquid)
Compound of the present invention 0.01 to 70 parts Liquid carrier 20 to 99.99 parts Others 0 to 10 parts Other examples include antifreezing agents and spreading agents.

〔粒剤〕
本発明化合物０.０１〜８０部
固体担体１０〜９９.９９部
その他０〜１０部
その他として、例えば結合剤、分解防止剤等が挙げられる。 [Granule]
Compound of the present invention 0.01 to 80 parts Solid carrier 10 to 99.99 parts Others 0 to 10 parts Others include, for example, binders, decomposition inhibitors and the like.

〔粉剤〕
本発明化合物０.０１〜３０部
固体担体６５〜９９.９９部
その他０〜５部
その他として、例えばドリフト防止剤、分解防止剤等が挙げられる。 [Dust]
Compound of the present invention 0.01 to 30 parts Solid support 65 to 99.99 parts Others 0 to 5 parts Other examples include a drift inhibitor and a decomposition inhibitor.

次に、本発明化合物を有効成分とする製剤例をより具体的に示すが、本発明はこれらに限定されるものではない。 Next, although the formulation example which uses this invention compound as an active ingredient is shown more concretely, this invention is not limited to these.

尚、以下の配合例において、「部」は重量部を意味する。 In the following formulation examples, “parts” means parts by weight.

〔配合例１〕水和剤
本発明化合物No.１-００１２０部
パイロフィライト７４部
ソルポール５０３９４部
（非イオン性界面活性剤とアニオン性界面活性剤との混合物：東邦化学工業（株）商品名）
カープレックス＃８０Ｄ２部
（合成含水珪酸：塩野義製薬（株）商品名）
以上を均一に混合粉砕して水和剤とする。 [Formulation Example 1] wettable powder Compound No.1-001 20 parts pyrophyllite 74 parts Solpol 5039 4 parts (mixture of nonionic surfactant and anionic surfactant: Toho Chemical Co., Ltd.) Product name)
Carplex # 80D 2 parts (Synthetic hydrous silicic acid: Shionogi & Co., Ltd. trade name)
The above is uniformly mixed and ground to obtain a wettable powder.

〔配合例２〕乳剤
本発明化合物No.１-００１５部
キシレン７５部
Ｎ−メチルピロリドン１５部
ソルポール２６８０５部
（非イオン性界面活性剤とアニオン性界面活性剤との混合物：東邦化学工業（株）商品名）
以上を均一に混合して乳剤とする。 [Formulation Example 2] Milk Compound of the present invention No.1-001 5 parts Xylene 75 parts N-methylpyrrolidone 15 parts Solpol 2680 5 parts (mixture of nonionic surfactant and anionic surfactant: Toho Chemical Industry (Product name)
The above is uniformly mixed to obtain an emulsion.

〔配合例３〕懸濁剤
本発明化合物No.１-００１２５部
アグリゾールＳ−７１０１０部
（非イオン性界面活性剤：花王（株）商品名）
ルノックス１０００Ｃ０.５部
（アニオン性界面活性剤：東邦化学工業（株）商品名）
キサンタンガム０.２部
水６４.３部
以上を均一に混合した後、湿式粉砕して懸濁剤とする。 [Formulation Example 3] Suspension Agent Compound No.1-001 25 parts Agrisol S-710 10 parts (Nonionic Surfactant: Kao Corporation trade name)
LUNOX 1000C 0.5 part (anionic surfactant: Toho Chemical Industries, Ltd. trade name)
Xanthan gum 0.2 parts water 64.3 parts After uniformly mixing the above, wet pulverize to make a suspension.

〔配合例４〕顆粒水和剤
本発明化合物No.１-００１７５部
ハイテノールNE-15 ５部
（アニオン性界面活性剤：第一工業製薬（株）商品名）
バニレックスＮ１０部
（アニオン性界面活性剤：日本製紙（株）商品名）
カープレックス＃８０Ｄ１０部
（合成含水珪酸：塩野義製薬（株）商品名）
以上を均一に混合粉砕した後、少量の水を加えて攪拌混合し、押出式造粒機で造粒し、乾燥して顆粒水和剤とする。 [Composition Example 4] Granule wettable powder Compound No.1-001 of the present invention 75 parts Hytenol NE-15 5 parts (anionic surfactant: Daiichi Kogyo Seiyaku Co., Ltd. trade name)
Vanillex N 10 parts (anionic surfactant: Nippon Paper Industries Co., Ltd. trade name)
Carplex # 80D 10 parts (Synthetic hydrous silicic acid: Shionogi Pharmaceutical Co., Ltd. trade name)
After uniformly mixing and pulverizing the above, a small amount of water is added, stirred and mixed, granulated with an extrusion granulator, and dried to obtain a granulated wettable powder.

〔配合例５〕粒剤
本発明化合物No.１-００１５部
ベントナイト５０部
タルク４５部
以上を均一に混合粉砕した後、少量の水を加えて攪拌混合し、押出式造粒機で造粒し、乾燥して粒剤とする。 [Formulation Example 5] Granules Invention compound No.1-001 5 parts Bentonite 50 parts Talc 45 parts After uniformly mixing and pulverizing the above, a small amount of water is added and mixed with stirring, and granulated with an extrusion granulator. And dried into granules.

〔配合例６〕粉剤
本発明化合物No.１-００１３部
カープレックス＃８０Ｄ０.５部
（合成含水珪酸：塩野義製薬（株）商品名）
カオリナイト９５部
リン酸ジイソプロピル１.５部
以上を均一に混合粉砕して粉剤とする。 [Composition Example 6] Powder Compound of the present invention No.1-001 3 parts Carplex # 80D 0.5 part (Synthetic hydrous silicic acid: Shionogi Pharmaceutical Co., Ltd. trade name)
Kaolinite 95 parts Diisopropyl phosphate 1.5 parts The above is uniformly mixed and ground to obtain a powder.

使用に際しては、上記製剤を水で１〜１００００倍に希釈して、又は希釈せずに直接散布する。 In use, the above preparation is diluted 1 to 10000 times with water or sprayed directly without dilution.

〔配合例７〕水和剤調製物
本発明化合物No.１-００１２５部
ジイソブチルナフタレンスルホン酸ナトリウム１部
ｎ−ドデシルベンゼンスルホン酸カルシウム１０部
アルキルアリールポリグリコールエーテル１２部
ナフタレンスルホン酸ホルマリン縮合物のナトリウム塩３部
エマルジョン型シリコーン１部
二酸化ケイ素３部
カオリン４５部
〔配合例８〕水溶性濃厚剤調製物
本発明化合物No.１-００１２０部
ポリオキシエチレンラウリルエーテル３部
ジオクチルスルホコハク酸ナトリウム３.５部
ジメチルスルホキシド３７部
２−プロパノール３６.５部
〔配合例９〕噴霧用液剤
本発明化合物No.１-００１２部
ジメチルスルホキシド１０部
２−プロパノール３５部
アセトン５３部
〔配合例１０〕経皮投与用液剤
本発明化合物No.１-００１５部
ヘキシレングリコール５０部
イソプロパノール４５部
〔配合例１１〕経皮投与用液剤
本発明化合物No.１-００１５部
プロピレングリコールモノメチルエーテル５０部
ジプロピレングリコール４５部
〔配合例１２〕経皮投与(滴下)用液剤
本発明化合物No.１-００１２部
軽質流動パラフィン９８部
〔配合例１３〕経皮投与(滴下)用液剤
本発明化合物No.１-００１２部
軽質流動パラフィン５８部
オリーブ油３０部
ＯＤＯ−Ｈ９部
信越シリコーン１部
また、本発明化合物を農薬として使用する場合には、必要に応じて製剤時又は散布時に他種の除草剤、各種殺虫剤、殺ダニ剤、殺線虫剤、殺菌剤、植物生長調節剤、共力剤、肥料、土壌改良剤等と混合施用しても良い。 [Formulation Example 7] wettable powder preparation Compound No. 1-001 of the present invention 25 parts sodium diisobutylnaphthalenesulfonate 1 part calcium n-dodecylbenzenesulfonate 10 parts alkylaryl polyglycol ether 12 parts naphthalenesulfonic acid formalin condensate Sodium salt 3 parts Emulsion type silicone 1 part Silicon dioxide 3 parts Kaolin 45 parts [Formulation Example 8] Water-soluble thickener preparation Compound No.1-001 20 parts Polyoxyethylene lauryl ether 3 parts Sodium dioctyl sulfosuccinate 3. 5 parts dimethyl sulfoxide 37 parts 2-propanol 36.5 parts [Formulation Example 9] Solution for spraying the present compound No.1-001 2 parts dimethyl sulfoxide 10 parts 2-propanol 35 parts acetone 53 parts [Formulation Example 10] transdermal Solution for administration The present compound No.1-001 5 Parts hexylene glycol 50 parts isopropanol 45 parts [Formulation Example 11] Solution for transdermal administration Compound No. 1-001 5 parts propylene glycol monomethyl ether 50 parts Dipropylene glycol 45 parts [Formulation example 12] transdermal administration (instillation) ) Solution for the Invention Compound No.1-001 2 parts Light Liquid Paraffin 98 parts [Formulation Example 13] Solution for the transdermal administration (drip) Compound No.1-001 2 parts Light Liquid Paraffin 58 parts Olive Oil 30 parts ODO -H 9 parts Shin-Etsu Silicone 1 part In addition, when the compound of the present invention is used as an agrochemical, other types of herbicides, various insecticides, acaricides, nematicides, You may mix and apply with a disinfectant, a plant growth regulator, a synergist, a fertilizer, a soil conditioner, etc.

特に他の農薬あるいは植物ホルモンと混合施用することにより、施用薬量の低減による低コスト化、混合薬剤の相乗作用による殺虫スペクトラムの拡大やより高い有害生物防除効果が期待できる。この際、同時に複数の公知農薬との組み合わせも可能である。本発明化合物と混合使用する農薬の種類としては、例えばザ・ペスティサイド・マニュアル（The Pesticide Manual）１５版、２００９年に記載されている化合物等が挙げられる。具体的にその一般名を例示すれば次の通りであるが、必ずしもこれらのみに限定されるものではない。 In particular, when mixed with other pesticides or plant hormones, the cost can be reduced by reducing the amount of applied medicine, the insecticidal spectrum can be expanded by the synergistic action of the mixed drugs, and higher pest control effects can be expected. At this time, a combination with a plurality of known agricultural chemicals is also possible. Examples of the type of agricultural chemical used in combination with the compound of the present invention include compounds described in The Pesticide Manual 15th edition, 2009, and the like. Specific examples of common names are as follows, but the general names are not necessarily limited to these.

殺菌剤：アシベンゾラルーＳ−メチル（acibenzolar-S-methyl）、アシルアミノベンザミド(acylaminobenzamide)、アシペタックス(acypetacs)、アルジモルフ(aldimorph) 、アメトクトラジン(ametoctradin)、アミスルブロム(amisulbrom)、アンバム(amobam)、アムプロピルホス（ampropyfos）、アニラジン（anilazine）、アザコナゾール（azaconazole）、アジチラム(azithiram)、アゾキシストロビン（azoxystrobin）、バリウムポリサルファイド(barium polysulfide)、ベナラキシル（benalaxyl）、ベナラキシル−Ｍ（benalaxyl-M）、ベノダニル（benodanil）、ベノミル（benomyl）、ベンキノックス(benquinox)、ベンタルロン(bentaluron)、ベンチアバリカルブ(benthiavalicarb)、ベンチアゾール(benthiazole)、ベンザマクリル（benzamacril）、ベンズアモルフ(benzamorf)、ベトキサジン（bethoxazine）、ビナパクリル（binapacryl）、ビフェニル（biphenyl）、ビテルタノール（bitertanol）、ブラストサイジン−Ｓ（blasticidin-S）、ビキサフェン（bixafen）、ボルドー液（bordeaux mixture）、ボスカリド(boscalid)、ブロモコナゾール（bromoconazole）、ブピリメート（bupirimate）、ブチオベート（buthiobate）、石灰硫黄合剤（calcium polysulfide）、カルシウムポリスルフィド（calcium polysulfide）、キャプタフォール（captafol）、キャプタン（captan）、カルプロパミド（carpropamid）、カルバモルフ(carbamorph)、カルベンダジン（carbendazim）、カルボキシン（carboxin）、カルボン(carvone)、チェシュントミクスチャ(cheshunt mixture)、キノメチオネート（chinomethionat）、クロベンチアゾン（chlobenthiazone）、クロラニフォルメタン(chloraniformethane)、クロラニル(chloranil)、クロルフェナゾール（chlorfenazol）、クロロネブ（chloroneb）、クロロピクリン(chloropicrin)、クロロタロニル（chlorothalonil）、クロロキノックス(chlorquinox)、クロゾリネート（chlozolinate）、クリムバゾール(climbazole)、クロトリマゾール(clotrimazole)、カッパーアセテイト(copper acetate)、塩基性炭酸銅(copper carbonate, basic)、水酸化第二銅(copper hydroxide)、カッパーナフタレン(copper naphthenate)、カッパーオルアイト(copper oleate)、カッパーオキシクロリド（copper oxychloride）、硫酸銅(copper sulfate)、塩基性硫酸銅(copper sulfate, basic)、カッパージンククロメイト(copper zinc chromate)、クフラネブ（cufraneb）、クプロバム(cuprobam)、シアゾファミド(cyazofamid)、シクラフルアミド(cyclafuramid)、シクロヘキシミド(cycloheximide)、シフルフェナミド(cyflufenamid)、シモキサニル（cymoxanil）、サイペンダゾール(cypendazole)、シプロコナゾール（cyproconazol）、シプロジニル（cyprodinil）、シプロフラム（cyprofuram）、ダゾメット(dazomet)、デバカルブ（debacarb）、デカフェンチン(decafentin)、デハイドロアセテイト(dehydroacetic acid)、ジクロフルアニド（dichlofluanid）、ジクロン(dichlone)、ジクロロフェン（dichlorophen）、ジクロゾリン(dichlozoline)、ジクロブトラゾール（diclobutrazol）、ジクロシメット（diclocymet）、ジクロメジン（diclomedine）、ジクロラン（dicloran）など。 Bactericides: acibenzolar-S-methyl, acylaminobenzamide, acypetacs, aldimorph, ametoctradin, amisulbrom, amobam, ampropyl Phos (ampropyfos), anilazine, azaconazole, azithiram, azoxystrobin, barium polysulfide, benalaxyl, benalaxyl-M, benodaril (Benodanil), benomyl, benquinox, bentaluron, benthiavalicarb, benthiazole, benzamacril, benzamorf, bethoxazine, Binapacryl Biphenyl, bitertanol, blasticidin-S, bixafen, bordeaux mixture, boscalid, bromoconazole, bupirimate, buthiobate (Buthiobate), calcium polysulfide, calcium polysulfide, captafol, captan, carpropamid, carbamorph, carbendazim, carboxin (Carboxin), carvone, cheshunt mixture, chinomethionat, clobenthiazone, chloraniformethane, chloranil, chlorfenazol, Chloroneb (c hloroneb), chloropicrin, chlorothalonil, chlorquinox, chlozolinate, climbazole, clotrimazole, copper acetate, basic copper carbonate (copper carbonate, basic), cupric hydroxide, copper naphthenate, copper oleate, copper oxychloride, copper sulfate, basic sulfuric acid Copper sulfate, basic, copper zinc chromate, cufraneb, cuprobam, cyazofamid, cyclafuramid, cycloheximide, cyflufenamid, Simoxanil, cypendazole, cyproconazole (cyp) roconazol), cyprodinil, cyprofuram, dazomet, debacarb, decaentin, dehydroacetic acid, dichlorfluanid, dichlone, Dichlorophen, dichlozoline, diclobutrazol, diclocymet, diclomedine, dicloran, etc.

殺菌剤（続き）：ジエトフェンカルブ（diethofencarb）、ジフェノコナゾール（difenoconazole）、ジフルメトリン（diflumetorim）、ジメチリモール（dimethirimol）、ジメトモルフ（dimethomorph）、ジモキシストロビン(dimoxystrobin)、ジニコナゾール（diniconazole）、ジニコナゾール−Ｍ（diniconazole-M）、ジノブトン(dinobuton)、ジノカップ（dinocap）、ジノカップ−４(dinocap-4)、ジノカップ−６(dinocap-6)、ジノクトン(dinocton)、ジノスルフォン(dinosulfon)、ジノテルボン(dinoterbon)、ジフェニルアミン（diphenylamine）、ジピリチオン（dipyrithione）、ジタリムホス（ditalimfos）、ジチアノン（dithianon）、ドデモルフ（dodemorph）、ドジン（dodine）、ドラゾクソロン（drazoxolon）、エデフェノホス（edifenphos）、エポキシコナゾール（epoxiconazole）、エタコナゾール（etaconazole）、エタボキサム（ethaboxam）、エテム(etem)、エチリモル（ethirimol）、エトキシキン(ethoxyquin)、エトリジアノール（etridiazole）、ファモキサゾン（famoxadone）、フェナリモル（fenarimol）、フェブコナゾール（febuconazole）、フェナミドン（fenamidone）、フェナミノスルフ(fenaminosulf)、フェナパニル(fenapanil)、フェンダゾスラム(fendazosulam)、フェンフラム（fenfuram）、フェンヘキサミド（fenhexamid）、フェニトロパン(fenitropan)、フェノキサニル(fenoxanil)、フェンピクロニル（fenpiclonil）、フェンプロピジン（fenpropidin）、フェンピラザミン(fenpyrazamine)、フェンプロピモルフ（fenpropimorph）、フェンチン（fentin）、フェルバン（ferbam）、フェリムゾン（ferimzone）、フルアジナム（fluazinam）、フルジオキソニル（fludioxonil）、フルメトベル(flumetover)、フルモルフ(flumorph)、フルオピコリド（fluopicolide）、フルオピラム（fluopyram）、フルオロイミド（fluoroimide）、フルオトリマゾール(fluotrimazole)、フルオキサストロビン(fluoxastrobin)、フルキンコナゾール（fluquinconazole）、フルシラゾール（flusilazole）、フルスルファミド（flusulfamide）、フルチアニル（flutianil）、フルトラニル（flutolanil）、フルトリアフォール（flutriafol）、フルキサピロキサド（fluxapyroxad）、フォルペット（folpet）、フォセチル−アルミニウム（fosetyl-aluminium）、フベリダゾール（fuberidazole）、フララキシル（furalaxyl）、フラメトピル(furametpyr)、フルカルバニル(furcarbanil)、フルコナゾール(furconazole)、フルコナゾール−シス(furconazole-cis)、フルメシクロックス(furmecyclox)、フルファネート(furphanate)、グリオジン(glyodin)、グリセオフルビン(griseofulvin)、グアザチン（guazatine）、ハラクリネイト(halacrinate)、ヘキサクロロベンゼン（hexachlorobenzene）、ヘキサコナゾール（hexaconazole）、ヘキシルチオフォス(hexylthiofos)、ハイドロキシキノリンサルフェイト(8-hydroxyquinoline sulfate)、ヒメキサゾール（hymexazol）、イマザリル（imazalil）、イミベンコナゾール（imibenconazole）、イミノクタジン（iminoctadine）、イプコナゾール（ipconazole）、イプロベンホス（iprobenfos）、イプロジオン（iprodione）、イプロバリカルブ（iprovalicarb）、イソプロチオラン（isoprothiolane）、イソバレジオン(isovaledione)など。 Bactericides (continued): diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole-M, diniconazole-M, diniconazole-M M), dinobuton, dinocap, dinocap-4, dinocap-6, dinoton, dinosulfon, dinoterbon, diphenylamine ), Dipyrithione, ditalimfos, dithianon, dodemorph, dodine, drazoxolon, edifenphos, epoxiconazole, etaconazole, etaconazole Xham (ethaboxam), etem, etirimol, ethoxyquin, etridianol, famoxadone, fenarimol, febuconazole, fenamidone, phenaminosulf ), Fenapanil, fendazosulam, fenfuram, fenhexamid, fenitropan, fenoxanil, fenpiclonil, fenpropidin, fenpyrazamine (fenpyrazamine), fenpropimorph, fentin, ferbam, ferimzone, fluazinam, fludioxonil, flumetover, flumorph, full Fluopicolide, fluopyram, fluoroimide, fluotrimazole, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, fluthianyl (fluoxanil) flutianil), flutolanil, flutriafol, fluxapyroxad, folpet, fosetyl-aluminium, fuberidazole, fluralaxyl, flametopyr ( furametpyr), furcarbanil, furconazole, fluconazole-cis, furmecyclox, furphanate, furyonate, glyodin, griseofulvin, guazachi (Guazatine), halacrinate, hexachlorobenzene, hexaconazole, hexylthiofos, hydroxyquinoline sulfate, hymexazol, imazalil, Imibenconazole, iminoctadine, ipconazole, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isovaledione, etc.

殺菌剤（続き）：カスガマイシン（kasugamycin）、クレソキシム−メチル（kresoxim-methyl）、マンカッパー（mancopper）、マンコゼブ（mancozeb）、マンジプロパミド（mandipropamid）、マンネブ（maneb）、メベニル（mebenil）、メカルビンジド（mecarbinzid）、メパニピリム（mepanipyrim）、メプロニル（mepronil）、メタラキシル（metalaxyl）、メタラキシル−Ｍ（metalaxyl-M）、メタム（metam）、メタゾキソロン（metazoxolon）、メトコナゾール（metconazole）、メタスルホカルブ(methasulfocarb)、メトフロキサム（methfuroxam）、メチルイソチオシアネイト（methyl isothiocyanate）、メチラム（metiram）、メトミノストロビン（metominostrobin）、メトラフェノン（metrafenone）、メトスルフォバックス（metsulfovax）、ミルネブ（milneb）、ミクロブタニル（myclobutanil）、ミクロゾリン（myclozolin）、ナバム（nabam）、ナタマイシン（natamycin）、ニッケルビス（ジメチルジチオカーバメート）（nickel bis(dimethyldithiocarbamate)）、ニトロスチレン（nitrostyrene）、ニトロタール−イソプロピル（nitrothal-isopropyl）、ヌアリモル（nuarimol）、オーシーエイチ（OCH）、オクチリノン（octhilinone）、オフレース（ofurace）、オリサストロビン（orysastrobin）、オキサジキシル（oxadixyl）、有機銅（oxine copper）、オキシカルボキシン（oxycarboxin）、オキスポコナゾールフマール酸塩（oxpoconazole fumarate）、ペフラゾエート（pefurzoate）、ペンコナゾール（penconazole）、ペンフルフェン（penflufen）、ペンシクロン（pencycuron）、ペンチオピラド（penthiopyrad）、オルソフェニルフェノール（o-phenylphenol）、フォスジフェン（phosdiphen）、フタライド（phthalide）、ピコキシストロビン（picoxystrobin）、ピペラリン（piperalin）、ポリカーバメート（polycarbamate）、ポリオキシン（polyoxins）、ポリオクソリム（polyoxorim）、ポタシウムアザイド（potassium azide）、炭酸水素カリウム(potassium hydrogen carbonate)、プロキナジド（proquinazid）、プロベナゾール（probenazole）、プロクロラズ（prochloraz）、プロシミドン（procymidone）、プロパモカルブ塩酸塩（propamocarb hydrochloride）、プロピコナゾール（propiconazole）、プロピネブ（propineb）、プロチオカルブ（prothiocarb）、プロチオコナゾール（prothioconazole）、ピラカルボリド（pyracarbolid）、ピラクロストロビン（pyraclostrobin）、ピラゾホス（pyrazophos）、ピリジニトリル（pyridinitril）、ピリフェノックス（pyrifenox）、ピリメタニル（pyrimethanil）、ピリオフェノン（pyriofenone）、ピロキュロン（pyroquilon）、ピロキシクロル（pyroxychlor）、ピロキシフル（pyroxyfur）、キノメチオネート(quinomethionate)、キノキシフェン（quinoxyfen）、キントゼン（quintozene）、キナセトール・スルフェート（quinacetol-sulfate）、キナザミド（quinazamid）、キンコナゾール（quinconazole）、ラベンザゾール（rabenzazole）など。 Fungicide (continued): kasugamycin, kresoxim-methyl, mancopper, mancozeb, mandipropamid, maneb, mebenil, mecarbinzid , Mepanipyrim, mepronil, metalaxyl, metalaxyl-M, metam, metazoxolon, metconazole, metasulfocarb, metoxasulfocarb, metoxafloxam ), Methyl isothiocyanate, metiram, metinominostrobin, metrafenone, metsulfovax, milneb, microbutanil, microzoline (myclozo) lin), nabam, natamycin, nickel bis (dimethyldithiocarbamate), nitrostyrene, nitrothal-isopropyl, nuarimol, OH (OCH), octhilinone, offurace, orysastrobin, oxadixyl, oxine copper, oxycarboxin, oxpoconazole fumarate , Pefurzoate, penconazole, penflufen, penencycuron, penthiopyrad, o-phenylphenol, phosdiphen, phthalide, picoxis Robin (picoxystrobin), piperalin (piperalin), polycarbamate (polycarbamate), polyoxins (polyoxins), polyoxorim (polyoxorim), potassium azide (potassium hydrogen carbonate) (potassium hydrogen carbonate), proquinazid (proquinazid) probenazole), prochloraz, procymidone, propamocarb hydrochloride, propiconazole, propineb, prothiocarb, prothioconazole, pyracarbolid, Pyraclostrobin, pyrazophos, pyridinitril, pyrifenox, pyrimethanil, pyriofenone, pyroculone (pyroq) uilon, pyroxychlor, pyroxyfur, quinomethionate, quinoxyfen, quintozene, quinacetol-sulfate, quinazamid, quinazaazole, quinconazole rabenzazole).

殺菌剤（続き）：アジ化ナトリウム（sodium azide）、炭酸水素ナトリウム(sodium hydrogen carbonate)、次亜塩素酸ナトリウム(sodium hypochlorite)、硫黄（sulfur）、スピロキサミン（spiroxamine）、サリチルアニリド（salycylanilide）、シルチオファム（silthiofam）、シメコナゾール（simeconazole）、テブコナゾール（tebuconazole）、テクナゼン（tecnazene）、テコラム（tecoram）、テトラコナゾール（tetraconazole）、チアベンダゾール（thiabendazole）、チアジフルオール（thiadifluor）、チシオフェン（thicyofen）、チフルザミド（thifluzamide）、チオクロルフェンフィム（thiochlorfenphim）、チオファネート（thiophanate）、チオファネート−メチル（thiophanate-methyl）、チオキノックス（thioquinox）、チラム（thiram）、チアジニル（tiadinil）、チオキシミド（tioxymid）、トルクロホス−メチル（tolclofos-methyl）、トリルフラニド（tolylfluanid）、トリアジメホン（triadimefon）、トリアジメノール（toriadimenol）、トリアミフォス（triamiphos）、トリアリモル（triarimol）、トリアゾキシド（triazoxide）、トリアズブチル（triazbutil）、トリブチルチンオキサイド（tributyltin oxide）、トリクラミド（trichlamide）、トリシクラゾール（tricyclazole）、トリデモルフ（tridemorph）、トリフロキシストロビン(trifloxystrobin)、トリフルミゾール（triflumizole）、トリホリン（triforine）、トリチコナゾール（triticonazole）、バリダマイシン（validamycin）、バリフェナレート（valifenalate）、ビンクロゾリン（vinclozolin）、ザリルアミド（zarilamide）、硫酸亜鉛(zinc sulfate)、ジネブ（zineb）、ジラム（ziram）、ゾキサミド（zoxamide）及びシイタケ菌糸体抽出物など。 Fungicide (continued): sodium azide, sodium hydrogen carbonate, sodium hypochlorite, sulfur, spiroxamine, salicylanilide, silthiofam (Silthiofam), simeconazole, tebuconazole, tecnazene, tecoram, tetraconazole, thiabendazole, thiadifluor, thicyofen, thifluzamide thifluzamide, thiochlorfenphim, thiophanate, thiophanate-methyl, thioquinox, thiram, thiadinyl, tioxymid, tolcrophos-me Tolclofos-methyl, tolylfluanid, triadimefon, triadimenol, triamiphos, triarimol, triazoxide, triazbutil, tributyltin oxide ), Trichlamide, tricyclazole, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, validamycin, validamycin Examples include valifenalate, vinclozolin, zarilamide, zinc sulfate, zineb, ziram, zoxamide and shiitake mycelium extract.

殺バクテリア剤：ベンザルコニウムクロライド(benzalkonium chloride)、ビチオノール(bithionol)、ブロノポール（bronopol）、クレゾール(cresol)、ホルムアルデヒド（formaldehyde）、ニトラピリン（nitrapyrin）、オキソリニックアシド（oxolinic acid）、オキシテトラサイクリン（oxyterracycline）、ストレプトマイシン（streptomycin）及びテクロフタラム(tecloftalam)など。 Bactericides: benzalkonium chloride, bithionol, bronopol, cresol, formaldehyde, nitrapyrin, oxolinic acid, oxyterracycline , Streptomycin and tecloftalam.

殺線虫剤：アルドキシカルブ（aldoxycarb）、カズサホス（cadusafos）、デービーシーピー(DBCP)、ジクロフェンチオン（dichlofenthion）、デーエスピー（DSP）、エトプロホス（ethoprophos）、フェナミホス（fenamiphos）、フェンスルホチオン（fensulfothion）、フルエンスルホン(fluensulfone)、フォスチアゼート（fosthiazate）、フォスチエタン（fosthietan）、イミシアホス（imicyafos）、イサミドホス（isamidofos）、イサゾホス（isazofos）、オキサミル（oxamyl）及びチオナジン（thionazin）など。 Nematicides: aldoxycarb, cadusafos, DCP, DBCH, dichlofenthion, DSP (DSP), etoprophos, fenamiphos, fensulfothion, fluene Sulfone (fluensulfone), fosthiazate (fosthiazate), fosthietan (fosthietan), imisiafos (imicyafos), isamidofos (isamidofos), isazofos (isazofos), oxamyl (oxamyl) and thionazin (thionazin) and the like.

殺ダニ剤：アセキノシル（acequinocyl）、アクリナトリン（acrinathrin）、アミトラズ（amitraz）、ＢＣＩ−０３３（試験名）、ビフェナゼート（bifenazate）、ブロモプロピレート（bromopropylate）、チノメチオネート（chinomethionat）、クロロベンジラート（chlorobezilate）、クロフェンテジン（clofentezine）、シエノピラフェン（cyenopyrafen）、シフルメトフェン（cyflumetofen）、サイヘキサチン（cyhexatine）、ジコフォール（dicofol）、ジエノクロール（dienochlor）、デーエヌオーシー(DNOC)、エトキサゾール（etoxazole）、フェナザキン（fenazaquin）、フェンブタチンオキシド（fenbutatin oxide）、フェノチオカルブ（fenothiocarb）、フェンプロパトリン（fenpropathrin）、フェンピロキシメート（fenpyroximate）、フルアクリピリム（fluacrypyrim）、ハルフェンプロックス（halfenprox）、ヘキシチアゾックス（hexythiazox）、ミルベメクチン（milbemectin）、プロパルギット（propargite）、ピリダベン（pyridaben）、ピリミジフェン（pyrimidifen）、Ｓ−１８７０（試験名）、スピロジクロフェン（spirodiclofen）、スピロメシフェン（spyromesifen）、ＮＮＩ−０７１１（試験名）、ＣＬ９００１６７（試験名）及びテブフェンピラド（tebufenpyrad）など。 Acaricide: acequinocyl, acrinathrin, amitraz, BCI-033 (test name), bifenazate, bromopropylate, chinomethionat, chlorobezilate , Clofentezine, cyenopyrafen, cyflumetofen, cyhexatine, dicofol, dienochlor, denochlor (DNOC), etoxazole, quinazaquin (fenaza) Fenbutatin oxide, fenothiocarb, fenpropathrin, fenpyroximate, fluacrypyrim, halfenprox (halfenpro) x), hexythiazox, milbemectin, propargite, pyridaben, pyrimidifen, S-1870 (test name), spirodiclofen, spiromesifen ( spyromesifen), NNI-0711 (test name), CL900187 (test name) and tebufenpyrad.

殺虫剤：アバメクチン（abamectin）、アセフェート（acephate）、アセタミピリド（acetamipirid）、アラニカルブ（alanycarb）、アルディカルブ（aldicarb）、アレスリン（allethrin）、アザメチホス(azamethiphos)、アジンホス−メチル（azinphos-methyl）、バチルスチューリンゲシス（bacillus thuringiensis）、ベンジオカルブ（bendiocarb）、ベンフルトリン(benfluthrin)、ベンフラカルブ（benfuracarb）、ベンスルタップ（bensultap）、ビフェントリン（bifenthrin）、ビオアレスリン(bioallethrin)、ビオレスメトリン(bioresmethrin)、ビストリフルロン(bistrifluron)、ブプロフェジン（buprofezin）、ブトカルボキシン（butocarboxim）、カルバリル（carbaryl）、カルボフラン（carbofuran）、カルボスルファン（carbosulfan）、カルタップ（cartap）、クロルアントラニリプロール（chlorantraniliprole）、クロルエトキシホス(chlorethxyfos)、クロルフェナピル（chlorfenapyr）、クロルフェンビンホス（chlorfenvinphos）、クロルフルアズロン（chlorfluazuron）、クロルメホス(chlormephos)、クロルピリホス（chlorpyrifos）、クロピリホス−メチル（chlorpyrifos-methyl）、クロマフェノジド（chromafenozide）、クロチアニジン（clothianidin）、シアントラニリプロール(cyantraniliprole)、シクロプロトリン（cycloprothrin）、シフルメトフェン（cyflumetofen）、シフルトリン（cyfluthrin）、ベータ−シフルトリン（beta-cyfluthrin）、シハロトリン（cyhalothrin）、ラムダ−シハロトリン（lambda-cyhalothrin）、シペルメトリン（cypermethrin）、アルファ−シペルメトリン（alpha-cypermethrin）、ベータ−シペルメトリン（beta-cypermethrin）、ゼタ−シペルメトリン（zeta-cypermethrin）、シロマジン（cyromazine）、デルタメトリン（deltamethrin）、ジアクロデン（diacloden）、ジアフェンチウロン（diafenthiuron）、ダイアジノン（diazinon）、ジクロルボス（dichlorvos）、ジフルベンズロン（diflubenzuron）、ジメチルビンホス（dimethylvinphos）、ジノテフラン（dinotefuran）、ジオフェノラン（diofenolan）、ジスルフォトン（disulfoton）、ジメトエート（dimethoate）、エマメクチンベンゾエート（emamectin-benzoate）、エンペントリン（empenthrin）、エンドスルファン（endosulfan）、アルファ−エンドスルファン（alpha-endosulfan）、イーピーエヌ（EPN）、エスフェンバレレート（esfenvalerate）、エチオフェンカルブ（ethiofencarb）、エチプロール（ethiprole）、エトフェンプロックス（etofenprox）、エトリムホス（etrimfos）、フェニトロチオン（fenitrothion）、フェノブカルブ（fenobucarb）、フェノキシカーブ（fenoxycarb）、フェンプロパトリン（fenpropathrin）、フェンチオン（fenthion）、フェンバレレート（fenvalerate）、フィプロニル（fipronil）、フロニカミド（flonicamid）、フルベンジアミド（flubendiamide）、フルシトリネート（flucythrinate）、フルフェネリム（flufenerim）、フルフェノクスウロン（flufenoxuron）、フルフェンプロックス（flufenprox）、フルメトリン（flumethrin）、フルバリネート（fluvalinate）、タウ−フルバリネート（tau-fluvalinate）、ホノホス（fonophos）、フォルメタネート（formetanate）、フォルモチオン（formothion）、フラチオカルブ（furathiocarb）、フルフィプロール(flufiprole)、フルピラジフロン(flupyradifurone)、フロメトキン(flometoquin)など。 Insecticides: abamectin, acephate, acetamipirid, alanamicarb, aldicarb, allethrin, azamethiphos, azinphos-methyl, bacillus tubulin Bacillus thuringiensis, bendiocarb, benfluthrin, benfuracarb, bensultap, bifenthrin, bioallethrin, bioresmethrin, bistrifluron, tris Buprofezin, butocarboxim, carbaryl, carbofuran, carbosulfan, cartap, chlorantraniliprole, Chlorethxyfos, chlorfenapyr, chlorfenvinphos, chlorfluazuron, chlormephos, chlorpyrifos, chlorpyrifos-methyl, chromafenozide, chromafenozide Clothianidin, cyantraniliprole, cycloprothrin, cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin cyhalothrin), cypermethrin, alpha-cypermethrin, beta-cypermethrin, zeta-cypermethrin, cyromazine, Deltamethrin, diacloden, diafenthiuron, diazinon, dichlorvos, diflubenzuron, dimethylvinphos, dinotefuran, diofenolan, diofenolan Disulfoton, dimethoate, emamectin-benzoate, empenthrin, endosulfan, alpha-endosulfan, EP-N, EPN, esfenvalerate, etiophencarb (Ethiofencarb), ethiprole, etofenprox, etrimfos, fenitrothion, fenobucarb, fenobucarb Fenoxycarb, fenpropathrin, fenthion, fenvalerate, fipronil, flonicamid, flubendiamide, flucythrinate, flufenerim , Flufenoxuron, flufenprox, flumethrin, fluvalinate, tau-fluvalinate, fonophos, formetanate, formotaion ( formothion), furathiocarb, flufiprole, flupyradifurone, flometoquin and the like.

殺虫剤（続き）：ハロフェノジド（halofenozide）、ヘキサフルムロン（hexaflumuron）、ヒドラメチルノン（hydramethylnon）、イミダクロプリド（imidacloprid）、イソフェンホス（isofenphos）、インドキサカルブ（indoxacarb）、イソプロカルブ（isoprocarb）、イソキサチオン（isoxathion）、レピメクチン（lepimectin）、ルフェヌウロン（lufenuron）、マラチオン（malathion）、メペルフルスリン（meperfluthrin）、メタフルミゾン（metaflumizone）、メタルデヒド（metaldehyde）、メタミドホス（methamidophos）、メチダチオン（methidathion）、メタクリホス（methacrifos）、メタフルミゾン（metaflumizone）、メタルカルブ（metalcarb）、メソミル（methomyl）、メソプレン（methoprene）、メトキシクロール（methoxychlor）、メトキシフェノジド（methoxyfenozide）、メチルブロマイド（methyl bromide）、モノクロトホス（monocrotophos）、ムスカルーレ（muscalure）、ニテンピラム（nitenpyram）、ノバルロン（novaluron）、ノビフルムロン（noviflumuron）、オメトエート（omethoate）、オキサミル（oxamyl）、オキシデメトン−メチル（oxydemeton-methyl）、オキシデプロホス（oxydeprofos）、パラチオン（parathion）、パラチオン−メチル（parathion-methyl）、ペンタクロロフェノール（pentachlorophenol(PCP)）、ペルメトリン（permethrin）、フェノトリン（phenothrin）、フェントエート（phenthoate）、フォキシム（phoxim）、ホレート（phorate）、ホサロン（phosalone）、ホスメット（phosmet）、ホスファミドン（phosphamidon）、ピリミカルブ（pirimicarb）、ピリミホス−メチル（pirimiphos-methyl）、プロフェノホス（profenofos）、プロチオホス（prothiofos）、プロパホス（propaphos）、プロトリフェンブト（protrifenbute）、ピメトロジン（pymetrozine）、ピラクロホス（pyraclofos）、ピレトリン（pyrethrins）、ピリダリル（pyridalyl）、ピリフルキナゾン（pyrifluquinazon）、ピリプロール（pyriprole）、ピラフルプロール(pyrafluprole)、、ピリプロキシフェン（pyriproxyfen）、レスメトリン（resmethrin）、ロテノン（rotenone）、ＳＩ−０４０５（試験名）、スルプロホス（sulprofos）、シラフルオフェン（silafluofen）、スピネトラム（spinetoram）、スピノサド（spinosad）、スピロテトラマート（spirotetramat）、スルホキサフロール(sulfoxaflor)、スルホテップ（sulfotep）、ＳＹＪ−１５９（試験名）、テブフェノジド（tebfenozide）、テフルベンズロン（teflubenzuron）、テフルトリン（tefluthorin）、テルブホス（terbufos）、テトラクロロビンホス（tetrachlorvinphos）、テトラメトリン（tetramethrin）、ｄ−Ｔ−８０−フタルスリン（d-tetramethrin）、テトラメチルフルスリン（tetramethylfluthrin）、チアクロプリド（thiacloprid）、チオシクラム（thiocyclam）、チオジカルブ（thiodicarb）、チアメトキサム（thiamethoxam）、チオファノックス（thiofanox）、チオメトン（thiometon）、トルフェンピラド（tolfenpyrad）、トラロメスリン（tralomethrin）、トリクロルホン（trichlorfon）、トリアズロン（triazuron）、トリフルムロン（triflumuron）、バミドチオン（vamidothion）及びＭＥ−５３４３（試験名）など。 Insecticides (continued): halofenozide, hexaflumuron, hydramethylnon, imidacloprid, isofenphos, indoxacarb, isoprocarb, isoxathion ), Lepimectin, lufenuron, malathion, meperfluthrin, metaflumizone, metalaldehyde, methamidophos, methidathion, methidathion, methacrifos (methacrifos) ), Metalcarb, methomyl, metoprene, methoxychlor, methoxyfenozide, methyl bromide , Monocrotophos, muscalure, nitenpyram, novaluron, noviflumuron, omethoate, oxamyl, oxydemeton-methyl, oxydemeton-methyl (oxydemeton-methyl) oxydeprofos, parathion, parathion-methyl, pentachlorophenol (PCP), permethrin, phenothrin, phenthoate, phoxim, phorate ), Phosalone, phosmet, phosphamidon, pirimicarb, pirimiphos-methyl, profenofos, prothiofos, propaphos, prototri Protrifenbute, pyrometrozine, pyraclofos, pyrethrins, pyridalalyl, pyrifluquinazon, pyriprole, pyrafluprole, proxy, pyrifiprofen, py Resmethrin, rotenone, SI-0405 (study name), sulprofos, silafluofen, spinetram, spinosad, spirotetramat, sulfoxaflor ), Sulfotep, SYJ-159 (test name), tebfenozide, teflubenzuron, tefluthorin, terbufos, tetrachlorvinphos, tetrame Trimethrin, dT-80-phthalthrin, d-tetramethrin, tetramethylfluthrin, thiacloprid, thiocyclam, thiodicarb, thiamethoxam, thiophanox ( thiofanox, thiometon, tolfenpyrad, tralomethrin, trichlorfon, triazuron, triflumuron, vamidomion and ME-5343 (test name).

以下に本発明化合物の合成例、試験例を実施例として具体的に述べることで、本発明をさらに詳しく説明するが、本発明はこれらによって限定されるものではない。 Hereinafter, the present invention will be described in more detail by specifically describing synthesis examples and test examples of the compounds of the present invention as examples, but the present invention is not limited thereto.

合成例に記載したプロトン核磁気共鳴ケミカルシフト値は、基準物質としてＭｅ_４Ｓｉ（テトラメチルシラン）を用い、３００ＭＨｚにて測定した。 The proton nuclear magnetic resonance chemical shift value described in the synthesis example was measured at 300 MHz using Me ₄ Si (tetramethylsilane) as a reference substance.

また、ｓ：シングレット、ｄ：ダブレット、ｔ：トリプレット、ｑ：カルテット、ｍ：マルチプレット、ｂｒｓ：ブロードピークの意味を表す。 Further, s: singlet, d: doublet, t: triplet, q: quartet, m: multiplet, and brs: broad peak.

［合成例］
合成例１
５−（１−（ターシャリーブチル）−３−［｛メチルチオ｝メチル］−１Ｈ−ピラゾール−５−イル）−４−メチル−２−（ピリジン−３−イル）チアゾールの製造（本発明化合物１−００１）
工程１
４−メチル−２（ピリジン−３−イル）−５−（４，４，５，５−テトラメチル−１，３，２−ジオキサボロラン−２−イル）チアゾールの製造
５−ブロモ−４−メチル−２−（ピリジン−３イル）チアゾール２．５ｇのテトラヒドロフラン５０ｍｌ溶液を−１０℃に冷却し、イソピロピルマグネシウムクロリド・リチウムクロリド錯体のテトラヒドロフラン溶液（１．３ｍｏｌ／Ｌ）８．３ｍｌを滴下した。滴下終了後、同温度にて５分間攪拌した。攪拌終了後、該反応混合物に２−メトキシ−４、４、５、５−テトラメチル−１、３、２−ジオキサボロラン１．７ｇを添加した。添加終了後、室温にて５時間撹拌した。反応終了後、該反応混合物に水５０ｍｌを添加し、酢酸エチル（８０ｍｌ）にて抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下溶媒を留去した。得られた残渣をｎ−ヘキサン−酢酸エチル{２：１（体積比、以下同じである。）}にて溶出するシリカゲルクロマトグラフィーで精製し、目的物１．１ｇを褐色固体として得た。
^１ＨＮＭＲ（測定溶媒ＣＤＣｌ_３）δ９．２５−９．１５（ｍ，１Ｈ），８．７０−８．６０（ｍ，１Ｈ），８．３０−８．２０（ｍ，１Ｈ），７．４５−７．３０（ｍ，１Ｈ），２．７０（ｓ，３Ｈ），１．３６（ｓ，１２Ｈ）。 [Synthesis example]
Synthesis example 1
Preparation of 5- (1- (tertiarybutyl) -3-[{methylthio} methyl] -1H-pyrazol-5-yl) -4-methyl-2- (pyridin-3-yl) thiazole (present compound 1 -001)
Process 1
Preparation of 4-methyl-2 (pyridin-3-yl) -5- (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) thiazole 5-bromo-4-methyl- A solution of 2.5 g of 2- (pyridin-3-yl) thiazole in 50 ml of tetrahydrofuran was cooled to −10 ° C., and 8.3 ml of a tetrahydrofuran solution (1.3 mol / L) of isopropylpyrrole magnesium chloride / lithium chloride complex was added dropwise. After completion of dropping, the mixture was stirred at the same temperature for 5 minutes. After the completion of stirring, 1.7 g of 2-methoxy-4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolane was added to the reaction mixture. After completion of the addition, the mixture was stirred at room temperature for 5 hours. After completion of the reaction, 50 ml of water was added to the reaction mixture and extracted with ethyl acetate (80 ml). The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel chromatography eluting with n-hexane-ethyl acetate {2: 1 (volume ratio, the same shall apply hereinafter)} to obtain 1.1 g of the desired product as a brown solid.
¹ H NMR (measurement solvent CDCl ₃ ) δ 9.25-9.15 (m, 1H), 8.70-8.60 (m, 1H), 8.30-8.20 (m, 1H), 7. 45-7.30 (m, 1H), 2.70 (s, 3H), 1.36 (s, 12H).

工程２
５−（１−（ターシャリーブチル）−３−［｛メチルチオ｝メチル］−１Ｈ−ピラゾール−５−イル）−４−メチル−２−（ピリジン−３−イル）チアゾールの製造
４−メチル−２（ピリジン−３−イル）−５−（４，４，５，５−テトラメチル−１，３，２−ジオキサボロラン−２−イル）チアゾール０．８ｇの１，４−ジオキサン２０ｍｌ溶液に、１−（ターシャリーブチル）−５−｛（メチルチオ）メチル｝−１Ｈ−ピラゾール−３−イル−トリフルオロメタンスルホナート０．８８ｇ、リン酸三カリウム１．７ｇ及び［１，１‘−ビス（ジフェニルホスフィノ）フェロセン］パラジウム（II）ジクロリドのジクロロメタン付加物０．２１ｇを順次添加した。添加終了後、反応容器内を窒素ガスで置換した後、１００℃にて４時間撹拌した。反応終了後、該反応混合物に水３０ｍｌを添加し、酢酸エチル（５０ｍｌ）にて抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下溶媒を留去した。得られた残渣をｎ−ヘキサン−酢酸エチル（１：１）にて溶出するシリカゲルカラムクロマトグラフィーで精製し、目的物０．５４ｇを褐色固体として得た。
^１ＨＮＭＲ（測定溶媒ＣＤＣｌ_３）δ９．１６（ｄ，Ｊ＝２．１Ｈｚ，１Ｈ），８．７０−８．６５（ｍ，１Ｈ），８．３０−８．２０（ｍ，１Ｈ），７．５０−７．３０（ｍ，１Ｈ），６．２７（ｓ，１Ｈ），３．７１（ｓ，２Ｈ），２．３３（ｓ，３Ｈ），２．１３（ｓ，３Ｈ），１．５４（ｓ，９Ｈ）。
融点；９５−９８℃。 Process 2
Preparation of 5- (1- (tertiarybutyl) -3-[{methylthio} methyl] -1H-pyrazol-5-yl) -4-methyl-2- (pyridin-3-yl) thiazole 4-methyl-2 To a 20 ml 1,4-dioxane solution of 0.8 g of (pyridin-3-yl) -5- (4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) thiazole, (Tertiarybutyl) -5-{(methylthio) methyl} -1H-pyrazol-3-yl-trifluoromethanesulfonate 0.88 g, tripotassium phosphate 1.7 g and [1,1′-bis (diphenylphosphino) ) Ferrocene] 0.21 g of a dichloromethane adduct of palladium (II) dichloride was sequentially added. After completion of the addition, the inside of the reaction vessel was replaced with nitrogen gas, followed by stirring at 100 ° C. for 4 hours. After completion of the reaction, 30 ml of water was added to the reaction mixture and extracted with ethyl acetate (50 ml). The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography eluting with n-hexane-ethyl acetate (1: 1) to obtain 0.54 g of the objective product as a brown solid.
¹ H NMR (measurement solvent CDCl ₃ ) δ 9.16 (d, J = 2.1 Hz, 1H), 8.70-8.65 (m, 1H), 8.30-8.20 (m, 1H), 7.50-7.30 (m, 1H), 6.27 (s, 1H), 3.71 (s, 2H), 2.33 (s, 3H), 2.13 (s, 3H), 1 .54 (s, 9H).
Melting point: 95-98 ° C.

合成例２
４−メチル−５−［５−｛（メチルチオ）メチル｝−１Ｈ−ピラゾール−３−イル］−２−（ピリジン−３−イル）チアゾールの製造（本発明化合物１−００２）
５−（１−（ターシャリーブチル）−３−［｛メチルチオ｝メチル］−１Ｈ−ピラゾール−５−イル）−４−メチル−２−（ピリジン−３−イル）チアゾール０．４９ｇに蟻酸３ｍｌを添加し、８０℃にて２時間撹拌した。反応終了後、減圧下にて、該反応混合物から蟻酸を留去した。得られた残渣に、飽和炭酸水素ナトリウム水溶液１０ｍｌを添加し、酢酸エチル（２０ｍｌ）にて抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下にて溶媒を留去し、目的物０．３５ｇを褐色固体として得た。
^１ＨＮＭＲ（測定溶媒ＣＤＣｌ_３）δ１０．５５（ｂｒｓ，１Ｈ），９．１７（ｄ，Ｊ＝２．１Ｈｚ，１Ｈ），８．７０−８．６０（ｍ，１Ｈ），８．３０−８．２０（ｍ，１Ｈ），７．５０−７．３０（ｍ，１Ｈ），６．４６（ｓ，１Ｈ），３．７８（ｓ，２Ｈ），２．６８（ｓ，３Ｈ），２．１１（ｓ，３Ｈ）。
融点；１６６−１６８℃。 Synthesis example 2
Preparation of 4-methyl-5- [5-{(methylthio) methyl} -1H-pyrazol-3-yl] -2- (pyridin-3-yl) thiazole (present compound 1-002)
3- (1- (tert-butyl) -3-[{methylthio} methyl] -1H-pyrazol-5-yl) -4-methyl-2- (pyridin-3-yl) thiazole (0.49 g) was mixed with 3 ml of formic acid. The mixture was added and stirred at 80 ° C. for 2 hours. After completion of the reaction, formic acid was distilled off from the reaction mixture under reduced pressure. To the obtained residue, 10 ml of saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate (20 ml). The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 0.35 g of the desired product as a brown solid.
¹ H NMR (measurement solvent CDCl ₃ ) δ 10.55 (brs, 1H), 9.17 (d, J = 2.1 Hz, 1H), 8.70-8.60 (m, 1H), 8.30- 8.20 (m, 1H), 7.50-7.30 (m, 1H), 6.46 (s, 1H), 3.78 (s, 2H), 2.68 (s, 3H), 2 .11 (s, 3H).
Melting point: 166-168 ° C.

合成例３
４−メチル−５−［５−｛（メチルチオ）メチル｝−１−（２，２，２−トリフルオロエチル）−１Ｈ−ピラゾール−３−イル］−２−（ピリジン−３−イル）チアゾールの製造（本発明化合物２−００１）
４−メチル−５−［５−｛（メチルチオ）メチル｝−１Ｈ−ピラゾール−３−イル］−２−（ピリジン−３−イル）チアゾール０．３ｇをＮ，Ｎ−ジメチルホルムアミド５ｍｌに溶解させた。該反応混合物に、０℃にて６０重量％水素化ナトリウム（鉱油中に分散）０．０５ｇを添加した。添加終了後、同温度で１０分間攪拌した。攪拌終了後、該反応混合物に０℃にて２，２，２−トリフルオロエチルトリフルオロメタンスルホナート０．２８ｇを添加した。添加終了後、室温にて３時間攪拌を継続した。反応終了後、該反応混合物に水２０ｍｌを添加し、酢酸エチル（３０ｍｌ）にて抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下にて溶媒を留去した。得られた残渣をｎ−ヘキサン−酢酸エチル（１：１）にて溶出するシリカゲルカラムクロマトグラフィーで精製し、目的物０．２５ｇを淡褐固体として得た。
^１ＨＮＭＲ（測定溶媒ＣＤＣｌ_３）δ９．１６（ｄ，Ｊ＝２．１Ｈｚ，１Ｈ），８．７０−８．６０（ｍ，１Ｈ），８．３０−８．２０（ｍ，１Ｈ），７．４５−７．３０（ｍ，１Ｈ），６．４７（ｓ，１Ｈ），４．９１（ｑ，Ｊ＝８．１Ｈｚ，２Ｈ），３．７８（ｓ，２Ｈ），２．６８（ｓ，３Ｈ），２．０８（ｓ，３Ｈ）。
融点；１０７−１０９℃。 Synthesis example 3
4-methyl-5- [5-{(methylthio) methyl} -1- (2,2,2-trifluoroethyl) -1H-pyrazol-3-yl] -2- (pyridin-3-yl) thiazole Production (Compound 2-001 of the present invention)
0.3 g of 4-methyl-5- [5-{(methylthio) methyl} -1H-pyrazol-3-yl] -2- (pyridin-3-yl) thiazole was dissolved in 5 ml of N, N-dimethylformamide. . To the reaction mixture was added 0.05 g of 60 wt% sodium hydride (dispersed in mineral oil) at 0 ° C. After completion of the addition, the mixture was stirred at the same temperature for 10 minutes. After completion of the stirring, 0.28 g of 2,2,2-trifluoroethyl trifluoromethanesulfonate was added to the reaction mixture at 0 ° C. After completion of the addition, stirring was continued at room temperature for 3 hours. After completion of the reaction, 20 ml of water was added to the reaction mixture and extracted with ethyl acetate (30 ml). The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography eluting with n-hexane-ethyl acetate (1: 1) to obtain 0.25 g of the desired product as a light brown solid.
¹ H NMR (measurement solvent CDCl ₃ ) δ 9.16 (d, J = 2.1 Hz, 1H), 8.70-8.60 (m, 1H), 8.30-8.20 (m, 1H), 7.45-7.30 (m, 1H), 6.47 (s, 1H), 4.91 (q, J = 8.1 Hz, 2H), 3.78 (s, 2H), 2.68 ( s, 3H), 2.08 (s, 3H).
Melting point: 107-109 ° C.

合成例４
４−メチル−５−［５−｛（メチルスルホニル）メチル｝−１−（２，２，２−トリフルオロエチル）−１Ｈ−ピラゾール−３−イル］−２−（ピリジン−３−イル）チアゾールの製造（本発明化合物２−００２）
４−メチル−５−［５−｛（メチルチオ）メチル｝−１−（２，２，２−トリフルオロエチル）−１Ｈ−ピラゾール−３−イル］−２−（ピリジン−３−イル）チアゾール０．１２ｇを酢酸２ｍｌに溶解させた。該反応混合物に３０重量％過酸化水素水０．０９ｇ及びタングステン酸ナトリウム二水和物５ｍｇを添加した。添加終了後、室温にて３時間撹拌した。反応終了後、該反応混合物に飽和亜硫酸水素ナトリウム水溶液５ｍｌを添加し、３０分間攪拌した。攪拌終了後、さらに飽和炭酸水素ナトリウム水溶液３０ｍｌを添加した後、酢酸エチル（５０ｍｌ）にて抽出した。得られた有機層を無水硫酸ナトリウムで脱水・乾燥し、減圧下にて溶媒を留去し、目的物０．１２ｇを白色固体として得た。
^１ＨＮＭＲ（測定溶媒ＣＤＣｌ_３）δ９．１７（ｓ，１Ｈ），８．７０−８．６０（ｍ，１Ｈ），８．３０−８．２０（ｍ，１Ｈ），７．４５−７．３５（ｍ，１Ｈ），６．６８（ｓ，１Ｈ），５．０４（ｑ，Ｊ＝８．４Ｈｚ，２Ｈ），４．４７（ｓ，２Ｈ），２．９９（ｓ，３Ｈ），２．６９（ｓ，３Ｈ）。
融点；２１４−２１７℃。 Synthesis example 4
4-Methyl-5- [5-{(methylsulfonyl) methyl} -1- (2,2,2-trifluoroethyl) -1H-pyrazol-3-yl] -2- (pyridin-3-yl) thiazole (Compound 2-002 of the present invention)
4-Methyl-5- [5-{(methylthio) methyl} -1- (2,2,2-trifluoroethyl) -1H-pyrazol-3-yl] -2- (pyridin-3-yl) thiazole 0 .12 g was dissolved in 2 ml acetic acid. To the reaction mixture, 0.09 g of 30% by weight hydrogen peroxide and 5 mg of sodium tungstate dihydrate were added. After completion of the addition, the mixture was stirred at room temperature for 3 hours. After completion of the reaction, 5 ml of a saturated aqueous sodium hydrogen sulfite solution was added to the reaction mixture and stirred for 30 minutes. After completion of the stirring, 30 ml of a saturated aqueous sodium hydrogen carbonate solution was further added, followed by extraction with ethyl acetate (50 ml). The obtained organic layer was dehydrated and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 0.12 g of the desired product as a white solid.
¹ H NMR (measurement solvent CDCl ₃ ) δ 9.17 (s, 1H), 8.70-8.60 (m, 1H), 8.30-8.20 (m, 1H), 7.45-7. 35 (m, 1H), 6.68 (s, 1H), 5.04 (q, J = 8.4 Hz, 2H), 4.47 (s, 2H), 2.99 (s, 3H), 2 .69 (s, 3H).
Melting point: 214-217 ° C.

本発明化合物は、前記製造法及び実施例に準じて製造することができる。合成例１〜４と同様に製造した本発明化合物の例を第２表乃至第３表に示すが、本発明はこれらのみに限定されるものではない。また、表中「m.p.」は融点を表す
〔第２表〕 This invention compound can be manufactured according to the said manufacturing method and an Example. Examples of the compounds of the present invention produced in the same manner as in Synthesis Examples 1 to 4 are shown in Tables 2 to 3, but the present invention is not limited to these. In the table, “mp” represents the melting point [Table 2].

―――――――――――――――――――――――――――――――――――
No. R³ X¹ X^1a m.p.(℃)
―――――――――――――――――――――――――――――――――――
1-001 CH₃ CH₂SCH₃ C(CH₃)₃ 95-98
1-002 CH₃ CH₂SCH₃ H 166-168
―――――――――――――――――――――――――――――――――――
〔第３表〕 ―――――――――――――――――――――――――――――――――――
No. R ³ X ¹ X ^1a mp (℃)
―――――――――――――――――――――――――――――――――――
1-001 CH ₃ CH ₂ SCH ₃ C (CH ₃ ) ₃ 95-98
1-002 CH ₃ CH ₂ SCH ₃ H 166-168
―――――――――――――――――――――――――――――――――――
[Table 3]

―――――――――――――――――――――――――――――――――――
No. R³ X¹ X^1a m.p.(℃)
―――――――――――――――――――――――――――――――――――
2-001 CH₃ CH₂SCH₃ CH₂CF₃ 107-109
2-002 CH₃ CH₂SO₂CH₃ CH₂CF₃ 214-217
―――――――――――――――――――――――――――――――――――
［試験例］
次に、本発明化合物の有害生物防除剤としての有用性について、以下の試験例において具体的に説明するが、本発明はこれらのみに限定されるものではない。
試験例１トビイロウンカに対する殺虫試験
本発明化合物の１０％乳剤（化合物によっては１０％水和剤を供試）を展着剤の入った水で希釈して、５００ｐｐｍ濃度の薬液を調製した。この薬液中にイネの葉鞘を約１０秒間浸漬し、風乾後試験管に入れ、この中にトビイロウンカ（Ｎｉｌａｐａｒｖａｔａｌｕｇｅｎｓ）の２齢幼虫を試験管当たり５頭放虫し、スポンジで蓋をして２５℃恒温室に収容した。６日後の死虫数を調査し、死虫率(％)(死虫数÷供試虫数×１００)を算出した。尚、試験は２連制で行なった。 ―――――――――――――――――――――――――――――――――――
No. R ³ X ¹ X ^1a mp (℃)
―――――――――――――――――――――――――――――――――――
2-001 CH ₃ CH ₂ SCH ₃ CH ₂ CF ₃ 107-109
2-002 CH ₃ CH ₂ SO ₂ CH ₃ CH ₂ CF ₃ 214-217
―――――――――――――――――――――――――――――――――――
[Test example]
Next, the usefulness of the compound of the present invention as a pest control agent will be specifically described in the following test examples, but the present invention is not limited to these.
Test Example 1 Insecticidal test against brown planthopper A 10% emulsion of the compound of the present invention (depending on the compound, 10% wettable powder) was diluted with water containing a spreading agent to prepare a chemical solution having a concentration of 500 ppm. Rice leaf sheaths are immersed in this chemical solution for about 10 seconds, air-dried and placed in a test tube, and 5 second-instar larvae of Nilaparvata lugens are released per test tube, covered with a sponge and 25 Housed in a constant temperature room. The number of dead insects after 6 days was investigated, and the death rate (%) (number of dead insects ÷ number of test insects × 100) was calculated. In addition, the test was performed by 2 continuous systems.

その結果、供試した化合物の内、下記の化合物が９０％以上の死虫率を示した。
本発明化合物：１−００１、１−００２、２−００１、２−００２
試験例２シルバーリーフコナジラミに対する殺虫試験
内径７ｃｍのスチロールカップに湿った濾紙を敷き、その上に３ｃｍに切り取ったインゲンの葉を置いた。本発明化合物の１０％乳剤（化合物によっては１０％水和剤を供試）を展着剤の入った水で希釈して、５００ｐｐｍ濃度の薬液を調製し、回転式散布塔を用いて薬液をスチロールカップ当たり２．５ｍｌずつ散布した（２．５ｍｇ／ｃｍ^２）。葉を風乾後、シルバーリーフコナジラミ（Ｂｅｍｉｓｉａａｒｇｅｎｔｉｆｏｌｉｉ）の成虫を放虫し、蓋をして２５℃恒温室に収容した。５日後の死虫数を調査し、試験例１と同様の計算式から死虫率を算出した。尚、試験は２連制で行なった。 As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compound of the present invention: 1-001, 1-002, 2-001, 2-002
Test Example 2 Insecticidal test for silver leaf whitefly A moist filter paper was laid on a styrene cup having an inner diameter of 7 cm, and a green leaf cut into 3 cm was placed thereon. A 10% emulsion of a compound of the present invention (depending on the compound, 10% wettable powder) is diluted with water containing a spreading agent to prepare a chemical solution with a concentration of 500 ppm, and the chemical solution is prepared using a rotary spray tower. 2.5 ml was sprayed per styrene cup (2.5 mg / cm ² ). After the leaves were air-dried, adults of silver leaf whiteflies (Bemisia argentifolii) were released, covered, and housed in a thermostatic chamber at 25 ° C. The number of dead insects after 5 days was investigated, and the dead insect rate was calculated from the same calculation formula as in Test Example 1. In addition, the test was performed by 2 continuous systems.

その結果、供試した化合物の内、下記の化合物が９０％以上の死虫率を示した。
本発明化合物：２−００１
試験例３モモアカアブラムシに対する殺虫試験
内径３ｃｍのガラスシャーレに湿った脱脂綿を敷き、その上に同径に切り取ったカンランの葉を置き、モモアカアブラムシ（Ｍｙｚｕｓｐｅｒｓｉｃａｅ）無翅成虫を４頭放虫した。１日後、本発明化合物の１０％乳剤（化合物によっては１０％水和剤を供試）を展着剤の入った水で希釈して、５００ｐｐｍ濃度の薬液を調製し、回転式散布塔にて薬液を散布（２．５ｍｇ/ｃｍ^２）、蓋をして２５℃恒温室に収容した。６日後の死虫数を調査し、試験例１と同様の計算式から死虫率を算出した。尚、試験は２連制で行なった。 As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
The compound of the present invention: 2-001
Test Example 3 Insecticidal test against peach aphid A moist absorbent cotton is laid on a glass petri dish with an inner diameter of 3 cm, and a kanran leaf cut out to the same diameter is placed thereon, and four mosquito aphids (Myzus persicae) adults are released. did. One day later, a 10% emulsion of the compound of the present invention (depending on the compound, 10% wettable powder was tested) was diluted with water containing a spreading agent to prepare a chemical solution with a concentration of 500 ppm. The chemical solution was sprayed (2.5 mg / cm ² ), covered, and stored in a constant temperature room at 25 ° C. The number of dead insects after 6 days was investigated, and the death rate was calculated from the same calculation formula as in Test Example 1. In addition, the test was performed by 2 continuous systems.

その結果、供試した化合物の内、下記の化合物が９０％以上の死虫率を示した。
本発明化合物：１−００１、１−００２、２−００１、２−００２
試験例４ワタアブラムシに対する殺虫試験
内径３ｃｍのガラスシャーレに湿った脱脂綿を敷き、その上に同径に切り取ったキュウリの葉を置き、ワタアブラムシ（Ａｐｈｉｓｇｏｓｓｙｐｉｉ）無翅成虫を４頭放虫した。１日後、本発明化合物の１０％乳剤（化合物によっては１０％水和剤を供試）を展着剤の入った水で希釈して、５００ｐｐｍ濃度の薬液を調製し、回転式散布塔にて薬液を散布（２．５ｍｇ/ｃｍ^２）、蓋をして２５℃恒温室に収容した。６日後の死虫数を調査し、試験例１と同様の計算式から死虫率を算出した。尚、試験は２連制で行なった。 As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compound of the present invention: 1-001, 1-002, 2-001, 2-002
Test Example 4 Insecticidal test for cotton aphids Wet cotton wool with a 3 cm inner diameter petri dish and a cucumber leaf cut out to the same diameter were placed on it, and four cotton aphids (Aphis gossypii) adults were released. One day later, a 10% emulsion of the compound of the present invention (depending on the compound, 10% wettable powder was tested) was diluted with water containing a spreading agent to prepare a chemical solution with a concentration of 500 ppm. The chemical solution was sprayed (2.5 mg / cm ² ), covered, and stored in a constant temperature room at 25 ° C. The number of dead insects after 6 days was investigated, and the death rate was calculated from the same calculation formula as in Test Example 1. In addition, the test was performed by 2 continuous systems.

その結果、供試した化合物の内、下記の化合物が９０％以上の死虫率を示した。
本発明化合物：１−００２、２−００１、２−００２
試験例５モモアカアブラムシに対する土壌潅注処理試験
本発明化合物の１０％乳剤を水道水で希釈して、濃度が１００ｐｐｍの薬液を調製した。 As a result, among the compounds tested, the following compounds showed a death rate of 90% or more.
Compound of the present invention: 1-002, 2-001, 2-002
Test Example 5 Soil irrigation treatment test for peach aphid A 10% emulsion of the compound of the present invention was diluted with tap water to prepare a chemical solution having a concentration of 100 ppm.

プラスチックカップ植えキャベツ苗（２．５本葉期）の株元土壌部分に１０ｍｌの薬液を潅注処理し、温室内に放置した。潅注処理１日後にモモアカアブラムシ（Ｍｙｚｕｓｐｅｒｓｉｃａｅ）の成虫を２０頭／株で放虫し、その後温室内に放置した。放虫６日後の生存虫数を調査し、下記の計算式から対照値を算出した。
対照値(％)＝｛１−（Ｃｂ×Ｔａｉ）／（Ｃａｉ×Ｔｂ）｝×１００
式中の文字は下記を表している。
Ｃｂ：無処理区における処理前の虫の数
Ｃａｉ：無処理区における最終調査時の生存虫数
Ｔｂ：処理区における処理前の虫の数
Ｔａｉ：処理区における最終調査時の生存虫数
その結果、供試した化合物の内、下記の化合物が９０％以上の対照値を示した。
本発明化合物：２−００１、２−００２ 10 ml of the chemical solution was irrigated to the stock soil portion of the plastic cup planted cabbage seedling (2.5 true leaf stage) and left in the greenhouse. One day after the irrigation treatment, 20 mosquitoes / strain of adult peach aphid (Myzus persicae) were released and then left in the greenhouse. The number of surviving insects 6 days after the release was examined, and a control value was calculated from the following formula.
Control value (%) = {1− (Cb × Tai) / (Cai × Tb)} × 100
The characters in the formula represent the following:
Cb: number of insects before treatment in the untreated group Cai: number of live insects at the time of final survey in the untreated group Tb: number of insects before treatment in the treated group Tai: number of live insects at the time of final survey in the treated group Among the compounds tested, the following compounds showed a control value of 90% or more.
Compound of the present invention: 2-001, 2-002

本発明における新規なチアゾール誘導体は、優れた有害生物防除活性、特に殺虫・殺ダニ活性を示し、且つ、ホ乳動物、魚類及び益虫等の非標的生物に対してほとんど悪影響の無い、極めて有用な化合物である。 The novel thiazole derivative in the present invention exhibits excellent pest control activity, particularly insecticidal / miticidal activity, and is extremely useful with little adverse effect on non-target organisms such as mammals, fish and beneficial insects. A compound.

Claims

Formula (1):

[Wherein A ¹ represents N (O) _m2 or CR ¹ ;
A ² represents D1-15, D1-16 or D1-17,
R ¹ is a hydrogen atom, a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , —CHO, —C (O) OH, —C (O) NH ₂ , —C (S) NH ₂ , _{_{_{-S (O) 2 NH 2,}}} C 1 ~C 6 _alkyl, C 1 -C ₆ _haloalkyl, C 1 -C ₆ _alkoxy, C 1 -C ₆ _haloalkoxy, C 1 -C ₆ _alkylthio, C 1 -C ₆ represents _{alkylsulfinyl,} C 1 -C ₆ _{alkylsulfonyl,} C 1 -C ₆ _{haloalkylthio,} a C 1 -C ₆ haloalkylsulfinyl or _C 1 -C ₆ haloalkylsulfonyl,
R ² is a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , —CHO, —C (O) OH, —C (O) NH ₂ , —C (S) NH ₂ , —S ( _{_{_{O) 2 NH 2, C 1}}} ~C 6 _alkyl, C 1 -C ₆ _haloalkyl, C 1 -C ₆ _alkoxy, C 1 -C ₆ _haloalkoxy, C 1 -C ₆ _alkylthio, C 1 -C ₆ alkylsulfinyl, C ₁ -C ₆ _{alkylsulfonyl,} C 1 -C ₆ represents _{haloalkylthio,} a C 1 -C ₆ haloalkylsulfinyl or _C 1 -C ₆ haloalkylsulfonyl, when n is 2 or more integer, each of ^{R 2} are each They may be the same or different from each other,
R ³ is a hydrogen atom, a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , —CHO, —C (O) OH, —C (O) NH ₂ , —C (S) NH ₂ , _{_{_{-S (O) 2 NH 2,}}} C 1 ~C 6 _alkyl, C 3 -C ₆ _cycloalkyl, C 2 -C ₆ _alkenyl, C 2 -C ₆ _alkynyl, C 1 -C ₆ _haloalkyl, C 1 -C ₆ _alkoxy, C 1 -C ₆ _haloalkoxy, C 1 -C ₆ _alkylthio, C 1 -C ₆ _{alkylsulfinyl,} C 1 -C ₆ _{alkylsulfonyl,} C 1 -C ₆ _{haloalkylthio,} C 1 -C ₆ haloalkylsulfinyl, C ₁ -C ₆ haloalkylsulfonyl, _cyano, C 1 -C ₆ _{alkoxycarbonyl,} C 1 -C ₆ _{alkylcarbonyl,} C 1 -C ₆ alkylaminocarbonyl or di _(C 1 -C ₆ A It represents Kill) aminocarbonyl,
D1-15, D1-16 and D1-17 each represent a ring represented by the following structural formula;

X ¹ represents (C ₁ -C ₆ ) alkyl optionally substituted with R ⁵ ;
X ^1a represents a hydrogen _atom, C 1 -C ₆ ^alkyl, optionally substituted by ^{R 5a} _(C 1 ~C ₆₎ _alkyl, C 2 -C ₆ ^alkenyl, optionally substituted by ^{R 5a} _(C 2 ~ C ₆₎ ^{_{^{^{alkenyl, -OH, -OR 6a, -SH,}}}} -S (O) g R 6a, -C (O) R 7a, -C (O) OR 6a, -C (O) N (R 8a) ^{^{^{R 9a, -C (S) N}}} (R 8a) R 9a, D2-32, D2-33, D2-34, D2-36, D2-37, D2-38, D2-81, D2-82, D2- 84, D2-85, D2-87, D2-92, D2-93, D2-95, D2-96 or D2-98,
D2-32, D2-33, D2-34, D2-36, D2-37, D2-38, D2-81, D2-82, D2-84, D2-85, D2-87, D2-92, D2- 93, D2-95, D2-96 and D2-98 each represent a ring represented by the following structural formula;

R ⁵ represents —S (O) _r R ¹¹ ,
R ^5a represents a halogen atom, cyano, —OH, —OR ^11a , —SH, —S (O) _r R ^11a , —C (R ^12a ) = NOH or —C (R ^12a ) = NOR ^11a ,
R ^6a represents C ₁ -C ₆ alkyl;
R ^7a represents a hydrogen atom or C ₁ -C ₆ alkyl;
R ^8a and R ^9a each independently represent a hydrogen atom or C ₁ -C ₆ alkyl;
R ¹¹ represents C ₁ -C ₆ alkyl or (C ₁ -C ₆ ) alkyl optionally substituted by R ¹⁴ ,
R ^11a represents C ₁ -C ₆ alkyl or (C ₁ -C ₆ ) alkyl optionally substituted with R ^14a ,
R ^12a represents a hydrogen atom or C ₁ -C ₆ alkyl;
R ¹⁴ represents a halogen atom, C ₃ -C ₆ cycloalkyl, —OH, —OR ¹⁵ , —SH or —S (O) _r R ¹⁵ ;
R ^14a represents a halogen atom, C ₃ -C ₆ cycloalkyl, —OH, —OR ^15a , —SH or —S (O) _r R ^15a ,
R ¹⁵ and R ^15a each independently represent C ₁ -C ₆ alkyl;
X ² and X ^2b are each independently a halogen atom, cyano, nitro, —OH, —SH, —NH ₂ , C ₁ -C ₆ alkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ alkynyl or C ₃ -C ₈ cycloalkyl,
n and t1 each independently represents an integer of 0 to 3,
p2 represents an integer of 0 to 2,
t4 represents an integer of 0 to 4,
u5 represents an integer of 0 to 5;
u7 represents an integer of 0 to 7,
u9 represents an integer of 0 to 9,
m1 and m2 each independently represent an integer of 0 or 1,
g and r each independently represents an integer of 0, 1 or 2. Or a salt thereof.

A ¹ represents CR ¹
R ¹ and R ³ each independently represent a hydrogen atom, a halogen atom or C ₁ -C ₆ alkyl;
The thiazole derivative or a salt thereof according to claim ₁ , wherein R ² represents a halogen atom or C ₁ -C ₆ alkyl.

A ² represents D1-15 or D1-17,
R ¹ represents a hydrogen atom,
R ³ represents C ₁ -C ₆ alkyl,
X ¹ represents (C ₁ -C ₆ ) alkyl optionally substituted with R ⁵ ;
X ^1a represents a hydrogen atom, C ₁ -C ₆ alkyl or (C ₁ -C ₆ ) alkyl optionally substituted with R ^5a ,
R ⁵ represents —S (O) _r R ¹¹ ,
R ^5a represents a halogen atom,
R ¹¹ represents C ₁ -C ₆ alkyl,
m1 and n represent 0;
The thiazole derivative or a salt thereof according to claim 2, wherein p2 represents an integer of 1.

The pest control agent which contains the 1 type (s) or 2 or more types chosen from the thiazole derivative and its salt of Claims 1-3 as an active ingredient.

The agrochemical which contains 1 type, or 2 or more types chosen from the thiazole derivative of Claims 1-3, and those salts as an active ingredient.

A control agent for inside or ectoparasites of mammals or birds containing one or more selected from the thiazole derivatives according to claim 1 and salts thereof as active ingredients.

An insecticide or acaricide containing as an active ingredient one or more selected from the thiazole derivatives according to claim 1 and a salt thereof.

The soil treatment agent which contains the 1 type (s) or 2 or more types chosen from the thiazole derivative of Claims 1-3, and those salts as an active ingredient.

The soil treatment agent according to claim 8, wherein the soil treatment method is soil irrigation treatment.