WO2012025460A1 - Oxadiazolinone derivatives and use thereof in pest control - Google Patents

Abstract

The present invention provides an oxadiazolinone derivative represented by the formula (I) suitable for use in pest control: wherein G represents a 5- or 6-membered heterocyclic ring containing at least one of oxygen, nitrogen and sulfur atoms, and the heterocyclic ring may be substituted by R³, with the proviso that when G represents a pyridine ring substituted by R³ and when the nitrogen atom in the pyridine ring is at an ortho position relative to the carbon atom bonded to the oxadiazolinone ring, the positions of the carbon atom bonded to R¹ and the carbon atom bonded to R³ are each limited to any positon selected from the ortho and meta positions relative to this nitrogen atom; R³ represents hydrogen, halogen, nitro, cyano, C_1-12 alkyl, C_1-12 haloalkyl, C_1-12 alkoxy, C_1-12 haloalkoxy, or the like; X represents an oxygen or sulfur atom; R1 represents C1-12 haloalkyl, C1-12 haloalkoxy, C_1-12 alkoxy, phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylsulfinyl, phenylsulfonyl, or the like; and R² represents hydrogen, -CH₂CN, C_1-12 alkyl, C_1-12 haloalkyl, or the like.

Description

OXADIAZOLINONE DERIVATIVES AND USE THEREOF IN PEST CONTROL

[0001] The present invention relates to a novel oxadiazolinone derivative and use thereof in pest control.

[0002] Oxadiazolinone compounds are known to be useful as pest control agents.

[0003] For example, WO 2010/035899 discloses a compound in which an oxadiazolinone ring and an aromatic group such as a phenyl group are bonded at ortho and para positions, respectively, relative to nitrogen in a pyridine ring.

[0004] Moreover, WO 2009/066786 discloses a compound in which an oxadiazolinone ring and a group such as a haloalkyl group are bonded at ortho and para positions, respectively, relative to nitrogen in a pyridine ring.

[0005] Furthermore, JP Patent Application Publication No. 2002-205991 discloses a compound in which an oxadiazolinone ring and a trifluoromethyl group are bonded at meta and para positions, respectively, relative to nitrogen in a pyridine ring.

[0006] Although conventional techniques typified by Patent Literatures 1 to 3 disclose oxadiazolinone compounds with various structures, as described above, there is still a great demand on oxadiazolinone derivatives with a novel structure having high activity.

[0007] Thus, the object of the present invention is to provide an oxadiazolinone derivative that has a novel structure and is suitable for use in pest control.

[0008] The present inventors have diligently studied to develop a novel compound that exhibits higher effect as an insecticide and has a broad spectrum thereas and have consequently accomplished the present invention this time by finding a novel oxadiazolinone derivative that is available for use in pest control. Specifically, the present invention relates to an

oxadiazolinone derivative represented by the formula (I):

( I )

wherein

G represents a 5- or 6-membered heterocyclic ring containing at least one of oxygen, nitrogen and sulfur atoms, and the heterocyclic ring may be substituted by R³, with the proviso that when G represents a pyridine ring substituted by R³ and when the nitrogen atom in the pyridine ring is at an ortho position relative to the carbon atom bonded to the oxadiazolinone ring, the positions of the carbon atom bonded to R¹ and the carbon atom bonded to R³ are each limited to any position selected from the ortho and meta positions relative to this nitrogen atom;

R³ represents hydrogen, halogen, nitro, cyano, C_M2 alkyl, C_M2 haloalkyi, C_M2 alkoxy, Ci-₁₂ haloalkoxy, C_M2 alkylsulfenyl, C_M2 alkylsulfinyl, C_M2 alkylsulfonyl, C_M2 haloalkylsulfenyl, Ci-₁₂ haloalkylsulfinyl, C_M2 haloalkylsulfonyl, hydroxy, mercapto or C₃.₈ cycloalkyl;

X represents an oxygen or sulfur atom;

R¹ represents C_M2 haloalkyi, C_M2 haloalkoxy, C_M2 alkoxy, phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylsulfinyl, phenylsulfonyl, phenylamino, (phenyl)(Ci_i₂ alkyl)amino, phenyl- Ci-₁₂ alkoxy, phenyl-Ci_i₂ alkylsulfenyl, phenyl-Ci_i₂ alkylsulfinyl, phenyl-Ci_i₂ alkylsulfonyl, phenyl-Ci-i₂ alkylamino, C_M2 alkylsulfenyl, C_M2 alkylsulfinyl, C_M2 alkylsulfonyl, C_{M 2}

haloalkylsulfenyl, C_M2 haloalkylsulfinyl, C_M2 haloalkylsulfonyl, C_M2 alkylsulfinyl-Ci-i₂ alkyl, Ci. 12 alkylsulfonyl-Ci-12 alkyl, CM₂ haloalkylsulfenyl-Ci-i₂ alkyl, CM₂ haloalkylsulfinyl-Ci-i₂ alkyl, Ci. 12 haloalkylsulfonyl-Ci-i2 alkyl, C2-12 alkenyloxy, C2-12 haloalkenyloxy, C2-12 alkynyloxy, C2-12 haloalkynyloxy, (C_M2 alkyl)₃ silyloxy or hydroxy, and these substituents can be optionally substituted by a substituent(s) selected from halogen, cyano, amino, mercapto, C_M2 alkyl, Ci- 12 haloalkyi, C_M2 haloalkoxy, C2-12 alkenyloxy, C2-12 haloalkenyloxy, C2-12 alkynyloxy, C2-12 haloalkynyloxy, C_M2 alkylsulfenyl-Ci.12 alkyl and hydroxy; and

R² represents hydrogen, -CH₂CN, C_M2 alkyl, C_M2 haloalkyi, C₃.₈ cycloalkyl which may be optionally substituted by a substituent(s) selected from halogen, C_M2 alkyl and C_{M 2} haloalkyi, benzyl which may be optionally substituted by a substituent selected from halogen, cyano, nitro, C_M2 alkyl, C_M2 haloalkyi and C_M2 alkoxy or a substituent represented by one selected from the following formulas Q1 , Q2, Q3, Q4, and Q5:

Q l Q 2 Q 3 Q 4 Q 5

wherein, in each of the formulas Q1 to Q5,

a bond marked with * represents a bond with the nitrogen atom bonded to R² in the formula (I);

R²¹ represents hydrogen, C_M2 alkyl, C_M2 haloalkyi or C₃.₈ cycloalkyl; R²² and R²³ individually represent hydrogen, CM₂ alkyl, CM₂ haloalkyl, CM₂ alkoxy, C₃.₈ cycloalkyl, C2-12 alkenyloxy or C2-12 alkynyloxy, or R²² and R²³ form a 3- to 8-membered heterocyclic ring together with the nitrogen atom bonded thereto, and the heterocyclic ring is constituted on the basis of these substituents capable of constituting R²² and R²³ and may further be optionally substituted by a substituent selected from halogen, CM₂ alkyl, CM₂ haloalkyl, nitro, CM₂ alkoxy, cyano, CM₂ haloalkoxy, CM₂ alkylsulfenyl, CM₂ alkylsulfinyl, CM₂ alkylsulfonyl, CM₂ haloalkylsulfenyl, CM₂ haloalkylsulfinyl, CM₂ haloalkylsulfonyl, hydroxy and mercapto;

R²⁴ and R²⁵ individually represent a substituent selected from CM₂ alkyl, CM₂ haloalkyl, C3.8 cycloalkyl, phenyl and phenyl-Ci.₃ alkyl, and these substituents can be optionally substituted by a substituent(s) selected from halogen, CM₂ alkyl, CM₂ haloalkyl, nitro, CM₂ alkoxy, cyano, CM₂ haloalkoxy, CM₂ alkylsulfenyl, CM₂ alkylsulfinyl, CM₂ alkylsulfonyl, CM₂ haloalkylsulfenyl, CM₂ haloalkylsulfinyl, CM₂ haloalkylsulfonyl, hydroxy and mercapto; and

R²⁶ represents a hydrogen atom or CM₂ alkyl.

[0009] In one embosiment, the present invention relates to the oxadiazolinone derivative represented by the formula (I), wherein when the heterocyclic ring constituting G is substituted by R³,

R³ represents hydrogen, halogen, nitro, cyano, Ci_₆ alkyl, Ci_₆ haloalkyl, Ci_₆ alkoxy, Ci_₆ haloalkoxy, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, hydroxy, mercapto or C₃.₇ cycloalkyl;

X represents an oxygen or sulfur atom;

R¹ represents Ci_₆ haloalkyl, Ci_₆ haloalkoxy, Ci_₆ alkoxy, phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylsulfinyl, phenylsulfonyl, phenylamino, (phenyl)(Ci_₆ alkyl)amino, phenyl- C1-3 alkoxy, phenyl-Ci.₃ alkylsulfenyl, phenyl-Ci.₃ alkylsulfinyl, phenyl-Ci.₃ alkylsulfonyl, phenyl- Ci-3 alkylamino, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, Ci_₆ alkylsulfinyl-Ci_₃ alkyl, Ci_₆ alkylsulfonyl-Ci_₃ alkyl, Ci-6 haloalkylsulfenyl-Ci-₃ alkyl, Ci_₆ haloalkylsulfinyl-Ci_-3 alkyl, Ci_₆ haloalkylsulfonyl-Ci_₃ alkyl, C₂-6 alkenyloxy, C₂.₆ haloalkenyloxy, C₂.₆ alkynyloxy, C₂.₆ haloalkynyloxy, (Ci_₆ alkyl)₃ silyloxy or hydroxy, and these substituents can be optionally substituted by a substituent(s) selected from halogen, cyano, amino, mercapto, Ci_₆ alkyl, Ci_₆ haloalkyl, Ci_₆ haloalkoxy, C₂.₆ alkenyloxy, C₂. 6 haloalkenyloxy, C₂.₆ alkynyloxy, C₂.₆ haloalkynyloxy, Ci_₆ alkylsulfenyl-Ci_₃ alkyl and hydroxy; and

R² represents hydrogen, -CH₂CN, Ci_₆ alkyl, Ci_₆ haloalkyl, C₃.₆ cycloalkyl optionally substituted by a substituent selected from halogen, Ci_₆ alkyl and Ci_₆ haloalkyl, benzyl optionally substituted by a substituent selected from halogen, cyano, nitro, Ci_₆ alkyl, Ci_₆ haloalkyl, and Ci_₆ alkoxy or a substituent represented by one selected from the following formulas Q1 , Q2, Q3, Q4, and Q5:

Q 1 Q 2 Q 3 Q 4 Q 5

wherein, in each of the formulas Q1 to Q5,

a bond marked with * represents a bond with the nitrogen atom bonded to R² in the formula (I);

R²¹ represents hydrogen, Ci_₆ alkyl, Ci_₆ haloalkyl or C₃.₆ cycloalkyl;

R²² and R²³ individually represent hydrogen, Ci_₆ alkyl, Ci_₆ haloalkyl, Ci_₆ alkoxy, C₃.₇ cycloalkyl, C₂-6 alkenyloxy or C₂-6 alkynyloxy, or R²² and R²³ form a 3- to 8-membered heterocyclic ring together with the nitrogen atom bonded thereto, and the heterocyclic ring is constituted on the basis of these substituents capable of constituting R²² and R²³ and may further be optionally substituted by a substituent selected from halogen, Ci_₆ alkyl, Ci_₆ haloalkyl, nitro, Ci_₆ alkoxy, cyano, Ci_₆ haloalkoxy, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, hydroxy and mercapto;

R²⁴ and R²⁵ individually represent a substituent selected from Ci_₆ alkyl, Ci_₆ haloalkyl, C₃.₇ cycloalkyl, phenyl and phenyl-Ci.₃ alkyl, and these substituents can be optionally substituted by a substituent(s) selected from halogen, Ci_₆ alkyl, Ci_₆ haloalkyl, nitro, Ci_₆ alkoxy, cyano, Ci_₆ haloalkoxy, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, hydroxy and mercapto; and

R²⁶ represents a hydrogen atom or Ci_₆ alkyl.

[0010] The present invention also relates to an insecticide containing the above oxadiazolinone derivative as an active ingredient and an animal parasite control agent containing the above oxadiazolinone derivative as an active ingredient, and use of the oxadiazolinone derivative as an insecticide or an animal parasite control agent.

[001 1] In the present invention, "C_x._y" is an abbreviation that means the number of carbon atoms in a substituent within the range of x to y.

[0012] The present invention provides an oxadiazolinone derivative that has high activity and is suitable for use in pest control.

[0013] In an oxadiazolinone derivative of the present invention, examples of CM₂ alkyl include linear or branched alkyl groups such as methyl, ethyl, n- or iso-propyl, n-, iso-, sec- or tert- butyl, n-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl and n-dodecyl.

Particularly, for example, linear or branched alkyl groups having 1 to 6 carbon atoms (Ci_₆ alkyl) such as methyl, ethyl, n- or iso-propyl, n-, iso-, sec- or tert-butyl, n-pentyl and n-hexyl are preferable.

[0014] A heteroatom means an atom other than a carbon atom, and examples thereof include hydrogen, oxygen, sulfur, nitrogen and phosphorus.

[0015] Examples of CM₂ haloalkyi include linear or branched haloalkyi such as CH₂F, CHF₂, CF₃, CF₂CI, CFCI₂, CF₂Br, CF₂CF₃, CFHCF₃, CH₂CF₃, CFCICF₃, CCI₂CF₃, CF₂CH₃, CF₂CH₂F, CF₂CHF₂, CF₂CF₂CI, CF₂CF₂Br, CFHCH₃, CFHCHF₂, CHFCF₃, CHFCF₂CI, CHFCF₂Br, CFCICF₃, CCI₂CF₃, CF₂CF₂CF₃, CH₂CF₂CF₃, CF₂CH₂CF₃, CF₂CF₂CH₃, CHFCF₂CF₃,

CF₂CHFCF₃, CF₂CF₂CHF₂, CF₂CF₂CH₂F, CF₂CF₂CF₂CI, CF₂CF₂CF₂Br, CH(CF₃)CF₃,

CF(CF₃)CF₃, CF(CF₃)CF₂Br, CF₂CF₂CF₂CF₃, CH(CF₃)CF₂CF₃ and CF(CF₃)CF₂CF₃. Of them, Ci-6 haloalkyi is preferable. Each of these CM₂ haloalkyi and Ci_₆ haloalkyi groups also includes perfluoroalkyi in which all replaceable hydrogen atoms on the corresponding alkyl have been substituted by fluorine. The haloalkyi may further be substituted by an optional substituent.

[0016] Examples of CM₂ alkoxy include linear or branched alkoxy such as methoxy, ethoxy, n- propoxy, i-propoxy, n-, iso-, sec- or tert-butoxy, pentyloxy and hexyloxy. Ci_₆ alkoxy is preferable. These alkoxy groups may further be substituted by a substituent.

[0017] Examples of halogen include fluorine, chlorine, bromine and iodine. Fluorine, chlorine and bromine are preferable.

[0018] Examples of C₃.₈ cycloalkyl include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl.

[0019] Examples of C₂_i₂ alkenyl include vinyl, allyl, 1-propenyl, 1- (or 2- or 3-)butenyl and 1- pentenyl. C₂.₄ alkenyl is more preferable.

[0020] Examples of C₂_i₂ alkynyl include ethynyl, propargyl, 1-propynyl, but-3-ynyl and pent-4- ynyl. C₂.₄ alkynyl is more preferable.

[0021] Aryl is preferably a C₆-i₂ aromatic hydrocarbon group, and examples thereof include phenyl, naphthyl, and biphenyl. C₆-io aromatic hydrocarbon groups are preferable, and C₆ aromatic hydrocarbon groups are more preferable. [0022] Specific examples of a 5- or 6-membered heterocyclic ring containing at least one of oxygen, nitrogen and sulfur atoms can include: saturated rings such as pyrrolidinyl, piperidinyl, morpholinyl, thiomorpholinyl, aziridinyl, oxiranyl, thiiranyl, azetidinyl, oxetanyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, tetrahydropyranyl and tetrahydrothiopyranyl; partially saturated rings such as dihydropyrrolyl, dihydroisoxazolyl, dihydropyrazolyl, dihydrooxazolyl and dihydrothiazolyl; and furyl, thienyl, pyrrolyl, isoxazolyl, pyrazolyl, oxazolyl, isothiazolyl, thiazolyl, imidazolyl, triazolyl, oxadiazolyl, thiadiazolyl, tetrazolyl, pyridyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, indolyl, benzoxazolyl, benzothiazolyl and quinolyl. These heterocyclic rings may further be substituted by substituent.

[0023] The substituent in the phrase "may be substituted by an optional substituent" refers to, for example, amino, hydroxy, oxo, thioxo, halogen, nitro, cyano, isocyano, mercapto, isothiocyanato, carboxy, carboxamido, SF₅, aminosulfonyl, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, monoalkylamino, dialkylamino, N-alkylcarbonyl-amino, alkoxy, alkenyloxy, alkynyloxy, cycloalkyloxy, cycloalkenyloxy, alkoxycarbonyl, alkenyloxycarbonyl, alkynyloxycarbonyl, aryloxycarbonyl, alkylcarbonyl, alkenylcarbonyl, alkynylcarbonyl, arylcarbonyl, alkylthio, cycloalkylthio, alkenylthio, cycloalkenylthio, alkynylthio, alkylsulfenyl, alkylsulfinyl, alkylsulfinyl including its isomers, alkylsulfonyl, monoalkylaminosulfonyl, dialkylaminosulfonyl, alkylphosphinyl, alkylphosphonyl, alkylphosphinyl including its isomers, alkylphosphonyl including its isomers, N-alkyl-aminocarbonyl, Ν,Ν-dialkyl-aminocarbonyl, N- alkylcarbonyl-aminocarbonyl, N-alkylcarbonyl-N-alkylaminocarbonyl, aryl, aryloxy, benzyl, benzyloxy, benzylthio, arylthio, arylamino, benzylamino, a heterocyclic ring, trialkylsilyl, alkoxyalkyl, alkylthioalkyl, alkylthioalkoxy, alkoxyalkoxy, phenethyl, benzyloxy, haloalkyl, haloalkoxy, haloalkylthio, haloalkylcarbonyl, haloalkoxycarbonyl, haloalkoxyalkoxy,

haloalkoxyalkylthio, haloalkoxyalkylcarbonyl or haloalkoxyalkyi and preferably refers to chloro, fluoro, bromo, iodo, amino, nitro, cyano, hydroxy, thio or carboxy.

[0024] Preferable subgroups of the oxadiazolinone derivative of the formula (I) according to the present invention are listed below.

1) an oxadiazolinone derivative wherein G is a 6-membered heterocyclic ring comprising, as constituent atoms, at least one nitrogen atom and at least one heteroatom selected from the group consisting of nitrogen, sulfur and oxygen. In this case, G is more preferably a 6-membered heterocyclic ring comprising at least two nitrogen atoms as constituent atoms, even more preferably a 6-membered heterocyclic ring comprising two nitrogen atoms and four carbon atoms as constituent atoms. Particularly, when G is a 6- membered heterocyclic ring comprising two nitrogen atoms and four carbon atoms as constituent atoms, it is preferred that the positions of the two nitrogen atoms should be ortho and para positions, respectively, relative to the site bonded to the oxadiazolinone ring and should also be ortho positions, relative to the site bonded to R¹. It is the most desirable that one of the two nitrogen atoms should be flanked by the site bonded to R¹ and the site bonded to the oxadiazolinone ring and the other nitrogen atom should be positioned at para position relative to the site bonded to the oxadiazolinone ring and simultaneously at ortho position relative to the site bonded to R¹ , wherein R¹ is positioned at para position relative to the site bonded to the oxadiazolinone ring.

(2) an oxadiazolinone derivative wherein G is a 5-membered heterocyclic ring comprising at least one nitrogen atom and, optionally, additional heteroatom(s) as constituent atoms. In this case, G is more desirably a 5-membered heterocyclic ring comprising one or two nitrogen atoms as constituent atoms and even more desirably comprises one nitrogen atom and four carbon atoms as constituent atoms or two nitrogen atoms and three carbon atoms as constituent atoms.

(3) an oxadiazolinone derivative wherein R¹ is CM₂ haloalkyl, CM₂ haloalkoxy, CM₂ alkoxy, phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylamino, (phenyl)(Ci_i₂ alkyl)amino, phenyl-Ci-i₂ alkoxy, CM₂ haloalkylsulfenyl or CM₂ alkylsulfenyl-Ci_i₂ alkyl, and these substituents may be substituted by a substituent selected from halogen, cyano, CM₂ haloalkyl, Ci-12 alkylsulfenyl-Ci-12 alkyl and CM₂ haloalkoxy.

(4) an oxadiazolinone derivative represented by the formula (I) wherein a moiety represented by the following formula:

R¹

I

wherein a bond marked with an asterisk (*) binds to a carbon atom marked with an asterisk (*) in the following formula:

is one of the following formulas G1 to G21 :

wherein R¹ and R³ are as defined above; and each ring of G1 to G21 may further be substituted by an optional substituent.

[0025] In one embodiment, the following groups 1 to 9 of novel oxadiazolinone derivatives are preferable, and they are understood to be the subgroups of the compound represented by the above formula (I) in any of the following groups:

Group 1 : Group 2:

wherein R¹ and R² are as defined above

wherein R¹ and R² are as defined above; Group 3: Group 4:

wherein R¹ and R² are as defined above; wherein R¹ , R², and R³ are as defined above; Group 5: Group 6:

wherein R¹ , R², and R³ are as defined above; wherein R¹ , R², and R³ are as defined above; Group 7: Group 8:

wherein R¹ and R² are as defined above; wherein R¹ and R² are as defined above; and

Group 9:

wherein R¹ and R² are as defined above.

[0026] In another embodiment, R¹ of compounds of formula (I) refers to a substituent comprising a halosubstituted Ci-i₂alkyl group, e.g. CM₂ haloalkyl; CM₂ haloalkoxy; with CM₂ haloalkyl, CM₂ haloalkoxy, C₂_i₂ haloalkenyloxy and/or C₂_i₂ haloalkynyloxy substituted phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylsulfinyl, phenylsulfonyl, phenylamino, (phenyl)(Ci_i₂ alkyl)amino, phenyl-Ci-i₂ alkoxy, phenyl-Ci-i₂ alkylsulfenyl, phenyl-Ci-i₂ alkylsulfinyl, phenyl-Ci. ₁₂ alkylsulfonyl or phenyl-Ci-i₂ alkylamino; CM₂ haloalkylsulfenyl; CM₂ haloalkylsulfinyl; CM₂ haloalkylsulfonyl; C₂_i₂ haloalkenyloxy; or C₂_i₂ haloalkynyloxy.

[0027] In yet another embodiment, R¹ is a substituent selected from the group consisting of Ci. ₁₂ haloalkyl; CM₂ haloalkoxy; with CM₂ haloalkyl, CM₂ haloalkoxy substituted phenyl, phenoxy or pyridyl.

[0028] In yet another embodiment, R¹ represents a substituent comprising a fluorosubstituted Ci_i₂alkyl group of any of the substituents described in paragraphs [0027] and [0026].

[0029] In another embodiment, R² represents H or Ci_i₂alkyl such as methyl.

[0030] Subsequently, a process for producing the oxadiazolinone derivative of the formula (I) of the present invention is described. The process for producing the oxadiazolinone derivative of the formula (I) is not particularly limited, and specifically, the oxadiazolinone derivative of the formula (I) can be produced by the following Production Process (A), (B) or (Β'):

Production Process (A):

[0031] This process comprises: <Step A-1 >

reacting a compound represented by the formula (lnt-1):

R

{ lnt-1)

CN

wherein R¹ and G are as defined above

with a hydroxyamine reagent, if necessary in the presence of an appropriate diluent and/or base to form a carboximidamide intermediate represented by the formula (lnt-2):

wherein R¹ and G are as defined above; subsequently

<Step A-2> reacting the carboximidamide intermediate with a carbonylating agent, if necessary in the presence of an appropriate diluent and/or base to prepare a compound represented by the formula (1-10):

wherein R¹ and G are as defined above

included in the compound of the present invention wherein R² represents hydrogen; and <Step A-3>

reacting the obtained compound with a compound represented by the following formula (r-1):

R²— L ( r-1)

wherein R² is as defined above, and L¹ represents a leaving group, for example, halogen, e.g., chlorine, bromine and fluorine or an alkylsulfonyl or arylsulfonyl group, e.g., methanesulfonyl, trifluoromethanesulfonyl, p-toluenesulfonyl and p-trifluoromethanephenylsulfonyl,

if necessary in the presence of an appropriate diluent and/or base to produce a compound represented by the formula (1-1 1) included in the compounds of the present invention:

wherein R¹ and G are as defined above, and R^2' is as defined in R² with the proviso that hydrogen is not included.

[0032] Each step of Production Process (A) can be performed in accordance with a usual organic synthesis process.

[0033] Examples of the hydroxyamine reagent in <Step A-1 > can include hydroxyamine hydrochloride, hydroxyamine sulfate, and aqueous hydroxyamine solutions.

[0034] The reaction of <Step A-1 > can be carried out in an appropriate diluent, and examples of the diluent used therein can include aliphatic hydrocarbons (hexane, cyclohexane, heptane, etc.), aliphatic halogenated hydrocarbons (dichloromethane, chloroform, carbon tetrachloride, dichloroethane, etc.), aromatic hydrocarbons (benzene, toluene, xylene, chlorobenzene, etc.), ethers (diethyl ether, dibutyl ether, dimethoxyethane (DME), tetrahydrofuran, dioxane, etc.), esters (ethyl acetate, ethyl propionate, etc.), acid amides (dimethylformamide (DMF), dimethylacetamide (DMA), N-methylpyrrolidone, etc.), nitriles (acetonitrile, propionitrile, etc.), dimethyl sulfoxide (DMSO), alcohols (methanol, ethanol, propanol, etc.), water, and mixed solvents thereof. Alcohols are desirable.

[0035] Examples of the appropriate base in <Step A-1 > can include: alkali metal bases such as sodium carbonate, potassium carbonate, sodium hydrogencarbonate, potassium

hydrogencarbonate, sodium acetate, potassium acetate, sodium methoxide, sodium ethoxide and potassium-tert-butoxide; and organic bases such as triethylamine, diisopropylethylamine, tributylamine, N-methylmorpholine, N,N-dimethylaniline, Ν,Ν-diethylaniline, 4-tert-butyl-N,N- dimethylaniline, pyridine, picoline, lutidine, diazabicycloundecene (DBU), diazabicyclooctane and imidazole.

[0036] <Step A-1 > can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately -20 and approximately 200°C, preferably 0 and approximately 120°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 0.1 to 48 hours, preferably 2 to 24 hours.

[0037] In carrying out <Step A-1 >, for example, a hydroxyamine reagent, e.g., hydroxylamine hydrochloride in an amount of 1 mol to 3 mol with respect to 1 mol of the compound of the formula (lnt-1) is reacted in a diluent, for example, ethanol, to obtain the corresponding compound of the formula (lnt-2).

[0038] Examples of novel compounds of the formula (lnt-1) used as a raw material in

Production Process (A) include 4-(pentafluoroethyl)pyrimidine-2-carbonitrile, 4-[2- (trifluoromethyl)phenyl]pyrimidine-2-carbonitrile, 4-[3-(trifluoromethyl)phenyl]pyrimidine-2- carbonitrile, 4-[4-(trifluoromethyl)phenyl]pyrimidine-2-carbonitrile, 6-(trifluoromethyl)-pyrimidine- 4-carbonitrile, 4-[2-(trifluoromethyl)phenoxy]pyrimidine-2-carbonitrile and 4-[4- (trifluoromethyl)phenoxy]pyrimidine-2-carbonitrile.

[0039] Examples of novel compounds of the formula (lnt-2) used as a raw material in

Production Process (A) include N'-hydroxy-4-(trifluoromethyl)pyrimidine-2-carboximidamide, N'-hydroxy-6-(trifluoromethyl)pyrimidine-4-carboximidamide, N'-hydroxy-2- (trifluoromethyl)pyrimidine-4-carboximidamide, N'-hydroxy-4-[2- (trifluoromethyl)phenyl]pyrimidine-2-carboximidamide, N'-hydroxy-4-[3- (trifluoromethyl)phenyl]pyrimidine-2-carboximidamide, N'-hydroxy-4-[4- (trifluoromethyl)phenyl]pyrimidine-2-carboximidarnide, N'-hydroxy-4-[2- (trifluoromethyl)phenoxy]pyrimidine-2-carboximidarTiide, N'-hydroxy-4-[3- (trifluoromethyl)phenoxy]pyrimidine-2-carboxirnidarTiide and N'-hydroxy-4-[4- (trifluoromethyl)phenoxy]pyrirnidine-2-carboxirnidarTiide.

[0040] Examples of the carbonylating agent in <Step A-2> of Production Process (A) can include carbonyldiimidazole, phenyl chlorocarbonate and phosgene.

[0041] The reaction of <Step A-2> of Production Process (A) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in <Step A-1 >. Tetrahydrofuran is desirable.

[0042] The reaction of <Step A-2> of Production Process (A) can be carried out in the presence of an appropriate base, and examples of the base used therein include the same as those exemplified in <Step A-1 >. Diazabicycloundecene (hereinafter, sometimes abbreviated to "DBU") is desirable.

[0043] <Step A-2> of Production Process (A) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately - 20 and approximately 100°C, preferably 0 and approximately 50°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 1 to 30 hours, preferably 3 to 12 hours.

[0044] In carrying out <Step A-2> of Production Process (A), for example, a carbonylating agent, for example, carbonyldiimidazole in an amount of 1 mol to 3 mol with respect to 1 mol of the compound of the formula (lnt-2) is reacted in a diluent, for example, tetrahydrofuran, and the obtained product is then reacted with a base, for example, DBU in an amount of 1 mol to 3 mol to obtain the corresponding compound of the formula (1-10).

[0045] The compound of the formula (1-10) in Production Process (A) is included in the compound (I) of the present invention. Examples thereof include 3-[4- (trifluoromethyl)pyrimidin-2-yl]-1 ,2,4-oxadiazolidin-5-one, 3-[6-(trifluoromethyl)pyrimidin-4-yl]- 1 ,2,4-oxadiazolidin-5-one and 3-[2-(trifluoromethyl)pyrimidin-4-yl]-1 ,2,4-oxadiazolidin-5-one.

[0046] The reaction of <Step A-3> of Production Process (A) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in <Step A-1 >. Dimethylformamide is desirable. [0047] The reaction of <Step A-3> of Production Process (A) can be carried out in the presence of an appropriate base, and examples of the base used therein include the same as those exemplified in <Step A-1 >. Sodium hydride is desirable.

[0048] <Step A-3> of Production Process (A) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately - 20 and approximately 200°C, preferably 20 and approximately 100°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 1 to 30 hours, preferably 3 to 15 hours.

[0049] In carrying out <Step A-3> of Production Process (A), for example, a compound of the formula (r-1), for example, iodomethyl benzoate in an amount of 1 mol to 3 mol with respect to 1 mol of the compound of the formula (1-10) is reacted in the presence of a base, for example, sodium hydride in an amount of 1 mol to 2 mol in a diluent, for example, dimethylformamide, to obtain the corresponding compound of the formula (1-1 1).

[0050] The compound of the formula (1-1 1) in Production Process (A) is included in the compound (I) of the present invention. Examples thereof include 4-methyl-3-[4- (trifluoromethyl)pyrimidin-2-yl]-1 ,2,4-oxadiazol-5(4H)-one, 4-methyl-3-[6- (trifluoromethyl)pyrimidin-4-yl]-1 ,2,4-oxadiazol-5(4H)-one, and 4-methyl-3-[2- (trifluoromethyl)pyrimidin-4-yl]-1 ,2,4-oxadiazol-5(4H)-one.

[0051] The compound of the formula (lnt-1) in Production Process (A) can be produced by Production Process (a), (b), (c), (d), (e), or (f).

Production Process (a):

[0052] This process comprises reacting a compound represented by the formula (a-1):

wherein R¹ , L¹ , and G are as defined above

with a cyanating agent, if necessary in the presence of an appropriate diluent and/or base. Production Process (b):

[0053] This process comprises:

<Step b-1 > reacting a compound represented by the formula (b-1):

wherein R¹ is as defined above, and R⁴ represents Ci.

with a compound represented by the formula (b-2):

wherein R⁵ represents Ci_₄ alkyl,

if necessary in the presence of an appropriate diluent and/or base to form a compound represented by the following formula (b-3):

wherein R¹ , R⁵ and G are as defined above; subsequently <Step b-2>

reacting the obtained compound with an oxidizing agent, if necessary in the presence of appropriate diluent to form a compound represented by the following formula (b-4):

(the compound of the formula (b-4) is included in the compound of the formula (a-1)); and <Step b-3>

reacting the obtained compound with a cyanating agent, if necessary in the presence of an appropriate diluent and/or base.

Production Process (c):

[0054] This process comprises reacting a compound represented by the formula (c-1): L¹

I (e-1)

CN

wherein L¹ and G are as defined above

with a compound represented by the formula (c-2): x-^R ( 0-2) wherein V represents S, O, or NH, and R⁶ represents phenyl, phenyl-Ci.₃ alkyl, Ci_₆ alkyl, Ci_₆ haloalkyl, C₂-6 alkenyl, C₂-6 haloalkenyl, C₂-6 alkynyl or C₂-6 haloalkynyl,

if necessary in the presence of an appropriate diluent and/or base.

Production Process (d): wherein G represents imidazole

[0055] A specific production process of the compound of the formula (lnt-1) is shown in Scheme 1.

Scheme 1

Step d-2

wherein in Step d-1 , a starting compound is reacted with an appropriate alkali metalizing reagent, for example, butyllithium at a temperature of -60°C or lower in an appropriate dehydrated diluent, for example, tetrahydrofuran, and then reacted with dimethylformamide to form aldehyde; and in Step d-2, the aldehyde can be made into a hydroxyimine form through reaction with hydroxyamine hydrochloride at a temperature between 0°C and 70°C in an appropriate diluent, for example, pyridine, and then reacted with acetic anhydride at a temperature between 80°C and 150°C to obtain the object compound.

Production Process (e): wherein G represents pyrazole

[0056] A specific production process of the compound of the formula (lnt-1) is shown in Scheme 2.

Scheme 2:

wherein in Step e-1 , a starting compound can be made into an acid chloride form through reaction with an appropriate halogenating agent, for example, oxalyl chloride in an appropriate diluent, for example, dichloromethane, and then reacted with ammonia water to form acid amide; and in Step e-2, the acid amide can be reacted with trifluoromethanesulfonic anhydride in the presence of an appropriate base, for example, triethylamine at a temperature between - 10°C and 30°C in an appropriate diluent, for example, dichloromethane to obtain the object compound.

Production Process (f): wherein G represents pyrazole

[0057] A specific production process of the compound of the formula (lnt-1) is shown in Scheme 3.

Scheme 3:

wherein in Step f-1 , a starting compound can be made into a 4,5-dihydropyrazole form through reaction in an appropriate diluent, for example, ethanol; in Step f-2, the 4,5-dihydropyrazole form is heat-refluxed in the presence of an appropriate acid catalyst, for example, hydrochloric acid and dehydrated to prepare a pyrazole form; in Step f-3, the pyrazole form is oxidized with an appropriate oxidizing agent, for example, potassium permanganate at a temperature between 10°C and 80°C in an appropriate diluent, for example, a water-acetone mixed solvent to prepare a carboxylic acid form; and in Steps f-4 and f-5, reaction can be performed in the same ways as in Steps b-1 and b-2, respectively, to obtain the object compound. [0058] Production processes (a), (b), (c), (d),(e), and (f) can be performed in accordance with a usual organic synthesis process.

[0059] Examples of the cyanating agent in Production Process (a) can include sodium cyanide, potassium cyanide, copper cyanide and zinc cyanide.

[0060] The reaction of Production Process (a) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in Production Process (A). Dimethyl sulfoxide is desirable.

[0061] Production Process (a) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately -20 and approximately 200°C, preferably 0 and approximately 100°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 0.1 to 48 hours, preferably 3 to 24 hours.

[0062] In carrying out Production Process (a), for example, a cyanating agent, for example, sodium cyanide, in an amount of 1 mol to 2 mol with respect to 1 mol of the compound of the formula (a-1) is reacted in a diluent, for example, DMSO, to obtain the corresponding compound of the formula (lnt-1).

[0063] Examples of the compound of the formula (a-1) in Production Process (a) include 2- chloro-4-(trifluoromethyl)pyrimidine, 4-chloro-6-(trifluoromethyl)pyrimidine, 4-chloro-2- (trifluoromethyl)pyrimidine, 2-(methylsulfonyl)-4-[2-(trifluoromethyl)phenyl]pyrimidine, 2- (methylsulfonyl)-4-[3-(trifluoromethyl)phenyl]pyrimidine and 2-(methylsulfonyl)-4-[4- (trifluoromethyl)phenyl]pyrimidine.

[0064] The compound of the formula (a-1) can be produced, for example, by halogenating or sulfonating a compound of the following formula (a-1-1):

R¹

I ( a -1 -1)

OH

in accordance with a usual organic chemical synthesis process.

[0065] Examples of the compound of the formula (a-1-1) include 4-hydroxy-6- (trifluoromethyl)pyrimidine and 4-hydroxy-2-(trifluoromethyl)pyrimidine.

[0066] The reaction of <Step b-1 > of Production Process (b) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in Production Process (A). Water is desirable. [0067] The reaction of <Step b-1 > of Production Process (b) can be carried out in the presence of an appropriate base, and examples of the base used therein include the same as those exemplified in Production Process (A). Pyridine is desirable.

[0068] <Step b-1 > of Production Process (b) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately - 20 and approximately 200°C, preferably 10 and approximately 120°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 1 to 100 hours, preferably 10 to 50 hours.

[0069] In carrying out <Step b-1 > of Production Process (b), for example, a compound of the formula (b-2), for example, S-methylisothiourea sulfate in an amount of 0.5 mol to 2 mol with respect to 1 mol of the compound of the formula (b-1) is reacted in the presence of pyridine as a base in a diluent, for example, water, to obtain the corresponding compound of the formula (b-3).

[0070] Examples of the compound of the formula (b-1) in Production Process (b) include (1 E)- 1-methoxy-4,4,5,5,5-pentafluoropent-1-en-3-one and (1 E)-1-ethoxy-4, 4,5,5, 5-pentafluoropent- 1-en-3-one.

[0071] Examples of the compound of the formula (b-2) in Production Process (b) include methylisothiourea sulfate and S-ethylisothiourea hydrobromide.

[0072] Examples of the compound of the formula (b-3) in Production Process (b) include 2- (methylsulfanyl)-4-(pentafluoroethyl)pyrimidine.

[0073] The reaction of <Step b-2> of Production Process (b) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified for Production Process (A). Dichloromethane is desirable.

[0074] Examples of the appropriate oxidizing agent in <Step b-2> of Production Process (b) include chromic acid, pyridium chromate, periodic acid, manganese dioxide, potassium permanganate and m-chloroperoxybenzoic acid (MCPBA). MCPBA is desirable.

[0075] <Step b-2> of Production Process (b) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately - 60 and approximately 100°C, preferably between approximately -20 and approximately 50°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. [0076] In carrying out <Step b-2> of Production Process (b), for example, an oxidizing agent, for example, MCPBA in an amount of 2 mol to 4 mol with respect to 1 mol of the compound of the formula (b-3) is reacted in a diluent, for example, dichloromethane, to obtain a compound of the formula (b-4).

[0077] Examples of the compound of the formula (b-4) in Production Process (b) include 2- (methylsulfonyl)-4-(pentafluoroethyl)pyrimidine.

[0078] The reaction conditions of <Step b-3> of Production Process (b) can be the same as those of Production Process (a).

[0079] The reaction of Production Process (c) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in Production Process (A). Dimethylformamide is desirable.

[0080] The reaction of Production Process (c) can be carried out in the presence of an appropriate base, and examples of the base used therein include the same as those exemplified in Production Process (A). Sodium hydride is desirable.

[0081] Production Process (c) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately -20 and approximately 200°C, preferably between 0 and approximately 100°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 0.1 to 24 hours, preferably 1 to 5 hours.

[0082] In carrying out Production Process (c), for example, a compound of the formula (e-2) in an amount of 1 mol to 3 mol with respect to 1 mol of the compound of the formula (c-1) is reacted in the presence of sodium hydride as a base in a diluent, for example, DMF, to obtain the corresponding compound of the formula (lnt-1).

[0083] Examples of the compound of the formula (c-1) in Production Process (c) include 2- chloropyrimidine-4-carbonitrile. Examples of the compound of the formula (c-2) in Production Process (c) include 2,2,2-trifluoroethanethiol.

[0084] The compound of the formula (b-3) in Production Process (b) can be produced by Production Process (g) or (h) shown below.

Production Process (g):

[0085] This process comprises: <Step g-1 >

reactin a compound represented by the formula (g-1):

wherein L¹ and R⁵ are as defined above

with a compound represented by the formula (g-2):

R— B(OH)₂ (g-2) wherein R¹ is as defined above,

if necessary in the presence of an appropriate diluent, catalyst and/or base to form a com ound represented by the following formula (b-3):

wherein R¹ , R⁵, and G are as defined above.

Production Process(h):

[0086] This process comprises reacting a compound represented by the formula (g-1):

wherein L¹ , G, and R⁵ are as defined above

with a compound represented by the formula (h-1):

wherein V represents O or NH, and R⁶ is as defined above,

if necessary in the presence of an appropriate diluent and/or base.

[0087] The reaction of Production Process (g) can be performed in accordance with the process disclosed in WO2004/762. The reaction of Production Process (g) can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in Production Process (A). Dimethoxyethane and water are desirable. [0088] The reaction of Production Process (g) can be carried out in the presence of an appropriate catalyst, and examples of the catalyst used therein include

tetrakis(triphenylphosphine)palladium and dichlorobis(triphenylphosphine)palladium.

Tetrakis(triphenylphosphine)palladium is desirable.

[0089] The reaction of Production Process (g) can be carried out in the presence of an appropriate base, and examples of the base used therein include the same as those exemplified in Production Process (A). Potassium carbonate is desirable.

[0090] The reaction of Production Process (g) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately - 20 and approximately 250°C, preferably between 50 and approximately 150°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 0.1 to 24 hours, preferably 1 to 5 hours.

[0091] In carrying out Production Process (g), for example, a compound of the formula (g-2) in an amount of 1 mol to 3 mol with respect to 1 mol of the compound of the formula (g-1) is reacted in the presence of tetrakis(triphenylphosphine)palladium as a catalyst and potassium carbonate as a base in a diluent, for example, dimethoxyethane and water, to obtain the corresponding compound of the formula (b-3).

[0092] The reaction conditions of Production Process (h) can be the same as those of

Production Process (b). Examples of the compound of the formula (g-1) in Production Process (h) include 4-chloro-2-(methylsulfanyl)pyrimidine.

[0093] Examples of the compound of the formula (h-1) in Production Process (h) include 2,2,2- trifluoroethanol.

Production Process (B): wherein X in the formula (I) represents sulfur

[0094] This process comprises reacting a compound represented by the formula (1-12):

wherein R¹ , R², and G are as defined above

with a sulfurizing agent, if necessary in the presence of an appropriate diluent to produce a compound represented by the formula (1-13):

wherein R¹ , R², and G are as defined above

included in the compound of the present invention.

Production Process (Β'): wherein X in the formula (I) represents sulfur

[0095] This process comprises reacting a carboximidamide intermediate represented by the formula (lnt-2):

wherein R¹ and G are as defined above

with a thiocarbonylating agent to produce a compound represented by the formula (1-13):

wherein R¹ , R², and G are as defined above

included in the compound of the present invention wherein R² represents hydrogen.

[0096] Examples of the sulfurizing agent used in Production Process (B) can include diphosphorus pentasulfide and Lawesson's reagents.

[0097] The reaction of Production Process (B) can be carried out in an appropriate diluent, and examples of the diluent used therein can include the same as those exemplified in Production Process (A), preferably toluene.

[0098] The reaction of Production Process (B) can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately 0 and approximately 200°C, preferably between 20 and approximately 150°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 1 to 20 hours, preferably 3 to 10 hours.

[0099] In carrying out Production Process (B), for example, a Lawesson's reagent in an amount of 0.5 mol to 3 mol with respect to 1 mol of the compound of the formula (1-12) is reacted in an appropriate diluent, for example, toluene, to obtain a compound of the formula (I- 13).

[0100] Examples of the thiocarbonylating agent in Production Process (Β') can include thiocarbonyldiimidazole and thiophosgene.

[0101] The reaction of Production Process (Β') can be carried out in an appropriate diluent, and examples of the diluent used therein include the same as those exemplified in Production Process (A). Tetrahydrofuran is desirable.

[0102] The reaction of Production Process (Β') can be carried out in the presence of an appropriate base, and examples of the base used therein include the same as those exemplified in Production Process (A). DBU is desirable.

[0103] Production Process (Β') can be carried out within a substantially wide temperature range. In general, it can be carried out at a temperature between approximately -20 and approximately 100°C, preferably between 0 and approximately 50°C. The reaction is desirably performed under normal pressure and can also be manipulated under pressure or under reduced pressure. The reaction time is 1 to 30 hours, preferably 3 to 12 hours.

[0104] In carrying out Production Process (Β'), for example, a thiocarbonylating agent, for example, thiocarbonyldiimidazole in an amount of 1 mol to 3 mol with respect to 1 mol of the compound of the formula (lnt-2) is reacted in a diluent, for example, tetrahydrofuran, and then the obtained product is reacted with a base, for example, DBU, in an amount of 1 mol to 3 mol to obtain the corresponding compound of the formula (1-13).

[0105] The compound of the formula (1-13) in Production Process (Β') is included in the compound (I) of the present invention. Examples thereof include 3-[4- (trifluoromethyl)pyrimidin-2-yl]-1 ,2,4-oxadiazole-5(4H)-thione.

[0106] The oxadiazolinone derivative of the present invention usually exhibits potent insecticidal effect and can be used as an insecticide. Furthermore, the oxadiazolinone derivative of the present invention usually exhibits potent disinfesting effect on harmful insects with no or little harmful adverse drug side effect to cultivated plants. Thus, the oxadiazolinone derivative of the present invention can be used for disinfesting a wide range of pest species, for example, harmful sucking insects, chewing insects, and other plant-parasitic pests, stored product insects, and hygiene pests, and can be applied for the purpose of disinfesting or exterminating them. Examples of the harmful pests include the following:

[0107] As for insects, coleopterans such as Callosobruchus chinensis, Sitophilus zeamais, Tribolium castaneum, Epilachna vigintioctomaculata, Agriotes fuscicollis, Anomala rufocuprea, Leptinotarsa decemlineata, Diabrotica spp., Monochamus alternatus, Lissorhoptrus oryzophilus, Lyctus bruneus and Aulacophora femoralis; lepidopterans such as Lymantria dispar, Malacosoma neustria, Pieris rapae, Spodoptera litura, Mamestra brassicae, Chilo suppressalis, Pyrausta nubilalis, Ephestia cautella, Adoxophyes orana, Carpocapsa pomonella, Agrotisfucosa, Galleria mellonella, Plutella maculipennis, Heliothis virescens, and Phyllocnistis citrella; hemipterans such as Nephotettix cincticeps, Nilaparvata lugens,

Pseudococcus comstocki, Unapsis yanonensis, Myzus persicas, Aphis pomi, Aphis gossypii, Rhopalosiphum pseudobrassicas, Stephanitis nashi, Nezara spp., Trialeurodes vaporariorm and Psylla spp.; thysanopterans such as Thrips palmi and Franklinella occidental; orthopterans such as Blatella germanica, Periplaneta americana, Gryllotalpa Africana and Locusta migratoria migratoriodes; isopterans such as Reticulitermes speratus and Coptotermes formosanus; dipterans such as Musca domestica, Aedes aegypti, Hylemia platura, Culex pipiens, Anopheles sinensis, Culex tritaeniorhynchus, Liriomyza torifolii.

[0108] As for the order Acari, for example, Tetranychus cinnabarinus, Tetranychus urticae, Panonychus citri, Aculops pelekassi and Tarsonemus spp.

[0109] As for nematodes, for example, Meloidogyne incognita, Bursaphelenchus lignicolus Mamiya et Kiyohara, Aphelenchoides besseyi, Heterodera glycines, and Pratylenchus spp.

[0110] Furthermore, the oxadiazolinone derivative of the present invention shows excellent plant tolerance and preferable toxicity to warm-blooded animals and is well tolerated by the environment, and thus is suitable for protecting plants and plant parts.

[011 1] The application of the oxadiazolinone derivative of the present invention can bring about increased harvest yields and improved quality of harvested materials. The compound is further suitable for disinfesting harmful pests, particularly, insects, arachnids, helminths, nematodes and mollusks, which are encountered in the protection of stored products and the protection of materials, in the hygiene field, agriculture, horticulture or the veterinary field and in forests, gardens or recreational facilities. The compound of the present invention can be used preferably as a plant protectant. The oxadiazolinone derivative of the present invention has activity against normally sensitive or resistant species and against all or some of stages of growth. The above pests particularly include the following: [0112] From the order Anoplura (Phthiraptera), for example, Damalinia spp., Haematopinus, Linognathus spp., Pediculus spp. and Trichodectes spp.

[0113] From the class Arachnida, for example, Acarus siro, Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus gallinae, Eotetranychus spp., Epitrimerus pyri, Eutetranyctus spp., Eriophyes spp., Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Oligonychus spp., Ornithodoros spp.,

Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Stenotarsonemus spp., Tarsonemus spp., Tetranychus spp. and Vasates lycopersici.

[0114] From the class Bivalvia, for example, Dreissena spp.

[0115] From the order Chilopoda, for example, Geophilus spp. and Scutigera spp.

[0116] From the order Coleoptera, for example, Acanthoscelides obtectus, Adoretus spp., Agelastica alni, Agriotes spp., Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., Anthonomus spp., Anthrenus spp., Apogonia spp., Atomaria spp., Attagenus spp., Bruchidius obtectus, Bruchus spp., Ceuthorhynchus spp., Cleonus mendicus, Conoderus spp.,

Cosmopolites spp., Costelytra zealandica, Curculio spp., Cryptorhynchus lapathi, Dermestes spp., Diabrotica spp., Epilachna spp., Faustinus cubae, Gibbium psylloides, Heteronychus arator, Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypothenemus spp., Lachnosterna consanguinea, Leptinotarsa decemlineata, Lissorhoptrus oryzophilus, Lixus spp., Lyctus spp., Meligethes aeneus, Melolontha melolontha, Migdolus spp., Monochamus spp., Naupactus xanthographus, Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Otiorrhynchus sulcatus, Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Popillia japonica, Premnotrypes spp., Psylliodes chrysocephala, Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Sitophilus spp., Sphenophorus spp., Sternechus spp., Symphyletes spp., Tenebrio molitor, Tribolium spp., Trogoderma spp., Tychius spp.,

Xylotrechus spp. and Zabrus spp.

[0117] From the order Collembola, for example, Onychiurus armatus.

[0118] From the order Dermaptera, for example, Forficula auricularia.

[0119] From the order Diplopoda, for example, Blaniulus guttulatus.

[0120] From the order Diptera, for example, Aedes spp., Anopheles spp., Bibio hortulanus, Calliphora erythrocephala, Ceratitis capitata, Chrysomyia spp., Cochliomyia spp., Cordylobia anthropophaga, Culex spp., Cuterebra spp., Dacus oleae, Dermatobia hominis, Drosophila spp., Fannia spp., Gastrophilus spp., Hylemyia spp., Hyppobosca spp., Hypoderma spp., Liriomyza spp., Lucilia spp., Musca spp., Nezara spp., Oestrus spp., Oscinella frit, Pegomyia hyoscyami, Phorbia spp., Stomoxys spp., Tabanus spp., Tannia spp., Tipula paludosa and Wohlfahrtia spp.

[0121] From the class Gastropoda, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp. and Succinea spp.

[0122] From the class of helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp., Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus

medeinensis, Echinococcus granulosus, Echinococcus multiocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp., Strongyloides fuelleborni,

Strongyloides stercoralis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria and Wuchereria bancrofti.

[0123] The compound of the present invention can further disinfest protozoans such as Eimeria.

[0124] From the order Heteroptera, for example, Anasa tristis, Antestiopsis spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercus.spp., Euschistus spp., Eurygaster spp., Heliopeltis spp., Horchias nobiellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus seriatus, Pseudacysta persea, Rhodonius spp., Sahlbergella singularis, Scotinophora spp., Stephanitis nashi, Tibraca spp. and Triatoma spp.

[0125] From the order Homoptera, for example, Acyrthosipon spp., Aeneolamia spp., Agonoscena spp., Aleurodes spp., Aleurolobus barodensis, Aleurothrixus spp., Amrasca spp., Anuraphis cardui, Aonidiella spp., Aphanostigma piri, Aphis spp., Arboridia apicalis, Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacorthum solani, Bemisia spp., Brachycaudus helichrysii, Brachycolus spp., Brevicoryne brassicae, Calligypona marginata, Carneocephala fulgida, Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus halli, Coccus spp., Chryptomyzus ribis, Dalbulus spp., Dialeurodes spp., Diaphorina spp., Diaspis spp., Doralis spp., Drosicha spp., Dysaphis spp., Dysmicoccus spp., Empoasca spp., Eriosoma spp., Erythroneura spp., Euscelis bilobatus, Geococcus coffeae, Homalodisca coagulata, Hyalopterus arundinis, lcerya spp., Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lepidosaphes spp., Lipaphis erysimi, Macrosiphum spp., Mahanarva fimbriolata, Melanaphis sacchari, Metcalfiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., Nasonovia ribisnigri, Nephotettix spp., Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Parabemisia myricae, Paratorioza spp., Parlatoria spp., Pemphigus spp., Peregrinus maidis, Phenacoccus spp., Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Pinnaspis aspidistrae, Planococcus spp., Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Psylla spp., Pteromalus spp., Pyrilla spp., Quadraspidiotus spp., Quesda gigas, Rastrococcus spp., Rhopalosiphum spp., Saissetia spp., Scaphoides titanus,

Schizaphis graminum, Selenaspidus articulatus, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephala festina, Tenalaphara malayensis, Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., Trialeurodes vaporariorum, Trioza spp., Typhlocyba spp., Unaspis spp. and Viteus vitifolii.

[0126] From the order Hymenoptera, for example, Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis and Vespa spp.

[0127] From the order Isopoda, for example, Armadillidium vulgare, Oniscus asellus and Porcellio scaber.

[0128] From the order Isoptera, for example, Reticulitermes spp. and Odontotermes spp.

[0129] From the order Lepidoptera, for example, Acronicta major, Aedia leucomelas, Agrotis spp., Alabama argillacea, Anticarsia spp., Barathra brassicae, Bucculatrix thurberiella, Bupalus piniarius, Cacoecia podana, Capua reticulana, Carpocapsa pomonella, Cheimatobia brumata, Chilo spp., Choristoneura fumiferana, Clysia ambiguella, Cnaphalocerus spp., Earias insulana, Ephestia kuehniella, Euproctis chrysorrhoea, Euxoa spp., Feltia spp., Galleria mellonella, Helicoverpa spp., Heliothis spp., Hofmannophila pseudospretella, Homona magnanima, Hyponomeuta padella, Laphygma spp., Lithocolletis blancardella, Lithophane antennata, Loxagrotis albicosta, Lymantria spp., Malacosoma neustria, Mamestra brassicae, Mods repanda, Mythimna separata, Oria spp., Oulema oryzae, Panolis flammea, Pectinophora gossypiella, Phyllocnistis citrella, Pieris spp., Plutella xylostella, Prodenia spp., Pseudaletia spp., Pseudoplusia includens, Pyrausta nubilalis, Spodoptera spp., Thermesia gemmatalis, Tinea pellionella, Tineola bisselliella, Tortrix viridana and Trichoplusia spp. [0130] From the order Orthoptera, for example, Acheta domesticus, Blatta orientalis, Blattella germanica, Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana and Schistocerca gregaria.

[0131] From the order Siphonaptera, for example, Ceratophyllus spp. and Xenopsylla cheopis.

[0132] From the order Symphyla, for example, Scutigerella immaculata.

[0133] From the order Thynsanoptera, for example, Baliothrips biformis, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Kakothrips spp.,

Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni and Thrips spp.

[0134] From the order Thysanura, for example, Lepisma saccharina.

[0135] Examples of phytoparasitic nematodes include Anguina spp., Aphelenchoides spp., Belonoaimus spp., Bursaphelenchus spp., Ditylenchus dipsaci, Globodera spp.,

Heliocotylenchus spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Rotylenchus spp., Trichodorus spp., Tylenchorhynchus spp., Tylenchulus spp., Thlenchulus semipenetrans and Xiphinema spp.

[0136] According to the present invention, every plant and every part of plants can be treated. In the present invention, it should be understood that the plants mean all plants and plant populations such as desirable or undesirable wild plants or grain plants (including naturally growing grain plants). The grain plants can be plants that can be obtained by routine plant breeding and optimization methods, by biotechnological and genetic engineering methods or by combinations of these methods. These grain plants include transgenic plants and encompass plant varieties that may or may not be protected by plant breeders' rights. It should be understood that the parts of plants mean every part or organ of plants above or below the ground, such as buds, leaves, flowers, and roots. Examples thereof can also include leaves, needles, stems, trunks, flowers, fruit bodies, fruits, seeds, roots, tubers and subterranean stems. The parts of plants also include collected substances, and vegetatively or reproductively propagating substances, for example, cuttings, tubers, subterranean stems, lateral braches and seeds.

[0137] The treatment of the plants or the parts of plants with the active compound according to the present invention is carried out either directly or by allowing the compound to act on the surroundings, habitats or storage areas of the plants or the parts of plants by routine treatment methods, for example, dipping, spraying, vaporization, atomization, scattering, application and injection, or for propagating substances particularly for seeds, by application of one or more coatings.

[0138] The compound of the present invention exhibits permeable effect, which means that the compound is capable of penetrating through a plant body and moving in the parts of plants from under to above the ground.

[0139] As already described above, all plants and their parts can be treated according to the present invention. In a preferred embodiment, wild plant species and plant cultivars or those obtained by traditional biological breeding methods such as hybridization or protoplast fusion and the parts thereof are treated. In a further preferred embodiment, transgenic plants and plant varieties (genetically modified organisms) obtained by appropriate combinations of genetic engineering methods with conventional methods and the parts thereof are treated. The terms "parts" and "parts of plants" are as described above.

[0140] Particularly preferably, plants of varieties which are commercially available or in use are treated according to the present invention in each case. It is understood that the plant varieties mean plants with novel properties ("traits"), which are obtained by conventional breeding, mutagenesis or recombinant DNA techniques. They can be plant varieties, biotypes or genotypes.

[0141] The treatment according to the present invention can bring about superadditive ("synergistic") effects depending on plant species or plant varieties, their locations and propagation conditions (soil, climate, growth period, and nutrition). Thus, the treatment according to the present invention can probably result in, for example, reduced application rates and/or expanded activity spectra and/or increased activities of substances and compositions available according to the present invention, improved plant growth, increased tolerance to high or low temperatures, increased tolerance to droughts or to water or soil salt contents, improved flowering performance, simplified collection, accelerated maturation, increased harvest yields, improved quality and/or increased nutritional values of collected products, and improved storage stability and/or processability of collected products, which exceed actually expected effects.

[0142] The preferable transgenic plants or plant varieties (obtained by genetic engineering) treated in accordance with the present invention include all plants that have received, by means of genetic modification, genetic materials imparting exceedingly advantageous and useful traits to these plants. Examples of such properties include improved plant growth, increased tolerance to high or low temperatures, increased tolerance to droughts or to water or soil salt contents, improved flowering performance, simplified collection, accelerated maturation, increased harvest yields, improved quality and/or increased nutritional values of collected products, and improved storage stability and/or processability of collected products. Examples where such traits are further and particularly emphasized include improved defense of plants against harmful pests and microorganisms such as insects, mites, phytopathogenic fungi, bacteria and/or viruses, and increased tolerance of plants to certain herbicidally active compounds. Examples of the transgenic plants can include: important grain plants such as grains (wheat and rice), maize, soy bean, potato, sugar beet, tomato, bean, and other vegetable cultivars, cotton, tobacco and rapeseed; and fruit plants such as those bearing fruits, for example, apples, pears, citrus fruits and grapes. Particularly, maize, soy bean, potato, cotton, tobacco and rapeseed are important. Traits that are emphasized are, particularly, increased defense of plants against insects, arachnids, nematodes, slugs and snails attributed to toxins formed in the plants, particularly, toxins formed in the plants by genetic materials derived from Bacillus thuringiensis (e.g., by genes CrylA(a), CrylA(b), CrylA(c), CryllA, CrylllA, CrylllB2, Cry9c, Cry2Ab, Cry3Bb and CrylF, and combinations thereof) (hereinafter, referred to as "Bt plants"). Traits that are also particularly emphasized are increased defense of plants against fungi, bacteria, and viruses attributed to systemic acquired resistance (SAR), systemin, phytoalexin, elicitors, and resistance genes, and corresponding expressed proteins and toxins. Further traits that are particularly emphasized are increased tolerance of plants to certain herbicidally active compounds, for example, imidazolinone, sulfonylurea, glyphosate or phosphinotricin (e.g., "PTA" genes). Genes that impart the desired traits may be allowed to exist in combination with one another in the transgenic plants. Examples of the "Bt plants" can include maize, cotton, soy bean and potato cultivars sold under the trade names YIELD GARD^(R) (e.g., maize, cotton and soy bean), KnockOut^(R) (e.g., maize), Starl_ink^(R) (e.g., maize), Bollgard^(R) (cotton), Nucotn^(R) (cotton) and NewLeaf^(R) (potato). Examples of the plants tolerant to herbicides can include maize, cotton and soy bean cultivars sold under the trade names Roundup Ready^(R) (tolerance to glyphosate; e.g., maize, cotton and soy beans), Liberty Link^(R) (tolerance to phosphinotricin; e.g., rapeseed), IMI^(R) (tolerance to imidazolinones) and STS^(R) (tolerance to sulfonylurea; e.g., maize). Examples of the plants resistant to herbicides (plants bred by conventional manners for imparting herbicide resistance) include cultivars sold under the name Clearfield^(R) (e.g., maize). Of course, these descriptions also hold true for plant varieties having these genetic traits or genetic traits to be developed in the future, and such plant varieties will be developed and/or marketed in the future.

[0143] The listed plants can be treated particularly advantageously with the oxadiazolinone derivative of the present invention at an appropriate concentration.

[0144] The novel compound of the present invention can further be used effectively against various harmful parasitic pests (entozoan and ectozoan), for example, insects and helminths, in the veterinary field. Examples of such harmful parasitic pests include those described below. Examples of insects include Gasterophilus spp., Stomoxys spp., Trichodectes spp., Rhodonius spp., Ctenocephalides canis, Cimx lecturius, Ctenocephalides felis and Lucilia cuprina. Examples of acari include Ornithodoros spp., Ixodes spp. and Boophilus spp.

[0145] The active compound of the present invention is active against parasitic animals, particularly, ectoparasites or endoparasites, in the field of veterinary specialists, i.e., in the veterinary field. The term endoparasite particularly includes helminths such as cestodes, nematodes and trematodes, and protozoans such as Coccidia. The ectoparasites are typically and preferably arthropods, particularly, insects such as flies (biting and licking flies), parasitic fly larvae, lice, hair lice, bird lice and flea, or Acarina such as mites, for example, hard ticks, soft ticks, scab mites, harvest mites and bird mites.

[0146] These parasites include the following:

[0147] From the order Anoplurida, for example, Haematopinus spp., Linognathus spp., Pediculus spp., Phtirus spp. and Solenopotes spp. Specific examples are Linognathus setosus, Linognathus vituli, Linognathus ovillus, Linognathus oviformis, Linognathus pedalis, Linognathus stenopsis, Haematopinus asini macrocephalus, Haematopinus eurysternus, Haematopinus suis, Pediculus humanus capitis, Pediculus humanus corporis, Phylloera vastatrix, Phthirus pubis and Solenopotes capillatus.

[0148] From the order Mallophagida and the suborders Amblycerina and Ischnocerina, for example, Trimenopon spp., Menopon spp., Trinoton spp., Bovicola spp., Werneckiella spp., Lepikentron spp., Damalina spp., Trichodectes spp. and Felicola spp. Specific examples are Bovicola bovis, Bovicola ovis, Bovicola limbata, Damalina bovis, Trichodectes canis, Felicola subrostratus, Bovicola caprae, Lepikentron ovis and Werneckiella equi.

[0149] From the order Diptera and the suborders Nematocerina and Brachycerina, for example, Aedes spp., Anopheles spp., Culex spp., Simulium spp., Eusimulium spp.,

Phlebotomus spp., Lutzomyia spp., Culicoides spp., Chrysops spp., Odagmia spp., Wilhelmia spp., Hybomitora spp., Atylotus spp., Tabanus spp., Haematopota spp., Philipomyia spp., Braula spp., Musca spp., Hydrotaea spp., Stomoxys spp., Haematobia spp., Morellia spp., Fannia spp., Glossina spp., Calliphora spp., Lucilia spp., Chrysomyia spp., Wohlfahrtia spp., Sarcophaga spp., Oestrus spp., Hypoderma spp., Gasterophilus spp., Hippobosca spp., Lipoptena spp., Melophagus spp., Rhinoestrus spp. and Tipula spp. Specific examples are Aedes aegypti, Aedes albopictus, Aedes taeniorhynchus, Anopheles gambiae, Anopheles maculipennis, Calliphora erythrocephala, Chrysozona pluvialis, Culex quinquefasciatus, Culex pipiens, Culex tarsalis, Fannia canicularis, Sarcophaga carnaria, Stomoxys calcitrans, Tipula paludosa, Lucilia cuprina, Lucilia sericata, Simulium reptans, Phlebotomus papatasi,

Phlebotomus longipalpis, Odagmia ornata, Wilhelmia equina, Boophthora erythrocephala, Tabanus bromius, Tabanus spodopterus, Tabanus atratus, Tabanus sudeticus, Hybomitra ciurea, Chrysops caecutiens, Chrysops relictus, Haematopota pluvialis, Haematopota italica, Musca autumnalis, Musca domestica, Haematobia irritans irritans, Haematobia irritans exigua, Haematobia stimulans, Hydrotaea irritans, Hydrotaea albipuncta, Chrysomya chloropyga, Chrysomya bezziana, Oestrus ovis, Hypoderma bovis, Hypoderma lineatum, Przhevalskiana silenus, Dermatobia hominis, Melphagus ovinus, Lipoptena capreoli, Lipoptena cervi,

Hippobosca variegata, Hippobosca equina, Gasterophilus intestinalis, Gasterophilus haemorroidalis, Gasterophilus inermis, Gasterophilus nasalis, Gasterophilus nigricornis, Gasterophilus pecorum and Braulra coeca;

[0150] From the order Siphonapterida, for example, Pulex spp., Ctenocephalides spp., Tunga spp., Xenopsylla spp. and Ceratophyllus spp., and specific examples are

Ctenocephalides canis, Ctenocephalides felis, Pulex irritans, Tunga penetrans and Xenopsylla cheopsis.

[0151] From the order Heteropterida, for example, Cimex spp., Triatoma spp., Rhodnius spp. and Panstrongylus spp.

[0152] From the order Blattarida, for example, Blatta orientalis, Periplaneta americana, Blattela germanica, and Supella spp. (e.g., Supella longipalpa).

[0153] From the subclass Acari (Acarina) and the orders Metastigmata and Mesostigmata, for example, Argas spp., Ornithodorus spp., Otobius spp., Ixodes spp., Amblyomma spp., Rhipicephalus (Boophilus) spp., Dermacentor spp., Haemophysalis spp., Hyalomma spp., Dermanyssus spp., Rhipicephalus spp. (the original genus of multi-host ticks), Ornithonyssus spp., Pneumonyssus spp., Raillietia spp., Pneumonyssus spp., Sternostoma spp., Varroa spp. and Acarapis spp. Specific examples are Argas persicus, Argas reflexus, Ornithodorus moubata, Otobius megnini, Rhipicephalus (Boophilus) microplus, Rhipicephalus (Boophilus) decoloratus, Rhipicephalus (Boophilus) annulatus, Rhipicephalus (Boophilus) calceratus, Hyalomma annatolicum, Hyalomma aegypticum, Hyalomma marginatum, Hyalomma transiens, Rhipicephalus evertsi, Ixodes ricinus, Ixodes hexagonus, Ixodes canisuga, Ixodes pilosus, Ixodes rubicundus, Ixodes scapularis, Ixodes holocyclus, Haemaphysalis concinna, Haemaphysalis punctata, Haemaphysalis cinnabarina, Haemaphysalis otophila,

Haemaphysalis leachi, Haemaphysalis longicorni, Dermacentor marginatus, Dermacentor reticulatus, Dermacentor pictus, Dermacentor albipictus, Dermacentor andersoni, Dermacentor variabilis, Hyalomma mauritanicum, Rhipicephalus sanguineus, Rhipicephalus bursa,

Rhipicephalus appendiculatus, Rhipicephalus capensis, Rhipicephalus turanicus, Rhipicephalus zambeziensis, Amblyomma americanum, Amblyomma variegatum, Amblyomma maculatum, Amblyomma hebraeum, Amblyomma cajennense, Dermanyssus gallinae, Ornithonyssus bursa, Ornithonyssus sylviarum and Varroa jacobsoni;

[0154] From the orders Actinedida (Prostigmata) and Acaridida (Astigmata), for example, Acarapis spp., Cheyletiella spp., Ornithocheyletia spp., Myobia spp., Psorergates spp., Demodex spp., Trombicula spp., Listrophorus spp., Acarus spp., Tyrophagus spp.,

Caloglyphus spp., Hypodectes spp., Pterolichus spp., Psoroptes spp., Chorioptes spp., Otodectes spp., Sarcoptes spp., Notoedres spp., Knemidocoptes spp., Cytodites spp. and Laminosioptes spp. Specific examples are Cheyletiella yasguri, Cheyletiella blakei, Demodex canis, Demodex bovis, Demodex ovis, Demodex caprae, Demodex equi, Demodex caballi, Demodex suis, Neotrombicula autumnalis, Neotrombicula desaleri, Neoschongastia xerothermobia, Trombicula akamushi, Otodectes cynotis, Notoedres cati, Sarcoptis canis, Sarcoptes bovis, Sarcoptes ovis, Sarcoptes rupicaprae (= S. caprae), Sarcoptes equi, Sarcoptes suis, Psoroptes ovis, Psoroptes cuniculi, Psoroptes equi, Chorioptes bovis, Psoergates ovis, Pneumonyssoidic mange, Pneumonyssoides caninum and Acarapis woodi.

[0155] The oxadiazolinone derivative of the present invention is also suitable for disinfesting arthropods, helminths and protozoans that attack animals. The animals include agricultural livestock such as cattle, sheep, goats, horses, pigs, donkeys, camels, buffaloes, rabbits, chickens, turkeys, ducks, geese, cultured fishes and honeybees. The animals further include, for example, pet animals (also referred to as companion animals) such as dogs, cats, cage birds and aquarium fishes, and animals known as experimental animals such as hamsters, guinea pigs, rats and mice.

[0156] The disinfestion of these arthropods, helminths, and/or protozoans is expected to reduce the mortality of animals and improve productivity (of meat, milk, wool, leather, eggs and honey, etc.) and the health of host animals. Thus, the use of the active compound of the present invention achieves the further economical and convenient raising of animals.

[0157] For example, it is desirable to suppress or interrupt the uptake of blood from hosts by parasites (when applicable). The disinfestion of parasites may also help suppress the transmittance of infectious agents.

[0158] The term "disinfest" used herein as to the veterinary field means that the active compound is effective in reducing the incidence of parasite in each animal infected with such a parasite to harmless levels. More specifically, the term "disinfest" used herein means that the active compound is effective in killing each parasite, inhibiting its growth or inhibiting its propagation. [0159] In general, the oxadiazolinone derivative of the present invention, when used in the treatment of animals, can be applied directly. Preferably, the compound of the present invention is applied as pharmaceutical compositions which may contain pharmaceutically acceptable excipients and/or auxiliaries publicly known in the art.

[0160] In the veterinary field and in livestock raising, the active compound is applied (= administered) in a manner known in the art by enteral administration in the form of, for example, tablets, capsules, drinks, drenches, granules, pastes, boluses, methods via feed or suppositories or by parenteral administration such as injections (intramuscular, subcutaneous, intravenous, intraperitoneal, etc.), implants or nasal application, for example, by dermal application in the form of dipping or immersion, spraying, pouring-on, spotting-on, washing or dusting or with the aid of active compound-containing molded articles such as collars, ear tags, tail tags, limb bands, halters and marking tools. The active compound may be formulated as shampoo, appropriate preparations available in aerosols or unpressurized sprays such as pump sprays and atomizer sprays.

[0161] The active compound of the present invention, when used for livestock, poultry, pet animals and the like, can be applied, either directly or after dilution (e.g., 100- to 10,000-fold dilution), as preparations (e.g., powders, wettable powders ["WP"], emulsions, emulsifiable concentrates ["EC"], flowables, homogeneous solutions and suspension concentrates ["SC"]) containing the active compound in an amount of 1 to 80% by weight (% by mass as an SI unit), or can be used as an immersion bath thereof.

[0162] The active compound of the present invention, when used in the veterinary field, may be used in combination with appropriate synergists or other active compounds, such as miticides, insecticides, anthelmintics and antiprotozoal drugs.

[0163] In the present invention, substances having insecticidal effect on pests including all of them are referred to as insecticides.

[0164] The active compound of the present invention can be prepared in conventional dosage forms, when used as an insecticide. Examples of the dosage forms include solutions, emulsions, wettable powders, water-dispersible granules, suspensions, powders, foams, pastes, tablets, granules, aerosols, active compound-impregnated natural and synthetic substances, microcapsules, seed coating agents, preparations used with a combustion apparatus (e.g., smoking or fuming cartridges, cans and coils as combustion apparatuses) and ULV (cold or warm mist). [0165] These preparations can be produced by a process publicly known per se in the art. The preparations can be produced, for example, by mixing the active compound with a developer i.e., a liquid diluent or carrier, a liquefied gas diluent or carrier, or a solid diluent or carrier, and optionally with a surfactant i.e., an emulsifier and/or a dispersant and/or a foaming agent.

[0166] When water is used as the developer, for example, an organic solvent can also be used as an auxiliary solvent.

[0167] Examples of the liquid diluent or carrier include aromatic hydrocarbons (e.g., xylene, toluene and alkylnaphthalene), chlorinated aromatic or chlorinated aliphatic hydrocarbons (e.g., chlorobenzene, ethylene chloride and methylene chloride), aliphatic hydrocarbons (e.g., cyclohexane), paraffin (e.g., mineral oil fractions), alcohols (e.g., butanol or glycol and their ethers or esters), ketones (e.g., acetone, methyl ethyl ketone, methyl isobutyl ketone and cyclohexanone), strong polar solvents (e.g., dimethylformamide and dimethyl sulfoxide) and water.

[0168] The liquefied gas diluent or carrier can be, for example, those in a gas state at normal temperature and normal pressure, such as aerosol propellants including butane, propane, nitrogen gas, carbon dioxide and halogenated hydrocarbon.

[0169] Examples of the solid diluent include pulverized natural minerals (e.g., kaolin, clay, talc, chalk, quartz, attapulgite, montmorillonite and diatomaceous earth) and pulverized synthetic minerals (e.g., highly dispersed silicic acid, alumina and silicate).

[0170] Examples of the solid carrier for granules include pulverized and sieved rocks (e.g., calcite, marble, pumice, sepiolite, and dolomite), synthetic granules of inorganic or organic powder and fine particles of organic materials (e.g., sawdust, coconuts, corncobs and tobacco stems).

[0171] Examples of the emulsifier and/or the foaming agent include: nonionic or anionic emulsifiers such as polyoxyethylene fatty acid ester, polyoxyethylene fatty acid alcohol ether (e.g., alkylaryl polyglycol ether), alkylsulfonate, alkylsulfate and arylsulfonate; and albumin hydrolysates.

[0172] Examples of the dispersant include lignin-sulfite waste liquors and methylcellulose.

[0173] A fixative may also be used in the preparations (powders, granules or emulsions), and examples of the fixative include carboxymethylcellulose and natural or synthetic polymers (e.g., gum arabic, polyvinyl alcohol and polyvinyl acetate). [0174] A colorant may also be used, and examples of the colorant include inorganic pigments (e.g., iron oxide, titanium oxide and Prussian Blue), organic dyes (e.g., alizarin dyes, azo dyes and metallophthalocyanine dyes), and further, trace elements such as iron, manganese, boron, copper, cobalt, molybdenum and zinc salts.

[0175] The preparations can generally contain the active ingredient in an amount ranging from 0.1 to 95% by weight, preferably 0.5 to 90% by weight.

[0176] The oxadiazolinone derivative of the present invention can also exist as mixtures with other active compounds, for example, insecticides, toxic feed, bactericides, miticides, nematicides, fungicides, growth regulators and herbicides, in their commercially useful preparation forms and in application forms prepared from these preparations.

[0177] The content of the compound of the present invention in a commercially useful application form can vary within a wide range.

[0178] The concentration of the active compound of the present invention in actual use can be, for example, in the range of 0.0000001 to 100% by weight, preferably 0.00001 to 1 % by weight.

[0179] The oxadiazolinone derivative of the present invention can be used through conventional methods suitable for usage patterns.

[0180] The oxadiazolinone derivative of the present invention has stability effective against alkali on lime materials when used against hygiene pests and pests infesting stored products, and also exhibits excellent residual effect on wood and soil.

[0181] The active compound of the present invention is also low toxic to warm-blooded animal and can be used safely.

Examples

[0182] Next, the present invention will be described further specifically on the basis of Examples. However, the present invention is not intended to be limited to them by any means.

Example 1 : Synthesis of 3-r4-(trifluoromethyl)pyrimidin-2-vn-1 ,2,4-oxadiazol-5-one

(Compound No. G1 -1 )

[0183] <Step 1-1 > Synthesis of N'-hydroxy-4-(trifluoromethyl)pyrimidine-2-carboxirnidarnide

[0184] Hydroxylamine hydrochloride (0.71 g) and sodium hydrogencarbonate (0.85 g) were heat-refluxed for 1 hour in ethanol and then cooled to 0°C, and an ethanol solution of 4- (trifluoromethyl)pyrimidine-2-carbonitrile (0.8 g) was dropped theron. The mixture was stirred at room temperature for 20 hours, and then, the solvent was concentrated. Water was added to the residue, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated and the residue was purified by silica gel column chromatography to obtain N'-hydroxy-4-(trifluoromethyl)pyrimidine-2- carboximidamide (0.73 g).

[0185] <Step 1-2> Synthesis of 3-[4-(trifluoromethyl)pyrimidin-2-yl]-1 ,2,4-oxadiazol-5-one (G1-1)

[0186] N'-hydroxy-4-(trifluoromethyl)pyrimidine-2-carboximidamide (0.5 g) was dissolved in tetrahydrofuran and carbonyldiimidazole (0.43 g) was added thereto. The mixture was stirred at room temperature for 2 hours. Then, DBU (0.43 ml_) was added thereto, and the mixture was stirred at room temperature for 20 hours. 2 N hydrochloric acid was added thereto, followed by extraction with ethyl acetate. Then, the organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 3-[4-(trifluoromethyl)pyrimidin-2-yl]-1 ,2,4-oxadiazol-5-one

(0.05 g). Example 2: Synthesis of 3-r4-(pentafluoroethyl)pyrimidin-2-vn-1 ,2,4-oxadiazol-5-one (Compound No. G1 -2)

[0187] <Step 2-1 > Synthesis of 2-(methylsulfanyl)-4-(pentafluoroethyl)pyrimidine

[0188] 1-Ethoxy-4,4,5,5,5-pentafluoropent-1-en-3-one (6.5 g) and S-methylisothiourea sulfate (4.2 g) were dissolved in water (60 ml). Pyridine (3.5 g) was added thereto, and then, the mixture was heat-refluxed for 40 hours. The reaction mixture was subjected to extraction with ethyl acetate, and then, the organic layer was washed with 1 N hydrochloric acid and saturated saline and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to obtain 2-(methylsulfanyl)-4-(pentafluoroethyl)pyrimidine (1.45 g).

[0189] <Step 2-2> Synthesis of 2-(methylsulfonyl)-4-(pentafluoroethyl)pyrimidine

[0190] 2-(Methylsulfanyl)-4-(pentafluoroethyl)pyrimidine (1.45 g) was dissolved in dichloromethane. m-Chloroperbenzoic acid (3.7 g) was added thereto at 0°C, and the mixture was stirred at room temperature for 5 hours. An aqueous sodium thiosulfate solution and a saturated aqueous solution of sodium hydrogencarbonate were added thereto, and the mixture was stirred for 30 minutes. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 2-(methylsulfonyl)-4-(pentafluoroethyl)pyrimidine (1.47 g).

[0191] <Step 2-3> Synthesis of 4-(pentafluoroethyl)pyrimidine-2-carbonitrile

[0192] 2-(Methylsulfonyl)-4-(pentafluoroethyl)pyrimidine (0.7 g) was dissolved in dimethyl sulfoxide, and sodium cyanide (0.12 g) was added thereto at 10°C. The mixture was stirred at room temperature for 30 minutes, and then, water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated sodium hydrogencarbonate and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 4- (pentafluoroethyl)pyrimidine-2-carbonitrile (0.29 g).

[0193] <Step 2-4> Synthesis of N'-hydroxy-4-(pentafluoroethyl)pyrimidine-2- carboximidamide

[0194] An aqueous hydroxylamine solution (0.16 g) was added to an ethanolic solution of 4- (pentafluoroethyl)pyrimidine-2-carbonitrile (0.29 g), and the mixture was stirred at room temperature for 5 hours. Water was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was washed with t-butylmethyl ether to obtain N'- hydroxy-4-(pentafluoroethyl)pyrimidine-2-carboximidamide (0.28 g).

<Step 2-5> Synthesis of 3-[4-(pentafluoroethyl)pyrimidin-2-yl]-1 ,2,4-oxadiazol-5-

[0196] N'-Hydroxy-4-(pentafluoroethyl)pyrimidine-2-carboximidamide (0.2 g) was dissolved in tetrahydrofuran, and carbonyldiimidazole (0.14 g) was added thereto. The mixture was stirred at room temperature for 2 hours. Then, DBU (0.14 g) was added thereto, and the mixture was stirred at room temperature for 5 hours. 2 N hydrochloric acid was added thereto, followed by extraction with ethyl acetate. Then, the organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated, and the precipitated crystal was filtered and washed with water and t-butylmethyl ether to obtain 3-[4-(pentafluoroethyl)pyrimidin-2-yl]- 1 ,2,4-oxadiazol-5-one (0.12 g).

Example 3: Synthesis of 3-r4-(2,2,2-trifluoroethoxy)pyrimidin-2-vni,2,4-oxadiazol-5(4H)- one (G1 -7)

[0197] <Step 3-1 > Synthesis of 4-(2,2,2-trifluoroethoxy)pyrimidine-2-carbonitrile

[0198] 2-(Methylsulfonyl)-4-(2,2,2-trifluoroethoxy)pyrimidine (0.8 g) was dissolved in dimethyl sulfoxide, and sodium cyanide (0.15 g) was added thereto at 10°C. The mixture was stirred at room temperature for 30 minutes, and then, water was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with saturated sodium hydrogencarbonate and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 4-(2,2,2- trifluoroethoxy)pyrimidine-2-carbonitrile (0.2 g).

[0199] <Step 3-2> Synthesis of N'-hydroxy-4-(2,2,2-trifluoroethoxy)pyrimidine-2- carboximidamide

[0200] An aqueous hydroxylamine solution (0.13 g) was added to an ethanolic solution of 4- (2,2,2-trifluoroethoxy)pyrimidine-2-carbonitrile (0.2 g), and the mixture was stirred at room temperature for 20 hours. Water was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was washed with t-butylmethyl ether to obtain N'- hydroxy-4-(2,2,2-trifluoroethoxy)pyrirnidine-2-carboxirnidarTiide (0.22 g).

[0201] <Step 3-3> Synthesis of 3-[4-(2,2,2-trifluoroethoxy)pyrimidin-2-yl]1 ,2,4-oxadiazol- 5(4H)-one (G1-7)

[0202] N'-Hydroxy-4-(2,2,2-trifluoroethoxy)pyrirnidine-2-carboxirnidarTiide (0.22 g) was dissolved in tetrahydrofuran. Carbonyldiimidazole (0.17 g) was added thereto, and the mixture was stirred at room temperature for 2 hours. 1 ,8-diazabicyclo[5.4.0]-7-undecene (0.17 g) was added thereto, and the mixture was stirred at room temperature for 5 hours. 2 N hydrochloric acid was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was washed with t-butylmethyl ether to obtain 3-[4-(2,2,2- trifluoroethoxy)pyrimidin-2-yl]1 ,2,4-oxadiazol-5(4H)-one (0.23 g).

Example 4: Synthesis of 3-r6-(trifluoromethyl)pyrimidin-4-vn-1 ,2,4-oxadiazol-5-one (G2- D

[0203] <Step 4-1 > Synthesis of 6-(trifluoromethyl)pyrimidine-4-carbonitrile

[0204] 4-Chloro-6-(trifluoromethyl)pyrimidine (0.98 g) and potassium cyanide (0.7 g) were added to acetonitrile, and the mixture was heat-refluxed for 20 hours. Insoluble matter was filtered off, and the solvent was distilled off. The residue was purified by silica gel column chromatography to obtain 6-(trifluoromethyl)pyrimidine-4-carbonitrile (0.18 g). [0205] <Step 4-2> Synthesis of N'-hydroxy-6-(trifluoromethyl)pyrimidine-4-carboxirnidarTiicle

[0206] Hydroxylamine hydrochloride (0.16 g) and sodium hydrogencarbonate (0.2 g) were heat-refluxed for 1 hour in ethanol and then cooled to 0°C, and an ethanol solution of 6- (trifluoromethyl)pyrimidine-4-carbonitrile (0.18 g) was dropped thereon. The mixture was stirred at room temperature for 20 hours, and then, the solvent was concentrated. Water was added to the residue, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated to obtain N'-hydroxy-4- (trifluoromethyl)pyrimidine-2-carboximidamide (0.19 g).

[0207] <Step 4-3> Synthesis of N'-[(phenoxycarbonyl)oxy]-6-(trifluoromethyl)pyrimidine-4- carboximidamide

[0208] N'-Hydroxy-4-(trifluoromethyl)pyrimidine-2-carboximidamide (0.19 g) and

triethylamine (0.13 g) were dissolved in DMF, and phenyl chlorocarbonate (0.16 g) was added thereto at 0°C. The mixture was stirred at room temperature for 4 hours, and then, 5% saline was added thereto, followed by extraction with ethyl acetate. The organic layer was washed with 5% saline and saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain N'-[(phenoxycarbonyl)oxy]-6-(trifluoromethyl)pyrimidine-4-carboximidamide (0.22 g).

[0209] <Step 4-4> Synthesis of 3-[6-(trifluoromethyl)pyrimidin-4-yl]-1 ,2,4-oxadiazol-5-one (G2-1)

[0210] N'-[(Phenoxycarbonyl)oxy]-6-(trifluoromethyl)pyrimidine-4-carboximidami (0.22 g) was dissolved in chlorobenzene, and the solution was irradiated with microwave at 180°C for 1.5 hours. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 3-[6-(trifluoromethyl)pyrimidin-4-yl]-1 ,2,4-oxadiazol-5-one (0.04 g).

Example 5: Synthesis of 3-r2-(trifluoromethyl)pyrimidin-4-vni,2,4-oxadiazol-5(4H)-one

(G3-1 )

[021 1] <Step 5-1 > Synthesis of N'-hydroxy-2-(trifluoromethyl)pyrimidine-4-carboximidamide

[0212] An aqueous hydroxylamine solution (0.16 g) was added to an ethanolic solution of 2- trifluoromethylpyrimidine-4-carbonitrile (0.22 g), and the mixture was stirred at room

temperature for 20 hours. Water was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was washed with t-butylmethyl ether to obtain N'- hydroxy-2-(trifluoromethyl)pyrimidine-4-carboximidamide (0.18 g).

[0213] <Step 5-2> Synthesis of 3-[2-(trifluoromethyl)pyrimidin-4-yl]1 ,2,4-oxadiazol-5(4H)-one (G3-1)

[0214] N'-Hydroxy-2-(trifluoromethyl)pyrimidine-4-carboximidamide (0.18 g) was dissolved in tetrahydrofuran. Carbonyldiimidazole (0.16 g) was added thereto, and the mixture was stirred at room temperature for 2 hours. 1 ,8-diazabicyclo[5.4.0]-7-undecene (0.16 g) was added thereto, and the mixture was stirred at room temperature for 5 hours. 2 N hydrochloric acid was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was washed with t-butylmethyl ether to obtain 3-[2-(trifluoromethyl)pyrimidin-4-yl]1 ,2,4- oxadiazol-5(4H)-one (0.14 g).

Example 6: Synthesis of 3-{2-r(2,2,2-trifluoroethyl)sulfanvnpyrimidin-4-yl)1 ,2,4- oxadiazol-5(4H)-one (G3-10)

[0215] <Step 6-1 > Synthesis of 2-[(2,2,2-trifluoroethyl)sulfanyl]pyrimidine-4-carbonitrile

[0216] A dimethylformamide solution of trifluoroethanethiol (0.3 g) was dropped onto a dimethylformamide suspension of sodium hydride (0.11 g) at 0°C. The mixture was stirred for 30 minutes, and then, a dimethylformamide solution of 2-chloropyrimidine-4-carbonitrile (0.3 g) was added thereto. The mixture was stirred at room temperature for 3 hours, and then, water was added thereto, followed by extraction with ethyl acetate. The organic layer was separated, then washed with water and saturated saline and dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 2-[(2,2,2-trifluoroethyl)sulfanyl]pyrimidine-4-carbonitrile (0.4 g).

[0217] <Step 6-2> Synthesis of N'-hydroxy-2-(2,2,2-trifluoroethyl)sulfanyl]pyrimidine-4- carboximidamide

[0218] An aqueous hydroxylamine solution (0.16 g) was added to an ethanolic solution of 2- [(2,2,2-trifluoroethyl)sulfanyl]pyrimidine-4-carbonitrile (0.32 g), and the mixture was stirred at room temperature for 20 hours. Water was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was washed with t-butylmethyl ether to obtain N'-hydroxy-2-(2,2,2-trifluoroethyl)sulfanyl]pyrimidine-4-carboximidamide (0.33 g).

[0219] <Step 6-3> Synthesis of 3-{2-[(2,2,2-trifluoroethyl)sulfanyl]pyrimidin-4-yl}1 ,2,4- oxadiazol-5(4H)-one (G3-10)

[0220] N'-Hydroxy-2-(2,2,2-trifluoroethyl)sulfanyl]pyrimidine-4-carboximidamide (0.2 g) was dissolved in tetrahydrofuran. Carbonyldiimidazole (0.14 g) was added thereto, and the mixture was stirred at room temperature for 2 hours. 1 ,8-diazabicyclo[5.4.0]-7-undecene (0.16 g) was added thereto, and the mixture was stirred at room temperature for 5 hours. 2 N hydrochloric acid was added thereto, followed by extraction with ethyl acetate. The organic layer was separated and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was washed with t-butylmethyl ether to obtain 3-{2-[(2,2,2- trifluoroethyl)sulfanyl]pyrimidin-4-yl}1 ,2,4-oxadiazol-5(4H)-one (0.22 g).

Example 7: Synthesis of 3-ri-methyl-5-(trifluoromethyl)-1 H-imidazol-2-vn-1 ,2,4- oxadiazol-5(4H)-one (G6-113)

[0221] <Step 7-1 > Synthesis of 1-methyl-5-(trifluoromethyl)-1 H-imidazole-2-carbaldehyde

[0222] n-Butyllithium (5 ml, 1.6 M hexane solution) was dropped onto a tetrahydrofuran solution of 1-methyl-5-(trifluoromethyl)-1 H-imidazole (1.1 g) at -78°C in an argon atmosphere. The mixture was stirred for 30 minutes, and then, a tetrahydrofuran solution (2 ml) of dimethylformamide (0.59 g) was dropped thereon. The mixture was stirred at 0°C for 2 hours, and then, the reaction solution was added to ice water, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 1-methyl-5-(trifluoromethyl)-1 H-imidazole-2- carbaldehyde (1.24 g).

[0223] <Step 7-2> Synthesis of 1-methyl-5-(trifluoromethyl)-1 H-imidazole-2-carbonitrile

[0224] 1-Methyl-5-(trifluoromethyl)-1 H-imidazole-2-carbaldehyde (1.24 g) was dissolved in pyridine (50 ml). Hydroxylamine hydrochloride (2.02 g) was added thereto, and the mixture was stirred at 50°C for 1 hour. After cooling to room temperature, the solvent was

concentrated. The residue was dissolved in acetic anhydride (70 ml), and the solution was stirred at 100°C for 3 hours and at 125°C for 1 hour. The solvent was concentrated, and water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with a saturated sodium hydrogencarbonate solution and saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 1-methyl-5- (trifluoromethyl)-1 H-imidazole-2-carbonitrile (1.17 g).

[0225] <Step 7-3> Synthesis of N'-hydroxy-1-methyl-5-(trifluoromethyl)-1 H-imidazole-2- carboximidamide

[0226] An ethanol suspension (13 ml) of hydroxylamine hydrochloride (1.01 g) and sodium hydrogencarbonate (1.22 g) was heat-refluxed for 45 minutes. After cooling to room temperature, an ethanolic solution (2 ml) of 1-methyl-5-(trifluoromethyl)-1 H-imidazole-2- carbonitrile (1.21 g) was added thereto at 0°C, and the mixture was stirred overnight at room temperature. The solvent was concentrated, and then, water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain N'-hydroxy-1-methyl-5- (trifluoromethyl)-1 H-imidazole-2-carboximidamide (0.98 g).

[0227] <Step 7-4> Synthesis of 3-[1-methyl-5-(trifluoromethyl)-1 H-imidazol-2-yl]-1 ,2,4- oxadiazol-5(4H)-one (G6-1 13)

[0228] Carbonyldiimidazole (0.39 g) was added to a tetrahydrofuran solution (8 ml) of N'- hydroxy-1-methyl-5-(trifluoromethyl)-1 H-imidazole-2-carboximidamide (0.42 g) in an argon atmosphere, and the mixture was stirred at room temperature for 2 hours. DBU (0.37 g) was added thereto, and stirring was continued for additional 6 hours. 10% hydrochloric acid was added thereto, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 3-[1-methyl-5-(trifluoromethyl)-1 H-imidazol-2-yl]- 1 ,2,4-oxadiazol-5(4H)-one (0.15 g).

Example 8: Synthesis of 3-ri-methyl-3-(trifluoromethyl)-1 H-pyrazol-5-vn-1 ,2,4-oxadiazol-

5(4H)-one (G4-113)

[0229] <Step 8-1 > Synthesis of 1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carboxamide

[0230] 1-Methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carboxylic acid (4.85 g) and dimethylformamide (0.04 g) were dissolved in dichloromethane (80 ml), and a dichloromethane solution (20 ml) of oxalyl chloride (3.33 g) was dropped thereon. The mixture was stirred at room temperature for 1 hour, and then, the solvent was concentrated. The residue was dissolved in dichloromethane (15 ml), and a mixed solution of 28% ammonia water (15.2 g) and dichloromethane (25 ml) was added thereto at 0°C. The mixture was stirred at room temperature for 1 hour, and then, the organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated to obtain crude 1-methyl-3- (trifluoromethyl)-1 H-pyrazole-5-carboxamide (4.29 g).

[0231] <Step 8-2> Synthesis of 1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carbonitrile

[0232] 1-Methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carboxamide (0.97 g) and triethylamine (1.52 g) were dissolved in dichloromethane (25 ml), and trifluoroacetic anhydride was added thereto at 0°C. The mixture was stirred at 0°C for 1 hour and then at room temperature for 2 hours. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carbonitrile (0.74 g).

[0233] <Step 8-3> Synthesis of N'-hydroxy-1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5- carboximidamide

[0234] An ethanol suspension (10 ml) of hydroxylamine hydrochloride (0.59 g) and sodium hydrogencarbonate (0.72 g) was heat-refluxed for 45 minutes. After cooling to room temperature, an ethanol solution (2 ml) of 1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5- carbonitrile (0.71 g) was added thereto at -5°C, and the mixture was stirred at room

temperature for 5 hours. The solvent was concentrated, and then, water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain N'- hydroxy-1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carboximidamide (0.81 g).

[0235] <Step 8-4> Synthesis of 3-[1-methyl-3-(trifluoromethyl)-1 H-pyrazol-5-yl]-1 ,2,4- oxadiazol-5(4H)-one (G4-1 13)

[0236] Carbonyldiimidazole (0.47 g) was added to a tetrahydrofuran solution (8 ml) of N'- hydroxy-1-methyl-3-(trifluoromethyl)-1 H-pyrazole-5-carboximidamide (0.5 g) in an argon atmosphere, and the mixture was stirred at room temperature for 2 hours. DBU (0.44 g) was added thereto, and stirring was continued for additional 6 hours. 10% hydrochloric acid was added thereto, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 3-[1-methyl-3-(trifluoromethyl)-1 H-pyrazol-5-yl]- 1 ,2,4-oxadiazol-5(4H)-one (0.3 g).

Example 9: Synthesis of 4-methyl-3-ri-methyl-5-(trifluoromethyl)-1 H-pyrazol-3-vn-1 ,2,4- oxadiazol-5(4H)-one (G5-354)

[0237] <Step 9-1 > Synthesis of 3-(2-furyl)-1-methyl-5-(trifluoromethyl)-4,5-dihydro-1 H- pyrazol-5-ol

[0238] Methylhydrazine (3.46 g) was dropped onto an ethanolic solution (100 ml) of 4,4,4- trifluoro-1-(2-furyl)butane-1 ,3-dione (10.31 g) at 0°C. The mixture was stirred at room temperature for 1 hour, and then, the solvent was concentrated. The residue was dissolved in ethyl acetate, and the solution was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 3-(2-furyl)-1-methyl-5-(trifluoromethyl)- 4,5-dihydro-1 H-pyrazol-5-ol (3.25 g).

[0239] <Step 9-2> Synthesis of 3-(2-furyl)-1-methyl-5-(trifluoromethyl)1 H-pyrazole

[0240] 3-(2-Furyl)-1-methyl-5-(trifluoromethyl)-4,5-dihydro-1 H-pyrazol-5-ol (3.25 g) and 3 N hydrochloric acid (16.2 ml) were dissolved in tetrahydrofuran (60 ml), and the solution was heat-refluxed for 30 minutes. After cooling to room temperature, the solvent was concentrated. The residue was subjected to extraction with ethyl acetate, and the organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 3-(2-furyl)-1-methyl-5-(trifluoromethyl)1 H-pyrazole (2.14 g).

[0241] <Step 9-3> Synthesis of 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboxylic acid

[0242] An aqueous solution (130 ml) of potassium permanganate (8.14 g) was added to an acetone solution (100 ml) of 3-(2-furyl)-1-methyl-5-(trifluoromethyl)1 H-pyrazole (2.1 g). The reaction mixture was stirred at 60°C for 4 hours and then cooled to room temperature.

Isopropanol (30 ml) was added thereto, and the mixture was stirred overnight at room temperature. The reaction mixture was filtered through celite, and the filtrate was concentrated to approximately 30 ml. 2 N aqueous sodium hydroxide solution (7 ml) was added to the residue, and the solution was washed with t-butylmethyl ether. 5 N hydrochloric acid (10 ml) was added to the aqueous layer, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate. The solvent was concentrated to obtain crude 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboxylic acid (1.59 g).

[0243] <Step 9-4> Synthesis of 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboxamide

[0244] 1-Methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboxylic acid (1.58 g) and

dimethylformamide (0.01 g) were dissolved in dichloromethane (20 ml), and a dichloromethane solution (5 ml) of oxalyl chloride (1.09 g) was dropped thereon. The mixture was stirred at room temperature for 1 hour, and then, the solvent was concentrated. The residue was dissolved in dichloromethane (50 ml), and a mixed solution of 28% ammonia water (4.95 g) and dichloromethane (50 ml) was added thereto at 0°C. The mixture was stirred at room temperature for 1 hour, and then, the organic layer was separated and dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboxamide

(0.91 g).

[0245] <Step 9-5> Synthesis of 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carbonitrile

[0246] 1-Methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboxamide (1.31 g) and triethylamine (2.06 g) were dissolved in dichloromethane (25 ml), and trifluoroacetic anhydride (2.14 g) was added thereto at 0°C. The mixture was stirred at 0°C for 1 hour and then at room temperature for 2 hours. The solvent was concentrated, and then, the residue was purified by silica gel column chromatography to obtain 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carbonitrile (1.1

[0247] <Step 9-6> Synthesis of N'-hydroxy-1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3- carboximidamide

[0248] An ethanol suspension (10 ml) of hydroxylamine hydrochloride (0.92 g) and sodium hydrogencarbonate (1.11 g) was heat-refluxed for 45 minutes. After cooling to room temperature, an ethanol solution (2 ml) of 1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3- carbonitrile (1.18 g) was added thereto at 0°C, and the mixture was stirred at room

temperature for 3 hours. The solvent was concentrated, and then, water was added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain N'- hydroxy-1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboximidamide (1.0 g).

[0249] <Step 9-7> Synthesis of 3-[1-methyl-5-(trifluoromethyl)-1 H-pyrazol-3-yl]-1 ,2,4- oxadiazol-5(4H)-one (G5-1 13)

[0250] Carbonyldiimidazole (1.67 g) was added to a tetrahydrofuran solution (28 ml) of N'- hydroxy-1-methyl-5-(trifluoromethyl)-1 H-pyrazole-3-carboximidamide (1.79g) in an argon atmosphere, and the mixture was stirred at room temperature for 2 hours. DBU (1.57 g) was added thereto, and stirring was continued for additional 6 hours. 2 N hydrochloric acid was added thereto at 0°C, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and the residue was purified by silica gel column chromatography to obtain 3-[1- methyl-5-(trifluoromethyl)-1 H-pyrazol-3-yl]-1 ,2,4-oxadiazol-5(4H)-one (1.13 g).

[0251] <Step 9-8> Synthesis of 4-methyl-3-[1-methyl-5-(trifluoromethyl)-1 H-pyrazol-3-yl]- 1 ,2,4-oxadiazol-5(4H)-one (G5-354)

[0252] 3-[1-Methyl-5-(trifluoromethyl)-1 H-pyrazol-3-yl]-1 ,2,4-oxadiazol-5(4H)-one (0.79 g) was added to a dimethylformamide (5 ml) suspension of 60% sodium hydride (0.14 g) at 0°C in an argon atmosphere. The mixture was stirred at room temperature. Again, the reaction solution was cooled to 0°C, and methyl iodide (0.58 g) was added thereto. The mixture was stirred at 0°C for 2 hours and then overnight at room temperature. The reaction solution was added to ice water, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated saline and then dried over anhydrous magnesium sulfate. The solvent was concentrated, and then, the residue was purified by silica gel column

chromatography to obtain 4-methyl-3-[1-methyl-5-(trifluoromethyl)-1 H-pyrazol-3-yl]-1 ,2,4- oxadiazol-5(4H)-one (0.78 g).

[0253] Compounds of the formula (I) of the present invention obtained by the same processes as employed in Examples 1 to 9 above or according to the processes described in detail above, and their physical property values are summarized in Tables 1 to 9 and NMR tables. In addition, each of the compounds obtained in the above synthetic examples is also shown in the corresponding table.

[0254] Abbreviations in the tables are as follows:

[0255] n-: normal-, c-hex: cyclohexyl, c-pen: cyclopentyl, c-hep: cycloheptyl, c-pro:

cyclopropyl, Ph: phenyl, pyridyl: pyridyl

Example 10: Biological Test

[0256] Drug samples were prepared as follows, unless otherwise specified.

Solvent: 3 parts by weight of dimethylformamide

Emulsifier: 1 part by weight of polyoxyethylene alkylphenyl ether

[0257] To prepare formulations of appropriate active compounds, 1 part by weight of active compound was mixed with the solvent in the amount above containing the emulsifier in the amount above, and the mixture was diluted with water to a predetermined concentration.

Ammonium salt or ammonium salt and penetration enhancer in a dosage of l OOOppm are added to the desired concentration if necessary.

10.1 Test on Myzus persicae resistant to organic phosphorus and carbamate agents Test Method

[0258] Eggplant leaves with two developed true leaves cultivated in a pot of 6 cm in diameter were inoculated with raised Myzus persicae resistant to organic phosphorus and carbamate agents at a dose of approximately 50 to 100 insects per seedling. One day after the inoculation, the prepared aqueous dilution of the active compound at the predetermined concentration was spreaded thereto in a sufficient amount using a spray gun. After the spreading, the seedlings were left in a greenhouse. Seven days after the spreading, insecticidal rates were calculated. The insecticidal rate of 100% means that all the insects (Myzus persicae) died. On the other hand, the insecticidal rate of 0% means that none of the insects (Myzus persicae) died.

Test Results

[0259] The compounds of Compound Nos. G1-1 , G1-7, G1-25, G2-1 , G3-1 , G4-1 13, and G8-1 as typical examples exhibited control effect with the insecticidal rate of 100% at an active ingredient concentration of 500 ppm.

10.2 Test 2 on Myzus persicae - spray test (MYZUPE - OP/Carb-resistant) Test Method 2

Solvent: 3 parts by weight dimethylformamide

Emulsifier: 1 part by weight polyoxyethylene alkyl phenyl ether

[0260] In order to make an appropriate formulation of an active compound, 1 part by weight of the active compound is mixed with the above mentioned amount of solvent and emulsifier and the mixture is diluted with water to a prescribed concentration. Ammonium salt or ammonium salt and penetration enhancer in a dosage of lOOOppm are added to the desired concentration if necessary.

[0261] 1 day before treatment, all instars of the green peach aphid (Myzus persicae) are inoculated onto the 2-leaf stage of eggplant seedlings (Solarium melongena). The compound solution is sprayed directly onto both insects and plants. After drying, the pots are placed in the greenhouse, at 20°C to 25°C.

[0262] After 2 days mortality in % is determined. An insecticidal activity of 100 % means that all larvae have been killed, an insecticidal activity of 0 % means that no larvae have been killed.

[0263] In this test the following compounds showed an insecticidal activity of 100% at an active compound concentration of 500ppm: G1-16

[0264] In this test the following compounds showed an insecticidal activity of 98% at an active compound concentration of 500ppm: G13-20, G15-103,

[0265] In this test the following compounds showed an insecticidal activity of 90% at an active compound concentration of 500ppm: G3-10 [0266] After 6 days mortality in % is determined. An insecticidal activity of 100 % means that all larvae have been killed, an insecticidal activity of 0 % means that no larvae have been killed.

[0267] In this test the following compounds showed an insecticidal activity of 100% at an active compound concentration of 500ppm: G1-1 , G1-7, G1-15, G1-25, G2-1 , G3-1 , G4-113, G8-1 , G9-1 , G16-1 , G18-1

[0268] In this test the following compounds showed an insecticidal activity of 98% at an active compound concentration of 500ppm: G1-2, G1-18, G4-1521 , G4-1557, G6-1 13

[0269] In this test the following compounds showed an insecticidal activity of 90% at an active compound concentration of 500ppm: G1-17, G3-45, G5-1 13, G7-19, G8-104

[0270] In this test the following compounds showed an insecticidal activity of 90% at an active compound concentration of 100ppm: G17-112

10.3 Two-spotted spider mite (TETRUR)

Solvent: 3 parts by weight dimethylformamide

Emulsifier: 1 part by weight polyoxyethylene alkyl phenyl ether

[0271] In order to make an appropriate formulation of an active compound, 1 part by weight of the active compound is mixed with the above mentioned amount of solvent and emulsifier and the mixture is diluted with water to a prescribed concentration. Ammonium salt or ammonium salt and penetration enhancer in a dosage of lOOOppm are added to the desired concentration if necessary.

[0272] 1 day before treatment, the apex parts of kidney bean seedlings (Phaseolus vulgaris) are pruned. About 20 adults of the two-spotted spider mite (Tetranychus urticae) are inoculated onto each leaf, about 40 adults and some nymphs per pot. A paper label is placed on each pot.

[0273] The solution is sprayed directly onto both mites and plants. After drying, pots are placed in the greenhouse at 20°C- 25°C.

[0274] After 2 days, the acaricidal activity is calculated. An acaricidal activity of 100 % means that all mites have been killed, an acaricidal activity of 0 % means that no mites have been killed. [0275] In this test the following compounds showed an acaricidal activity of 98% at an active compound concentration of 500ppm: G1-52, G15-103

[0276] In this test the following compounds showed an acaricidal activity of 90% at an active compound concentration of 500ppm: G1-90, G4-1557, G18-1 , G14-49

[0277] After 6 days, the acaricidal activity is calculated. An acaricidal activity of 100 % means that all mites have been killed, an acaricidal activity of 0 % means that no mites have been killed.

[0278] In this test the following compounds showed an acaricidal activity of 100% at an active compound concentration of 500ppm: G2-1 , G9-1 , G14-103

[0279] In this test the following compounds showed an acaricidal activity of 98% at an active compound concentration of 500ppm: G5-113

[0280] In this test the following compounds showed an acaricidal activity of 90% at an active compound concentration of 500ppm: G1-18, G4-1534, G8-20, G16-1

10.4 Bemisia spray-test (BEMIAR)

Solvent: 3 parts by weight dimethylformamide

Emulsifier: 1 part by weight polyoxyethylene alkyl phenyl ether

[0281] In order to make an appropriate formulation of an active compound, 1 part by weight of the active compound is mixed with the above mentioned amount of solvent and emulsifier and the mixture is diluted with water to a prescribed concentration. Ammonium salt or ammonium salt and penetration enhancer in a dosage of lOOOppm are added to the desired concentration if necessary.

[0282] Tomato seedlings (Lycopersicon esculentum) are treated by being sprayed with the desired concentration of the compound solution. After drying, the treated pots are placed in the greenhouse where they are inoculated with the silverleaf whitefly (Bemisia argentifolii) for an infection-time of 24h. Afterwards, the plants are placed in a room at 25°C and 50-60 % r.h., with 16L8D lighting conditions.

[0283] After 14 days, the insecticidal activity is calculated. An insecticidal activity of 100 % means that all whiteflies have been killed, an insecticidal activity of 0 % means that no whiteflies have been killed. [0284] In this test the following compounds showed an insecticidal activity of 90% at an active compound concentration of 100ppm: G16-1.

10.5 Thrips palmi - spraytest (THRIPL)

Solvent: Dimethylformamide, 3 parts by weight

Emulsifier: Polyoxyethylene alkyl phenyl ether, 1 part by weight

[0285] In order to make an appropriate formulation of an active compound, 1 part by weight of the active compound is mixed with the above mentioned amount of solvent and emulsifier and the mixture is diluted with water to a prescribed concentration. Ammonium salt or ammonium salt and penetration enhancer in a dosage of lOOOppm are added to the desired concentration if necessary.

[0286] The compound solutions are sprayed to a cucumber seedling (Cucumis sativus). After drying, the treated plant is placed in a plastic stand. About 100 thrips-eggs (Thrips palmi) on a piece of filter paper are attached to the plant and covered with a cage to keep 100% humidity. The plant is kept in a room at 23°C.

[0287] After 6 days activity in % is evaluated by feeding damage degree. An activity of 100 % means that there is no feeding damage, an activity of 0 % means that there is no difference to the untreated control.

[0288] In this test the following compounds showed an insecticidal activity of 98% at an active compound concentration of 500ppm: G5-354

Example 11 : Formulation Preparation Example

Preparation Example 1 (Granule)

[0289] 25 parts of water are added to a mixture of 10 parts of the compound of the present invention (No. G1-1), 30 parts of bentonite (montmorillonite), 58 parts of talc, and 2 parts of lignin sulfonate, and the mixture is well kneaded, then granulated with 10- to 40-mesh size using an extrusion granulator, and dried at 40 to 50°C to form a granule.

Preparation Example 2 (Granule)

[0290] 95 parts of clay mineral particles having particle size distribution within the range of 0.2 to 2 mm are fed to a rotational mixing machine, then uniformly moistened by the spraying of 5 parts of the compound of the present invention (No. G1-1) together with a liquid diluent under rotation, and then dried at 40 to 50°C to form a granule.

Preparation Example 3 (Emulsifiable Concentrate)

[0291] 30 parts of the compound of the present invention (No. G1-1), 55 parts of xylene, 8 parts of polyoxyethylene alkylphenyl ether and 7 parts of calcium alkylbenzenesulfonate are mixed and stirred to form an emulsifiable concentrate.

Preparation Example 4 (Wettable Powder)

[0292] 15 parts of the compound of the present invention (No. G1-1), 80 parts of a mixture of white carbon (fine powder of hydrous amorphous silicon oxide) and clay powder (1 :5), 2 parts of sodium alkylbenzenesulfonate, and 3 parts of sodium alkylnaphthalenesulfonate-formalin condensate are pulverized and mixed to form a wettable powder.

Preparation Example 5 (Wettable Granule)

[0293] 20 parts of the compound of the present invention (No. G1-1), 30 parts of sodium salt of lignin sulfonic acid, 15 parts of bentonite and 35 parts of calcined diatomaceous earth powder are sufficiently mixed. After addition of water, the mixture is extruded with a 0.3 mm screen and dried to form wettable granules.

[0294] Table 1

G1-285 2-CF₃Ph (2-FPh)OCH₂

G 1-286 2-CF₃Ph (3-FPh)OCH₂

G1-287 2-CF₃Ph (4-FPh)OCH₂

G1-288 2-CF₃Ph (2-CIPh)OCH₂

G1-289 2-CF₃Ph (3-CIPh)OCH₂

G1-290 2-CF₃Ph (4-CIPh)OCH₂

G1-291 2-CF₃Ph (2-BrPh)OCH₂

G 1-292 2-CF₃Ph (3-BrPh)OCH₂

G1-293 2-CF₃Ph (4-BrPh)OCH₂

G 1-294 2-CF₃Ph (2-CF₃OPh)OCH₂

G1-295 2-CF₃Ph (3-CF₃OPh)OCH₂

G 1-296 2-CF₃Ph (4-CF₃OPh)OCH₂

G1-297 2-CF₃Ph (2-CNPh)OCH₂

G1-298 2-CF₃Ph (3-CNPh)OCH₂

G1-299 2-CF₃Ph (4-CNPh)OCH₂

G1-300 2-CF₃Ph (2-N0₂Ph)OCH₂

G1-301 2-CF₃Ph (3-N0₂Ph)OCH₂

G1-302 2-CF₃Ph (4-N0₂Ph)OCH₂

G1-303 2-CF₃Ph (2-CF₃Ph)OCH₂

G1-304 2-CF₃Ph (3-CF₃Ph)OCH₂

G1-305 2-CF₃Ph (4-CF₃Ph)OCH₂

G1-306 2-CF₃Ph PhCH₂OCH₂

G1-307 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G1-308 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G1-309 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G1-310 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G1-311 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G1-312 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G1-313 2-CF₃Ph (2-FPh)CH₂OCH₂

G1-314 2-CF₃Ph (3-FPh)CH₂OCH₂

G1-315 2-CF₃Ph (4-FPh)CH₂OCH₂

G1-316 2-CF₃Ph (2-CIPh)CH₂OCH₂

G1-317 2-CF₃Ph (3-CIPh)CH₂OCH₂

G1-318 2-CF₃Ph (4-CIPh)CH₂OCH₂

G1-319 2-CF₃Ph (2-BrPh)CH₂OCH₂

G1-320 2-CF₃Ph (3-BrPh)CH₂OCH₂

G1-321 2-CF₃Ph (4-BrPh)CH₂OCH₂

G 1-322 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G1-323 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 1-324 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G1-325 2-CF₃Ph (2-CNPh)CH₂OCH₂

G 1-326 2-CF₃Ph (3-CNPh)CH₂OCH₂

G1-327 2-CF₃Ph (4-CNPh)CH₂OCH₂

G1-328 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G1-329 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G1-330 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G1-331 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G1-332 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G1-381 3-CF₃Ph (CH₃)₂CHCH₂C(=0)

G1-382 3-CF₃Ph (CH₃)₃CCH₂CH₂C(=0)

G1-383 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)

G1-384 3-CF₃Ph (c-hex)C(=0)

G1-385 3-CF₃Ph (c-pen)C(=0)

G1-386 3-CF₃Ph (c-hep)C(=0)

G1-387 3-CF₃Ph (c-pro)C(=0)

G1-388 3-CF₃Ph CF₃C(=0)

G1-389 3-CF₃Ph (CH₃)₂NC(=0)

G1-390 3-CF₃Ph (CH₃CH₂)₂NC(=0)

G1-391 3-CF₃Ph (CH₃CH₂CH₂)₂NC(=0)

G1-392 3-CF₃Ph CH₃CH₂N(CH₃)C(=0)

G1-393 3-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0)

G1-394 3-CF₃Ph CH₃ON(CH₃)C(=0)

G1-395 3-CF₃Ph (CH₂=CHCH₂)₂N C(=0)

G1-396 3-CF₃Ph (CHCCH₂)₂NC(=0)

CO-N^]

G1-397 3-CF₃Ph

CO-N^

G1-398 3-CF₃Ph

CO-N^O

G1-399 3-CF₃Ph

G1-400 3-CF₃Ph CH₃OCH₂

G1-401 3-CF₃Ph CH₃CH₂OCH₂

G 1-402 3-CF₃Ph (CH₃)₂CHOCH₂

G1-403 3-CF₃Ph (CH₃)₃COCH₂

G 1-404 3-CF₃Ph (CH₃)₃CCH₂0CH₂

G1-405 3-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂

G 1-406 3-CF₃Ph (c-hex)OCH₂

G1-407 3-CF₃Ph PhOCH₂

G1-408 3-CF₃Ph (2-CH₃Ph)OCH₂

G1-409 3-CF₃Ph (3-CH₃Ph)OCH₂

G1-410 3-CF₃Ph (4-CH₃Ph)OCH₂

G1-411 3-CF₃Ph (2-CH₃OPh)OCH₂

G1-412 3-CF₃Ph (3-CH₃OPh)OCH₂

G1-413 3-CF₃Ph (4-CH₃OPh)OCH₂

G1-414 3-CF₃Ph (2-FPh)OCH₂

G1-415 3-CF₃Ph (3-FPh)OCH₂

G1-416 3-CF₃Ph (4-FPh)OCH₂

G1-417 3-CF₃Ph (2-CIPh)OCH₂

G1-418 3-CF₃Ph (3-CIPh)OCH₂

G1-419 3-CF₃Ph (4-CIPh)OCH₂

G 1-420 3-CF₃Ph (2-BrPh)OCH₂

G1-421 3-CF₃Ph (3-BrPh)OCH₂

G 1-422 3-CF₃Ph (4-BrPh)OCH₂ G 1-423 3-CF₃Ph (2-CF₃OPh)OCH₂

G 1-424 3-CF₃Ph (3-CF₃OPh)OCH₂

G 1-425 3-CF₃Ph (4-CF₃OPh)OCH₂

G 1-426 3-CF₃Ph (2-CNPh)OCH₂

G 1-427 3-CF₃Ph (3-CNPh)OCH₂

G 1-428 3-CF₃Ph (4-CNPh)OCH₂

G 1-429 3-CF₃Ph (2-N0₂Ph)OCH₂

G1-430 3-CF₃Ph (3-N0₂Ph)OCH₂

G1-431 3-CF₃Ph (4-N0₂Ph)OCH₂

G 1-432 3-CF₃Ph (2-CF₃Ph)OCH₂

G1-433 3-CF₃Ph (3-CF₃Ph)OCH₂

G 1-434 3-CF₃Ph (4-CF₃Ph)OCH₂

G1-435 3-CF₃Ph PhCH₂OCH₂

G 1-436 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G1-437 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G1-438 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G1-439 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 1-440 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G1-441 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 1-442 3-CF₃Ph (2-FPh)CH₂OCH₂

G 1-443 3-CF₃Ph (3-FPh)CH₂OCH₂

G 1-444 3-CF₃Ph (4-FPh)CH₂OCH₂

G 1-445 3-CF₃Ph (2-CIPh)CH₂OCH₂

G 1-446 3-CF₃Ph (3-CIPh)CH₂OCH₂

G 1-447 3-CF₃Ph (4-CIPh)CH₂OCH₂

G 1-448 3-CF₃Ph (2-BrPh)CH₂OCH₂

G 1-449 3-CF₃Ph (3-BrPh)CH₂OCH₂

G1-450 3-CF₃Ph (4-BrPh)CH₂OCH₂

G1-451 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 1-452 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G1-453 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 1-454 3-CF₃Ph (2-CNPh)CH₂OCH₂

G1-455 3-CF₃Ph (3-CNPh)CH₂OCH₂

G 1-456 3-CF₃Ph (4-CNPh)CH₂OCH₂

G1-457 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G1-458 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G1-459 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 1-460 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G1-461 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 1-462 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G 1-463 3-CF₃Ph CH₃C(=0)OCH₂

G 1-464 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G 1-465 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 1-466 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G 1-467 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G 1-468 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 1-469 3-CF₃Ph CF₃C(=0)OCH₂

G1-470 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G1-561 4-CF₃Ph (2-CF₃Ph)OCH₂

G 1-562 4-CF₃Ph (3-CF₃Ph)OCH₂

G1-563 4-CF₃Ph (4-CF₃Ph)OCH₂

G 1-564 4-CF₃Ph PhCH₂OCH₂

G1-565 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 1-566 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G1-567 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G1-568 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G1-569 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G1-570 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G1-571 4-CF₃Ph (2-FPh)CH₂OCH₂

G1-572 4-CF₃Ph (3-FPh)CH₂OCH₂

G1-573 4-CF₃Ph (4-FPh)CH₂OCH₂

G1-574 4-CF₃Ph (2-CIPh)CH₂OCH₂

G1-575 4-CF₃Ph (3-CIPh)CH₂OCH₂

G1-576 4-CF₃Ph (4-CIPh)CH₂OCH₂

G1-577 4-CF₃Ph (2-BrPh)CH₂OCH₂

G1-578 4-CF₃Ph (3-BrPh)CH₂OCH₂

G1-579 4-CF₃Ph (4-BrPh)CH₂OCH₂

G1-580 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G1-581 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G1-582 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G1-583 4-CF₃Ph (2-CNPh)CH₂OCH₂

G1-584 4-CF₃Ph (3-CNPh)CH₂OCH₂

G1-585 4-CF₃Ph (4-CNPh)CH₂OCH₂

G1-586 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G1-587 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G1-588 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G1-589 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G1-590 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G1-591 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G1-592 4-CF₃Ph CH₃C(=0)OCH₂

G1-593 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G1-594 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G1-595 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G1-596 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G1-597 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G1-598 4-CF₃Ph CF₃C(=0)OCH₂

G1-599 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G1-600 4-CF₃Ph (c-hex)C(=0)OCH₂

G1-601 4-CF₃Ph PhC(=0)OCH₂

G 1-602 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G1-603 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 1-604 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G1-605 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 1-606 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G1-607 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G1-608 4-CF₃Ph (2-FPh)C(=0)OCH₂ G1-609 4-CF₃Ph (3-FPh)C(=0)OCH₂

G1-610 4-CF₃Ph (4-FPh)C(=0)OCH₂

G1-611 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G1-612 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G1-613 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G1-614 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G1-615 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G1-616 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G1-617 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G1-618 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G1-619 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G 1-620 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G1-621 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G 1-622 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G 1-623 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G 1-624 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G 1-625 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G 1-626 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G 1-627 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G 1-628 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂

G 1-629 3,5-(CF₃)₂Ph CH₃

G1-630 3,5-(CF₃)₂Ph CH3CH2

G1-631 3,5-(CF₃)₂Ph CH3CH2CH2

G 1-632 3,5-(CF₃)₂Ph (CH₃)₂CH

G1-633 3,5-(CF₃)₂Ph CH₃C(=0)

G 1-634 3,5-(CF₃)₂Ph CH₃CH₂C(=0)

G1-635 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0)

G 1-636 3,5-(CF₃)₂Ph (CH₃)₃CC(=0)

G1-637 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0)

G1-638 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0)

G1-639 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0)

G 1-640 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0)

G1-641 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)

G 1-642 3,5-(CF₃)₂Ph (c-hex)C(=0)

G 1-643 3,5-(CF₃)₂Ph (c-pen)C(=0)

G 1-644 3,5-(CF₃)₂Ph (c-hep)C(=0)

G 1-645 3,5-(CF₃)₂Ph (c-pro)C(=0)

G 1-646 3,5-(CF₃)₂Ph CF₃C(=0)

G 1-647 3,5-(CF₃)₂Ph (CH₃)₂NC(=0)

G 1-648 3,5-(CF₃)₂Ph (CH₃CH₂)₂NC(=0)

G 1-649 3,5-(CF₃)₂Ph (CH₃CH₂CH₂)₂NC(=0)

G1-650 3,5-(CF₃)₂Ph CH₃CH₂N(CH₃)C(=0)

G1-651 3,5-(CF₃)₂Ph [(CH₃)₂CHCH₂]₂NC(=0)

G 1-652 3,5-(CF₃)₂Ph CH₃ON(CH₃)C(=0)

G1-653 3,5-(CF₃)₂Ph (CH₂=CHCH₂)₂N C(=0)

G 1-654 3,5-(CF₃)₂Ph (CHCCH₂)₂NC(=0)

G1-697 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G1-698 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G1-699 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G1-700 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G1-701 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G1-702 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G1-703 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G1-704 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G1-705 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G1-706 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G1-707 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G1-708 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G1-709 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G1-710 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G1-711 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G1-712 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G1-713 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G1-714 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G1-715 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G1-716 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G1-717 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G1-718 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G1-719 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G1-720 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G1-721 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G 1-722 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G1-723 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G 1-724 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G1-725 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G 1-726 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G1-727 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G1-728 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G1-729 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G1-730 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G1-731 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G1-732 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G1-733 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G1-734 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G1-735 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G1-736 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G1-737 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G1-738 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G1-739 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G1-740 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G1-741 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G 1-742 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G1-743 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G 1-744 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ G1-745 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G 1-746 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G1-747 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G1-748 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G1-749 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G1-750 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G1-751 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G1-752 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G1-753 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G1-754 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G1-755 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G1-756 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G1-757 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0295] Table 2

G2-296 2-CF₃Ph (4-CF₃OPh)OCH₂

G2-297 2-CF₃Ph (2-CNPh)OCH₂

G2-298 2-CF₃Ph (3-CNPh)OCH₂

G2-299 2-CF₃Ph (4-CNPh)OCH₂

G2-300 2-CF₃Ph (2-N0₂Ph)OCH₂

G2-301 2-CF₃Ph (3-N0₂Ph)OCH₂

G2-302 2-CF₃Ph (4-N0₂Ph)OCH₂

G2-303 2-CF₃Ph (2-CF₃Ph)OCH₂

G2-304 2-CF₃Ph (3-CF₃Ph)OCH₂

G2-305 2-CF₃Ph (4-CF₃Ph)OCH₂

G2-306 2-CF₃Ph PhCH₂OCH₂

G2-307 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G2-308 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G2-309 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G2-310 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G2-311 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G2-312 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G2-313 2-CF₃Ph (2-FPh)CH₂OCH₂

G2-314 2-CF₃Ph (3-FPh)CH₂OCH₂

G2-315 2-CF₃Ph (4-FPh)CH₂OCH₂

G2-316 2-CF₃Ph (2-CIPh)CH₂OCH₂

G2-317 2-CF₃Ph (3-CIPh)CH₂OCH₂

G2-318 2-CF₃Ph (4-CIPh)CH₂OCH₂

G2-319 2-CF₃Ph (2-BrPh)CH₂OCH₂

G2-320 2-CF₃Ph (3-BrPh)CH₂OCH₂

G2-321 2-CF₃Ph (4-BrPh)CH₂OCH₂

G2-322 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G2-323 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G2-324 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G2-325 2-CF₃Ph (2-CNPh)CH₂OCH₂

G2-326 2-CF₃Ph (3-CNPh)CH₂OCH₂

G2-327 2-CF₃Ph (4-CNPh)CH₂OCH₂

G2-328 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G2-329 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G2-330 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G2-331 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G2-332 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G2-333 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G2-334 2-CF₃Ph CH₃C(=0)OCH₂

G2-335 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G2-336 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G2-337 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G2-338 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G2-339 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G2-340 2-CF₃Ph CF₃C(=0)OCH₂

G2-341 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G2-342 2-CF₃Ph (c-hex)C(=0)OCH₂

G2-343 2-CF₃Ph PhC(=0)OCH₂

G2-434 3-CF₃Ph (4-CF₃Ph)OCH₂

G2-435 3-CF₃Ph PhCH₂OCH₂

G2-436 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G2-437 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G2-438 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G2-439 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G2-440 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G2-441 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G2-442 3-CF₃Ph (2-FPh)CH₂OCH₂

G2-443 3-CF₃Ph (3-FPh)CH₂OCH₂

G2-444 3-CF₃Ph (4-FPh)CH₂OCH₂

G2-445 3-CF₃Ph (2-CIPh)CH₂OCH₂

G2-446 3-CF₃Ph (3-CIPh)CH₂OCH₂

G2-447 3-CF₃Ph (4-CIPh)CH₂OCH₂

G2-448 3-CF₃Ph (2-BrPh)CH₂OCH₂

G2-449 3-CF₃Ph (3-BrPh)CH₂OCH₂

G2-450 3-CF₃Ph (4-BrPh)CH₂OCH₂

G2-451 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G2-452 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G2-453 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G2-454 3-CF₃Ph (2-CNPh)CH₂OCH₂

G2-455 3-CF₃Ph (3-CNPh)CH₂OCH₂

G2-456 3-CF₃Ph (4-CNPh)CH₂OCH₂

G2-457 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G2-458 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G2-459 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G2-460 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G2-461 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G2-462 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G2-463 3-CF₃Ph CH₃C(=0)OCH₂

G2-464 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G2-465 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G2-466 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G2-467 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G2-468 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G2-469 3-CF₃Ph CF₃C(=0)OCH₂

G2-470 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G2-471 3-CF₃Ph (c-hex)C(=0)OCH₂

G2-472 3-CF₃Ph PhC(=0)OCH₂

G2-473 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G2-474 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G2-475 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G2-476 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G2-477 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G2-478 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G2-479 3-CF₃Ph (2-FPh)C(=0)OCH₂

G2-480 3-CF₃Ph (3-FPh)C(=0)OCH₂

G2-481 3-CF₃Ph (4-FPh)C(=0)OCH₂

G2-571 4-CF₃Ph (2-FPh)CH₂OCH₂

G2-572 4-CF₃Ph (3-FPh)CH₂OCH₂

G2-573 4-CF₃Ph (4-FPh)CH₂OCH₂

G2-574 4-CF₃Ph (2-CIPh)CH₂OCH₂

G2-575 4-CF₃Ph (3-CIPh)CH₂OCH₂

G2-576 4-CF₃Ph (4-CIPh)CH₂OCH₂

G2-577 4-CF₃Ph (2-BrPh)CH₂OCH₂

G2-578 4-CF₃Ph (3-BrPh)CH₂OCH₂

G2-579 4-CF₃Ph (4-BrPh)CH₂OCH₂

G2-580 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G2-581 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G2-582 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G2-583 4-CF₃Ph (2-CNPh)CH₂OCH₂

G2-584 4-CF₃Ph (3-CNPh)CH₂OCH₂

G2-585 4-CF₃Ph (4-CNPh)CH₂OCH₂

G2-586 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G2-587 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G2-588 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G2-589 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G2-590 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G2-591 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G2-592 4-CF₃Ph CH₃C(=0)OCH₂

G2-593 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G2-594 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G2-595 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G2-596 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G2-597 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G2-598 4-CF₃Ph CF₃C(=0)OCH₂

G2-599 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G2-600 4-CF₃Ph (c-hex)C(=0)OCH₂

G2-601 4-CF₃Ph PhC(=0)OCH₂

G2-602 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G2-603 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G2-604 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G2-605 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G2-606 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G2-607 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G2-608 4-CF₃Ph (2-FPh)C(=0)OCH₂

G2-609 4-CF₃Ph (3-FPh)C(=0)OCH₂

G2-610 4-CF₃Ph (4-FPh)C(=0)OCH₂

G2-611 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G2-612 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G2-613 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G2-614 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G2-615 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G2-616 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G2-617 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G2-618 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G2-661 3,5-(CF₃)₂Ph (CH₃)₃COCH₂

G2-662 3,5-(CF₃)₂Ph (CH₃)₃CCH₂0CH₂

G2-663 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂OCH₂

G2-664 3,5-(CF₃)₂Ph (c-hex)OCH₂

G2-665 3,5-(CF₃)₂Ph PhOCH₂

G2-666 3,5-(CF₃)₂Ph (2-CH₃Ph)OCH₂

G2-667 3,5-(CF₃)₂Ph (3-CH₃Ph)OCH₂

G2-668 3,5-(CF₃)₂Ph (4-CH₃Ph)OCH₂

G2-669 3,5-(CF₃)₂Ph (2-CH₃OPh)OCH₂

G2-670 3,5-(CF₃)₂Ph (3-CH₃OPh)OCH₂

G2-671 3,5-(CF₃)₂Ph (4-CH₃OPh)OCH₂

G2-672 3,5-(CF₃)₂Ph (2-FPh)OCH₂

G2-673 3,5-(CF₃)₂Ph (3-FPh)OCH₂

G2-674 3,5-(CF₃)₂Ph (4-FPh)OCH₂

G2-675 3,5-(CF₃)₂Ph (2-CIPh)OCH₂

G2-676 3,5-(CF₃)₂Ph (3-CIPh)OCH₂

G2-677 3,5-(CF₃)₂Ph (4-CIPh)OCH₂

G2-678 3,5-(CF₃)₂Ph (2-BrPh)OCH₂

G2-679 3,5-(CF₃)₂Ph (3-BrPh)OCH₂

G2-680 3,5-(CF₃)₂Ph (4-BrPh)OCH₂

G2-681 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂

G2-682 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂

G2-683 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂

G2-684 3,5-(CF₃)₂Ph (2-CNPh)OCH₂

G2-685 3,5-(CF₃)₂Ph (3-CNPh)OCH₂

G2-686 3,5-(CF₃)₂Ph (4-CNPh)OCH₂

G2-687 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂

G2-688 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G2-689 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G2-690 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G2-691 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G2-692 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G2-693 3,5-(CF₃)₂Ph PhCH₂OCH₂

G2-694 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G2-695 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G2-696 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G2-697 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G2-698 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G2-699 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G2-700 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G2-701 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G2-702 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G2-703 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G2-704 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G2-705 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G2-706 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G2-707 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G2-708 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂ G2-709 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G2-710 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G2-711 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G2-712 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G2-713 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G2-714 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G2-715 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G2-716 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G2-717 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G2-718 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G2-719 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G2-720 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G2-721 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G2-722 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G2-723 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G2-724 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G2-725 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G2-726 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G2-727 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G2-728 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G2-729 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G2-730 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G2-731 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G2-732 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G2-733 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G2-734 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G2-735 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G2-736 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G2-737 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G2-738 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G2-739 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G2-740 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G2-741 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G2-742 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G2-743 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G2-744 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G2-745 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G2-746 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G2-747 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G2-748 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G2-749 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G2-750 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G2-751 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G2-752 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G2-753 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G2-754 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G2-755 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G2-756 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂ G2-757 I 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0296] Table 3

G3-309 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G3-310 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G3-311 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G3-312 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G3-313 2-CF₃Ph (2-FPh)CH₂OCH₂

G3-314 2-CF₃Ph (3-FPh)CH₂OCH₂

G3-315 2-CF₃Ph (4-FPh)CH₂OCH₂

G3-316 2-CF₃Ph (2-CIPh)CH₂OCH₂

G3-317 2-CF₃Ph (3-CIPh)CH₂OCH₂

G3-318 2-CF₃Ph (4-CIPh)CH₂OCH₂

G3-319 2-CF₃Ph (2-BrPh)CH₂OCH₂

G3-320 2-CF₃Ph (3-BrPh)CH₂OCH₂

G3-321 2-CF₃Ph (4-BrPh)CH₂OCH₂

G3-322 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G3-323 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G3-324 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G3-325 2-CF₃Ph (2-CNPh)CH₂OCH₂

G3-326 2-CF₃Ph (3-CNPh)CH₂OCH₂

G3-327 2-CF₃Ph (4-CNPh)CH₂OCH₂

G3-328 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G3-329 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G3-330 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G3-331 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G3-332 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G3-333 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G3-334 2-CF₃Ph CH₃C(=0)OCH₂

G3-335 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G3-336 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G3-337 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G3-338 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G3-339 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G3-340 2-CF₃Ph CF₃C(=0)OCH₂

G3-341 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G3-342 2-CF₃Ph (c-hex)C(=0)OCH₂

G3-343 2-CF₃Ph PhC(=0)OCH₂

G3-344 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G3-345 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G3-346 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G3-347 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G3-348 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G3-349 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G3-350 2-CF₃Ph (2-FPh)C(=0)OCH₂

G3-351 2-CF₃Ph (3-FPh)C(=0)OCH₂

G3-352 2-CF₃Ph (4-FPh)C(=0)OCH₂

G3-353 2-CF₃Ph (2-CIPh)C(=0)OCH₂

G3-354 2-CF₃Ph (3-CIPh)C(=0)OCH₂

G3-355 2-CF₃Ph (4-CIPh)C(=0)OCH₂

G3-356 2-CF₃Ph (2-BrPh)C(=0)OCH₂

G3-445 3-CF₃Ph (2-CIPh)CH₂OCH₂

G3-446 3-CF₃Ph (3-CIPh)CH₂OCH₂

G3-447 3-CF₃Ph (4-CIPh)CH₂OCH₂

G3-448 3-CF₃Ph (2-BrPh)CH₂OCH₂

G3-449 3-CF₃Ph (3-BrPh)CH₂OCH₂

G3-450 3-CF₃Ph (4-BrPh)CH₂OCH₂

G3-451 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G3-452 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G3-453 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G3-454 3-CF₃Ph (2-CNPh)CH₂OCH₂

G3-455 3-CF₃Ph (3-CNPh)CH₂OCH₂

G3-456 3-CF₃Ph (4-CNPh)CH₂OCH₂

G3-457 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G3-458 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G3-459 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G3-460 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G3-461 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G3-462 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G3-463 3-CF₃Ph CH₃C(=0)OCH₂

G3-464 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G3-465 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G3-466 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G3-467 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G3-468 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G3-469 3-CF₃Ph CF₃C(=0)OCH₂

G3-470 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G3-471 3-CF₃Ph (c-hex)C(=0)OCH₂

G3-472 3-CF₃Ph PhC(=0)OCH₂

G3-473 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G3-474 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G3-475 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G3-476 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G3-477 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G3-478 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G3-479 3-CF₃Ph (2-FPh)C(=0)OCH₂

G3-480 3-CF₃Ph (3-FPh)C(=0)OCH₂

G3-481 3-CF₃Ph (4-FPh)C(=0)OCH₂

G3-482 3-CF₃Ph (2-CIPh)C(=0)OCH₂

G3-483 3-CF₃Ph (3-CIPh)C(=0)OCH₂

G3-484 3-CF₃Ph (4-CIPh)C(=0)OCH₂

G3-485 3-CF₃Ph (2-BrPh)C(=0)OCH₂

G3-486 3-CF₃Ph (3-BrPh)C(=0)OCH₂

G3-487 3-CF₃Ph (4-BrPh)C(=0)OCH₂

G3-488 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G3-489 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G3-490 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G3-491 3-CF₃Ph (2-CNPh)C(=0)OCH₂

G3-492 3-CF₃Ph (3-CNPh)C(=0)OCH₂

G3-535 4-CF₃Ph (c-hex)OCH₂

G3-536 4-CF₃Ph PhOCH₂

G3-537 4-CF₃Ph (2-CH₃Ph)OCH₂

G3-538 4-CF₃Ph (3-CH₃Ph)OCH₂

G3-539 4-CF₃Ph (4-CH₃Ph)OCH₂

G3-540 4-CF₃Ph (2-CH₃OPh)OCH₂

G3-541 4-CF₃Ph (3-CH₃OPh)OCH₂

G3-542 4-CF₃Ph (4-CH₃OPh)OCH₂

G3-543 4-CF₃Ph (2-FPh)OCH₂

G3-544 4-CF₃Ph (3-FPh)OCH₂

G3-545 4-CF₃Ph (4-FPh)OCH₂

G3-546 4-CF₃Ph (2-CIPh)OCH₂

G3-547 4-CF₃Ph (3-CIPh)OCH₂

G3-548 4-CF₃Ph (4-CIPh)OCH₂

G3-549 4-CF₃Ph (2-BrPh)OCH₂

G3-550 4-CF₃Ph (3-BrPh)OCH₂

G3-551 4-CF₃Ph (4-BrPh)OCH₂

G3-552 4-CF₃Ph (2-CF₃OPh)OCH₂

G3-553 4-CF₃Ph (3-CF₃OPh)OCH₂

G3-554 4-CF₃Ph (4-CF₃OPh)OCH₂

G3-555 4-CF₃Ph (2-CNPh)OCH₂

G3-556 4-CF₃Ph (3-CNPh)OCH₂

G3-557 4-CF₃Ph (4-CNPh)OCH₂

G3-558 4-CF₃Ph (2-N0₂Ph)OCH₂

G3-559 4-CF₃Ph (3-N0₂Ph)OCH₂

G3-560 4-CF₃Ph (4-N0₂Ph)OCH₂

G3-561 4-CF₃Ph (2-CF₃Ph)OCH₂

G3-562 4-CF₃Ph (3-CF₃Ph)OCH₂

G3-563 4-CF₃Ph (4-CF₃Ph)OCH₂

G3-564 4-CF₃Ph PhCH₂OCH₂

G3-565 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G3-566 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G3-567 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G3-568 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G3-569 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G3-570 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G3-571 4-CF₃Ph (2-FPh)CH₂OCH₂

G3-572 4-CF₃Ph (3-FPh)CH₂OCH₂

G3-573 4-CF₃Ph (4-FPh)CH₂OCH₂

G3-574 4-CF₃Ph (2-CIPh)CH₂OCH₂

G3-575 4-CF₃Ph (3-CIPh)CH₂OCH₂

G3-576 4-CF₃Ph (4-CIPh)CH₂OCH₂

G3-577 4-CF₃Ph (2-BrPh)CH₂OCH₂

G3-578 4-CF₃Ph (3-BrPh)CH₂OCH₂

G3-579 4-CF₃Ph (4-BrPh)CH₂OCH₂

G3-580 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G3-581 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G3-582 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ G3-583 4-CF₃Ph (2-CNPh)CH₂OCH₂

G3-584 4-CF₃Ph (3-CNPh)CH₂OCH₂

G3-585 4-CF₃Ph (4-CNPh)CH₂OCH₂

G3-586 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G3-587 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G3-588 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G3-589 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G3-590 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G3-591 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G3-592 4-CF₃Ph CH₃C(=0)OCH₂

G3-593 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G3-594 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G3-595 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G3-596 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G3-597 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G3-598 4-CF₃Ph CF₃C(=0)OCH₂

G3-599 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G3-600 4-CF₃Ph (c-hex)C(=0)OCH₂

G3-601 4-CF₃Ph PhC(=0)OCH₂

G3-602 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G3-603 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G3-604 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G3-605 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G3-606 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G3-607 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G3-608 4-CF₃Ph (2-FPh)C(=0)OCH₂

G3-609 4-CF₃Ph (3-FPh)C(=0)OCH₂

G3-610 4-CF₃Ph (4-FPh)C(=0)OCH₂

G3-611 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G3-612 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G3-613 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G3-614 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G3-615 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G3-616 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G3-617 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G3-618 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G3-619 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G3-620 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G3-621 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G3-622 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G3-623 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G3-624 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G3-625 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G3-626 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G3-627 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G3-628 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂

G3-629 3,5-(CF₃)₂Ph CH₃

G3-630 3,5-(CF₃)₂Ph CH3CH2

G3-673 3,5-(CF₃)₂Ph (3-FPh)OCH₂

G3-674 3,5-(CF₃)₂Ph (4-FPh)OCH₂

G3-675 3,5-(CF₃)₂Ph (2-CIPh)OCH₂

G3-676 3,5-(CF₃)₂Ph (3-CIPh)OCH₂

G3-677 3,5-(CF₃)₂Ph (4-CIPh)OCH₂

G3-678 3,5-(CF₃)₂Ph (2-BrPh)OCH₂

G3-679 3,5-(CF₃)₂Ph (3-BrPh)OCH₂

G3-680 3,5-(CF₃)₂Ph (4-BrPh)OCH₂

G3-681 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂

G3-682 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂

G3-683 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂

G3-684 3,5-(CF₃)₂Ph (2-CNPh)OCH₂

G3-685 3,5-(CF₃)₂Ph (3-CNPh)OCH₂

G3-686 3,5-(CF₃)₂Ph (4-CNPh)OCH₂

G3-687 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂

G3-688 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G3-689 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G3-690 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G3-691 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G3-692 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G3-693 3,5-(CF₃)₂Ph PhCH₂OCH₂

G3-694 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G3-695 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G3-696 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G3-697 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G3-698 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G3-699 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G3-700 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G3-701 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G3-702 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G3-703 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G3-704 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G3-705 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G3-706 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G3-707 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G3-708 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G3-709 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G3-710 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G3-711 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G3-712 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G3-713 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G3-714 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G3-715 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G3-716 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G3-717 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G3-718 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G3-719 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G3-720 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ G3-721 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G3-722 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G3-723 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G3-724 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G3-725 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G3-726 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G3-727 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G3-728 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G3-729 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G3-730 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G3-731 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G3-732 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G3-733 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G3-734 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G3-735 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G3-736 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G3-737 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G3-738 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G3-739 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G3-740 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G3-741 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G3-742 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G3-743 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G3-744 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G3-745 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G3-746 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G3-747 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G3-748 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G3-749 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G3-750 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G3-751 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G3-752 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G3-753 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G3-754 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G3-755 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G3-756 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G3-757 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0297] Table 4

G4-133 2-CF₃CF₂Ph H CH₃

G4-134 3-CF₃CF₂Ph H CH₃

G4-135 4-CF₃CF₂Ph H CH₃

G4-136 2-CF₃OPh H CH₃

G4-137 3-CF₃OPh H CH₃

G4-138 4-CF₃OPh H CH₃

G4-139 2-CF₃CH₂OPh H CH₃

G4-140 3-CF₃CH₂OPh H CH₃

G4-141 4-CF₃CH₂OPh H CH₃

G4-142 2-CF₃-3-F-Ph H CH₃

G4-143 2-CF₃-4-F-Ph H CH₃

G4-144 2-CF₃-5-F-Ph H CH₃

G4-145 2-CF₃-6-F-Ph H CH₃

G4-146 2-CF₃-3-CI-Ph H CH₃

G4-147 2-CF₃-4-CI-Ph H CH₃

G4-148 2-CF₃-5-CI-Ph H CH₃

G4-149 2-CF₃-6-CI-Ph H CH₃

G4-150 2-CF₃-3-CH₃-Ph H CH₃

G4-151 2-CF₃-4-CH₃-Ph H CH₃

G4-152 2-CF₃-5-CH₃-Ph H CH₃

G4-153 2-CF₃-6-CH₃-Ph H CH₃

G4-154 2,3-(CF₃)₂Ph H CH₃

G4-155 2,4-(CF₃)₂Ph H CH₃

G4-156 2,6-(CF₃)₂Ph H CH₃

G4-157 3,5-(CF₃)₂Ph H CH₃

G4-158 2-CF₃-3-CN-Ph H CH₃

G4-159 2-CF₃-4-CNPh H CH₃

G4-160 2-CF₃-5-CN-Ph H CH₃

G4-161 2-CF₃-6-CN-Ph H CH₃

G4-162 PhO H CH₃

G4-163 2-CF₃PhO H CH₃

G4-164 3-CF₃PhO H CH₃

G4-165 4-CF₃PhO H CH₃

G4-166 2-CF₃CF₂PhO H CH₃

G4-167 3-CF₃CF₂PhO H CH₃

G4-168 4-CF₃CF₂PhO H CH₃

G4-169 2-CF₃OPhO H CH₃

G4-170 3-CF₃OPhO H CH₃

G4-171 4-CF₃OPhO H CH₃

G4-172 2-CF₃-3-F-PhO H CH₃

G4-173 2-CF₃-4-F-PhO H CH₃

G4-174 2-CF₃-5-F-PhO H CH₃

G4-175 2-CF₃-6-F-PhO H CH₃

G4-176 2-CF₃-3-CI-PhO H CH₃

G4-177 2-CF₃-4-CI-PhO H CH₃

G4-178 2-CF₃-5-CI-PhO H CH₃

G4-179 2-CF₃-6-CI-PhO H CH₃ G4-180 2-CF₃-3-CH₃-PhO H CH₃

G4-181 2-CF₃-4-CH₃-PhO H CH₃

G4-182 2-CF₃-5-CH₃-PhO H CH₃

G4-183 2-CF₃-6-CH₃-PhO H CH₃

G4-184 2,3-(CF₃)₂PhO H CH₃

G4-185 2,4-(CF₃)₂PhO H CH₃

G4-186 2,6-(CF₃)₂PhO H CH₃

G4-187 3,5-(CF₃)₂PhO H CH₃

G4-188 PhCH₂0 H CH₃

G4-189 2-CF₃PhCH₂0 H CH₃

G4-190 3-CF₃PhCH₂0 H CH₃

G4-191 4-CF₃PhCH₂0 H CH₃

G4-192 2-CF₃CF₂PhCH₂0 H CH₃

G4-193 3-CF₃CF₂PhCH₂0 H CH₃

G4-194 4-CF₃CF₂PhCH₂0 H CH₃

G4-195 2-CF₃OPhCH₂0 H CH₃

G4-196 3-CF₃OPhCH₂0 H CH₃

G4-197 4-CF₃OPhCH₂0 H CH₃

G4-198 2-CF₃-3-F-PhCH₂0 H CH₃

G4-199 2-CF₃-4-F-PhCH₂0 H CH₃

G4-200 2-CF₃-5-F-PhCH₂0 H CH₃

G4-201 2-CF₃-6-F-PhCH₂0 H CH₃

G4-202 2-CF₃-3-CI-PhCH₂0 H CH₃

G4-203 2-CF₃-4-CI-PhCH₂0 H CH₃

G4-204 2-CF₃-5-CI-PhCH₂0 H CH₃

G4-205 2-CF₃-6-CI-PhCH₂0 H CH₃

G4-206 2-CF₃-3-CH₃-PhCH₂0 H CH₃

G4-207 2-CF₃-4-CH₃-PhCH₂0 H CH₃

G4-208 2-CF₃-5-CH₃-PhCH₂0 H CH₃

G4-209 2-CF₃-6-CH₃-PhCH₂0 H CH₃

G4-210 2,3-(CF₃)₂PhCH₂0 H CH₃

G4-211 2,4-(CF₃)₂PhCH₂0 H CH₃

G4-212 2,6-(CF₃)₂PhCH₂0 H CH₃

G4-213 3,5-(CF₃)₂PhCH₂0 H CH₃

G4-214 PhS H CH₃

G4-215 2-CF₃PhS H CH₃

G4-216 3-CF₃PhS H CH₃

G4-217 4-CF₃PhS H CH₃

G4-218 PhNCH₃ H CH₃

G4-219 2-CF₃PhNCH₃ H CH₃

G4-220 3-CF₃PhNCH₃ H CH₃

G4-221 4-CF₃PhNCH₃ H CH₃

G4-222 2-Pyridyl H CH₃

G4-223 3-Pyridyl H CH₃

G4-224 4-Pyridyl H CH₃

G4-225 CF₃ CH₃ H

G4-226 CF₃ CH3CH2 H

G4-269 CF₃ (3-FPh)OCH₂ H

G4-270 CF₃ (4-FPh)OCH₂ H

G4-271 CF₃ (2-CIPh)OCH₂ H

G4-272 CF₃ (3-CIPh)OCH₂ H

G4-273 CF₃ (4-CIPh)OCH₂ H

G4-274 CF₃ (2-BrPh)OCH₂ H

G4-275 CF₃ (3-BrPh)OCH₂ H

G4-276 CF₃ (4-BrPh)OCH₂ H

G4-277 CF₃ (2-CF₃OPh)OCH₂ H

G4-278 CF₃ (3-CF₃OPh)OCH₂ H

G4-279 CF₃ (4-CF₃OPh)OCH₂ H

G4-280 CF₃ (2-CNPh)OCH₂ H

G4-281 CF₃ (3-CNPh)OCH₂ H

G4-282 CF₃ (4-CNPh)OCH₂ H

G4-283 CF₃ (2-N0₂Ph)OCH₂ H

G4-284 CF₃ (3-N0₂Ph)OCH₂ H

G4-285 CF₃ (4-N0₂Ph)OCH₂ H

G4-286 CF₃ (2-CF₃Ph)OCH₂ H

G4-287 CF₃ (3-CF₃Ph)OCH₂ H

G4-288 CF₃ (4-CF₃Ph)OCH₂ H

G4-289 CF₃ PhCH₂OCH₂ H

G4-290 CF₃ (2-CH₃Ph)CH₂OCH₂ H

G4-291 CF₃ (3-CH₃Ph)CH₂OCH₂ H

G4-292 CF₃ (4-CH₃Ph)CH₂OCH₂ H

G4-293 CF₃ (2-CH₃OPh)CH₂OCH₂ H

G4-294 CF₃ (3-CH₃OPh)CH₂OCH₂ H

G4-295 CF₃ (4-CH₃OPh)CH₂OCH₂ H

G4-296 CF₃ (2-FPh)CH₂OCH₂ H

G4-297 CF₃ (3-FPh)CH₂OCH₂ H

G4-298 CF₃ (4-FPh)CH₂OCH₂ H

G4-299 CF₃ (2-CIPh)CH₂OCH₂ H

G4-300 CF₃ (3-CIPh)CH₂OCH₂ H

G4-301 CF₃ (4-CIPh)CH₂OCH₂ H

G4-302 CF₃ (2-BrPh)CH₂OCH₂ H

G4-303 CF₃ (3-BrPh)CH₂OCH₂ H

G4-304 CF₃ (4-BrPh)CH₂OCH₂ H

G4-305 CF₃ (2-CF₃OPh)CH₂OCH₂ H

G4-306 CF₃ (3-CF₃OPh)CH₂OCH₂ H

G4-307 CF₃ (4-CF₃OPh)CH₂OCH₂ H

G4-308 CF₃ (2-CNPh)CH₂OCH₂ H

G4-309 CF₃ (3-CNPh)CH₂OCH₂ H

G4-310 CF₃ (4-CNPh)CH₂OCH₂ H

G4-311 CF₃ (2-N0₂Ph)CH₂OCH₂ H

G4-312 CF₃ (3-N0₂Ph)CH₂OCH₂ H

G4-313 CF₃ (4-N0₂Ph)CH₂OCH₂ H

G4-314 CF₃ (2-CF₃Ph)CH₂OCH₂ H

G4-315 CF₃ (3-CF₃Ph)CH₂OCH₂ H

G4-316 CF₃ (4-CF₃Ph)CH₂OCH₂ H

G4-407 CF₃ (3-CF₃OPh)OCH₂ CH₃

G4-408 CF₃ (4-CF₃OPh)OCH₂ CH₃

G4-409 CF₃ (2-CNPh)OCH₂ CH₃

G4-410 CF₃ (3-CNPh)OCH₂ CH₃

G4-411 CF₃ (4-CNPh)OCH₂ CH₃

G4-412 CF₃ (2-N0₂Ph)OCH₂ CH₃

G4-413 CF₃ (3-N0₂Ph)OCH₂ CH₃

G4-414 CF₃ (4-N0₂Ph)OCH₂ CH₃

G4-415 CF₃ (2-CF₃Ph)OCH₂ CH₃

G4-416 CF₃ (3-CF₃Ph)OCH₂ CH₃

G4-417 CF₃ (4-CF₃Ph)OCH₂ CH₃

G4-418 CF₃ PhCH₂OCH₂ CH₃

G4-419 CF₃ (2-CH₃Ph)CH₂OCH₂ CH₃

G4-420 CF₃ (3-CH₃Ph)CH₂OCH₂ CH₃

G4-421 CF₃ (4-CH₃Ph)CH₂OCH₂ CH₃

G4-422 CF₃ (2-CH₃OPh)CH₂OCH₂ CH₃

G4-423 CF₃ (3-CH₃OPh)CH₂OCH₂ CH₃

G4-424 CF₃ (4-CH₃OPh)CH₂OCH₂ CH₃

G4-425 CF₃ (2-FPh)CH₂OCH₂ CH₃

G4-426 CF₃ (3-FPh)CH₂OCH₂ CH₃

G4-427 CF₃ (4-FPh)CH₂OCH₂ CH₃

G4-428 CF₃ (2-CIPh)CH₂OCH₂ CH₃

G4-429 CF₃ (3-CIPh)CH₂OCH₂ CH₃

G4-430 CF₃ (4-CIPh)CH₂OCH₂ CH₃

G4-431 CF₃ (2-BrPh)CH₂OCH₂ CH₃

G4-432 CF₃ (3-BrPh)CH₂OCH₂ CH₃

G4-433 CF₃ (4-BrPh)CH₂OCH₂ CH₃

G4-434 CF₃ (2-CF₃OPh)CH₂OCH₂ CH₃

G4-435 CF₃ (3-CF₃OPh)CH₂OCH₂ CH₃

G4-436 CF₃ (4-CF₃OPh)CH₂OCH₂ CH₃

G4-437 CF₃ (2-CNPh)CH₂OCH₂ CH₃

G4-438 CF₃ (3-CNPh)CH₂OCH₂ CH₃

G4-439 CF₃ (4-CNPh)CH₂OCH₂ CH₃

G4-440 CF₃ (2-N0₂Ph)CH₂OCH₂ CH₃

G4-441 CF₃ (3-N0₂Ph)CH₂OCH₂ CH₃

G4-442 CF₃ (4-N0₂Ph)CH₂OCH₂ CH₃

G4-443 CF₃ (2-CF₃Ph)CH₂OCH₂ CH₃

G4-444 CF₃ (3-CF₃Ph)CH₂OCH₂ CH₃

G4-445 CF₃ (4-CF₃Ph)CH₂OCH₂ CH₃

G4-446 CF₃ CH₃C(=0)OCH₂ CH₃

G4-447 CF₃ CH₃CH₂C(=0)OCH₂ CH₃

G4-448 CF₃ CH(CH₃)₂C(=0)OCH₂ CH₃

G4-449 CF₃ (CH₃)₃C(=0)OCH₂ CH₃

G4-450 CF₃ (CH₃)₃CCH₂(=0)OCH₂ CH₃

G4-451 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G4-452 CF₃ CF₃C(=0)OCH₂ CH₃

G4-453 CF₃ CF₃CF₂C(=0)OCH₂ CH₃

G4-454 CF₃ (c-hex)C(=0)OCH₂ CH₃

G4-545 2-CF₃Ph (3-CF₃Ph)OCH₂ H

G4-546 2-CF₃Ph (4-CF₃Ph)OCH₂ H

G4-547 2-CF₃Ph PhCH₂OCH₂ H

G4-548 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G4-549 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G4-550 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G4-551 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G4-552 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G4-553 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G4-554 2-CF₃Ph (2-FPh)CH₂OCH₂ H

G4-555 2-CF₃Ph (3-FPh)CH₂OCH₂ H

G4-556 2-CF₃Ph (4-FPh)CH₂OCH₂ H

G4-557 2-CF₃Ph (2-CIPh)CH₂OCH₂ H

G4-558 2-CF₃Ph (3-CIPh)CH₂OCH₂ H

G4-559 2-CF₃Ph (4-CIPh)CH₂OCH₂ H

G4-560 2-CF₃Ph (2-BrPh)CH₂OCH₂ H

G4-561 2-CF₃Ph (3-BrPh)CH₂OCH₂ H

G4-562 2-CF₃Ph (4-BrPh)CH₂OCH₂ H

G4-563 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G4-564 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G4-565 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G4-566 2-CF₃Ph (2-CNPh)CH₂OCH₂ H

G4-567 2-CF₃Ph (3-CNPh)CH₂OCH₂ H

G4-568 2-CF₃Ph (4-CNPh)CH₂OCH₂ H

G4-569 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G4-570 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G4-571 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G4-572 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G4-573 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G4-574 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G4-575 2-CF₃Ph CH₃C(=0)OCH₂ H

G4-576 2-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G4-577 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G4-578 2-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G4-579 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G4-580 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G4-581 2-CF₃Ph CF₃C(=0)OCH₂ H

G4-582 2-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G4-583 2-CF₃Ph (c-hex)C(=0)OCH₂ H

G4-584 2-CF₃Ph PhC(=0)OCH₂ H

G4-585 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G4-586 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G4-587 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G4-588 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G4-589 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G4-590 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G4-591 2-CF₃Ph (2-FPh)C(=0)OCH₂ H

G4-592 2-CF₃Ph (3-FPh)C(=0)OCH₂ H G4-593 2-CF₃Ph (4-FPh)C(=0)OCH₂ H

G4-594 2-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G4-595 2-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G4-596 2-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G4-597 2-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G4-598 2-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G4-599 2-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G4-600 2-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G4-601 2-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G4-602 2-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G4-603 2-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G4-604 2-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G4-605 2-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G4-606 2-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G4-607 2-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G4-608 2-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G4-609 2-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G4-610 2-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G4-611 2-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G4-612 2-CF₃Ph CH₃ CH₃

G4-613 2-CF₃Ph CH3CH2 CH₃

G4-614 2-CF₃Ph CH3CH2CH2 CH₃

G4-615 2-CF₃Ph (CH₃)₂CH CH₃

G4-616 2-CF₃Ph CH₃C(=0) CH₃

G4-617 2-CF₃Ph CH₃CH₂C(=0) CH₃

G4-618 2-CF₃Ph (CH₃)₂CHC(=0) CH₃

G4-619 2-CF₃Ph (CH₃)₃CC(=0) CH₃

G4-620 2-CF₃Ph (CH₃)₃CCH₂C(=0) CH₃

G4-621 2-CF₃Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G4-622 2-CF₃Ph (CH₃)₂CHCH₂C(=0) CH₃

G4-623 2-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G4-624 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G4-625 2-CF₃Ph (c-hex)C(=0) CH₃

G4-626 2-CF₃Ph (c-pen)C(=0) CH₃

G4-627 2-CF₃Ph (c-hep)C(=0) CH₃

G4-628 2-CF₃Ph (c-pro)C(=0) CH₃

G4-629 2-CF₃Ph CF₃C(=0) CH₃

G4-630 2-CF₃Ph (CH₃)₂NC(=0) CH₃

G4-631 2-CF₃Ph (CH₃CH₂)₂NC(=0) CH₃

G4-632 2-CF₃Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G4-633 2-CF₃Ph CH₃CH₂N(CH₃)C(=0) CH₃

G4-634 2-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃

G4-635 2-CF₃Ph CH₃ON(CH₃)C(=0) CH₃

G4-636 2-CF₃Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G4-637 2-CF₃Ph (CHCCH₂)₂NC(=0) CH₃

G4-638 2-CF₃Ph CH₃

G4-683 2-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G4-684 2-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G4-685 2-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G4-686 2-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G4-687 2-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G4-688 2-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G4-689 2-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G4-690 2-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G4-691 2-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G4-692 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G4-693 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G4-694 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G4-695 2-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G4-696 2-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G4-697 2-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G4-698 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G4-699 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G4-700 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G4-701 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G4-702 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G4-703 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G4-704 2-CF₃Ph CH₃C(=0)OCH₂ CH₃

G4-705 2-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G4-706 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G4-707 2-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G4-708 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G4-709 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G4-710 2-CF₃Ph CF₃C(=0)OCH₂ CH₃

G4-711 2-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G4-712 2-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G4-713 2-CF₃Ph PhC(=0)OCH₂ CH₃

G4-714 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G4-715 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G4-716 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G4-717 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G4-718 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G4-719 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G4-720 2-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G4-721 2-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G4-722 2-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G4-723 2-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G4-724 2-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G4-725 2-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G4-726 2-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G4-727 2-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G4-728 2-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G4-729 2-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G4-730 2-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G4-773 3-CF₃Ph (CH₃)₃COCH₂ H

G4-774 3-CF₃Ph (CH₃)3CCH20CH2 H

G4-775 3-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂ H

G4-776 3-CF₃Ph (c-hex)OCH₂ H

G4-777 3-CF₃Ph PhOCH₂ H

G4-778 3-CF₃Ph (2-CH₃Ph)OCH₂ H

G4-779 3-CF₃Ph (3-CH₃Ph)OCH₂ H

G4-780 3-CF₃Ph (4-CH₃Ph)OCH₂ H

G4-781 3-CF₃Ph (2-CH₃OPh)OCH₂ H

G4-782 3-CF₃Ph (3-CH₃OPh)OCH₂ H

G4-783 3-CF₃Ph (4-CH₃OPh)OCH₂ H

G4-784 3-CF₃Ph (2-FPh)OCH₂ H

G4-785 3-CF₃Ph (3-FPh)OCH₂ H

G4-786 3-CF₃Ph (4-FPh)OCH₂ H

G4-787 3-CF₃Ph (2-CIPh)OCH₂ H

G4-788 3-CF₃Ph (3-CIPh)OCH₂ H

G4-789 3-CF₃Ph (4-CIPh)OCH₂ H

G4-790 3-CF₃Ph (2-BrPh)OCH₂ H

G4-791 3-CF₃Ph (3-BrPh)OCH₂ H

G4-792 3-CF₃Ph (4-BrPh)OCH₂ H

G4-793 3-CF₃Ph (2-CF₃OPh)OCH₂ H

G4-794 3-CF₃Ph (3-CF₃OPh)OCH₂ H

G4-795 3-CF₃Ph (4-CF₃OPh)OCH₂ H

G4-796 3-CF₃Ph (2-CNPh)OCH₂ H

G4-797 3-CF₃Ph (3-CNPh)OCH₂ H

G4-798 3-CF₃Ph (4-CNPh)OCH₂ H

G4-799 3-CF₃Ph (2-N0₂Ph)OCH₂ H

G4-800 3-CF₃Ph (3-N0₂Ph)OCH₂ H

G4-801 3-CF₃Ph (4-N0₂Ph)OCH₂ H

G4-802 3-CF₃Ph (2-CF₃Ph)OCH₂ H

G4-803 3-CF₃Ph (3-CF₃Ph)OCH₂ H

G4-804 3-CF₃Ph (4-CF₃Ph)OCH₂ H

G4-805 3-CF₃Ph PhCH₂OCH₂ H

G4-806 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G4-807 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G4-808 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G4-809 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G4-810 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G4-81 1 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G4-812 3-CF₃Ph (2-FPh)CH₂OCH₂ H

G4-813 3-CF₃Ph (3-FPh)CH₂OCH₂ H

G4-814 3-CF₃Ph (4-FPh)CH₂OCH₂ H

G4-815 3-CF₃Ph (2-CIPh)CH₂OCH₂ H

G4-816 3-CF₃Ph (3-CIPh)CH₂OCH₂ H

G4-817 3-CF₃Ph (4-CIPh)CH₂OCH₂ H

G4-818 3-CF₃Ph (2-BrPh)CH₂OCH₂ H

G4-819 3-CF₃Ph (3-BrPh)CH₂OCH₂ H

G4-820 3-CF₃Ph (4-BrPh)CH₂OCH₂ H G4-821 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G4-822 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G4-823 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G4-824 3-CF₃Ph (2-CNPh)CH₂OCH₂ H

G4-825 3-CF₃Ph (3-CNPh)CH₂OCH₂ H

G4-826 3-CF₃Ph (4-CNPh)CH₂OCH₂ H

G4-827 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G4-828 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G4-829 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G4-830 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G4-831 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G4-832 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G4-833 3-CF₃Ph CH₃C(=0)OCH₂ H

G4-834 3-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G4-835 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G4-836 3-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G4-837 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G4-838 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G4-839 3-CF₃Ph CF₃C(=0)OCH₂ H

G4-840 3-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G4-841 3-CF₃Ph (c-hex)C(=0)OCH₂ H

G4-842 3-CF₃Ph PhC(=0)OCH₂ H

G4-843 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G4-844 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G4-845 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G4-846 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G4-847 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G4-848 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G4-849 3-CF₃Ph (2-FPh)C(=0)OCH₂ H

G4-850 3-CF₃Ph (3-FPh)C(=0)OCH₂ H

G4-851 3-CF₃Ph (4-FPh)C(=0)OCH₂ H

G4-852 3-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G4-853 3-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G4-854 3-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G4-855 3-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G4-856 3-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G4-857 3-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G4-858 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G4-859 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G4-860 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G4-861 3-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G4-862 3-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G4-863 3-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G4-864 3-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G4-865 3-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G4-866 3-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G4-867 3-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G4-868 3-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G4-911 3-CF₃Ph (3-CH₃OPh)OCH₂ CH₃

G4-912 3-CF₃Ph (4-CH₃OPh)OCH₂ CH₃

G4-913 3-CF₃Ph (2-FPh)OCH₂ CH₃

G4-914 3-CF₃Ph (3-FPh)OCH₂ CH₃

G4-915 3-CF₃Ph (4-FPh)OCH₂ CH₃

G4-916 3-CF₃Ph (2-CIPh)OCH₂ CH₃

G4-917 3-CF₃Ph (3-CIPh)OCH₂ CH₃

G4-918 3-CF₃Ph (4-CIPh)OCH₂ CH₃

G4-919 3-CF₃Ph (2-BrPh)OCH₂ CH₃

G4-920 3-CF₃Ph (3-BrPh)OCH₂ CH₃

G4-921 3-CF₃Ph (4-BrPh)OCH₂ CH₃

G4-922 3-CF₃Ph (2-CF₃OPh)OCH₂ CH₃

G4-923 3-CF₃Ph (3-CF₃OPh)OCH₂ CH₃

G4-924 3-CF₃Ph (4-CF₃OPh)OCH₂ CH₃

G4-925 3-CF₃Ph (2-CNPh)OCH₂ CH₃

G4-926 3-CF₃Ph (3-CNPh)OCH₂ CH₃

G4-927 3-CF₃Ph (4-CNPh)OCH₂ CH₃

G4-928 3-CF₃Ph (2-N0₂Ph)OCH₂ CH₃

G4-929 3-CF₃Ph (3-N0₂Ph)OCH₂ CH₃

G4-930 3-CF₃Ph (4-N0₂Ph)OCH₂ CH₃

G4-931 3-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G4-932 3-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G4-933 3-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G4-934 3-CF₃Ph PhCH₂OCH₂ CH₃

G4-935 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G4-936 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G4-937 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G4-938 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G4-939 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G4-940 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G4-941 3-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G4-942 3-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G4-943 3-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G4-944 3-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G4-945 3-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G4-946 3-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G4-947 3-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G4-948 3-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G4-949 3-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G4-950 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G4-951 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G4-952 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G4-953 3-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G4-954 3-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G4-955 3-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G4-956 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G4-957 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G4-958 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃ G4-959 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G4-960 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G4-961 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G4-962 3-CF₃Ph CH₃C(=0)OCH₂ CH₃

G4-963 3-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G4-964 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G4-965 3-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G4-966 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G4-967 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G4-968 3-CF₃Ph CF₃C(=0)OCH₂ CH₃

G4-969 3-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G4-970 3-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G4-971 3-CF₃Ph PhC(=0)OCH₂ CH₃

G4-972 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G4-973 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G4-974 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G4-975 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G4-976 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G4-977 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G4-978 3-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G4-979 3-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G4-980 3-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G4-981 3-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G4-982 3-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G4-983 3-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G4-984 3-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G4-985 3-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G4-986 3-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G4-987 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G4-988 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G4-989 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G4-990 3-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G4-991 3-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G4-992 3-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G4-993 3-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G4-994 3-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G4-995 3-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G4-996 3-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G4-997 3-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G4-998 3-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

G4-999 4-CF₃Ph CH₃ H

G4-1000 4-CF₃Ph CH3CH2 H

G4-1001 4-CF₃Ph CH3CH2CH2 H

G4-1002 4-CF₃Ph (CH₃)₂CH H

G4-1003 4-CF₃Ph CH₃C(=0) H

G4-1004 4-CF₃Ph CH₃CH₂C(=0) H

G4-1005 4-CF₃Ph (CH₃)₂CHC(=0) H

G4-1006 4-CF₃Ph (CH₃)₃CC(=0) H

G4-1049 4-CF₃Ph (3-BrPh)OCH₂ H

G4-1050 4-CF₃Ph (4-BrPh)OCH₂ H

G4-1051 4-CF₃Ph (2-CF₃OPh)OCH₂ H

G4-1052 4-CF₃Ph (3-CF₃OPh)OCH₂ H

G4-1053 4-CF₃Ph (4-CF₃OPh)OCH₂ H

G4-1054 4-CF₃Ph (2-CNPh)OCH₂ H

G4-1055 4-CF₃Ph (3-CNPh)OCH₂ H

G4-1056 4-CF₃Ph (4-CNPh)OCH₂ H

G4-1057 4-CF₃Ph (2-N0₂Ph)OCH₂ H

G4-1058 4-CF₃Ph (3-N0₂Ph)OCH₂ H

G4-1059 4-CF₃Ph (4-N0₂Ph)OCH₂ H

G4-1060 4-CF₃Ph (2-CF₃Ph)OCH₂ H

G4-1061 4-CF₃Ph (3-CF₃Ph)OCH₂ H

G4-1062 4-CF₃Ph (4-CF₃Ph)OCH₂ H

G4-1063 4-CF₃Ph PhCH₂OCH₂ H

G4-1064 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G4-1065 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G4-1066 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G4-1067 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G4-1068 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G4-1069 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G4-1070 4-CF₃Ph (2-FPh)CH₂OCH₂ H

G4-1071 4-CF₃Ph (3-FPh)CH₂OCH₂ H

G4-1072 4-CF₃Ph (4-FPh)CH₂OCH₂ H

G4-1073 4-CF₃Ph (2-CIPh)CH₂OCH₂ H

G4-1074 4-CF₃Ph (3-CIPh)CH₂OCH₂ H

G4-1075 4-CF₃Ph (4-CIPh)CH₂OCH₂ H

G4-1076 4-CF₃Ph (2-BrPh)CH₂OCH₂ H

G4-1077 4-CF₃Ph (3-BrPh)CH₂OCH₂ H

G4-1078 4-CF₃Ph (4-BrPh)CH₂OCH₂ H

G4-1079 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G4-1080 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G4-1081 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G4-1082 4-CF₃Ph (2-CNPh)CH₂OCH₂ H

G4-1083 4-CF₃Ph (3-CNPh)CH₂OCH₂ H

G4-1084 4-CF₃Ph (4-CNPh)CH₂OCH₂ H

G4-1085 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G4-1086 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G4-1087 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G4-1088 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G4-1089 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G4-1090 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G4-1091 4-CF₃Ph CH₃C(=0)OCH₂ H

G4-1092 4-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G4-1093 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G4-1094 4-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G4-1095 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G4-1096 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H G4-1097 4-CF₃Ph CF₃C(=0)OCH₂ H

G4-1098 4-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G4-1099 4-CF₃Ph (c-hex)C(=0)OCH₂ H

G4-1100 4-CF₃Ph PhC(=0)OCH₂ H

G4-1101 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G4-1102 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G4-1103 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G4-1104 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G4-1105 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G4-1106 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G4-1107 4-CF₃Ph (2-FPh)C(=0)OCH₂ H

G4-1108 4-CF₃Ph (3-FPh)C(=0)OCH₂ H

G4-1109 4-CF₃Ph (4-FPh)C(=0)OCH₂ H

G4-1110 4-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G4-1111 4-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G4-1112 4-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G4-1113 4-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G4-1114 4-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G4-1115 4-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G4-1116 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G4-1117 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G4-1118 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G4-1119 4-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G4-1120 4-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G4-1121 4-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G4-1122 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G4-1123 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G4-1124 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G4-1125 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G4-1126 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G4-1127 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G4-1128 4-CF₃Ph CH₃ CH₃

G4-1129 4-CF₃Ph CH3CH2 CH₃

G4-1130 4-CF₃Ph CH3CH2CH2 CH₃

G4-1131 4-CF₃Ph (CH₃)₂CH CH₃

G4-1132 4-CF₃Ph CH₃C(=0) CH₃

G4-1133 4-CF₃Ph CH₃CH₂C(=0) CH₃

G4-1134 4-CF₃Ph (CH₃)₂CHC(=0) CH₃

G4-1135 4-CF₃Ph (CH₃)₃CC(=0) CH₃

G4-1136 4-CF₃Ph (CH₃)₃CCH₂C(=0) CH₃

G4-1137 4-CF₃Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G4-1138 4-CF₃Ph (CH₃)₂CHCH₂C(=0) CH₃

G4-1139 4-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G4-1140 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G4-1141 4-CF₃Ph (c-hex)C(=0) CH₃

G4-1142 4-CF₃Ph (c-pen)C(=0) CH₃

G4-1143 4-CF₃Ph (c-hep)C(=0) CH₃

G4-1144 4-CF₃Ph (c-pro)C(=0) CH₃

G4-1187 4-CF₃Ph (3-N0₂Ph)OCH₂ CH₃

G4-1188 4-CF₃Ph (4-N0₂Ph)OCH₂ CH₃

G4-1189 4-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G4-1190 4-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G4-1191 4-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G4-1192 4-CF₃Ph PhCH₂OCH₂ CH₃

G4-1193 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G4-1194 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G4-1195 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G4-1196 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G4-1197 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G4-1198 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G4-1199 4-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G4-1200 4-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G4-1201 4-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G4-1202 4-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G4-1203 4-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G4-1204 4-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G4-1205 4-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G4-1206 4-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G4-1207 4-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G4-1208 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G4-1209 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G4-1210 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G4-1211 4-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G4-1212 4-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G4-1213 4-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G4-1214 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G4-1215 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G4-1216 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G4-1217 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G4-1218 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G4-1219 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G4-1220 4-CF₃Ph CH₃C(=0)OCH₂ CH₃

G4-1221 4-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G4-1222 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G4-1223 4-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G4-1224 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G4-1225 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G4-1226 4-CF₃Ph CF₃C(=0)OCH₂ CH₃

G4-1227 4-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G4-1228 4-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G4-1229 4-CF₃Ph PhC(=0)OCH₂ CH₃

G4-1230 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G4-1231 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G4-1232 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G4-1233 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G4-1234 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃ G4-1235 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G4-1236 4-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G4-1237 4-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G4-1238 4-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G4-1239 4-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G4-1240 4-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G4-1241 4-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G4-1242 4-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G4-1243 4-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G4-1244 4-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G4-1245 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G4-1246 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G4-1247 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G4-1248 4-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G4-1249 4-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G4-1250 4-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G4-1251 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G4-1252 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G4-1253 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G4-1254 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G4-1255 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G4-1256 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

G4-1257 3,5-(CF₃)₂Ph CH₃ H

G4-1258 3,5-(CF₃)₂Ph CH3CH2 H

G4-1259 3,5-(CF₃)₂Ph CH3CH2CH2 H

G4-1260 3,5-(CF₃)₂Ph (CH₃)₂CH H

G4-1261 3,5-(CF₃)₂Ph CH₃C(=0) H

G4-1262 3,5-(CF₃)₂Ph CH₃CH₂C(=0) H

G4-1263 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0) H

G4-1264 3,5-(CF₃)₂Ph (CH₃)₃CC(=0) H

G4-1265 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0) H

G4-1266 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0) H

G4-1267 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0) H

G4-1268 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0) H

G4-1269 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0) H

G4-1270 3,5-(CF₃)₂Ph (c-hex)C(=0) H

G4-1271 3,5-(CF₃)₂Ph (c-pen)C(=0) H

G4-1272 3,5-(CF₃)₂Ph (c-hep)C(=0) H

G4-1273 3,5-(CF₃)₂Ph (c-pro)C(=0) H

G4-1274 3,5-(CF₃)₂Ph CF₃C(=0) H

G4-1275 3,5-(CF₃)₂Ph (CH₃)₂NC(=0) H

G4-1276 3,5-(CF₃)₂Ph (CH₃CH₂)₂NC(=0) H

G4-1277 3,5-(CF₃)₂Ph (CH₃CH₂CH₂)₂NC(=0) H

G4-1278 3,5-(CF₃)₂Ph CH₃CH₂N(CH₃)C(=0) H

G4-1279 3,5-(CF₃)₂Ph [(CH₃)₂CHCH₂]₂NC(=0) H

G4-1280 3,5-(CF₃)₂Ph CH₃ON(CH₃)C(=0) H

G4-1281 3,5-(CF₃)₂Ph (CH₂=CHCH₂)₂N C(=0) H

G4-1282 3,5-(CF₃)₂Ph (CHCCH₂)₂NC(=0) H

G4-1325 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂ H

G4-1326 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂ H

G4-1327 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂ H

G4-1328 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂ H

G4-1329 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂ H

G4-1330 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂ H

G4-1331 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂ H

G4-1332 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂ H

G4-1333 3,5-(CF₃)₂P (4-CIPh)CH₂OCH₂ H

G4-1334 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂ H

G4-1335 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂ H

G4-1336 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂ H

G4-1337 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂ H

G4-1338 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂ H

G4-1339 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂ H

G4-1340 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂ H

G4-1341 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂ H

G4-1342 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂ H

G4-1343 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂ H

G4-1344 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂ H

G4-1345 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂ H

G4-1346 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂ H

G4-1347 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂ H

G4-1348 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ H

G4-1349 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂ H

G4-1350 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂ H

G4-1351 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂ H

G4-1352 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂ H

G4-1353 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂ H

G4-1354 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G4-1355 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂ H

G4-1356 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂ H

G4-1357 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂ H

G4-1358 3,5-(CF₃)₂Ph PhC(=0)OCH₂ H

G4-1359 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂ H

G4-1360 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂ H

G4-1361 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂ H

G4-1362 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂ H

G4-1363 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂ H

G4-1364 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂ H

G4-1365 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂ H

G4-1366 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂ H

G4-1367 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂ H

G4-1368 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂ H

G4-1369 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂ H

G4-1370 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂ H

G4-1371 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂ H

G4-1372 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ H G4-1373 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂ H

G4-1374 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂ H

G4-1375 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂ H

G4-1376 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂ H

G4-1377 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂ H

G4-1378 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂ H

G4-1379 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂ H

G4-1380 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂ H

G4-1381 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂ H

G4-1382 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂ H

G4-1383 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂ H

G4-1384 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂ H

G4-1385 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂ H

G4-1386 3,5-(CF₃)₂Ph CH₃ CH₃

G4-1387 3,5-(CF₃)₂Ph CH3CH2 CH₃

G4-1388 3,5-(CF₃)₂Ph CH3CH2CH2 CH₃

G4-1389 3,5-(CF₃)₂Ph (CH₃)₂CH CH₃

G4-1390 3,5-(CF₃)₂Ph CH₃C(=0) CH₃

G4-1391 3,5-(CF₃)₂Ph CH₃CH₂C(=0) CH₃

G4-1392 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0) CH₃

G4-1393 3,5-(CF₃)₂Ph (CH₃)₃CC(=0) CH₃

G4-1394 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0) CH₃

G4-1395 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G4-1396 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0) CH₃

G4-1397 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G4-1398 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G4-1399 3,5-(CF₃)₂Ph (c-hex)C(=0) CH₃

G4-1400 3,5-(CF₃)₂Ph (c-pen)C(=0) CH₃

G4-1401 3,5-(CF₃)₂Ph (c-hep)C(=0) CH₃

G4-1402 3,5-(CF₃)₂Ph (c-pro)C(=0) CH₃

G4-1403 3,5-(CF₃)₂Ph CF₃C(=0) CH₃

G4-1404 3,5-(CF₃)₂Ph (CH₃)₂NC(=0) CH₃

G4-1405 3,5-(CF₃)₂Ph (CH₃CH₂)₂NC(=0) CH₃

G4-1406 3,5-(CF₃)₂Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G4-1407 3,5-(CF₃)₂Ph CH₃CH₂N(CH₃)C(=0) CH₃

G4-1408 3,5-(CF₃)₂Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃

G4-1409 3,5-(CF₃)₂Ph CH₃ON(CH₃)C(=0) CH₃

G4-1410 3,5-(CF₃)₂Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G4-1411 3,5-(CF₃)₂Ph (CHCCH₂)₂NC(=0) CH₃

G4-1412 3,5-(CF₃)₂Ph CH₃

G4-1413 3,5-(CF₃)₂Ph CH₃

G4-1414 3,5-(CF₃)₂Ph CH₃ G4-1415 3,5-(CF₃)₂Ph CH₃OCH₂ CH₃

G4-1416 3,5-(CF₃)₂Ph CH₃CH₂OCH₂ CH₃

G4-1417 3,5-(CF₃)₂Ph (CH₃)₂CHOCH₂ CH₃

G4-1418 3,5-(CF₃)₂Ph (CH₃)₃COCH₂ CH₃

G4-1419 3,5-(CF₃)₂Ph (CH₃)3CCH20CH2 CH₃

G4-1420 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂OCH₂ CH₃

G4-1421 3,5-(CF₃)₂Ph (c-hex)OCH₂ CH₃

G4-1422 3,5-(CF₃)₂Ph PhOCH₂ CH₃

G4-1423 3,5-(CF₃)₂Ph (2-CH₃Ph)OCH₂ CH₃

G4-1424 3,5-(CF₃)₂Ph (3-CH₃Ph)OCH₂ CH₃

G4-1425 3,5-(CF₃)₂Ph (4-CH₃Ph)OCH₂ CH₃

G4-1426 3,5-(CF₃)₂Ph (2-CH₃OPh)OCH₂ CH₃

G4-1427 3,5-(CF₃)₂Ph (3-CH₃OPh)OCH₂ CH₃

G4-1428 3,5-(CF₃)₂Ph (4-CH₃OPh)OCH₂ CH₃

G4-1429 3,5-(CF₃)₂Ph (2-FPh)OCH₂ CH₃

G4-1430 3,5-(CF₃)₂Ph (3-FPh)OCH₂ CH₃

G4-1431 3,5-(CF₃)₂Ph (4-FPh)OCH₂ CH₃

G4-1432 3,5-(CF₃)₂Ph (2-CIPh)OCH₂ CH₃

G4-1433 3,5-(CF₃)₂Ph (3-CIPh)OCH₂ CH₃

G4-1434 3,5-(CF₃)₂Ph (4-CIPh)OCH₂ CH₃

G4-1435 3,5-(CF₃)₂Ph (2-BrPh)OCH₂ CH₃

G4-1436 3,5-(CF₃)₂Ph (3-BrPh)OCH₂ CH₃

G4-1437 3,5-(CF₃)₂Ph (4-BrPh)OCH₂ CH₃

G4-1438 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂ CH₃

G4-1439 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂ CH₃

G4-1440 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂ CH₃

G4-1441 3,5-(CF₃)₂Ph (2-CNPh)OCH₂ CH₃

G4-1442 3,5-(CF₃)₂Ph (3-CNPh)OCH₂ CH₃

G4-1443 3,5-(CF₃)₂Ph (4-CNPh)OCH₂ CH₃

G4-1444 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂ CH₃

G4-1445 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂ CH₃

G4-1446 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂ CH₃

G4-1447 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂ CH₃

G4-1448 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂ CH₃

G4-1449 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂ CH₃

G4-1450 3,5-(CF₃)₂Ph PhCH₂OCH₂ CH₃

G4-1451 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G4-1452 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G4-1453 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G4-1454 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G4-1455 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G4-1456 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G4-1457 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂ CH₃

G4-1458 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂ CH₃

G4-1459 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂ CH₃

G4-1460 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂ CH₃

G4-1461 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂ CH₃

G4-1462 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂ CH₃

G4-1559 CF₃ CH₃ 3-Pyridyl

G4-1560 CF₃ CH₃ 4-Pyridyl

G4-1561 CF₃ CH₃ 3-CI-Pyridin-2-yl

G4-1562 CF₃ CF₃CH₂ 2-Pyridyl

G4-1563 CF₃ CF₃CH₂ 3-Pyridyl

G4-1564 CF₃ CF₃CH₂ 4-Pyridyl

G4-1565 CF₃ CF₃CH₂ 3-CI-Pyridin-2-yl

[0298] Table 5

G5-123 Ph H CH₃

G5-124 2-FPh H CH₃

G5-125 3-FPh H CH₃

G5-126 4-FPh H CH₃

G5-127 2-CIPh H CH₃

G5-128 3-CIPh H CH₃

G5-129 4-CIPh H CH₃

G5-130 2-CF₃Ph H CH₃

G5-131 3-CF₃Ph H CH₃

G5-132 4-CF₃Ph H CH₃

G5-133 2-CF₃CF₂Ph H CH₃

G5-134 3-CF₃CF₂Ph H CH₃

G5-135 4-CF₃CF₂Ph H CH₃

G5-136 2-CF₃OPh H CH₃

G5-137 3-CF₃OPh H CH₃

G5-138 4-CF₃OPh H CH₃

G5-139 2-CF₃CH₂OPh H CH₃

G5-140 3-CF₃CH₂OPh H CH₃

G5-141 4-CF₃CH₂OPh H CH₃

G5-142 2-CF₃-3-F-Ph H CH₃

G5-143 2-CF₃-4-F-Ph H CH₃

G5-144 2-CF₃-5-F-Ph H CH₃

G5-145 2-CF₃-6-F-Ph H CH₃

G5-146 2-CF₃-3-CI-Ph H CH₃

G5-147 2-CF₃-4-CI-Ph H CH₃

G5-148 2-CF₃-5-CI-Ph H CH₃

G5-149 2-CF₃-6-CI-Ph H CH₃

G5-150 2-CF₃-3-CH₃-Ph H CH₃

G5-151 2-CF₃-4-CH₃-Ph H CH₃

G5-152 2-CF₃-5-CH₃-Ph H CH₃

G5-153 2-CF₃-6-CH₃-Ph H CH₃

G5-154 2,3-(CF₃)₂Ph H CH₃

G5-155 2,4-(CF₃)₂Ph H CH₃

G5-156 2,6-(CF₃)₂Ph H CH₃

G5-157 3,5-(CF₃)₂Ph H CH₃

G5-158 2-CF₃-3-CN-Ph H CH₃

G5-159 2-CF₃-4-CNPh H CH₃

G5-160 2-CF₃-5-CN-Ph H CH₃

G5-161 2-CF₃-6-CN-Ph H CH₃

G5-162 PhO H CH₃

G5-163 2-CF₃PhO H CH₃

G5-164 3-CF₃PhO H CH₃

G5-165 4-CF₃PhO H CH₃

G5-166 2-CF₃CF₂PhO H CH₃

G5-167 3-CF₃CF₂PhO H CH₃

G5-168 4-CF₃CF₂PhO H CH₃

G5-169 2-CF₃OPhO H CH₃ G5-170 3-CF₃OPhO H CH₃

G5-171 4-CF₃OPhO H CH₃

G5-172 2-CF₃-3-F-PhO H CH₃

G5-173 2-CF₃-4-F-PhO H CH₃

G5-174 2-CF₃-5-F-PhO H CH₃

G5-175 2-CF₃-6-F-PhO H CH₃

G5-176 2-CF₃-3-CI-PhO H CH₃

G5-177 2-CF₃-4-CI-PhO H CH₃

G5-178 2-CF₃-5-CI-PhO H CH₃

G5-179 2-CF₃-6-CI-PhO H CH₃

G5-180 2-CF₃-3-CH₃-PhO H CH₃

G5-181 2-CF₃-4-CH₃-PhO H CH₃

G5-182 2-CF₃-5-CH₃-PhO H CH₃

G5-183 2-CF₃-6-CH₃-PhO H CH₃

G5-184 2,3-(CF₃)₂PhO H CH₃

G5-185 2,4-(CF₃)₂PhO H CH₃

G5-186 2,6-(CF₃)₂PhO H CH₃

G5-187 3,5-(CF₃)₂PhO H CH₃

G5-188 PhCH₂0 H CH₃

G5-189 2-CF₃PhCH₂0 H CH₃

G5-190 3-CF₃PhCH₂0 H CH₃

G5-191 4-CF₃PhCH₂0 H CH₃

G5-192 2-CF₃CF₂PhCH₂0 H CH₃

G5-193 3-CF₃CF₂PhCH₂0 H CH₃

G5-194 4-CF₃CF₂PhCH₂0 H CH₃

G5-195 2-CF₃OPhCH₂0 H CH₃

G5-196 3-CF₃OPhCH₂0 H CH₃

G5-197 4-CF₃OPhCH₂0 H CH₃

G5-198 2-CF₃-3-F-PhCH₂0 H CH₃

G5-199 2-CF₃-4-F-PhCH₂0 H CH₃

G5-200 2-CF₃-5-F-PhCH₂0 H CH₃

G5-201 2-CF₃-6-F-PhCH₂0 H CH₃

G5-202 2-CF₃-3-CI-PhCH₂0 H CH₃

G5-203 2-CF₃-4-CI-PhCH₂0 H CH₃

G5-204 2-CF₃-5-CI-PhCH₂0 H CH₃

G5-205 2-CF₃-6-CI-PhCH₂0 H CH₃

G5-206 2-CF₃-3-CH₃-PhCH₂0 H CH₃

G5-207 2-CF₃-4-CH₃-PhCH₂0 H CH₃

G5-208 2-CF₃-5-CH₃-PhCH₂0 H CH₃

G5-209 2-CF₃-6-CH₃-PhCH₂0 H CH₃

G5-210 2,3-(CF₃)₂PhCH₂0 H CH₃

G5-21 1 2,4-(CF₃)₂PhCH₂0 H CH₃

G5-212 2,6-(CF₃)₂PhCH₂0 H CH₃

G5-213 3,5-(CF₃)₂PhCH₂0 H CH₃

G5-214 PhS H CH₃

G5-215 2-CF₃PhS H CH₃

G5-216 3-CF₃PhS H CH₃

G5-259 CF₃ CH₃CH₂C(CH₃)₂OCH₂ H

G5-260 CF₃ (c-hex)OCH₂ H

G5-261 CF₃ PhOCH₂ H

G5-262 CF₃ (2-CH₃Ph)OCH₂ H

G5-263 CF₃ (3-CH₃Ph)OCH₂ H

G5-264 CF₃ (4-CH₃Ph)OCH₂ H

G5-265 CF₃ (2-CH₃OPh)OCH₂ H

G5-266 CF₃ (3-CH₃OPh)OCH₂ H

G5-267 CF₃ (4-CH₃OPh)OCH₂ H

G5-268 CF₃ (2-FPh)OCH₂ H

G5-269 CF₃ (3-FPh)OCH₂ H

G5-270 CF₃ (4-FPh)OCH₂ H

G5-271 CF₃ (2-CIPh)OCH₂ H

G5-272 CF₃ (3-CIPh)OCH₂ H

G5-273 CF₃ (4-CIPh)OCH₂ H

G5-274 CF₃ (2-BrPh)OCH₂ H

G5-275 CF₃ (3-BrPh)OCH₂ H

G5-276 CF₃ (4-BrPh)OCH₂ H

G5-277 CF₃ (2-CF₃OPh)OCH₂ H

G5-278 CF₃ (3-CF₃OPh)OCH₂ H

G5-279 CF₃ (4-CF₃OPh)OCH₂ H

G5-280 CF₃ (2-CNPh)OCH₂ H

G5-281 CF₃ (3-CNPh)OCH₂ H

G5-282 CF₃ (4-CNPh)OCH₂ H

G5-283 CF₃ (2-N0₂Ph)OCH₂ H

G5-284 CF₃ (3-N0₂Ph)OCH₂ H

G5-285 CF₃ (4-N0₂Ph)OCH₂ H

G5-286 CF₃ (2-CF₃Ph)OCH₂ H

G5-287 CF₃ (3-CF₃Ph)OCH₂ H

G5-288 CF₃ (4-CF₃Ph)OCH₂ H

G5-289 CF₃ PhCH₂OCH₂ H

G5-290 CF₃ (2-CH₃Ph)CH₂OCH₂ H

G5-291 CF₃ (3-CH₃Ph)CH₂OCH₂ H

G5-292 CF₃ (4-CH₃Ph)CH₂OCH₂ H

G5-293 CF₃ (2-CH₃OPh)CH₂OCH₂ H

G5-294 CF₃ (3-CH₃OPh)CH₂OCH₂ H

G5-295 CF₃ (4-CH₃OPh)CH₂OCH₂ H

G5-296 CF₃ (2-FPh)CH₂OCH₂ H

G5-297 CF₃ (3-FPh)CH₂OCH₂ H

G5-298 CF₃ (4-FPh)CH₂OCH₂ H

G5-299 CF₃ (2-CIPh)CH₂OCH₂ H

G5-300 CF₃ (3-CIPh)CH₂OCH₂ H

G5-301 CF₃ (4-CIPh)CH₂OCH₂ H

G5-302 CF₃ (2-BrPh)CH₂OCH₂ H

G5-303 CF₃ (3-BrPh)CH₂OCH₂ H

G5-304 CF₃ (4-BrPh)CH₂OCH₂ H

G5-305 CF₃ (2-CF₃OPh)CH₂OCH₂ H

G5-306 CF₃ (3-CF₃OPh)CH₂OCH₂ H G5-307 CF₃ (4-CF₃OPh)CH₂OCH₂ H

G5-308 CF₃ (2-CNPh)CH₂OCH₂ H

G5-309 CF₃ (3-CNPh)CH₂OCH₂ H

G5-310 CF₃ (4-CNPh)CH₂OCH₂ H

G5-311 CF₃ (2-N0₂Ph)CH₂OCH₂ H

G5-312 CF₃ (3-N0₂Ph)CH₂OCH₂ H

G5-313 CF₃ (4-N0₂Ph)CH₂OCH₂ H

G5-314 CF₃ (2-CF₃Ph)CH₂OCH₂ H

G5-315 CF₃ (3-CF₃Ph)CH₂OCH₂ H

G5-316 CF₃ (4-CF₃Ph)CH₂OCH₂ H

G5-317 CF₃ CH₃C(=0)OCH₂ H

G5-318 CF₃ CH₃CH₂C(=0)OCH₂ H

G5-319 CF₃ CH(CH₃)₂C(=0)OCH₂ H

G5-320 CF₃ (CH₃)₃C(=0)OCH₂ H

G5-321 CF₃ (CH₃)₃CCH₂(=0)OCH₂ H

G5-322 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G5-323 CF₃ CF₃C(=0)OCH₂ H

G5-324 CF₃ CF₃CF₂C(=0)OCH₂ H

G5-325 CF₃ (c-hex)C(=0)OCH₂ H

G5-326 CF₃ PhC(=0)OCH₂ H

G5-327 CF₃ (2-CH₃Ph)C(=0)OCH₂ H

G5-328 CF₃ (3-CH₃Ph)C(=0)OCH₂ H

G5-329 CF₃ (4-CH₃Ph)C(=0)OCH₂ H

G5-330 CF₃ (2-CH₃OPh)C(=0)OCH₂ H

G5-331 CF₃ (3-CH₃OPh)C(=0)OCH₂ H

G5-332 CF₃ (4-CH₃OPh)C(=0)OCH₂ H

G5-333 CF₃ (2-FPh)C(=0)OCH₂ H

G5-334 CF₃ (3-FPh)C(=0)OCH₂ H

G5-335 CF₃ (4-FPh)C(=0)OCH₂ H

G5-336 CF₃ (2-CIPh)C(=0)OCH₂ H

G5-337 CF₃ (3-CIPh)C(=0)OCH₂ H

G5-338 CF₃ (4-CIPh)C(=0)OCH₂ H

G5-339 CF₃ (2-BrPh)C(=0)OCH₂ H

G5-340 CF₃ (3-BrPh)C(=0)OCH₂ H

G5-341 CF₃ (4-BrPh)C(=0)OCH₂ H

G5-342 CF₃ (2-CF₃OPh)C(=0)OCH₂ H

G5-343 CF₃ (3-CF₃OPh)C(=0)OCH₂ H

G5-344 CF₃ (4-CF₃OPh)C(=0)OCH₂ H

G5-345 CF₃ (2-CNPh)C(=0)OCH₂ H

G5-346 CF₃ (3-CNPh)C(=0)OCH₂ H

G5-347 CF₃ (4-CNPh)C(=0)OCH₂ H

G5-348 CF₃ (2-N0₂Ph)C(=0)OCH₂ H

G5-349 CF₃ (3-N0₂Ph)C(=0)OCH₂ H

G5-350 CF₃ (4-N0₂Ph)C(=0)OCH₂ H

G5-351 CF₃ (2-CF₃Ph)C(=0)OCH₂ H

G5-352 CF₃ (3-CF₃Ph)C(=0)OCH₂ H

G5-353 CF₃ (4-CF₃Ph)C(=0)OCH₂ H

G5-354 CF₃ CH₃ CH₃

G5-397 CF₃ (2-FPh)OCH₂ CH₃

G5-398 CF₃ (3-FPh)OCH₂ CH₃

G5-399 CF₃ (4-FPh)OCH₂ CH₃

G5-400 CF₃ (2-CIPh)OCH₂ CH₃

G5-401 CF₃ (3-CIPh)OCH₂ CH₃

G5-402 CF₃ (4-CIPh)OCH₂ CH₃

G5-403 CF₃ (2-BrPh)OCH₂ CH₃

G5-404 CF₃ (3-BrPh)OCH₂ CH₃

G5-405 CF₃ (4-BrPh)OCH₂ CH₃

G5-406 CF₃ (2-CF₃OPh)OCH₂ CH₃

G5-407 CF₃ (3-CF₃OPh)OCH₂ CH₃

G5-408 CF₃ (4-CF₃OPh)OCH₂ CH₃

G5-409 CF₃ (2-CNPh)OCH₂ CH₃

G5-410 CF₃ (3-CNPh)OCH₂ CH₃

G5-411 CF₃ (4-CNPh)OCH₂ CH₃

G5-412 CF₃ (2-N0₂Ph)OCH₂ CH₃

G5-413 CF₃ (3-N0₂Ph)OCH₂ CH₃

G5-414 CF₃ (4-N0₂Ph)OCH₂ CH₃

G5-415 CF₃ (2-CF₃Ph)OCH₂ CH₃

G5-416 CF₃ (3-CF₃Ph)OCH₂ CH₃

G5-417 CF₃ (4-CF₃Ph)OCH₂ CH₃

G5-418 CF₃ PhCH₂OCH₂ CH₃

G5-419 CF₃ (2-CH₃Ph)CH₂OCH₂ CH₃

G5-420 CF₃ (3-CH₃Ph)CH₂OCH₂ CH₃

G5-421 CF₃ (4-CH₃Ph)CH₂OCH₂ CH₃

G5-422 CF₃ (2-CH₃OPh)CH₂OCH₂ CH₃

G5-423 CF₃ (3-CH₃OPh)CH₂OCH₂ CH₃

G5-424 CF₃ (4-CH₃OPh)CH₂OCH₂ CH₃

G5-425 CF₃ (2-FPh)CH₂OCH₂ CH₃

G5-426 CF₃ (3-FPh)CH₂OCH₂ CH₃

G5-427 CF₃ (4-FPh)CH₂OCH₂ CH₃

G5-428 CF₃ (2-CIPh)CH₂OCH₂ CH₃

G5-429 CF₃ (3-CIPh)CH₂OCH₂ CH₃

G5-430 CF₃ (4-CIPh)CH₂OCH₂ CH₃

G5-431 CF₃ (2-BrPh)CH₂OCH₂ CH₃

G5-432 CF₃ (3-BrPh)CH₂OCH₂ CH₃

G5-433 CF₃ (4-BrPh)CH₂OCH₂ CH₃

G5-434 CF₃ (2-CF₃OPh)CH₂OCH₂ CH₃

G5-435 CF₃ (3-CF₃OPh)CH₂OCH₂ CH₃

G5-436 CF₃ (4-CF₃OPh)CH₂OCH₂ CH₃

G5-437 CF₃ (2-CNPh)CH₂OCH₂ CH₃

G5-438 CF₃ (3-CNPh)CH₂OCH₂ CH₃

G5-439 CF₃ (4-CNPh)CH₂OCH₂ CH₃

G5-440 CF₃ (2-N0₂Ph)CH₂OCH₂ CH₃

G5-441 CF₃ (3-N0₂Ph)CH₂OCH₂ CH₃

G5-442 CF₃ (4-N0₂Ph)CH₂OCH₂ CH₃

G5-443 CF₃ (2-CF₃Ph)CH₂OCH₂ CH₃

G5-444 CF₃ (3-CF₃Ph)CH₂OCH₂ CH₃

G5-535 2-CF₃Ph (2-CF₃OPh)OCH₂ H

G5-536 2-CF₃Ph (3-CF₃OPh)OCH₂ H

G5-537 2-CF₃Ph (4-CF₃OPh)OCH₂ H

G5-538 2-CF₃Ph (2-CNPh)OCH₂ H

G5-539 2-CF₃Ph (3-CNPh)OCH₂ H

G5-540 2-CF₃Ph (4-CNPh)OCH₂ H

G5-541 2-CF₃Ph (2-N0₂Ph)OCH₂ H

G5-542 2-CF₃Ph (3-N0₂Ph)OCH₂ H

G5-543 2-CF₃Ph (4-N0₂Ph)OCH₂ H

G5-544 2-CF₃Ph (2-CF₃Ph)OCH₂ H

G5-545 2-CF₃Ph (3-CF₃Ph)OCH₂ H

G5-546 2-CF₃Ph (4-CF₃Ph)OCH₂ H

G5-547 2-CF₃Ph PhCH₂OCH₂ H

G5-548 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G5-549 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G5-550 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G5-551 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G5-552 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G5-553 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G5-554 2-CF₃Ph (2-FPh)CH₂OCH₂ H

G5-555 2-CF₃Ph (3-FPh)CH₂OCH₂ H

G5-556 2-CF₃Ph (4-FPh)CH₂OCH₂ H

G5-557 2-CF₃Ph (2-CIPh)CH₂OCH₂ H

G5-558 2-CF₃Ph (3-CIPh)CH₂OCH₂ H

G5-559 2-CF₃Ph (4-CIPh)CH₂OCH₂ H

G5-560 2-CF₃Ph (2-BrPh)CH₂OCH₂ H

G5-561 2-CF₃Ph (3-BrPh)CH₂OCH₂ H

G5-562 2-CF₃Ph (4-BrPh)CH₂OCH₂ H

G5-563 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G5-564 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G5-565 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G5-566 2-CF₃Ph (2-CNPh)CH₂OCH₂ H

G5-567 2-CF₃Ph (3-CNPh)CH₂OCH₂ H

G5-568 2-CF₃Ph (4-CNPh)CH₂OCH₂ H

G5-569 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G5-570 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G5-571 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G5-572 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G5-573 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G5-574 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G5-575 2-CF₃Ph CH₃C(=0)OCH₂ H

G5-576 2-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G5-577 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G5-578 2-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G5-579 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G5-580 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G5-581 2-CF₃Ph CF₃C(=0)OCH₂ H

G5-582 2-CF₃Ph CF₃CF₂C(=0)OCH₂ H G5-583 2-CF₃Ph (c-hex)C(=0)OCH₂ H

G5-584 2-CF₃Ph PhC(=0)OCH₂ H

G5-585 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G5-586 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G5-587 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G5-588 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G5-589 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G5-590 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G5-591 2-CF₃Ph (2-FPh)C(=0)OCH₂ H

G5-592 2-CF₃Ph (3-FPh)C(=0)OCH₂ H

G5-593 2-CF₃Ph (4-FPh)C(=0)OCH₂ H

G5-594 2-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G5-595 2-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G5-596 2-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G5-597 2-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G5-598 2-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G5-599 2-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G5-600 2-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G5-601 2-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G5-602 2-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G5-603 2-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G5-604 2-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G5-605 2-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G5-606 2-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G5-607 2-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G5-608 2-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G5-609 2-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G5-610 2-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G5-611 2-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G5-612 2-CF₃Ph CH₃ CH₃

G5-613 2-CF₃Ph CH3CH2 CH₃

G5-614 2-CF₃Ph CH3CH2CH2 CH₃

G5-615 2-CF₃Ph (CH₃)₂CH CH₃

G5-616 2-CF₃Ph CH₃C(=0) CH₃

G5-617 2-CF₃Ph CH₃CH₂C(=0) CH₃

G5-618 2-CF₃Ph (CH₃)₂CHC(=0) CH₃

G5-619 2-CF₃Ph (CH₃)₃CC(=0) CH₃

G5-620 2-CF₃Ph (CH₃)₃CCH₂C(=0) CH₃

G5-621 2-CF₃Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G5-622 2-CF₃Ph (CH₃)₂CHCH₂C(=0) CH₃

G5-623 2-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G5-624 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G5-625 2-CF₃Ph (c-hex)C(=0) CH₃

G5-626 2-CF₃Ph (c-pen)C(=0) CH₃

G5-627 2-CF₃Ph (c-hep)C(=0) CH₃

G5-628 2-CF₃Ph (c-pro)C(=0) CH₃

G5-629 2-CF₃Ph CF₃C(=0) CH₃

G5-630 2-CF₃Ph (CH₃)₂NC(=0) CH₃

G5-673 2-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G5-674 2-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G5-675 2-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G5-676 2-CF₃Ph PhCH₂OCH₂ CH₃

G5-677 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G5-678 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G5-679 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G5-680 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G5-681 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G5-682 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G5-683 2-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G5-684 2-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G5-685 2-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G5-686 2-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G5-687 2-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G5-688 2-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G5-689 2-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G5-690 2-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G5-691 2-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G5-692 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G5-693 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G5-694 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G5-695 2-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G5-696 2-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G5-697 2-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G5-698 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G5-699 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G5-700 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G5-701 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G5-702 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G5-703 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G5-704 2-CF₃Ph CH₃C(=0)OCH₂ CH₃

G5-705 2-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G5-706 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G5-707 2-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G5-708 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G5-709 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G5-710 2-CF₃Ph CF₃C(=0)OCH₂ CH₃

G5-711 2-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G5-712 2-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G5-713 2-CF₃Ph PhC(=0)OCH₂ CH₃

G5-714 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G5-715 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G5-716 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G5-717 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G5-718 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G5-719 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G5-720 2-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G5-809 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G5-810 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G5-811 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G5-812 3-CF₃Ph (2-FPh)CH₂OCH₂ H

G5-813 3-CF₃Ph (3-FPh)CH₂OCH₂ H

G5-814 3-CF₃Ph (4-FPh)CH₂OCH₂ H

G5-815 3-CF₃Ph (2-CIPh)CH₂OCH₂ H

G5-816 3-CF₃Ph (3-CIPh)CH₂OCH₂ H

G5-817 3-CF₃Ph (4-CIPh)CH₂OCH₂ H

G5-818 3-CF₃Ph (2-BrPh)CH₂OCH₂ H

G5-819 3-CF₃Ph (3-BrPh)CH₂OCH₂ H

G5-820 3-CF₃Ph (4-BrPh)CH₂OCH₂ H

G5-821 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G5-822 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G5-823 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G5-824 3-CF₃Ph (2-CNPh)CH₂OCH₂ H

G5-825 3-CF₃Ph (3-CNPh)CH₂OCH₂ H

G5-826 3-CF₃Ph (4-CNPh)CH₂OCH₂ H

G5-827 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G5-828 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G5-829 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G5-830 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G5-831 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G5-832 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G5-833 3-CF₃Ph CH₃C(=0)OCH₂ H

G5-834 3-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G5-835 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G5-836 3-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G5-837 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G5-838 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G5-839 3-CF₃Ph CF₃C(=0)OCH₂ H

G5-840 3-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G5-841 3-CF₃Ph (c-hex)C(=0)OCH₂ H

G5-842 3-CF₃Ph PhC(=0)OCH₂ H

G5-843 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G5-844 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G5-845 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G5-846 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G5-847 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G5-848 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G5-849 3-CF₃Ph (2-FPh)C(=0)OCH₂ H

G5-850 3-CF₃Ph (3-FPh)C(=0)OCH₂ H

G5-851 3-CF₃Ph (4-FPh)C(=0)OCH₂ H

G5-852 3-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G5-853 3-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G5-854 3-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G5-855 3-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G5-856 3-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G5-947 3-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G5-948 3-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G5-949 3-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G5-950 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G5-951 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G5-952 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G5-953 3-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G5-954 3-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G5-955 3-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G5-956 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G5-957 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G5-958 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G5-959 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G5-960 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G5-961 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G5-962 3-CF₃Ph CH₃C(=0)OCH₂ CH₃

G5-963 3-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G5-964 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G5-965 3-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G5-966 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G5-967 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G5-968 3-CF₃Ph CF₃C(=0)OCH₂ CH₃

G5-969 3-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G5-970 3-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G5-971 3-CF₃Ph PhC(=0)OCH₂ CH₃

G5-972 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G5-973 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G5-974 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G5-975 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G5-976 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G5-977 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G5-978 3-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G5-979 3-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G5-980 3-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G5-981 3-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G5-982 3-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G5-983 3-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G5-984 3-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G5-985 3-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G5-986 3-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G5-987 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G5-988 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G5-989 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G5-990 3-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G5-991 3-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G5-992 3-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G5-993 3-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G5-994 3-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G5-1037 4-CF₃Ph (3-CH₃Ph)OCH₂ H

G5-1038 4-CF₃Ph (4-CH₃Ph)OCH₂ H

G5-1039 4-CF₃Ph (2-CH₃OPh)OCH₂ H

G5-1040 4-CF₃Ph (3-CH₃OPh)OCH₂ H

G5-1041 4-CF₃Ph (4-CH₃OPh)OCH₂ H

G5-1042 4-CF₃Ph (2-FPh)OCH₂ H

G5-1043 4-CF₃Ph (3-FPh)OCH₂ H

G5-1044 4-CF₃Ph (4-FPh)OCH₂ H

G5-1045 4-CF₃Ph (2-CIPh)OCH₂ H

G5-1046 4-CF₃Ph (3-CIPh)OCH₂ H

G5-1047 4-CF₃Ph (4-CIPh)OCH₂ H

G5-1048 4-CF₃Ph (2-BrPh)OCH₂ H

G5-1049 4-CF₃Ph (3-BrPh)OCH₂ H

G5-1050 4-CF₃Ph (4-BrPh)OCH₂ H

G5-1051 4-CF₃Ph (2-CF₃OPh)OCH₂ H

G5-1052 4-CF₃Ph (3-CF₃OPh)OCH₂ H

G5-1053 4-CF₃Ph (4-CF₃OPh)OCH₂ H

G5-1054 4-CF₃Ph (2-CNPh)OCH₂ H

G5-1055 4-CF₃Ph (3-CNPh)OCH₂ H

G5-1056 4-CF₃Ph (4-CNPh)OCH₂ H

G5-1057 4-CF₃Ph (2-N0₂Ph)OCH₂ H

G5-1058 4-CF₃Ph (3-N0₂Ph)OCH₂ H

G5-1059 4-CF₃Ph (4-N0₂Ph)OCH₂ H

G5-1060 4-CF₃Ph (2-CF₃Ph)OCH₂ H

G5-1061 4-CF₃Ph (3-CF₃Ph)OCH₂ H

G5-1062 4-CF₃Ph (4-CF₃Ph)OCH₂ H

G5-1063 4-CF₃Ph PhCH₂OCH₂ H

G5-1064 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G5-1065 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G5-1066 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G5-1067 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G5-1068 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G5-1069 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G5-1070 4-CF₃Ph (2-FPh)CH₂OCH₂ H

G5-1071 4-CF₃Ph (3-FPh)CH₂OCH₂ H

G5-1072 4-CF₃Ph (4-FPh)CH₂OCH₂ H

G5-1073 4-CF₃Ph (2-CIPh)CH₂OCH₂ H

G5-1074 4-CF₃Ph (3-CIPh)CH₂OCH₂ H

G5-1075 4-CF₃Ph (4-CIPh)CH₂OCH₂ H

G5-1076 4-CF₃Ph (2-BrPh)CH₂OCH₂ H

G5-1077 4-CF₃Ph (3-BrPh)CH₂OCH₂ H

G5-1078 4-CF₃Ph (4-BrPh)CH₂OCH₂ H

G5-1079 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G5-1080 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G5-1081 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G5-1082 4-CF₃Ph (2-CNPh)CH₂OCH₂ H

G5-1083 4-CF₃Ph (3-CNPh)CH₂OCH₂ H

G5-1084 4-CF₃Ph (4-CNPh)CH₂OCH₂ H G5-1085 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G5-1086 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G5-1087 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G5-1088 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G5-1089 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G5-1090 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G5-1091 4-CF₃Ph CH₃C(=0)OCH₂ H

G5-1092 4-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G5-1093 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G5-1094 4-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G5-1095 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G5-1096 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G5-1097 4-CF₃Ph CF₃C(=0)OCH₂ H

G5-1098 4-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G5-1099 4-CF₃Ph (c-hex)C(=0)OCH₂ H

G5-1100 4-CF₃Ph PhC(=0)OCH₂ H

G5-1101 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G5-1102 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G5-1103 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G5-1104 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G5-1105 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G5-1106 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G5-1107 4-CF₃Ph (2-FPh)C(=0)OCH₂ H

G5-1108 4-CF₃Ph (3-FPh)C(=0)OCH₂ H

G5-1109 4-CF₃Ph (4-FPh)C(=0)OCH₂ H

G5-1110 4-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G5-1111 4-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G5-1112 4-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G5-1113 4-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G5-1114 4-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G5-1115 4-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G5-1116 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G5-1117 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G5-1118 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G5-1119 4-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G5-1120 4-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G5-1121 4-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G5-1122 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G5-1123 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G5-1124 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G5-1125 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G5-1126 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G5-1127 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G5-1128 4-CF₃Ph CH₃ CH₃

G5-1129 4-CF₃Ph CH3CH2 CH₃

G5-1130 4-CF₃Ph CH3CH2CH2 CH₃

G5-1131 4-CF₃Ph (CH₃)₂CH CH₃

G5-1132 4-CF₃Ph CH₃C(=0) CH₃

G5-1175 4-CF₃Ph (3-CIPh)OCH₂ CH₃

G5-1176 4-CF₃Ph (4-CIPh)OCH₂ CH₃

G5-1177 4-CF₃Ph (2-BrPh)OCH₂ CH₃

G5-1178 4-CF₃Ph (3-BrPh)OCH₂ CH₃

G5-1179 4-CF₃Ph (4-BrPh)OCH₂ CH₃

G5-1180 4-CF₃Ph (2-CF₃OPh)OCH₂ CH₃

G5-1181 4-CF₃Ph (3-CF₃OPh)OCH₂ CH₃

G5-1182 4-CF₃Ph (4-CF₃OPh)OCH₂ CH₃

G5-1183 4-CF₃Ph (2-CNPh)OCH₂ CH₃

G5-1184 4-CF₃Ph (3-CNPh)OCH₂ CH₃

G5-1185 4-CF₃Ph (4-CNPh)OCH₂ CH₃

G5-1186 4-CF₃Ph (2-N0₂Ph)OCH₂ CH₃

G5-1187 4-CF₃Ph (3-N0₂Ph)OCH₂ CH₃

G5-1188 4-CF₃Ph (4-N0₂Ph)OCH₂ CH₃

G5-1189 4-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G5-1190 4-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G5-1191 4-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G5-1192 4-CF₃Ph PhCH₂OCH₂ CH₃

G5-1193 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G5-1194 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G5-1195 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G5-1196 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G5-1197 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G5-1198 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G5-1199 4-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G5-1200 4-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G5-1201 4-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G5-1202 4-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G5-1203 4-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G5-1204 4-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G5-1205 4-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G5-1206 4-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G5-1207 4-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G5-1208 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G5-1209 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G5-1210 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G5-1211 4-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G5-1212 4-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G5-1213 4-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G5-1214 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G5-1215 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G5-1216 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G5-1217 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G5-1218 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G5-1219 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G5-1220 4-CF₃Ph CH₃C(=0)OCH₂ CH₃

G5-1221 4-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G5-1222 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃ G5-1223 4-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G5-1224 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G5-1225 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G5-1226 4-CF₃Ph CF₃C(=0)OCH₂ CH₃

G5-1227 4-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G5-1228 4-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G5-1229 4-CF₃Ph PhC(=0)OCH₂ CH₃

G5-1230 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G5-1231 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G5-1232 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G5-1233 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G5-1234 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G5-1235 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G5-1236 4-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G5-1237 4-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G5-1238 4-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G5-1239 4-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G5-1240 4-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G5-1241 4-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G5-1242 4-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G5-1243 4-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G5-1244 4-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G5-1245 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G5-1246 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G5-1247 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G5-1248 4-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G5-1249 4-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G5-1250 4-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G5-1251 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G5-1252 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G5-1253 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G5-1254 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G5-1255 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G5-1256 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

G5-1257 3,5-(CF₃)₂Ph CH₃ H

G5-1258 3,5-(CF₃)₂Ph CH3CH2 H

G5-1259 3,5-(CF₃)₂Ph CH3CH2CH2 H

G5-1260 3,5-(CF₃)₂Ph (CH₃)₂CH H

G5-1261 3,5-(CF₃)₂Ph CH₃C(=0) H

G5-1262 3,5-(CF₃)₂Ph CH₃CH₂C(=0) H

G5-1263 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0) H

G5-1264 3,5-(CF₃)₂Ph (CH₃)₃CC(=0) H

G5-1265 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0) H

G5-1266 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0) H

G5-1267 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0) H

G5-1268 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0) H

G5-1269 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0) H

G5-1270 3,5-(CF₃)₂Ph (c-hex)C(=Q) H

G5-1313 3,5-(CF₃)₂Ph (3-CNPh)OCH₂ H

G5-1314 3,5-(CF₃)₂Ph (4-CNPh)OCH₂ H

G5-1315 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂ H

G5-1316 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂ H

G5-1317 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂ H

G5-1318 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂ H

G5-1319 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂ H

G5-1320 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂ H

G5-1321 3,5-(CF₃)₂Ph PhCH₂OCH₂ H

G5-1322 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂ H

G5-1323 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂ H

G5-1324 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂ H

G5-1325 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂ H

G5-1326 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂ H

G5-1327 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂ H

G5-1328 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂ H

G5-1329 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂ H

G5-1330 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂ H

G5-1331 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂ H

G5-1332 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂ H

G5-1333 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂ H

G5-1334 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂ H

G5-1335 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂ H

G5-1336 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂ H

G5-1337 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂ H

G5-1338 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂ H

G5-1339 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂ H

G5-1340 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂ H

G5-1341 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂ H

G5-1342 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂ H

G5-1343 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂ H

G5-1344 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂ H

G5-1345 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂ H

G5-1346 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂ H

G5-1347 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂ H

G5-1348 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ H

G5-1349 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂ H

G5-1350 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂ H

G5-1351 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂ H

G5-1352 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂ H

G5-1353 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂ H

G5-1354 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G5-1355 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂ H

G5-1356 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂ H

G5-1357 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂ H

G5-1358 3,5-(CF₃)₂Ph PhC(=0)OCH₂ H

G5-1359 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂ H

G5-1360 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂ H G5-1361 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂ H

G5-1362 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂ H

G5-1363 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂ H

G5-1364 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂ H

G5-1365 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂ H

G5-1366 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂ H

G5-1367 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂ H

G5-1368 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂ H

G5-1369 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂ H

G5-1370 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂ H

G5-1371 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂ H

G5-1372 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ H

G5-1373 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂ H

G5-1374 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂ H

G5-1375 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂ H

G5-1376 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂ H

G5-1377 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂ H

G5-1378 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂ H

G5-1379 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂ H

G5-1380 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂ H

G5-1381 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂ H

G5-1382 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂ H

G5-1383 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂ H

G5-1384 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂ H

G5-1385 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂ H

G5-1386 3,5-(CF₃)₂Ph CH₃ CH₃

G5-1387 3,5-(CF₃)₂Ph CH3CH2 CH₃

G5-1388 3,5-(CF₃)₂Ph CH3CH2CH2 CH₃

G5-1389 3,5-(CF₃)₂Ph (CH₃)₂CH CH₃

G5-1390 3,5-(CF₃)₂Ph CH₃C(=0) CH₃

G5-1391 3,5-(CF₃)₂Ph CH₃CH₂C(=0) CH₃

G5-1392 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0) CH₃

G5-1393 3,5-(CF₃)₂Ph (CH₃)₃CC(=0) CH₃

G5-1394 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0) CH₃

G5-1395 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G5-1396 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0) CH₃

G5-1397 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G5-1398 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G5-1399 3,5-(CF₃)₂Ph (c-hex)C(=0) CH₃

G5-1400 3,5-(CF₃)₂Ph (c-pen)C(=0) CH₃

G5-1401 3,5-(CF₃)₂Ph (c-hep)C(=0) CH₃

G5-1402 3,5-(CF₃)₂Ph (c-pro)C(=0) CH₃

G5-1403 3,5-(CF₃)₂Ph CF₃C(=0) CH₃

G5-1404 3,5-(CF₃)₂Ph (CH₃)₂NC(=0) CH₃

G5-1405 3,5-(CF₃)₂Ph (CH₃CH₂)₂NC(=0) CH₃

G5-1406 3,5-(CF₃)₂Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G5-1407 3,5-(CF₃)₂Ph CH₃CH₂N(CH₃)C(=0) CH₃

G5-1408 3,5-(CF₃)₂Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃ G5-1409 3,5-(CF₃)₂Ph CH₃ON(CH₃)C(=0) CH₃

G5-1410 3,5-(CF₃)₂Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G5-141 1 3,5-(CF₃)₂Ph (CHCCH₂)₂NC(=0) CH₃

G5-1412 3,5-(CF₃)₂Ph hO CH₃

G5-1413 3,5-(CF₃)₂Ph hO CH₃

G5-1414 3,5-(CF₃)₂Ph CH₃

G5-1415 3,5-(CF₃)₂Ph CH₃OCH₂ CH₃

G5-1416 3,5-(CF₃)₂Ph CH₃CH₂OCH₂ CH₃

G5-1417 3,5-(CF₃)₂Ph (CH₃)₂CHOCH₂ CH₃

G5-1418 3,5-(CF₃)₂Ph (CH₃)₃COCH₂ CH₃

G5-1419 3,5-(CF₃)₂Ph (CH₃)3CCH20CH2 CH₃

G5-1420 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂OCH₂ CH₃

G5-1421 3,5-(CF₃)₂Ph (c-hex)OCH₂ CH₃

G5-1422 3,5-(CF₃)₂Ph PhOCH₂ CH₃

G5-1423 3,5-(CF₃)₂Ph (2-CH₃Ph)OCH₂ CH₃

G5-1424 3,5-(CF₃)₂Ph (3-CH₃Ph)OCH₂ CH₃

G5-1425 3,5-(CF₃)₂Ph (4-CH₃Ph)OCH₂ CH₃

G5-1426 3,5-(CF₃)₂Ph (2-CH₃OPh)OCH₂ CH₃

G5-1427 3,5-(CF₃)₂Ph (3-CH₃OPh)OCH₂ CH₃

G5-1428 3,5-(CF₃)₂Ph (4-CH₃OPh)OCH₂ CH₃

G5-1429 3,5-(CF₃)₂Ph (2-FPh)OCH₂ CH₃

G5-1430 3,5-(CF₃)₂Ph (3-FPh)OCH₂ CH₃

G5-1431 3,5-(CF₃)₂Ph (4-FPh)OCH₂ CH₃

G5-1432 3,5-(CF₃)₂Ph (2-CIPh)OCH₂ CH₃

G5-1433 3,5-(CF₃)₂Ph (3-CIPh)OCH₂ CH₃

G5-1434 3,5-(CF₃)₂Ph (4-CIPh)OCH₂ CH₃

G5-1435 3,5-(CF₃)₂Ph (2-BrPh)OCH₂ CH₃

G5-1436 3,5-(CF₃)₂Ph (3-BrPh)OCH₂ CH₃

G5-1437 3,5-(CF₃)₂Ph (4-BrPh)OCH₂ CH₃

G5-1438 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂ CH₃

G5-1439 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂ CH₃

G5-1440 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂ CH₃

G5-1441 3,5-(CF₃)₂Ph (2-CNPh)OCH₂ CH₃

G5-1442 3,5-(CF₃)₂Ph (3-CNPh)OCH₂ CH₃

G5-1443 3,5-(CF₃)₂Ph (4-CNPh)OCH₂ CH₃

G5-1444 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂ CH₃

G5-1445 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂ CH₃

G5-1446 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂ CH₃

G5-1447 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂ CH₃

G5-1448 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂ CH₃

G5-1449 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂ CH₃

G5-1450 3,5-(CF₃)₂Ph PhCH₂OCH₂ CH₃ G5-1451 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G5-1452 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G5-1453 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G5-1454 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G5-1455 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G5-1456 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G5-1457 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂ CH₃

G5-1458 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂ CH₃

G5-1459 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂ CH₃

G5-1460 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂ CH₃

G5-1461 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂ CH₃

G5-1462 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂ CH₃

G5-1463 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂ CH₃

G5-1464 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂ CH₃

G5-1465 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂ CH₃

G5-1466 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G5-1467 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G5-1468 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G5-1469 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂ CH₃

G5-1470 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂ CH₃

G5-1471 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂ CH₃

G5-1472 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G5-1473 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G5-1474 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G5-1475 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G5-1476 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G5-1477 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G5-1478 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂ CH₃

G5-1479 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂ CH₃

G5-1480 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G5-1481 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂ CH₃

G5-1482 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G5-1483 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G5-1484 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂ CH₃

G5-1485 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂ CH₃

G5-1486 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂ CH₃

G5-1487 3,5-(CF₃)₂Ph PhC(=0)OCH₂ CH₃

G5-1488 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G5-1489 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G5-1490 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G5-1491 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G5-1492 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G5-1493 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G5-1494 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂ CH₃

G5-1495 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂ CH₃

G5-1496 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂ CH₃

G5-1497 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂ CH₃

G5-1498 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂ CH₃ G5-1499 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂ CH₃

G5-1500 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂ CH₃

G5-1501 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ CH₃

G5-1502 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂ CH₃

G5-1503 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G5-1504 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G5-1505 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G5-1506 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂ CH₃

G5-1507 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂ CH₃

G5-1508 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂ CH₃

G5-1509 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G5-1510 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G5-1511 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G5-1512 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G5-1513 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G5-1514 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

[0299] Table 6

G6-160 2-CF₃-5-CN-Ph H CH₃

G6-161 2-CF₃-6-CN-Ph H CH₃

G6-162 PhO H CH₃

G6-163 2-CFsPhO H CH₃

G6-164 3-CFsPhO H CH₃

G6-165 4-CFsPhO H CH₃

G6-166 2-CF₃CF₂PhO H CH₃

G6-167 3-CF₃CF₂PhO H CH₃

G6-168 4-CF₃CF₂PhO H CH₃

G6-169 2-CFsOPhO H CH₃

G6-170 3-CFsOPhO H CH₃

G6-171 4-CFsOPhO H CH₃

G6-172 2-CF₃-3-F-PhO H CH₃

G6-173 2-CF₃-4-F-PhO H CH₃

G6-174 2-CF₃-5-F-PhO H CH₃

G6-175 2-CF₃-6-F-PhO H CH₃

G6-176 2-CF₃-3-CI-PhO H CH₃

G6-177 2-CF₃-4-CI-PhO H CH₃

G6-178 2-CF₃-5-CI-PhO H CH₃

G6-179 2-CF₃-6-CI-PhO H CH₃

G6-180 2-CF₃-3-CH₃-PhO H CH₃

G6-181 2-CF₃-4-CH₃-PhO H CH₃

G6-182 2-CF₃-5-CH₃-PhO H CH₃

G6-183 2-CF₃-6-CH₃-PhO H CH₃

G6-184 2,3-(CF₃)₂PhO H CH₃

G6-185 2,4-(CF₃)₂PhO H CH₃

G6-186 2,6-(CF₃)₂PhO H CH₃

G6-187 3,5-(CF₃)₂PhO H CH₃

G6-188 PhCH₂0 H CH₃

G6-189 2-CF₃PhCH₂0 H CH₃

G6-190 3-CF₃PhCH₂0 H CH₃

G6-191 4-CF₃PhCH₂0 H CH₃

G6-192 2-CF₃CF₂PhCH₂0 H CH₃

G6-193 3-CF₃CF₂PhCH₂0 H CH₃

G6-194 4-CF₃CF₂PhCH₂0 H CH₃

G6-195 2-CF₃OPhCH₂0 H CH₃

G6-196 3-CF₃OPhCH₂0 H CH₃

G6-197 4-CF₃OPhCH₂0 H CH₃

G6-198 2-CF₃-3-F-PhCH₂0 H CH₃

G6-199 2-CF₃-4-F-PhCH₂0 H CH₃

G6-200 2-CF₃-5-F-PhCH₂0 H CH₃

G6-201 2-CF₃-6-F-PhCH₂0 H CH₃

G6-202 2-CF₃-3-CI-PhCH₂0 H CH₃

G6-203 2-CF₃-4-CI-PhCH₂0 H CH₃

G6-204 2-CF₃-5-CI-PhCH₂0 H CH₃

G6-205 2-CF₃-6-CI-PhCH₂0 H CH₃

G6-206 2-CF₃-3-CH₃-PhCH₂0 H CH₃

G6-296 CF₃ (2-FPh)CH₂OCH₂ H

G6-297 CF₃ (3-FPh)CH₂OCH₂ H

G6-298 CF₃ (4-FPh)CH₂OCH₂ H

G6-299 CF₃ (2-CIPh)CH₂OCH₂ H

G6-300 CF₃ (3-CIPh)CH₂OCH₂ H

G6-301 CF₃ (4-CIPh)CH₂OCH₂ H

G6-302 CF₃ (2-BrPh)CH₂OCH₂ H

G6-303 CF₃ (3-BrPh)CH₂OCH₂ H

G6-304 CF₃ (4-BrPh)CH₂OCH₂ H

G6-305 CF₃ (2-CF₃OPh)CH₂OCH₂ H

G6-306 CF₃ (3-CF₃OPh)CH₂OCH₂ H

G6-307 CF₃ (4-CF₃OPh)CH₂OCH₂ H

G6-308 CF₃ (2-CNPh)CH₂OCH₂ H

G6-309 CF₃ (3-CNPh)CH₂OCH₂ H

G6-310 CF₃ (4-CNPh)CH₂OCH₂ H

G6-311 CF₃ (2-N0₂Ph)CH₂OCH₂ H

G6-312 CF₃ (3-N0₂Ph)CH₂OCH₂ H

G6-313 CF₃ (4-N0₂Ph)CH₂OCH₂ H

G6-314 CF₃ (2-CF₃Ph)CH₂OCH₂ H

G6-315 CF₃ (3-CF₃Ph)CH₂OCH₂ H

G6-316 CF₃ (4-CF₃Ph)CH₂OCH₂ H

G6-317 CF₃ CH₃C(=0)OCH₂ H

G6-318 CF₃ CH₃CH₂C(=0)OCH₂ H

G6-319 CF₃ CH(CH₃)₂C(=0)OCH₂ H

G6-320 CF₃ (CH₃)₃C(=0)OCH₂ H

G6-321 CF₃ (CH₃)₃CCH₂(=0)OCH₂ H

G6-322 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G6-323 CF₃ CF₃C(=0)OCH₂ H

G6-324 CF₃ CF₃CF₂C(=0)OCH₂ H

G6-325 CF₃ (c-hex)C(=0)OCH₂ H

G6-326 CF₃ PhC(=0)OCH₂ H

G6-327 CF₃ (2-CH₃Ph)C(=0)OCH₂ H

G6-328 CF₃ (3-CH₃Ph)C(=0)OCH₂ H

G6-329 CF₃ (4-CH₃Ph)C(=0)OCH₂ H

G6-330 CF₃ (2-CH₃OPh)C(=0)OCH₂ H

G6-331 CF₃ (3-CH₃OPh)C(=0)OCH₂ H

G6-332 CF₃ (4-CH₃OPh)C(=0)OCH₂ H

G6-333 CF₃ (2-FPh)C(=0)OCH₂ H

G6-334 CF₃ (3-FPh)C(=0)OCH₂ H

G6-335 CF₃ (4-FPh)C(=0)OCH₂ H

G6-336 CF₃ (2-CIPh)C(=0)OCH₂ H

G6-337 CF₃ (3-CIPh)C(=0)OCH₂ H

G6-338 CF₃ (4-CIPh)C(=0)OCH₂ H

G6-339 CF₃ (2-BrPh)C(=0)OCH₂ H

G6-340 CF₃ (3-BrPh)C(=0)OCH₂ H

G6-341 CF₃ (4-BrPh)C(=0)OCH₂ H

G6-342 CF₃ (2-CF₃OPh)C(=0)OCH₂ H

G6-343 CF₃ (3-CF₃OPh)C(=0)OCH₂ H

G6-386 CF₃ (CH₃)₃COCH₂ CH₃

G6-387 CF₃ (CH₃)₃CCH20CH2 CH₃

G6-388 CF₃ CH₃CH₂C(CH₃)₂OCH₂ CH₃

G6-389 CF₃ (c-hex)OCH₂ CH₃

G6-390 CF₃ PhOCH₂ CH₃

G6-391 CF₃ (2-CH₃Ph)OCH₂ CH₃

G6-392 CF₃ (3-CH₃Ph)OCH₂ CH₃

G6-393 CF₃ (4-CH₃Ph)OCH₂ CH₃

G6-394 CF₃ (2-CH₃OPh)OCH₂ CH₃

G6-395 CF₃ (3-CH₃OPh)OCH₂ CH₃

G6-396 CF₃ (4-CH₃OPh)OCH₂ CH₃

G6-397 CF₃ (2-FPh)OCH₂ CH₃

G6-398 CF₃ (3-FPh)OCH₂ CH₃

G6-399 CF₃ (4-FPh)OCH₂ CH₃

G6-400 CF₃ (2-CIPh)OCH₂ CH₃

G6-401 CF₃ (3-CIPh)OCH₂ CH₃

G6-402 CF₃ (4-CIPh)OCH₂ CH₃

G6-403 CF₃ (2-BrPh)OCH₂ CH₃

G6-404 CF₃ (3-BrPh)OCH₂ CH₃

G6-405 CF₃ (4-BrPh)OCH₂ CH₃

G6-406 CF₃ (2-CF₃OPh)OCH₂ CH₃

G6-407 CF₃ (3-CF₃OPh)OCH₂ CH₃

G6-408 CF₃ (4-CF₃OPh)OCH₂ CH₃

G6-409 CF₃ (2-CNPh)OCH₂ CH₃

G6-410 CF₃ (3-CNPh)OCH₂ CH₃

G6-41 1 CF₃ (4-CNPh)OCH₂ CH₃

G6-412 CF₃ (2-N0₂Ph)OCH₂ CH₃

G6-413 CF₃ (3-N0₂Ph)OCH₂ CH₃

G6-414 CF₃ (4-N0₂Ph)OCH₂ CH₃

G6-415 CF₃ (2-CF₃Ph)OCH₂ CH₃

G6-416 CF₃ (3-CF₃Ph)OCH₂ CH₃

G6-417 CF₃ (4-CF₃Ph)OCH₂ CH₃

G6-418 CF₃ PhCH₂OCH₂ CH₃

G6-419 CF₃ (2-CH₃Ph)CH₂OCH₂ CH₃

G6-420 CF₃ (3-CH₃Ph)CH₂OCH₂ CH₃

G6-421 CF₃ (4-CH₃Ph)CH₂OCH₂ CH₃

G6-422 CF₃ (2-CH₃OPh)CH₂OCH₂ CH₃

G6-423 CF₃ (3-CH₃OPh)CH₂OCH₂ CH₃

G6-424 CF₃ (4-CH₃OPh)CH₂OCH₂ CH₃

G6-425 CF₃ (2-FPh)CH₂OCH₂ CH₃

G6-426 CF₃ (3-FPh)CH₂OCH₂ CH₃

G6-427 CF₃ (4-FPh)CH₂OCH₂ CH₃

G6-428 CF₃ (2-CIPh)CH₂OCH₂ CH₃

G6-429 CF₃ (3-CIPh)CH₂OCH₂ CH₃

G6-430 CF₃ (4-CIPh)CH₂OCH₂ CH₃

G6-431 CF₃ (2-BrPh)CH₂OCH₂ CH₃

G6-432 CF₃ (3-BrPh)CH₂OCH₂ CH₃

G6-433 CF₃ (4-BrPh)CH₂OCH₂ CH₃ G6-434 CF₃ (2-CF₃OPh)CH₂OCH₂ CH₃

G6-435 CF₃ (3-CF₃OPh)CH₂OCH₂ CH₃

G6-436 CF₃ (4-CF₃OPh)CH₂OCH₂ CH₃

G6-437 CF₃ (2-CNPh)CH₂OCH₂ CH₃

G6-438 CF₃ (3-CNPh)CH₂OCH₂ CH₃

G6-439 CF₃ (4-CNPh)CH₂OCH₂ CH₃

G6-440 CF₃ (2-N0₂Ph)CH₂OCH₂ CH₃

G6-441 CF₃ (3-N0₂Ph)CH₂OCH₂ CH₃

G6-442 CF₃ (4-N0₂Ph)CH₂OCH₂ CH₃

G6-443 CF₃ (2-CF₃Ph)CH₂OCH₂ CH₃

G6-444 CF₃ (3-CF₃Ph)CH₂OCH₂ CH₃

G6-445 CF₃ (4-CF₃Ph)CH₂OCH₂ CH₃

G6-446 CF₃ CH₃C(=0)OCH₂ CH₃

G6-447 CF₃ CH₃CH₂C(=0)OCH₂ CH₃

G6-448 CF₃ CH(CH₃)₂C(=0)OCH₂ CH₃

G6-449 CF₃ (CH₃)₃C(=0)OCH₂ CH₃

G6-450 CF₃ (CH₃)₃CCH₂(=0)OCH₂ CH₃

G6-451 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G6-452 CF₃ CF₃C(=0)OCH₂ CH₃

G6-453 CF₃ CF₃CF₂C(=0)OCH₂ CH₃

G6-454 CF₃ (c-hex)C(=0)OCH₂ CH₃

G6-455 CF₃ PhC(=0)OCH₂ CH₃

G6-456 CF₃ (2-CH₃Ph)C(=0)OCH₂ CH₃

G6-457 CF₃ (3-CH₃Ph)C(=0)OCH₂ CH₃

G6-458 CF₃ (4-CH₃Ph)C(=0)OCH₂ CH₃

G6-459 CF₃ (2-CH₃OPh)C(=0)OCH₂ CH₃

G6-460 CF₃ (3-CH₃OPh)C(=0)OCH₂ CH₃

G6-461 CF₃ (4-CH₃OPh)C(=0)OCH₂ CH₃

G6-462 CF₃ (2-FPh)C(=0)OCH₂ CH₃

G6-463 CF₃ (3-FPh)C(=0)OCH₂ CH₃

G6-464 CF₃ (4-FPh)C(=0)OCH₂ CH₃

G6-465 CF₃ (2-CIPh)C(=0)OCH₂ CH₃

G6-466 CF₃ (3-CIPh)C(=0)OCH₂ CH₃

G6-467 CF₃ (4-CIPh)C(=0)OCH₂ CH₃

G6-468 CF₃ (2-BrPh)C(=0)OCH₂ CH₃

G6-469 CF₃ (3-BrPh)C(=0)OCH₂ CH₃

G6-470 CF₃ (4-BrPh)C(=0)OCH₂ CH₃

G6-471 CF₃ (2-CF₃OPh)C(=0)OCH₂ CH₃

G6-472 CF₃ (3-CF₃OPh)C(=0)OCH₂ CH₃

G6-473 CF₃ (4-CF₃OPh)C(=0)OCH₂ CH₃

G6-474 CF₃ (2-CNPh)C(=0)OCH₂ CH₃

G6-475 CF₃ (3-CNPh)C(=0)OCH₂ CH₃

G6-476 CF₃ (4-CNPh)C(=0)OCH₂ CH₃

G6-477 CF₃ (2-N0₂Ph)C(=0)OCH₂ CH₃

G6-478 CF₃ (3-N0₂Ph)C(=0)OCH₂ CH₃

G6-479 CF₃ (4-N0₂Ph)C(=0)OCH₂ CH₃

G6-480 CF₃ (2-CF₃Ph)C(=0)OCH₂ CH₃

G6-481 CF₃ (3-CF₃Ph)C(=0)OCH₂ CH₃

G6-524 2-CF₃Ph (3-CH₃OPh)OCH₂ H

G6-525 2-CF₃Ph (4-CH₃OPh)OCH₂ H

G6-526 2-CF₃Ph (2-FPh)OCH₂ H

G6-527 2-CF₃Ph (3-FPh)OCH₂ H

G6-528 2-CF₃Ph (4-FPh)OCH₂ H

G6-529 2-CF₃Ph (2-CIPh)OCH₂ H

G6-530 2-CF₃Ph (3-CIPh)OCH₂ H

G6-531 2-CF₃Ph (4-CIPh)OCH₂ H

G6-532 2-CF₃Ph (2-BrPh)OCH₂ H

G6-533 2-CF₃Ph (3-BrPh)OCH₂ H

G6-534 2-CF₃Ph (4-BrPh)OCH₂ H

G6-535 2-CF₃Ph (2-CF₃OPh)OCH₂ H

G6-536 2-CF₃Ph (3-CF₃OPh)OCH₂ H

G6-537 2-CF₃Ph (4-CF₃OPh)OCH₂ H

G6-538 2-CF₃Ph (2-CNPh)OCH₂ H

G6-539 2-CF₃Ph (3-CNPh)OCH₂ H

G6-540 2-CF₃Ph (4-CNPh)OCH₂ H

G6-541 2-CF₃Ph (2-N0₂Ph)OCH₂ H

G6-542 2-CF₃Ph (3-N0₂Ph)OCH₂ H

G6-543 2-CF₃Ph (4-N0₂Ph)OCH₂ H

G6-544 2-CF₃Ph (2-CF₃Ph)OCH₂ H

G6-545 2-CF₃Ph (3-CF₃Ph)OCH₂ H

G6-546 2-CF₃Ph (4-CF₃Ph)OCH₂ H

G6-547 2-CF₃Ph PhCH₂OCH₂ H

G6-548 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G6-549 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G6-550 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G6-551 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G6-552 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G6-553 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G6-554 2-CF₃Ph (2-FPh)CH₂OCH₂ H

G6-555 2-CF₃Ph (3-FPh)CH₂OCH₂ H

G6-556 2-CF₃Ph (4-FPh)CH₂OCH₂ H

G6-557 2-CF₃Ph (2-CIPh)CH₂OCH₂ H

G6-558 2-CF₃Ph (3-CIPh)CH₂OCH₂ H

G6-559 2-CF₃Ph (4-CIPh)CH₂OCH₂ H

G6-560 2-CF₃Ph (2-BrPh)CH₂OCH₂ H

G6-561 2-CF₃Ph (3-BrPh)CH₂OCH₂ H

G6-562 2-CF₃Ph (4-BrPh)CH₂OCH₂ H

G6-563 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G6-564 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G6-565 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G6-566 2-CF₃Ph (2-CNPh)CH₂OCH₂ H

G6-567 2-CF₃Ph (3-CNPh)CH₂OCH₂ H

G6-568 2-CF₃Ph (4-CNPh)CH₂OCH₂ H

G6-569 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G6-570 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G6-571 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H G6-572 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G6-573 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G6-574 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G6-575 2-CF₃Ph CH₃C(=0)OCH₂ H

G6-576 2-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G6-577 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G6-578 2-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G6-579 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G6-580 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G6-581 2-CF₃Ph CF₃C(=0)OCH₂ H

G6-582 2-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G6-583 2-CF₃Ph (c-hex)C(=0)OCH₂ H

G6-584 2-CF₃Ph PhC(=0)OCH₂ H

G6-585 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G6-586 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G6-587 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G6-588 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G6-589 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G6-590 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G6-591 2-CF₃Ph (2-FPh)C(=0)OCH₂ H

G6-592 2-CF₃Ph (3-FPh)C(=0)OCH₂ H

G6-593 2-CF₃Ph (4-FPh)C(=0)OCH₂ H

G6-594 2-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G6-595 2-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G6-596 2-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G6-597 2-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G6-598 2-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G6-599 2-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G6-600 2-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G6-601 2-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G6-602 2-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G6-603 2-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G6-604 2-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G6-605 2-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G6-606 2-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G6-607 2-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G6-608 2-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G6-609 2-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G6-610 2-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G6-611 2-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G6-612 2-CF₃Ph CH₃ CH₃

G6-613 2-CF₃Ph CH₃CH₂ CH₃

G6-614 2-CF₃Ph CH₃CH₂CH₂ CH₃

G6-615 2-CF₃Ph (CH₃)₂CH CH₃

G6-616 2-CF₃Ph CH₃C(=0) CH₃

G6-617 2-CF₃Ph CH₃CH₂C(=0) CH₃

G6-618 2-CF₃Ph (CH₃)₂CHC(=0) CH₃

G6-619 2-CF₃Ph (CH₃)₃CC(=0) CH₃ G6-620 2-CF₃Ph (CH₃)₃CCH₂C(=0) CH₃

G6-621 2-CF₃Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G6-622 2-CF₃Ph (CH₃)₂CHCH₂C(=0) CH₃

G6-623 2-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G6-624 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G6-625 2-CF₃Ph (c-hex)C(=0) CH₃

G6-626 2-CF₃Ph (c-pen)C(=0) CH₃

G6-627 2-CF₃Ph (c-hep)C(=0) CH₃

G6-628 2-CF₃Ph (c-pro)C(=0) CH₃

G6-629 2-CF₃Ph CF₃C(=0) CH₃

G6-630 2-CF₃Ph (CH₃)₂NC(=0) CH₃

G6-631 2-CF₃Ph (CH₃CH₂)₂NC(=0) CH₃

G6-632 2-CF₃Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G6-633 2-CF₃Ph CH₃CH₂N(CH₃)C(=0) CH₃

G6-634 2-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃

G6-635 2-CF₃Ph CH₃ON(CH₃)C(=0) CH₃

G6-636 2-CF₃Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G6-637 2-CF₃Ph (CHCCH₂)₂NC(=0) CH₃

G6-638 2-CF₃Ph CH₃

G6-639 2-CF₃Ph CH₃

G6-640 2-CF₃Ph CH₃

G6-641 2-CF₃Ph CH₃OCH₂ CH₃

G6-642 2-CF₃Ph CH₃CH₂OCH₂ CH₃

G6-643 2-CF₃Ph (CH₃)₂CHOCH₂ CH₃

G6-644 2-CF₃Ph (CH₃)₃COCH₂ CH₃

G6-645 2-CF₃Ph (CH₃)₃CCH₂OCH₂ CH₃

G6-646 2-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂ CH₃

G6-647 2-CF₃Ph (c-hex)OCH₂ CH₃

G6-648 2-CF₃Ph PhOCH₂ CH₃

G6-649 2-CF₃Ph (2-CH₃Ph)OCH₂ CH₃

G6-650 2-CF₃Ph (3-CH₃Ph)OCH₂ CH₃

G6-651 2-CF₃Ph (4-CH₃Ph)OCH₂ CH₃

G6-652 2-CF₃Ph (2-CH₃OPh)OCH₂ CH₃

G6-653 2-CF₃Ph (3-CH₃OPh)OCH₂ CH₃

G6-654 2-CF₃Ph (4-CH₃OPh)OCH₂ CH₃

G6-655 2-CF₃Ph (2-FPh)OCH₂ CH₃

G6-656 2-CF₃Ph (3-FPh)OCH₂ CH₃

G6-657 2-CF₃Ph (4-FPh)OCH₂ CH₃

G6-658 2-CF₃Ph (2-CIPh)OCH₂ CH₃

G6-659 2-CF₃Ph (3-CIPh)OCH₂ CH₃

G6-660 2-CF₃Ph (4-CIPh)OCH₂ CH₃

G6-661 2-CF₃Ph (2-BrPh)OCH₂ CH₃ G6-662 2-CF₃Ph (3-BrPh)OCH₂ CH₃

G6-663 2-CF₃Ph (4-BrPh)OCH₂ CH₃

G6-664 2-CF₃Ph (2-CF₃OPh)OCH₂ CH₃

G6-665 2-CF₃Ph (3-CF₃OPh)OCH₂ CH₃

G6-666 2-CF₃Ph (4-CF₃OPh)OCH₂ CH₃

G6-667 2-CF₃Ph (2-CNPh)OCH₂ CH₃

G6-668 2-CF₃Ph (3-CNPh)OCH₂ CH₃

G6-669 2-CF₃Ph (4-CNPh)OCH₂ CH₃

G6-670 2-CF₃Ph (2-N0₂Ph)OCH₂ CH₃

G6-671 2-CF₃Ph (3-N0₂Ph)OCH₂ CH₃

G6-672 2-CF₃Ph (4-N0₂Ph)OCH₂ CH₃

G6-673 2-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G6-674 2-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G6-675 2-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G6-676 2-CF₃Ph PhCH₂OCH₂ CH₃

G6-677 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G6-678 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G6-679 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G6-680 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G6-681 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G6-682 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G6-683 2-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G6-684 2-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G6-685 2-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G6-686 2-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G6-687 2-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G6-688 2-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G6-689 2-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G6-690 2-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G6-691 2-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G6-692 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G6-693 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G6-694 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G6-695 2-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G6-696 2-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G6-697 2-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G6-698 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G6-699 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G6-700 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G6-701 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G6-702 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G6-703 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G6-704 2-CF₃Ph CH₃C(=0)OCH₂ CH₃

G6-705 2-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G6-706 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G6-707 2-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G6-708 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G6-709 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃ G6-710 2-CF₃Ph CF₃C(=0)OCH₂ CH₃

G6-711 2-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G6-712 2-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G6-713 2-CF₃Ph PhC(=0)OCH₂ CH₃

G6-714 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G6-715 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G6-716 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G6-717 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G6-718 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G6-719 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G6-720 2-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G6-721 2-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G6-722 2-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G6-723 2-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G6-724 2-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G6-725 2-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G6-726 2-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G6-727 2-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G6-728 2-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G6-729 2-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G6-730 2-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G6-731 2-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G6-732 2-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G6-733 2-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G6-734 2-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G6-735 2-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G6-736 2-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G6-737 2-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G6-738 2-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G6-739 2-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G6-740 2-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

G6-741 3-CF₃Ph CH₃ H

G6-742 3-CF₃Ph CH₃CH₂ H

G6-743 3-CF₃Ph CH₃CH₂CH₂ H

G6-744 3-CF₃Ph (CH₃)₂CH H

G6-745 3-CF₃Ph CH₃C(=0) H

G6-746 3-CF₃Ph CH₃CH₂C(=0) H

G6-747 3-CF₃Ph (CH₃)₂CHC(=0) H

G6-748 3-CF₃Ph (CH₃)₃CC(=0) H

G6-749 3-CF₃Ph (CH₃)₃CCH₂C(=0) H

G6-750 3-CF₃Ph CH₃CH₂CH(CH₃)C(=0) H

G6-751 3-CF₃Ph (CH₃)₂CHCH₂C(=0) H

G6-752 3-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) H

G6-753 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) H

G6-754 3-CF₃Ph (c-hex)C(=0) H

G6-755 3-CF₃Ph (c-pen)C(=0) H

G6-756 3-CF₃Ph (c-hep)C(=0) H

G6-757 3-CF₃Ph (c-pro)C(=0) H G6-758 3-CF₃Ph CF₃C(=0) H

G6-759 3-CF₃Ph (CH₃)₂NC(=0) H

G6-760 3-CF₃Ph (CH₃CH₂)₂NC(=0) H

G6-761 3-CF₃Ph (CH₃CH₂CH₂)₂NC(=0) H

G6-762 3-CF₃Ph CH₃CH₂N(CH₃)C(=0) H

G6-763 3-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0) H

G6-764 3-CF₃Ph CH₃ON(CH₃)C(=0) H

G6-765 3-CF₃Ph (CH₂=CHCH₂)₂N C(=0) H

G6-766 3-CF₃Ph (CHCCH₂)₂NC(=0) H

G6-767 3-CF₃Ph H

G6-768 3-CF₃Ph H

G6-769 3-CF₃Ph H

G6-770 3-CF₃Ph CH₃OCH₂ H

G6-771 3-CF₃Ph CH₃CH₂OCH₂ H

G6-772 3-CF₃Ph (CH₃)₂CHOCH₂ H

G6-773 3-CF₃Ph (CH₃)₃COCH₂ H

G6-774 3-CF₃Ph (CH₃)₃CCH₂OCH₂ H

G6-775 3-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂ H

G6-776 3-CF₃Ph (c-hex)OCH₂ H

G6-777 3-CF₃Ph PhOCH₂ H

G6-778 3-CF₃Ph (2-CH₃Ph)OCH₂ H

G6-779 3-CF₃Ph (3-CH₃Ph)OCH₂ H

G6-780 3-CF₃Ph (4-CH₃Ph)OCH₂ H

G6-781 3-CF₃Ph (2-CH₃OPh)OCH₂ H

G6-782 3-CF₃Ph (3-CH₃OPh)OCH₂ H

G6-783 3-CF₃Ph (4-CH₃OPh)OCH₂ H

G6-784 3-CF₃Ph (2-FPh)OCH₂ H

G6-785 3-CF₃Ph (3-FPh)OCH₂ H

G6-786 3-CF₃Ph (4-FPh)OCH₂ H

G6-787 3-CF₃Ph (2-CIPh)OCH₂ H

G6-788 3-CF₃Ph (3-CIPh)OCH₂ H

G6-789 3-CF₃Ph (4-CIPh)OCH₂ H

G6-790 3-CF₃Ph (2-BrPh)OCH₂ H

G6-791 3-CF₃Ph (3-BrPh)OCH₂ H

G6-792 3-CF₃Ph (4-BrPh)OCH₂ H

G6-793 3-CF₃Ph (2-CF₃OPh)OCH₂ H

G6-794 3-CF₃Ph (3-CF₃OPh)OCH₂ H

G6-795 3-CF₃Ph (4-CF₃OPh)OCH₂ H

G6-796 3-CF₃Ph (2-CNPh)OCH₂ H

G6-797 3-CF₃Ph (3-CNPh)OCH₂ H

G6-798 3-CF₃Ph (4-CNPh)OCH₂ H

G6-799 3-CF₃Ph (2-N0₂Ph)OCH₂ H G6-800 3-CF₃Ph (3-N0₂Ph)OCH₂ H

G6-801 3-CF₃Ph (4-N0₂Ph)OCH₂ H

G6-802 3-CF₃Ph (2-CF₃Ph)OCH₂ H

G6-803 3-CF₃Ph (3-CF₃Ph)OCH₂ H

G6-804 3-CF₃Ph (4-CF₃Ph)OCH₂ H

G6-805 3-CF₃Ph PhCH₂OCH₂ H

G6-806 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G6-807 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G6-808 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G6-809 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G6-810 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G6-811 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G6-812 3-CF₃Ph (2-FPh)CH₂OCH₂ H

G6-813 3-CF₃Ph (3-FPh)CH₂OCH₂ H

G6-814 3-CF₃Ph (4-FPh)CH₂OCH₂ H

G6-815 3-CF₃Ph (2-CIPh)CH₂OCH₂ H

G6-816 3-CF₃Ph (3-CIPh)CH₂OCH₂ H

G6-817 3-CF₃Ph (4-CIPh)CH₂OCH₂ H

G6-818 3-CF₃Ph (2-BrPh)CH₂OCH₂ H

G6-819 3-CF₃Ph (3-BrPh)CH₂OCH₂ H

G6-820 3-CF₃Ph (4-BrPh)CH₂OCH₂ H

G6-821 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G6-822 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G6-823 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G6-824 3-CF₃Ph (2-CNPh)CH₂OCH₂ H

G6-825 3-CF₃Ph (3-CNPh)CH₂OCH₂ H

G6-826 3-CF₃Ph (4-CNPh)CH₂OCH₂ H

G6-827 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G6-828 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G6-829 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G6-830 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G6-831 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G6-832 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G6-833 3-CF₃Ph CH₃C(=0)OCH₂ H

G6-834 3-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G6-835 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G6-836 3-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G6-837 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G6-838 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G6-839 3-CF₃Ph CF₃C(=0)OCH₂ H

G6-840 3-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G6-841 3-CF₃Ph (c-hex)C(=0)OCH₂ H

G6-842 3-CF₃Ph PhC(=0)OCH₂ H

G6-843 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G6-844 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G6-845 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G6-846 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G6-847 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H G6-848 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G6-849 3-CF₃Ph (2-FPh)C(=0)OCH₂ H

G6-850 3-CF₃Ph (3-FPh)C(=0)OCH₂ H

G6-851 3-CF₃Ph (4-FPh)C(=0)OCH₂ H

G6-852 3-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G6-853 3-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G6-854 3-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G6-855 3-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G6-856 3-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G6-857 3-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G6-858 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G6-859 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G6-860 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G6-861 3-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G6-862 3-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G6-863 3-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G6-864 3-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G6-865 3-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H

G6-866 3-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G6-867 3-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G6-868 3-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G6-869 3-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G6-870 3-CF₃Ph CH₃ CH₃

G6-871 3-CF₃Ph CH₃CH₂ CH₃

G6-872 3-CF₃Ph CH₃CH₂CH₂ CH₃

G6-873 3-CF₃Ph (CH₃)₂CH CH₃

G6-874 3-CF₃Ph CH₃C(=0) CH₃

G6-875 3-CF₃Ph CH₃CH₂C(=0) CH₃

G6-876 3-CF₃Ph (CH₃)₂CHC(=0) CH₃

G6-877 3-CF₃Ph (CH₃)₃CC(=0) CH₃

G6-878 3-CF₃Ph (CH₃)₃CCH₂C(=0) CH₃

G6-879 3-CF₃Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G6-880 3-CF₃Ph (CH₃)₂CHCH₂C(=0) CH₃

G6-881 3-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G6-882 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G6-883 3-CF₃Ph (c-hex)C(=0) CH₃

G6-884 3-CF₃Ph (c-pen)C(=0) CH₃

G6-885 3-CF₃Ph (c-hep)C(=0) CH₃

G6-886 3-CF₃Ph (c-pro)C(=0) CH₃

G6-887 3-CF₃Ph CF₃C(=0) CH₃

G6-888 3-CF₃Ph (CH₃)₂NC(=0) CH₃

G6-889 3-CF₃Ph (CH₃CH₂)₂NC(=0) CH₃

G6-890 3-CF₃Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G6-891 3-CF₃Ph CH₃CH₂N(CH₃)C(=0) CH₃

G6-892 3-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃

G6-893 3-CF₃Ph CH₃ON(CH₃)C(=0) CH₃

G6-894 3-CF₃Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G6-895 3-CF₃Ph (CHCCH₂)₂NC(=0) CH₃ G6-896 3-CF₃Ph CH₃

G6-897 3-CF₃Ph CH₃

G6-898 3-CF₃Ph CH₃

G6-899 3-CF₃Ph CH₃OCH₂ CH₃

G6-900 3-CF₃Ph CH₃CH20CH2 CH₃

G6-901 3-CF₃Ph (CH₃)₂CHOCH₂ CH₃

G6-902 3-CF₃Ph (CH₃)₃COCH₂ CH₃

G6-903 3-CF₃Ph (CH₃)₃CCH20CH2 CH₃

G6-904 3-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂ CH₃

G6-905 3-CF₃Ph (c-hex)OCH₂ CH₃

G6-906 3-CF₃Ph PhOCH₂ CH₃

G6-907 3-CF₃Ph (2-CH₃Ph)OCH₂ CH₃

G6-908 3-CF₃Ph (3-CH₃Ph)OCH₂ CH₃

G6-909 3-CF₃Ph (4-CH₃Ph)OCH₂ CH₃

G6-910 3-CF₃Ph (2-CH₃OPh)OCH₂ CH₃

G6-911 3-CF₃Ph (3-CH₃OPh)OCH₂ CH₃

G6-912 3-CF₃Ph (4-CH₃OPh)OCH₂ CH₃

G6-913 3-CF₃Ph (2-FPh)OCH₂ CH₃

G6-914 3-CF₃Ph (3-FPh)OCH₂ CH₃

G6-915 3-CF₃Ph (4-FPh)OCH₂ CH₃

G6-916 3-CF₃Ph (2-CIPh)OCH₂ CH₃

G6-917 3-CF₃Ph (3-CIPh)OCH₂ CH₃

G6-918 3-CF₃Ph (4-CIPh)OCH₂ CH₃

G6-919 3-CF₃Ph (2-BrPh)OCH₂ CH₃

G6-920 3-CF₃Ph (3-BrPh)OCH₂ CH₃

G6-921 3-CF₃Ph (4-BrPh)OCH₂ CH₃

G6-922 3-CF₃Ph (2-CF₃OPh)OCH₂ CH₃

G6-923 3-CF₃Ph (3-CF₃OPh)OCH₂ CH₃

G6-924 3-CF₃Ph (4-CF₃OPh)OCH₂ CH₃

G6-925 3-CF₃Ph (2-CNPh)OCH₂ CH₃

G6-926 3-CF₃Ph (3-CNPh)OCH₂ CH₃

G6-927 3-CF₃Ph (4-CNPh)OCH₂ CH₃

G6-928 3-CF₃Ph (2-N0₂Ph)OCH₂ CH₃

G6-929 3-CF₃Ph (3-N0₂Ph)OCH₂ CH₃

G6-930 3-CF₃Ph (4-N0₂Ph)OCH₂ CH₃

G6-931 3-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G6-932 3-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G6-933 3-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G6-934 3-CF₃Ph PhCH₂OCH₂ CH₃

G6-935 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G6-936 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G6-937 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃ G6-938 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G6-939 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G6-940 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G6-941 3-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G6-942 3-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G6-943 3-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G6-944 3-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G6-945 3-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G6-946 3-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G6-947 3-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G6-948 3-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G6-949 3-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G6-950 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G6-951 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G6-952 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G6-953 3-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G6-954 3-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G6-955 3-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃

G6-956 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G6-957 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G6-958 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G6-959 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G6-960 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G6-961 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G6-962 3-CF₃Ph CH₃C(=0)OCH₂ CH₃

G6-963 3-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G6-964 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G6-965 3-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G6-966 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G6-967 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G6-968 3-CF₃Ph CF₃C(=0)OCH₂ CH₃

G6-969 3-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G6-970 3-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G6-971 3-CF₃Ph PhC(=0)OCH₂ CH₃

G6-972 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G6-973 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G6-974 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G6-975 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G6-976 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G6-977 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G6-978 3-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G6-979 3-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G6-980 3-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G6-981 3-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G6-982 3-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G6-983 3-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G6-984 3-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G6-985 3-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃ G6-986 3-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G6-987 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G6-988 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G6-989 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G6-990 3-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G6-991 3-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G6-992 3-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G6-993 3-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G6-994 3-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G6-995 3-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G6-996 3-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G6-997 3-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G6-998 3-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

G6-999 4-CF₃Ph CH₃ H

G6-1000 4-CF₃Ph CH₃CH₂ H

G6-1001 4-CF₃Ph CH₃CH₂CH₂ H

G6-1002 4-CF₃Ph (CH₃)₂CH H

G6-1003 4-CF₃Ph CH₃C(=0) H

G6-1004 4-CF₃Ph CH₃CH₂C(=0) H

G6-1005 4-CF₃Ph (CH₃)₂CHC(=0) H

G6-1006 4-CF₃Ph (CH₃)₃CC(=0) H

G6-1007 4-CF₃Ph (CH₃)₃CCH₂C(=0) H

G6-1008 4-CF₃Ph CH₃CH₂CH(CH₃)C(=0) H

G6-1009 4-CF₃Ph (CH₃)₂CHCH₂C(=0) H

G6-1010 4-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) H

G6-1011 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) H

G6-1012 4-CF₃Ph (c-hex)C(=0) H

G6-1013 4-CF₃Ph (c-pen)C(=0) H

G6-1014 4-CF₃Ph (c-hep)C(=0) H

G6-1015 4-CF₃Ph (c-pro)C(=0) H

G6-1016 4-CF₃Ph CF₃C(=0) H

G6-1017 4-CF₃Ph (CH₃)₂NC(=0) H

G6-1018 4-CF₃Ph (CH₃CH₂)₂NC(=0) H

G6-1019 4-CF₃Ph (CH₃CH₂CH₂)₂NC(=0) H

G6-1020 4-CF₃Ph CH₃CH₂N(CH₃)C(=0) H

G6-1021 4-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0) H

G6-1022 4-CF₃Ph CH₃ON(CH₃)C(=0) H

G6-1023 4-CF₃Ph (CH₂=CHCH₂)₂N C(=0) H

G6-1024 4-CF₃Ph (CHCCH₂)₂NC(=0) H

G6-1025 4-CF₃Ph H

G6-1026 4-CF₃Ph H

G6-1027 4-CF₃Ph H G6-1028 4-CF₃Ph CH₃OCH₂ H

G6-1029 4-CF₃Ph CH₃CH20CH2 H

G6-1030 4-CF₃Ph (CH₃)₂CHOCH₂ H

G6-1031 4-CF₃Ph (CH₃)₃COCH₂ H

G6-1032 4-CF₃Ph (CH₃)₃CCH20CH2 H

G6-1033 4-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂ H

G6-1034 4-CF₃Ph (c-hex)OCH₂ H

G6-1035 4-CF₃Ph PhOCH₂ H

G6-1036 4-CF₃Ph (2-CH₃Ph)OCH₂ H

G6-1037 4-CF₃Ph (3-CH₃Ph)OCH₂ H

G6-1038 4-CF₃Ph (4-CH₃Ph)OCH₂ H

G6-1039 4-CF₃Ph (2-CH₃OPh)OCH₂ H

G6-1040 4-CF₃Ph (3-CH₃OPh)OCH₂ H

G6-1041 4-CF₃Ph (4-CH₃OPh)OCH₂ H

G6-1042 4-CF₃Ph (2-FPh)OCH₂ H

G6-1043 4-CF₃Ph (3-FPh)OCH₂ H

G6-1044 4-CF₃Ph (4-FPh)OCH₂ H

G6-1045 4-CF₃Ph (2-CIPh)OCH₂ H

G6-1046 4-CF₃Ph (3-CIPh)OCH₂ H

G6-1047 4-CF₃Ph (4-CIPh)OCH₂ H

G6-1048 4-CF₃Ph (2-BrPh)OCH₂ H

G6-1049 4-CF₃Ph (3-BrPh)OCH₂ H

G6-1050 4-CF₃Ph (4-BrPh)OCH₂ H

G6-1051 4-CF₃Ph (2-CF₃OPh)OCH₂ H

G6-1052 4-CF₃Ph (3-CF₃OPh)OCH₂ H

G6-1053 4-CF₃Ph (4-CF₃OPh)OCH₂ H

G6-1054 4-CF₃Ph (2-CNPh)OCH₂ H

G6-1055 4-CF₃Ph (3-CNPh)OCH₂ H

G6-1056 4-CF₃Ph (4-CNPh)OCH₂ H

G6-1057 4-CF₃Ph (2-N0₂Ph)OCH₂ H

G6-1058 4-CF₃Ph (3-N0₂Ph)OCH₂ H

G6-1059 4-CF₃Ph (4-N0₂Ph)OCH₂ H

G6-1060 4-CF₃Ph (2-CF₃Ph)OCH₂ H

G6-1061 4-CF₃Ph (3-CF₃Ph)OCH₂ H

G6-1062 4-CF₃Ph (4-CF₃Ph)OCH₂ H

G6-1063 4-CF₃Ph PhCH₂OCH₂ H

G6-1064 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂ H

G6-1065 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂ H

G6-1066 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂ H

G6-1067 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂ H

G6-1068 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂ H

G6-1069 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂ H

G6-1070 4-CF₃Ph (2-FPh)CH₂OCH₂ H

G6-1071 4-CF₃Ph (3-FPh)CH₂OCH₂ H

G6-1072 4-CF₃Ph (4-FPh)CH₂OCH₂ H

G6-1073 4-CF₃Ph (2-CIPh)CH₂OCH₂ H

G6-1074 4-CF₃Ph (3-CIPh)CH₂OCH₂ H

G6-1075 4-CF₃Ph (4-CIPh)CH₂OCH₂ H G6-1076 4-CF₃Ph (2-BrPh)CH₂OCH₂ H

G6-1077 4-CF₃Ph (3-BrPh)CH₂OCH₂ H

G6-1078 4-CF₃Ph (4-BrPh)CH₂OCH₂ H

G6-1079 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂ H

G6-1080 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂ H

G6-1081 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ H

G6-1082 4-CF₃Ph (2-CNPh)CH₂OCH₂ H

G6-1083 4-CF₃Ph (3-CNPh)CH₂OCH₂ H

G6-1084 4-CF₃Ph (4-CNPh)CH₂OCH₂ H

G6-1085 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂ H

G6-1086 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂ H

G6-1087 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂ H

G6-1088 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂ H

G6-1089 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂ H

G6-1090 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂ H

G6-1091 4-CF₃Ph CH₃C(=0)OCH₂ H

G6-1092 4-CF₃Ph CH₃CH₂C(=0)OCH₂ H

G6-1093 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂ H

G6-1094 4-CF₃Ph (CH₃)₃C(=0)OCH₂ H

G6-1095 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ H

G6-1096 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G6-1097 4-CF₃Ph CF₃C(=0)OCH₂ H

G6-1098 4-CF₃Ph CF₃CF₂C(=0)OCH₂ H

G6-1099 4-CF₃Ph (c-hex)C(=0)OCH₂ H

G6-1100 4-CF₃Ph PhC(=0)OCH₂ H

G6-1101 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ H

G6-1102 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ H

G6-1103 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ H

G6-1104 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ H

G6-1105 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ H

G6-1106 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ H

G6-1107 4-CF₃Ph (2-FPh)C(=0)OCH₂ H

G6-1108 4-CF₃Ph (3-FPh)C(=0)OCH₂ H

G6-1109 4-CF₃Ph (4-FPh)C(=0)OCH₂ H

G6-1110 4-CF₃Ph (2-CIPh)C(=0)OCH₂ H

G6-1111 4-CF₃Ph (3-CIPh)C(=0)OCH₂ H

G6-1112 4-CF₃Ph (4-CIPh)C(=0)OCH₂ H

G6-1113 4-CF₃Ph (2-BrPh)C(=0)OCH₂ H

G6-1114 4-CF₃Ph (3-BrPh)C(=0)OCH₂ H

G6-1115 4-CF₃Ph (4-BrPh)C(=0)OCH₂ H

G6-1116 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ H

G6-1117 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ H

G6-1118 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ H

G6-1119 4-CF₃Ph (2-CNPh)C(=0)OCH₂ H

G6-1120 4-CF₃Ph (3-CNPh)C(=0)OCH₂ H

G6-1121 4-CF₃Ph (4-CNPh)C(=0)OCH₂ H

G6-1122 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ H

G6-1123 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ H G6-1124 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ H

G6-1125 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ H

G6-1126 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ H

G6-1127 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ H

G6-1128 4-CF₃Ph CH₃ CH₃

G6-1129 4-CF₃Ph CH₃CH₂ CH₃

G6-1130 4-CF₃Ph CH₃CH₂CH₂ CH₃

G6-1131 4-CF₃Ph (CH₃)₂CH CH₃

G6-1132 4-CF₃Ph CH₃C(=0) CH₃

G6-1133 4-CF₃Ph CH₃CH₂C(=0) CH₃

G6-1134 4-CF₃Ph (CH₃)₂CHC(=0) CH₃

G6-1135 4-CF₃Ph (CH₃)₃CC(=0) CH₃

G6-1136 4-CF₃Ph (CH₃)₃CCH₂C(=0) CH₃

G6-1137 4-CF₃Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G6-1138 4-CF₃Ph (CH₃)₂CHCH₂C(=0) CH₃

G6-1139 4-CF₃Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G6-1140 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G6-1141 4-CF₃Ph (c-hex)C(=0) CH₃

G6-1142 4-CF₃Ph (c-pen)C(=0) CH₃

G6-1143 4-CF₃Ph (c-hep)C(=0) CH₃

G6-1144 4-CF₃Ph (c-pro)C(=0) CH₃

G6-1145 4-CF₃Ph CF₃C(=0) CH₃

G6-1146 4-CF₃Ph (CH₃)₂NC(=0) CH₃

G6-1147 4-CF₃Ph (CH₃CH₂)₂NC(=0) CH₃

G6-1148 4-CF₃Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G6-1149 4-CF₃Ph CH₃CH₂N(CH₃)C(=0) CH₃

G6-1150 4-CF₃Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃

G6-1151 4-CF₃Ph CH₃ON(CH₃)C(=0) CH₃

G6-1152 4-CF₃Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G6-1153 4-CF₃Ph (CHCCH₂)₂NC(=0) CH₃

G6-1154 4-CF₃Ph CH₃

G6-1155 4-CF₃Ph CH₃

G6-1156 4-CF₃Ph CH₃

G6-1157 4-CF₃Ph CH₃OCH₂ CH₃

G6-1158 4-CF₃Ph CH₃CH₂OCH₂ CH₃

G6-1159 4-CF₃Ph (CH₃)₂CHOCH₂ CH₃

G6-1160 4-CF₃Ph (CH₃)₃COCH₂ CH₃

G6-1161 4-CF₃Ph (CH₃)₃CCH₂OCH₂ CH₃

G6-1162 4-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂ CH₃

G6-1163 4-CF₃Ph (c-hex)OCH₂ CH₃

G6-1164 4-CF₃Ph PhOCH₂ CH₃

G6-1165 4-CF₃Ph (2-CH₃Ph)OCH₂ CH₃ G6-1166 4-CF₃Ph (3-CH₃Ph)OCH₂ CH₃

G6-1167 4-CF₃Ph (4-CH₃Ph)OCH₂ CH₃

G6-1168 4-CF₃Ph (2-CH₃OPh)OCH₂ CH₃

G6-1169 4-CF₃Ph (3-CH₃OPh)OCH₂ CH₃

G6-1170 4-CF₃Ph (4-CH₃OPh)OCH₂ CH₃

G6-1171 4-CF₃Ph (2-FPh)OCH₂ CH₃

G6-1172 4-CF₃Ph (3-FPh)OCH₂ CH₃

G6-1173 4-CF₃Ph (4-FPh)OCH₂ CH₃

G6-1174 4-CF₃Ph (2-CIPh)OCH₂ CH₃

G6-1175 4-CF₃Ph (3-CIPh)OCH₂ CH₃

G6-1176 4-CF₃Ph (4-CIPh)OCH₂ CH₃

G6-1177 4-CF₃Ph (2-BrPh)OCH₂ CH₃

G6-1178 4-CF₃Ph (3-BrPh)OCH₂ CH₃

G6-1179 4-CF₃Ph (4-BrPh)OCH₂ CH₃

G6-1180 4-CF₃Ph (2-CF₃OPh)OCH₂ CH₃

G6-1181 4-CF₃Ph (3-CF₃OPh)OCH₂ CH₃

G6-1182 4-CF₃Ph (4-CF₃OPh)OCH₂ CH₃

G6-1183 4-CF₃Ph (2-CNPh)OCH₂ CH₃

G6-1184 4-CF₃Ph (3-CNPh)OCH₂ CH₃

G6-1185 4-CF₃Ph (4-CNPh)OCH₂ CH₃

G6-1186 4-CF₃Ph (2-N0₂Ph)OCH₂ CH₃

G6-1187 4-CF₃Ph (3-N0₂Ph)OCH₂ CH₃

G6-1188 4-CF₃Ph (4-N0₂Ph)OCH₂ CH₃

G6-1189 4-CF₃Ph (2-CF₃Ph)OCH₂ CH₃

G6-1190 4-CF₃Ph (3-CF₃Ph)OCH₂ CH₃

G6-1191 4-CF₃Ph (4-CF₃Ph)OCH₂ CH₃

G6-1192 4-CF₃Ph PhCH₂OCH₂ CH₃

G6-1193 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G6-1194 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G6-1195 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G6-1196 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G6-1197 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G6-1198 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G6-1199 4-CF₃Ph (2-FPh)CH₂OCH₂ CH₃

G6-1200 4-CF₃Ph (3-FPh)CH₂OCH₂ CH₃

G6-1201 4-CF₃Ph (4-FPh)CH₂OCH₂ CH₃

G6-1202 4-CF₃Ph (2-CIPh)CH₂OCH₂ CH₃

G6-1203 4-CF₃Ph (3-CIPh)CH₂OCH₂ CH₃

G6-1204 4-CF₃Ph (4-CIPh)CH₂OCH₂ CH₃

G6-1205 4-CF₃Ph (2-BrPh)CH₂OCH₂ CH₃

G6-1206 4-CF₃Ph (3-BrPh)CH₂OCH₂ CH₃

G6-1207 4-CF₃Ph (4-BrPh)CH₂OCH₂ CH₃

G6-1208 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G6-1209 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G6-1210 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G6-1211 4-CF₃Ph (2-CNPh)CH₂OCH₂ CH₃

G6-1212 4-CF₃Ph (3-CNPh)CH₂OCH₂ CH₃

G6-1213 4-CF₃Ph (4-CNPh)CH₂OCH₂ CH₃ G6-1214 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G6-1215 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G6-1216 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G6-1217 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G6-1218 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G6-1219 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G6-1220 4-CF₃Ph CH₃C(=0)OCH₂ CH₃

G6-1221 4-CF₃Ph CH₃CH₂C(=0)OCH₂ CH₃

G6-1222 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G6-1223 4-CF₃Ph (CH₃)₃C(=0)OCH₂ CH₃

G6-1224 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G6-1225 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G6-1226 4-CF₃Ph CF₃C(=0)OCH₂ CH₃

G6-1227 4-CF₃Ph CF₃CF₂C(=0)OCH₂ CH₃

G6-1228 4-CF₃Ph (c-hex)C(=0)OCH₂ CH₃

G6-1229 4-CF₃Ph PhC(=0)OCH₂ CH₃

G6-1230 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G6-1231 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂ CH₃

G6-1232 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G6-1233 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G6-1234 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G6-1235 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G6-1236 4-CF₃Ph (2-FPh)C(=0)OCH₂ CH₃

G6-1237 4-CF₃Ph (3-FPh)C(=0)OCH₂ CH₃

G6-1238 4-CF₃Ph (4-FPh)C(=0)OCH₂ CH₃

G6-1239 4-CF₃Ph (2-CIPh)C(=0)OCH₂ CH₃

G6-1240 4-CF₃Ph (3-CIPh)C(=0)OCH₂ CH₃

G6-1241 4-CF₃Ph (4-CIPh)C(=0)OCH₂ CH₃

G6-1242 4-CF₃Ph (2-BrPh)C(=0)OCH₂ CH₃

G6-1243 4-CF₃Ph (3-BrPh)C(=0)OCH₂ CH₃

G6-1244 4-CF₃Ph (4-BrPh)C(=0)OCH₂ CH₃

G6-1245 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G6-1246 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G6-1247 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G6-1248 4-CF₃Ph (2-CNPh)C(=0)OCH₂ CH₃

G6-1249 4-CF₃Ph (3-CNPh)C(=0)OCH₂ CH₃

G6-1250 4-CF₃Ph (4-CNPh)C(=0)OCH₂ CH₃

G6-1251 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G6-1252 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G6-1253 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G6-1254 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G6-1255 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G6-1256 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

G6-1257 3,5-(CF₃)₂Ph CH₃ H

G6-1258 3,5-(CF₃)₂Ph CH₃CH₂ H

G6-1259 3,5-(CF₃)₂Ph CH₃CH₂CH₂ H

G6-1260 3,5-(CF₃)₂Ph (CH₃)₂CH H

G6-1261 3,5-(CF₃)₂Ph CH₃C(=0) H

G6-1304 3,5-(CF₃)₂Ph (3-CIPh)OCH₂ H

G6-1305 3,5-(CF₃)₂Ph (4-CIPh)OCH₂ H

G6-1306 3,5-(CF₃)₂Ph (2-BrPh)OCH₂ H

G6-1307 3,5-(CF₃)₂Ph (3-BrPh)OCH₂ H

G6-1308 3,5-(CF₃)₂Ph (4-BrPh)OCH₂ H

G6-1309 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂ H

G6-1310 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂ H

G6-1311 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂ H

G6-1312 3,5-(CF₃)₂Ph (2-CNPh)OCH₂ H

G6-1313 3,5-(CF₃)₂Ph (3-CNPh)OCH₂ H

G6-1314 3,5-(CF₃)₂Ph (4-CNPh)OCH₂ H

G6-1315 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂ H

G6-1316 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂ H

G6-1317 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂ H

G6-1318 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂ H

G6-1319 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂ H

G6-1320 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂ H

G6-1321 3,5-(CF₃)₂Ph PhCH₂OCH₂ H

G6-1322 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂ H

G6-1323 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂ H

G6-1324 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂ H

G6-1325 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂ H

G6-1326 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂ H

G6-1327 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂ H

G6-1328 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂ H

G6-1329 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂ H

G6-1330 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂ H

G6-1331 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂ H

G6-1332 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂ H

G6-1333 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂ H

G6-1334 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂ H

G6-1335 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂ H

G6-1336 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂ H

G6-1337 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂ H

G6-1338 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂ H

G6-1339 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂ H

G6-1340 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂ H

G6-1341 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂ H

G6-1342 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂ H

G6-1343 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂ H

G6-1344 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂ H

G6-1345 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂ H

G6-1346 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂ H

G6-1347 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂ H

G6-1348 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ H

G6-1349 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂ H

G6-1350 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂ H

G6-1351 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂ H G6-1352 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂ H

G6-1353 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂ H

G6-1354 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ H

G6-1355 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂ H

G6-1356 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂ H

G6-1357 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂ H

G6-1358 3,5-(CF₃)₂Ph PhC(=0)OCH₂ H

G6-1359 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂ H

G6-1360 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂ H

G6-1361 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂ H

G6-1362 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂ H

G6-1363 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂ H

G6-1364 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂ H

G6-1365 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂ H

G6-1366 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂ H

G6-1367 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂ H

G6-1368 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂ H

G6-1369 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂ H

G6-1370 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂ H

G6-1371 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂ H

G6-1372 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ H

G6-1373 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂ H

G6-1374 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂ H

G6-1375 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂ H

G6-1376 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂ H

G6-1377 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂ H

G6-1378 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂ H

G6-1379 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂ H

G6-1380 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂ H

G6-1381 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂ H

G6-1382 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂ H

G6-1383 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂ H

G6-1384 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂ H

G6-1385 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂ H

G6-1386 3,5-(CF₃)₂Ph CH₃ CH₃

G6-1387 3,5-(CF₃)₂Ph CH₃CH₂ CH₃

G6-1388 3,5-(CF₃)₂Ph CH₃CH₂CH₂ CH₃

G6-1389 3,5-(CF₃)₂Ph (CH₃)₂CH CH₃

G6-1390 3,5-(CF₃)₂Ph CH₃C(=0) CH₃

G6-1391 3,5-(CF₃)₂Ph CH₃CH₂C(=0) CH₃

G6-1392 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0) CH₃

G6-1393 3,5-(CF₃)₂Ph (CH₃)₃CC(=0) CH₃

G6-1394 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0) CH₃

G6-1395 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0) CH₃

G6-1396 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0) CH₃

G6-1397 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0) CH₃

G6-1398 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0) CH₃

G6-1399 3,5-(CF₃)₂Ph (c-hex)C(=0) CH₃ G6-1400 3,5-(CF₃)₂Ph (c-pen)C(=0) CH₃

G6-1401 3,5-(CF₃)₂Ph (c-hep)C(=0) CH₃

G6-1402 3,5-(CF₃)₂Ph (c-pro)C(=0) CH₃

G6-1403 3,5-(CF₃)₂Ph CF₃C(=0) CH₃

G6-1404 3,5-(CF₃)₂Ph (CH₃)₂NC(=0) CH₃

G6-1405 3,5-(CF₃)₂Ph (CH₃CH₂)₂NC(=0) CH₃

G6-1406 3,5-(CF₃)₂Ph (CH₃CH₂CH₂)₂NC(=0) CH₃

G6-1407 3,5-(CF₃)₂Ph CH₃CH₂N(CH₃)C(=0) CH₃

G6-1408 3,5-(CF₃)₂Ph [(CH₃)₂CHCH₂]₂NC(=0) CH₃

G6-1409 3,5-(CF₃)₂Ph CH₃ON(CH₃)C(=0) CH₃

G6-1410 3,5-(CF₃)₂Ph (CH₂=CHCH₂)₂N C(=0) CH₃

G6-1411 3,5-(CF₃)₂Ph (CHCCH₂)₂NC(=0) CH₃

CO-N^]

G6-1412 3,5-(CF₃)₂Ph CH₃

CO-N^

G6-1413 3,5-(CF₃)₂Ph CH₃

CO-N^O

G6-1414 3 5-(CF₃)₂Ph CH₃

G6-1415 3 5-(CF₃)₂Ph CH₃OCH₂ CH₃

G6-1416 3 5-(CF₃)₂Ph CH₃CH₂OCH₂ CH₃

G6-1417 3 5-(CF₃)₂Ph (CH₃)₂CHOCH₂ CH₃

G6-1418 3 5-(CF₃)₂Ph (CH₃)₃COCH₂ CH₃

G6-1419 3 5-(CF₃)₂Ph (CH₃)₃CCH₂OCH₂ CH₃

G6-1420 3 5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂OCH₂ CH₃

G6-1421 3 5-(CF₃)₂Ph (c-hex)OCH₂ CH₃

G6-1422 3 5-(CF₃)₂Ph PhOCH₂ CH₃

G6-1423 3 5-(CF₃)₂Ph (2-CH₃Ph)OCH₂ CH₃

G6-1424 3 5-(CF₃)₂Ph (3-CH₃Ph)OCH₂ CH₃

G6-1425 3 5-(CF₃)₂Ph (4-CH₃Ph)OCH₂ CH₃

G6-1426 3 5-(CF₃)₂Ph (2-CH₃OPh)OCH₂ CH₃

G6-1427 3 5-(CF₃)₂Ph (3-CH₃OPh)OCH₂ CH₃

G6-1428 3 5-(CF₃)₂Ph (4-CH₃OPh)OCH₂ CH₃

G6-1429 3 5-(CF₃)₂Ph (2-FPh)OCH₂ CH₃

G6-1430 3 5-(CF₃)₂Ph (3-FPh)OCH₂ CH₃

G6-1431 3 5-(CF₃)₂Ph (4-FPh)OCH₂ CH₃

G6-1432 3 5-(CF₃)₂Ph (2-CIPh)OCH₂ CH₃

G6-1433 3 5-(CF₃)₂Ph (3-CIPh)OCH₂ CH₃

G6-1434 3 5-(CF₃)₂Ph (4-CIPh)OCH₂ CH₃

G6-1435 3 5-(CF₃)₂Ph (2-BrPh)OCH₂ CH₃

G6-1436 3 5-(CF₃)₂Ph (3-BrPh)OCH₂ CH₃

G6-1437 3 5-(CF₃)₂Ph (4-BrPh)OCH₂ CH₃

G6-1438 3 5-(CF₃)₂Ph (2-CF₃OPh)OCH₂ CH₃

G6-1439 3 5-(CF₃)₂Ph (3-CF₃OPh)OCH₂ CH₃

G6-1440 3 5-(CF₃)₂Ph (4-CF₃OPh)OCH₂ CH₃

G6-1441 3 5-(CF₃)₂Ph (2-CNPh)OCH₂ CH₃ G6-1442 3,5-(CF₃)₂Ph (3-CNPh)OCH₂ CH₃

G6-1443 3,5-(CF₃)₂Ph (4-CNPh)OCH₂ CH₃

G6-1444 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂ CH₃

G6-1445 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂ CH₃

G6-1446 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂ CH₃

G6-1447 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂ CH₃

G6-1448 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂ CH₃

G6-1449 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂ CH₃

G6-1450 3,5-(CF₃)₂Ph PhCH₂OCH₂ CH₃

G6-1451 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂ CH₃

G6-1452 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂ CH₃

G6-1453 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂ CH₃

G6-1454 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂ CH₃

G6-1455 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂ CH₃

G6-1456 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂ CH₃

G6-1457 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂ CH₃

G6-1458 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂ CH₃

G6-1459 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂ CH₃

G6-1460 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂ CH₃

G6-1461 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂ CH₃

G6-1462 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂ CH₃

G6-1463 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂ CH₃

G6-1464 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂ CH₃

G6-1465 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂ CH₃

G6-1466 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂ CH₃

G6-1467 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂ CH₃

G6-1468 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂ CH₃

G6-1469 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂ CH₃

G6-1470 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂ CH₃

G6-1471 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂ CH₃

G6-1472 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂ CH₃

G6-1473 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂ CH₃

G6-1474 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂ CH₃

G6-1475 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂ CH₃

G6-1476 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂ CH₃

G6-1477 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ CH₃

G6-1478 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂ CH₃

G6-1479 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂ CH₃

G6-1480 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂ CH₃

G6-1481 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂ CH₃

G6-1482 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂ CH₃

G6-1483 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ CH₃

G6-1484 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂ CH₃

G6-1485 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂ CH₃

G6-1486 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂ CH₃

G6-1487 3,5-(CF₃)₂Ph PhC(=0)OCH₂ CH₃

G6-1488 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂ CH₃

G6-1489 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂ CH₃ G6-1490 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂ CH₃

G6-1491 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂ CH₃

G6-1492 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂ CH₃

G6-1493 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂ CH₃

G6-1494 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂ CH₃

G6-1495 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂ CH₃

G6-1496 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂ CH₃

G6-1497 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂ CH₃

G6-1498 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂ CH₃

G6-1499 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂ CH₃

G6-1500 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂ CH₃

G6-1501 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ CH₃

G6-1502 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂ CH₃

G6-1503 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂ CH₃

G6-1504 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂ CH₃

G6-1505 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂ CH₃

G6-1506 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂ CH₃

G6-1507 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂ CH₃

G6-1508 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂ CH₃

G6-1509 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂ CH₃

G6-1510 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂ CH₃

G6-1511 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂ CH₃

G6-1512 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂ CH₃

G6-1513 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂ CH₃

G6-1514 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂ CH₃

[0300] [Table 7]

G7-287 2-CF₃Ph (4-CH₃OPh)OCH₂

G7-288 2-CF₃Ph (2-FPh)OCH₂

G7-289 2-CF₃Ph (3-FPh)OCH₂

G7-290 2-CF₃Ph (4-FPh)OCH₂

G7-291 2-CF₃Ph (2-CIPh)OCH₂

G7-292 2-CF₃Ph (3-CIPh)OCH₂

G7-293 2-CF₃Ph (4-CIPh)OCH₂

G7-294 2-CF₃Ph (2-BrPh)OCH₂

G7-295 2-CF₃Ph (3-BrPh)OCH₂

G7-296 2-CF₃Ph (4-BrPh)OCH₂

G7-297 2-CF₃Ph (2-CF₃OPh)OCH₂

G7-298 2-CF₃Ph (3-CF₃OPh)OCH₂

G7-299 2-CF₃Ph (4-CF₃OPh)OCH₂

G7-300 2-CF₃Ph (2-CNPh)OCH₂

G7-301 2-CF₃Ph (3-CNPh)OCH₂

G7-302 2-CF₃Ph (4-CNPh)OCH₂

G7-303 2-CF₃Ph (2-N0₂Ph)OCH₂

G7-304 2-CF₃Ph (3-N0₂Ph)OCH₂

G7-305 2-CF₃Ph (4-N0₂Ph)OCH₂

G7-306 2-CF₃Ph (2-CF₃Ph)OCH₂

G7-307 2-CF₃Ph (3-CF₃Ph)OCH₂

G7-308 2-CF₃Ph (4-CF₃Ph)OCH₂

G7-309 2-CF₃Ph PhCH₂OCH₂

G7-310 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G7-311 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G7-312 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G7-313 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G7-314 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G7-315 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G7-316 2-CF₃Ph (2-FPh)CH₂OCH₂

G7-317 2-CF₃Ph (3-FPh)CH₂OCH₂

G7-318 2-CF₃Ph (4-FPh)CH₂OCH₂

G7-319 2-CF₃Ph (2-CIPh)CH₂OCH₂

G7-320 2-CF₃Ph (3-CIPh)CH₂OCH₂

G7-321 2-CF₃Ph (4-CIPh)CH₂OCH₂

G7-322 2-CF₃Ph (2-BrPh)CH₂OCH₂

G7-323 2-CF₃Ph (3-BrPh)CH₂OCH₂

G7-324 2-CF₃Ph (4-BrPh)CH₂OCH₂

G7-325 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G7-326 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G7-327 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G7-328 2-CF₃Ph (2-CNPh)CH₂OCH₂

G7-329 2-CF₃Ph (3-CNPh)CH₂OCH₂

G7-330 2-CF₃Ph (4-CNPh)CH₂OCH₂

G7-331 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G7-332 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G7-333 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G7-334 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G7-425 3-CF₃Ph (4-BrPh)OCH₂

G7-426 3-CF₃Ph (2-CF₃OPh)OCH₂

G7-427 3-CF₃Ph (3-CF₃OPh)OCH₂

G7-428 3-CF₃Ph (4-CF₃OPh)OCH₂

G7-429 3-CF₃Ph (2-CNPh)OCH₂

G7-430 3-CF₃Ph (3-CNPh)OCH₂

G7-431 3-CF₃Ph (4-CNPh)OCH₂

G7-432 3-CF₃Ph (2-N0₂Ph)OCH₂

G7-433 3-CF₃Ph (3-N0₂Ph)OCH₂

G7-434 3-CF₃Ph (4-N0₂Ph)OCH₂

G7-435 3-CF₃Ph (2-CF₃Ph)OCH₂

G7-436 3-CF₃Ph (3-CF₃Ph)OCH₂

G7-437 3-CF₃Ph (4-CF₃Ph)OCH₂

G7-438 3-CF₃Ph PhCH₂OCH₂

G7-439 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G7-440 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G7-441 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G7-442 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G7-443 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G7-444 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G7-445 3-CF₃Ph (2-FPh)CH₂OCH₂

G7-446 3-CF₃Ph (3-FPh)CH₂OCH₂

G7-447 3-CF₃Ph (4-FPh)CH₂OCH₂

G7-448 3-CF₃Ph (2-CIPh)CH₂OCH₂

G7-449 3-CF₃Ph (3-CIPh)CH₂OCH₂

G7-450 3-CF₃Ph (4-CIPh)CH₂OCH₂

G7-451 3-CF₃Ph (2-BrPh)CH₂OCH₂

G7-452 3-CF₃Ph (3-BrPh)CH₂OCH₂

G7-453 3-CF₃Ph (4-BrPh)CH₂OCH₂

G7-454 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G7-455 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G7-456 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G7-457 3-CF₃Ph (2-CNPh)CH₂OCH₂

G7-458 3-CF₃Ph (3-CNPh)CH₂OCH₂

G7-459 3-CF₃Ph (4-CNPh)CH₂OCH₂

G7-460 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G7-461 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G7-462 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G7-463 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G7-464 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G7-465 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G7-466 3-CF₃Ph CH₃C(=0)OCH₂

G7-467 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G7-468 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G7-469 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G7-470 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G7-471 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G7-472 3-CF₃Ph CF₃C(=0)OCH₂

G7-563 4-CF₃Ph (4-N0₂Ph)OCH₂

G7-564 4-CF₃Ph (2-CF₃Ph)OCH₂

G7-565 4-CF₃Ph (3-CF₃Ph)OCH₂

G7-566 4-CF₃Ph (4-CF₃Ph)OCH₂

G7-567 4-CF₃Ph PhCH₂OCH₂

G7-568 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G7-569 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G7-570 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G7-571 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G7-572 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G7-573 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G7-574 4-CF₃Ph (2-FPh)CH₂OCH₂

G7-575 4-CF₃Ph (3-FPh)CH₂OCH₂

G7-576 4-CF₃Ph (4-FPh)CH₂OCH₂

G7-577 4-CF₃Ph (2-CIPh)CH₂OCH₂

G7-578 4-CF₃Ph (3-CIPh)CH₂OCH₂

G7-579 4-CF₃Ph (4-CIPh)CH₂OCH₂

G7-580 4-CF₃Ph (2-BrPh)CH₂OCH₂

G7-581 4-CF₃Ph (3-BrPh)CH₂OCH₂

G7-582 4-CF₃Ph (4-BrPh)CH₂OCH₂

G7-583 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G7-584 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G7-585 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G7-586 4-CF₃Ph (2-CNPh)CH₂OCH₂

G7-587 4-CF₃Ph (3-CNPh)CH₂OCH₂

G7-588 4-CF₃Ph (4-CNPh)CH₂OCH₂

G7-589 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G7-590 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G7-591 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G7-592 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G7-593 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G7-594 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G7-595 4-CF₃Ph CH₃C(=0)OCH₂

G7-596 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G7-597 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G7-598 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G7-599 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G7-600 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G7-601 4-CF₃Ph CF₃C(=0)OCH₂

G7-602 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G7-603 4-CF₃Ph (c-hex)C(=0)OCH₂

G7-604 4-CF₃Ph PhC(=0)OCH₂

G7-605 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G7-606 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G7-607 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G7-608 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G7-609 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G7-610 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂ G7-611 4-CF₃Ph (2-FPh)C(=0)OCH₂

G7-612 4-CF₃Ph (3-FPh)C(=0)OCH₂

G7-613 4-CF₃Ph (4-FPh)C(=0)OCH₂

G7-614 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G7-615 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G7-616 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G7-617 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G7-618 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G7-619 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G7-620 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G7-621 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G7-622 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G7-623 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G7-624 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G7-625 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G7-626 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G7-627 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G7-628 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G7-629 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G7-630 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G7-631 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂

G7-632 3,5-(CF₃)₂Ph CH₃

G7-633 3,5-(CF₃)₂Ph CH3CH2

G7-634 3,5-(CF₃)₂Ph CH3CH2CH2

G7-635 3,5-(CF₃)₂Ph (CH₃)₂CH

G7-636 3,5-(CF₃)₂Ph CH₃C(=0)

G7-637 3,5-(CF₃)₂Ph CH₃CH₂C(=0)

G7-638 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0)

G7-639 3,5-(CF₃)₂Ph (CH₃)₃CC(=0)

G7-640 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0)

G7-641 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0)

G7-642 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0)

G7-643 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0)

G7-644 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)

G7-645 3,5-(CF₃)₂Ph (c-hex)C(=0)

G7-646 3,5-(CF₃)₂Ph (c-pen)C(=0)

G7-647 3,5-(CF₃)₂Ph (c-hep)C(=0)

G7-648 3,5-(CF₃)₂Ph (c-pro)C(=0)

G7-649 3,5-(CF₃)₂Ph CF₃C(=0)

G7-650 3,5-(CF₃)₂Ph (CH₃)₂NC(=0)

G7-651 3,5-(CF₃)₂Ph (CH₃CH₂)₂NC(=0)

G7-652 3,5-(CF₃)₂Ph (CH₃CH₂CH₂)₂NC(=0)

G7-653 3,5-(CF₃)₂Ph CH₃CH₂N(CH₃)C(=0)

G7-654 3,5-(CF₃)₂Ph [(CH₃)₂CHCH₂]₂NC(=0)

G7-655 3,5-(CF₃)₂Ph CH₃ON(CH₃)C(=0)

G7-656 3,5-(CF₃)₂Ph (CH₂=CHCH₂)₂N C(=0)

G7-657 3,5-(CF₃)₂Ph (CHCCH₂)₂NC(=0)

G7-700 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G7-701 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G7-702 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G7-703 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G7-704 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G7-705 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G7-706 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G7-707 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G7-708 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G7-709 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G7-710 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G7-711 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G7-712 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G7-713 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G7-714 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G7-715 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G7-716 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G7-717 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G7-718 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G7-719 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G7-720 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G7-721 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G7-722 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G7-723 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G7-724 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G7-725 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G7-726 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G7-727 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G7-728 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G7-729 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G7-730 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G7-731 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G7-732 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G7-733 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G7-734 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G7-735 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G7-736 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G7-737 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G7-738 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G7-739 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G7-740 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G7-741 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G7-742 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G7-743 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G7-744 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G7-745 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G7-746 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G7-747 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂ G7-748 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G7-749 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G7-750 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G7-751 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G7-752 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G7-753 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G7-754 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G7-755 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G7-756 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G7-757 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G7-758 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G7-759 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G7-760 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0301] Table 8

G8-160 CF₃ (3-CIPh)OCH₂

G8-161 CF₃ (4-CIPh)OCH₂

G8-162 CF₃ (2-BrPh)OCH₂

G8-163 CF₃ (3-BrPh)OCH₂

G8-164 CF₃ (4-BrPh)OCH₂

G8-165 CF₃ (2-CF₃OPh)OCH₂

G8-166 CF₃ (3-CF₃OPh)OCH₂

G8-167 CF₃ (4-CF₃OPh)OCH₂

G8-168 CF₃ (2-CNPh)OCH₂

G8-169 CF₃ (3-CNPh)OCH₂

G8-170 CF₃ (4-CNPh)OCH₂

G8-171 CF₃ (2-N0₂Ph)OCH₂

G8-172 CF₃ (3-N0₂Ph)OCH₂

G8-173 CF₃ (4-N0₂Ph)OCH₂

G8-174 CF₃ (2-CF₃Ph)OCH₂

G8-175 CF₃ (3-CF₃Ph)OCH₂

G8-176 CF₃ (4-CF₃Ph)OCH₂

G8-177 CF₃ PhCH₂OCH₂

G8-178 CF₃ (2-CH₃Ph)CH₂OCH₂

G8-179 CF₃ (3-CH₃Ph)CH₂OCH₂

G8-180 CF₃ (4-CH₃Ph)CH₂OCH₂

G8-181 CF₃ (2-CH₃OPh)CH₂OCH₂

G8-182 CF₃ (3-CH₃OPh)CH₂OCH₂

G8-183 CF₃ (4-CH₃OPh)CH₂OCH₂

G8-184 CF₃ (2-FPh)CH₂OCH₂

G8-185 CF₃ (3-FPh)CH₂OCH₂

G8-186 CF₃ (4-FPh)CH₂OCH₂

G8-187 CF₃ (2-CIPh)CH₂OCH₂

G8-188 CF₃ (3-CIPh)CH₂OCH₂

G8-189 CF₃ (4-CIPh)CH₂OCH₂

G8-190 CF₃ (2-BrPh)CH₂OCH₂

G8-191 CF₃ (3-BrPh)CH₂OCH₂

G8-192 CF₃ (4-BrPh)CH₂OCH₂

G8-193 CF₃ (2-CF₃OP )CH₂OCH₂

G8-194 CF₃ (3-CF₃OPh)CH₂OCH₂

G8-195 CF₃ (4-CF₃OPh)CH₂OCH₂

G8-196 CF₃ (2-CNPh)CH₂OCH₂

G8-197 CF₃ (3-CNPh)CH₂OCH₂

G8-198 CF₃ (4-CNPh)CH₂OCH₂

G8-199 CF₃ (2-N0₂Ph)CH₂OCH₂

G8-200 CF₃ (3-N0₂P )CH₂OCH₂

G8-201 CF₃ (4-N0₂Ph)CH₂OCH₂

G8-202 CF₃ (2-CF₃Ph)CH₂OCH₂

G8-203 CF₃ (3-CF₃Ph)CH₂OCH₂

G8-204 CF₃ (4-CF₃Ph)CH₂OCH₂

G8-205 CF₃ CH₃C(=0)OCH₂

G8-206 CF₃ CH₃CH₂C(=0)OCH₂

G8-207 CF₃ CH(CH₃)₂C(=0)OCH₂

G8-298 2-CF₃Ph (3-CNPh)OCH₂

G8-299 2-CF₃Ph (4-CNPh)OCH₂

G8-300 2-CF₃Ph (2-N0₂Ph)OCH₂

G8-301 2-CF₃Ph (3-N0₂Ph)OCH₂

G8-302 2-CF₃Ph (4-N0₂Ph)OCH₂

G8-303 2-CF₃Ph (2-CF₃Ph)OCH₂

G8-304 2-CF₃Ph (3-CF₃Ph)OCH₂

G8-305 2-CF₃Ph (4-CF₃Ph)OCH₂

G8-306 2-CF₃Ph PhCH₂OCH₂

G8-307 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G8-308 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G8-309 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G8-310 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G8-311 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G8-312 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G8-313 2-CF₃Ph (2-FP )CH₂OCH₂

G8-314 2-CF₃Ph (3-FPh)CH₂OCH₂

G8-315 2-CF₃Ph (4-FPh)CH₂OCH₂

G8-316 2-CF₃Ph (2-CIPh)CH₂OCH₂

G8-317 2-CF₃Ph (3-CIPh)CH₂OCH₂

G8-318 2-CF₃Ph (4-CIPh)CH₂OCH₂

G8-319 2-CF₃Ph (2-BrPh)CH₂OCH₂

G8-320 2-CF₃Ph (3-BrPh)CH₂OCH₂

G8-321 2-CF₃Ph (4-BrPh)CH₂OCH₂

G8-322 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G8-323 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G8-324 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G8-325 2-CF₃Ph (2-CNPh)CH₂OCH₂

G8-326 2-CF₃Ph (3-CNPh)CH₂OCH₂

G8-327 2-CF₃Ph (4-CNPh)CH₂OCH₂

G8-328 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G8-329 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G8-330 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G8-331 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G8-332 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G8-333 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G8-334 2-CF₃Ph CH₃C(=0)OCH₂

G8-335 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G8-336 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G8-337 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G8-338 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G8-339 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G8-340 2-CF₃Ph CF₃C(=0)OCH₂

G8-341 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G8-342 2-CF₃Ph (c-hex)C(=0)OCH₂

G8-343 2-CF₃Ph PhC(=0)OCH₂

G8-344 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G8-345 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G8-664 3,5-(CF₃)₂Ph (c-hex)OCH₂

G8-665 3,5-(CF₃)₂Ph PhOCH₂

G8-666 3,5-(CF₃)₂Ph (2-CH₃Ph)OCH₂

G8-667 3,5-(CF₃)₂Ph (3-CH₃Ph)OCH₂

G8-668 3,5-(CF₃)₂Ph (4-CH₃Ph)OCH₂

G8-669 3,5-(CF₃)₂Ph (2-CH₃OPh)OCH₂

G8-670 3,5-(CF₃)₂Ph (3-CH₃OPh)OCH₂

G8-671 3,5-(CF₃)₂Ph (4-CH₃OPh)OCH₂

G8-672 3,5-(CF₃)₂Ph (2-FPh)OCH₂

G8-673 3,5-(CF₃)₂Ph (3-FPh)OCH₂

G8-674 3,5-(CF₃)₂Ph (4-FPh)OCH₂

G8-675 3,5-(CF₃)₂Ph (2-CIPh)OCH₂

G8-676 3,5-(CF₃)₂Ph (3-CIPh)OCH₂

G8-677 3,5-(CF₃)₂Ph (4-CIPh)OCH₂

G8-678 3,5-(CF₃)₂Ph (2-BrPh)OCH₂

G8-679 3,5-(CF₃)₂Ph (3-BrPh)OCH₂

G8-680 3,5-(CF₃)₂Ph (4-BrPh)OCH₂

G8-681 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂

G8-682 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂

G8-683 3,5-(CF₃)₂P (4-CF₃OPh)OCH₂

G8-684 3,5-(CF₃)₂Ph (2-CNPh)OCH₂

G8-685 3,5-(CF₃)₂Ph (3-CNPh)OCH₂

G8-686 3,5-(CF₃)₂Ph (4-CNPh)OCH₂

G8-687 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂

G8-688 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G8-689 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G8-690 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G8-691 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G8-692 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G8-693 3,5-(CF₃)₂Ph PhCH₂OCH₂

G8-694 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G8-695 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G8-696 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G8-697 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G8-698 3,5-(CF₃)₂Ph (3-CH₃OP )CH₂OCH₂

G8-699 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G8-700 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G8-701 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G8-702 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G8-703 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G8-704 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G8-705 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G8-706 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G8-707 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G8-708 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G8-709 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G8-710 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G8-711 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G8-760 4-CIPhO H

G8-761 2-CIPhS H

G8-762 3-CIPhS H

G8-763 4-CIPhS H

[0302] Table 9

G9-308 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G9-309 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G9-310 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G9-311 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G9-312 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G9-313 2-CF₃Ph (2-FPh)CH₂OCH₂

G9-314 2-CF₃Ph (3-FPh)CH₂OCH₂

G9-315 2-CF₃Ph (4-FPh)CH₂OCH₂

G9-316 2-CF₃Ph (2-CIPh)CH₂OCH₂

G9-317 2-CF₃Ph (3-CIPh)CH₂OCH₂

G9-318 2-CF₃Ph (4-CIPh)CH₂OCH₂

G9-319 2-CF₃Ph (2-BrPh)CH₂OCH₂

G9-320 2-CF₃Ph (3-BrPh)CH₂OCH₂

G9-321 2-CF₃Ph (4-BrPh)CH₂OCH₂

G9-322 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G9-323 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G9-324 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G9-325 2-CF₃Ph (2-CNPh)CH₂OCH₂

G9-326 2-CF₃Ph (3-CNPh)CH₂OCH₂

G9-327 2-CF₃Ph (4-CNPh)CH₂OCH₂

G9-328 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G9-329 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G9-330 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G9-331 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G9-332 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G9-333 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G9-334 2-CF₃Ph CH₃C(=0)OCH₂

G9-335 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G9-336 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G9-337 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G9-338 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G9-339 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G9-340 2-CF₃Ph CF₃C(=0)OCH₂

G9-341 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G9-342 2-CF₃Ph (c-hex)C(=0)OCH₂

G9-343 2-CF₃Ph PhC(=0)OCH₂

G9-344 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G9-345 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G9-346 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G9-347 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G9-348 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G9-349 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G9-350 2-CF₃Ph (2-FPh)C(=0)OCH₂

G9-351 2-CF₃Ph (3-FPh)C(=0)OCH₂

G9-352 2-CF₃Ph (4-FPh)C(=0)OCH₂

G9-353 2-CF₃Ph (2-CIPh)C(=0)OCH₂

G9-354 2-CF₃Ph (3-CIPh)C(=0)OCH₂

G9-355 2-CF₃Ph (4-CIPh)C(=0)OCH₂

G9-445 3-CF₃Ph (2-CIPh)CH₂OCH₂

G9-446 3-CF₃Ph (3-CIPh)CH₂OCH₂

G9-447 3-CF₃Ph (4-CIPh)CH₂OCH₂

G9-448 3-CF₃Ph (2-BrPh)CH₂OCH₂

G9-449 3-CF₃Ph (3-BrPh)CH₂OCH₂

G9-450 3-CF₃Ph (4-BrPh)CH₂OCH₂

G9-451 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G9-452 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G9-453 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G9-454 3-CF₃Ph (2-CNPh)CH₂OCH₂

G9-455 3-CF₃Ph (3-CNPh)CH₂OCH₂

G9-456 3-CF₃Ph (4-CNPh)CH₂OCH₂

G9-457 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G9-458 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G9-459 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G9-460 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G9-461 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G9-462 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G9-463 3-CF₃Ph CH₃C(=0)OCH₂

G9-464 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G9-465 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G9-466 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G9-467 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G9-468 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G9-469 3-CF₃Ph CF₃C(=0)OCH₂

G9-470 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G9-471 3-CF₃Ph (c-hex)C(=0)OCH₂

G9-472 3-CF₃Ph PhC(=0)OCH₂

G9-473 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G9-474 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G9-475 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G9-476 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G9-477 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G9-478 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G9-479 3-CF₃Ph (2-FPh)C(=0)OCH₂

G9-480 3-CF₃Ph (3-FPh)C(=0)OCH₂

G9-481 3-CF₃Ph (4-FPh)C(=0)OCH₂

G9-482 3-CF₃Ph (2-CIPh)C(=0)OCH₂

G9-483 3-CF₃Ph (3-CIPh)C(=0)OCH₂

G9-484 3-CF₃Ph (4-CIPh)C(=0)OCH₂

G9-485 3-CF₃Ph (2-BrPh)C(=0)OCH₂

G9-486 3-CF₃Ph (3-BrPh)C(=0)OCH₂

G9-487 3-CF₃Ph (4-BrPh)C(=0)OCH₂

G9-488 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G9-489 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G9-490 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G9-491 3-CF₃Ph (2-CNPh)C(=0)OCH₂

G9-492 3-CF₃Ph (3-CNPh)C(=0)OCH₂

G9-535 4-CF₃Ph (c-hex)OCH₂

G9-536 4-CF₃Ph PhOCH₂

G9-537 4-CF₃Ph (2-CH₃Ph)OCH₂

G9-538 4-CF₃Ph (3-CH₃Ph)OCH₂

G9-539 4-CF₃Ph (4-CH₃Ph)OCH₂

G9-540 4-CF₃Ph (2-CH₃OPh)OCH₂

G9-541 4-CF₃Ph (3-CH₃OPh)OCH₂

G9-542 4-CF₃Ph (4-CH₃OPh)OCH₂

G9-543 4-CF₃Ph (2-FPh)OCH₂

G9-544 4-CF₃Ph (3-FPh)OCH₂

G9-545 4-CF₃Ph (4-FPh)OCH₂

G9-546 4-CF₃Ph (2-CIPh)OCH₂

G9-547 4-CF₃Ph (3-CIPh)OCH₂

G9-548 4-CF₃Ph (4-CIPh)OCH₂

G9-549 4-CF₃Ph (2-BrPh)OCH₂

G9-550 4-CF₃Ph (3-BrPh)OCH₂

G9-551 4-CF₃Ph (4-BrPh)OCH₂

G9-552 4-CF₃Ph (2-CF₃OPh)OCH₂

G9-553 4-CF₃Ph (3-CF₃OPh)OCH₂

G9-554 4-CF₃Ph (4-CF₃OPh)OCH₂

G9-555 4-CF₃Ph (2-CNPh)OCH₂

G9-556 4-CF₃Ph (3-CNPh)OCH₂

G9-557 4-CF₃Ph (4-CNPh)OCH₂

G9-558 4-CF₃Ph (2-N0₂Ph)OCH₂

G9-559 4-CF₃Ph (3-N0₂Ph)OCH₂

G9-560 4-CF₃Ph (4-N0₂Ph)OCH₂

G9-561 4-CF₃Ph (2-CF₃Ph)OCH₂

G9-562 4-CF₃Ph (3-CF₃Ph)OCH₂

G9-563 4-CF₃Ph (4-CF₃Ph)OCH₂

G9-564 4-CF₃Ph PhCH₂OCH₂

G9-565 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G9-566 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G9-567 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G9-568 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G9-569 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G9-570 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G9-571 4-CF₃Ph (2-FPh)CH₂OCH₂

G9-572 4-CF₃Ph (3-FPh)CH₂OCH₂

G9-573 4-CF₃Ph (4-FPh)CH₂OCH₂

G9-574 4-CF₃Ph (2-CIPh)CH₂OCH₂

G9-575 4-CF₃Ph (3-CIPh)CH₂OCH₂

G9-576 4-CF₃Ph (4-CIPh)CH₂OCH₂

G9-577 4-CF₃Ph (2-BrPh)CH₂OCH₂

G9-578 4-CF₃Ph (3-BrPh)CH₂OCH₂

G9-579 4-CF₃Ph (4-BrPh)CH₂OCH₂

G9-580 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G9-581 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G9-582 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂ G9-583 4-CF₃Ph (2-CNPh)CH₂OCH₂

G9-584 4-CF₃Ph (3-CNPh)CH₂OCH₂

G9-585 4-CF₃Ph (4-CNPh)CH₂OCH₂

G9-586 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G9-587 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G9-588 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G9-589 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G9-590 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G9-591 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G9-592 4-CF₃Ph CH₃C(=0)OCH₂

G9-593 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G9-594 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G9-595 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G9-596 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G9-597 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G9-598 4-CF₃Ph CF₃C(=0)OCH₂

G9-599 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G9-600 4-CF₃Ph (c-hex)C(=0)OCH₂

G9-601 4-CF₃Ph PhC(=0)OCH₂

G9-602 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G9-603 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G9-604 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G9-605 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G9-606 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G9-607 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G9-608 4-CF₃Ph (2-FPh)C(=0)OCH₂

G9-609 4-CF₃Ph (3-FPh)C(=0)OCH₂

G9-610 4-CF₃Ph (4-FPh)C(=0)OCH₂

G9-611 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G9-612 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G9-613 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G9-614 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G9-615 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G9-616 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G9-617 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G9-618 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G9-619 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G9-620 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G9-621 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G9-622 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G9-623 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G9-624 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G9-625 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G9-626 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G9-627 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G9-628 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂

G9-629 3,5-(CF₃)₂Ph CH₃

G9-630 3,5-(CF₃)₂Ph CH3CH2

G9-673 3,5-(CF₃)₂Ph (3-FPh)OCH₂

G9-674 3,5-(CF₃)₂Ph (4-FPh)OCH₂

G9-675 3,5-(CF₃)₂Ph (2-CIPh)OCH₂

G9-676 3,5-(CF₃)₂Ph (3-CIPh)OCH₂

G9-677 3,5-(CF₃)₂Ph (4-CIPh)OCH₂

G9-678 3,5-(CF₃)₂Ph (2-BrPh)OCH₂

G9-679 3,5-(CF₃)₂Ph (3-BrPh)OCH₂

G9-680 3,5-(CF₃)₂Ph (4-BrPh)OCH₂

G9-681 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂

G9-682 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂

G9-683 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂

G9-684 3,5-(CF₃)₂Ph (2-CNPh)OCH₂

G9-685 3,5-(CF₃)₂Ph (3-CNPh)OCH₂

G9-686 3,5-(CF₃)₂Ph (4-CNPh)OCH₂

G9-687 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂

G9-688 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G9-689 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G9-690 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G9-691 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G9-692 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G9-693 3,5-(CF₃)₂Ph PhCH₂OCH₂

G9-694 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G9-695 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G9-696 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G9-697 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G9-698 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G9-699 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G9-700 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G9-701 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G9-702 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G9-703 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G9-704 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G9-705 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G9-706 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G9-707 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G9-708 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G9-709 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G9-710 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G9-711 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G9-712 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G9-713 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G9-714 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G9-715 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G9-716 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G9-717 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G9-718 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G9-719 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G9-720 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂ G9-721 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G9-722 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G9-723 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G9-724 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G9-725 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G9-726 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G9-727 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G9-728 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G9-729 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G9-730 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G9-731 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G9-732 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G9-733 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G9-734 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G9-735 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G9-736 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G9-737 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G9-738 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G9-739 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G9-740 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G9-741 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G9-742 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G9-743 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G9-744 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G9-745 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G9-746 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G9-747 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G9-748 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G9-749 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G9-750 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G9-751 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G9-752 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G9-753 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G9-754 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G9-755 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G9-756 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G9-757 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0303] Table 9a

G13-184 CF₃ (2-FPh)CH₂OCH₂

G13-185 CF₃ (3-FPh)CH₂OCH₂

G13-186 CF₃ (4-FPh)CH₂OCH₂

G13-187 CF₃ (2-CIPh)CH₂OCH₂

G13-188 CF₃ (3-CIPh)CH₂OCH₂

G13-189 CF₃ (4-CIPh)CH₂OCH₂

G13-190 CF₃ (2-BrPh)CH₂OCH₂

G13-191 CF₃ (3-BrPh)CH₂OCH₂

G13-192 CF₃ (4-BrPh)CH₂OCH₂

G13-193 CF₃ (2-CF₃OPh)CH₂OCH₂

G13-194 CF₃ (3-CF₃OPh)CH₂OCH₂

G13-195 CF₃ (4-CF₃OPh)CH₂OCH₂

G13-196 CF₃ (2-CNPh)CH₂OCH₂

G13-197 CF₃ (3-CNPh)CH₂OCH₂

G13-198 CF₃ (4-CNPh)CH₂OCH₂

G13-199 CF₃ (2-N0₂Ph)CH₂OCH₂

G 13-200 CF₃ (3-N0₂Ph)CH₂OCH₂

G13-201 CF₃ (4-N0₂Ph)CH₂OCH₂

G 13-202 CF₃ (2-CF₃Ph)CH₂OCH₂

G 13-203 CF₃ (3-CF₃Ph)CH₂OCH₂

G 13-204 CF₃ (4-CF₃Ph)CH₂OCH₂

G 13-205 CF₃ CH₃C(=0)OCH₂

G 13-206 CF₃ CH₃CH₂C(=0)OCH₂

G 13-207 CF₃ CH(CH₃)₂C(=0)OCH₂

G 13-208 CF₃ (CH₃)₃C(=0)OCH₂

G 13-209 CF₃ (CH₃)₃CCH₂(=0)OCH₂

G13-210 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂

G13-211 CF₃ CF₃C(=0)OCH₂

G13-212 CF₃ CF₃CF₂C(=0)OCH₂

G13-213 CF₃ (c-hex)C(=0)OCH₂

G13-214 CF₃ PhC(=0)OCH₂

G13-215 CF₃ (2-CH₃Ph)C(=0)OCH₂

G13-216 CF₃ (3-CH₃Ph)C(=0)OCH₂

G13-217 CF₃ (4-CH₃Ph)C(=0)OCH₂

G13-218 CF₃ (2-CH₃OPh)C(=0)OCH₂

G13-219 CF₃ (3-CH₃OPh)C(=0)OCH₂

G 13-220 CF₃ (4-CH₃OPh)C(=0)OCH₂

G 13-221 CF₃ (2-FPh)C(=0)OCH₂

G 13-222 CF₃ (3-FPh)C(=0)OCH₂

G 13-223 CF₃ (4-FPh)C(=0)OCH₂

G 13-224 CF₃ (2-CIPh)C(=0)OCH₂

G 13-225 CF₃ (3-CIPh)C(=0)OCH₂

G 13-226 CF₃ (4-CIPh)C(=0)OCH₂

G 13-227 CF₃ (2-BrPh)C(=0)OCH₂

G 13-228 CF₃ (3-BrPh)C(=0)OCH₂

G 13-229 CF₃ (4-BrPh)C(=0)OCH₂

G 13-230 CF₃ (2-CF₃OPh)C(=0)OCH₂

G13-231 CF₃ (3-CF₃OPh)C(=0)OCH₂

G 13-274 2-CF₃Ph (CH₃)₃COCH₂

G 13-275 2-CF₃Ph (CH₃)₃CCH₂0CH₂

G 13-276 2-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂

G 13-277 2-CF₃Ph (c-hex)OCH₂

G 13-278 2-CF₃Ph PhOCH₂

G 13-279 2-CF₃Ph (2-CH₃Ph)OCH₂

G 13-280 2-CF₃Ph (3-CH₃Ph)OCH₂

G13-281 2-CF₃Ph (4-CH₃Ph)OCH₂

G 13-282 2-CF₃Ph (2-CH₃OPh)OCH₂

G 13-283 2-CF₃Ph (3-CH₃OPh)OCH₂

G 13-284 2-CF₃Ph (4-CH₃OPh)OCH₂

G 13-285 2-CF₃Ph (2-FPh)OCH₂

G 13-286 2-CF₃Ph (3-FPh)OCH₂

G 13-287 2-CF₃Ph (4-FPh)OCH₂

G 13-288 2-CF₃Ph (2-CIPh)OCH₂

G 13-289 2-CF₃Ph (3-CIPh)OCH₂

G 13-290 2-CF₃Ph (4-CIPh)OCH₂

G13-291 2-CF₃Ph (2-BrPh)OCH₂

G 13-292 2-CF₃Ph (3-BrPh)OCH₂

G 13-293 2-CF₃Ph (4-BrPh)OCH₂

G 13-294 2-CF₃Ph (2-CF₃OPh)OCH₂

G 13-295 2-CF₃Ph (3-CF₃OPh)OCH₂

G 13-296 2-CF₃Ph (4-CF₃OPh)OCH₂

G 13-297 2-CF₃Ph (2-CNPh)OCH₂

G 13-298 2-CF₃Ph (3-CNPh)OCH₂

G 13-299 2-CF₃Ph (4-CNPh)OCH₂

G13-300 2-CF₃Ph (2-N0₂Ph)OCH₂

G13-301 2-CF₃Ph (3-N0₂Ph)OCH₂

G 13-302 2-CF₃Ph (4-N0₂Ph)OCH₂

G13-303 2-CF₃Ph (2-CF₃Ph)OCH₂

G 13-304 2-CF₃Ph (3-CF₃Ph)OCH₂

G13-305 2-CF₃Ph (4-CF₃Ph)OCH₂

G 13-306 2-CF₃Ph PhCH₂OCH₂

G13-307 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G13-308 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G13-309 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G13-310 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G13-311 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G13-312 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G13-313 2-CF₃Ph (2-FPh)CH₂OCH₂

G13-314 2-CF₃Ph (3-FPh)CH₂OCH₂

G13-315 2-CF₃Ph (4-FPh)CH₂OCH₂

G13-316 2-CF₃Ph (2-CIPh)CH₂OCH₂

G13-317 2-CF₃Ph (3-CIPh)CH₂OCH₂

G13-318 2-CF₃Ph (4-CIPh)CH₂OCH₂

G13-319 2-CF₃Ph (2-BrPh)CH₂OCH₂

G 13-320 2-CF₃Ph (3-BrPh)CH₂OCH₂

G13-321 2-CF₃Ph (4-BrPh)CH₂OCH₂ G 13-322 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 13-323 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 13-324 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 13-325 2-CF₃Ph (2-CNPh)CH₂OCH₂

G 13-326 2-CF₃Ph (3-CNPh)CH₂OCH₂

G 13-327 2-CF₃Ph (4-CNPh)CH₂OCH₂

G 13-328 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 13-329 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G13-330 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G13-331 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G 13-332 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G13-333 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G 13-334 2-CF₃Ph CH₃C(=0)OCH₂

G13-335 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G 13-336 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G13-337 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G13-338 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G13-339 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 13-340 2-CF₃Ph CF₃C(=0)OCH₂

G13-341 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G 13-342 2-CF₃Ph (c-hex)C(=0)OCH₂

G 13-343 2-CF₃Ph PhC(=0)OCH₂

G 13-344 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 13-345 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 13-346 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 13-347 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 13-348 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G 13-349 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G13-350 2-CF₃Ph (2-FPh)C(=0)OCH₂

G13-351 2-CF₃Ph (3-FPh)C(=0)OCH₂

G 13-352 2-CF₃Ph (4-FPh)C(=0)OCH₂

G13-353 2-CF₃Ph (2-CIPh)C(=0)OCH₂

G 13-354 2-CF₃Ph (3-CIPh)C(=0)OCH₂

G13-355 2-CF₃Ph (4-CIPh)C(=0)OCH₂

G 13-356 2-CF₃Ph (2-BrPh)C(=0)OCH₂

G13-357 2-CF₃Ph (3-BrPh)C(=0)OCH₂

G13-358 2-CF₃Ph (4-BrPh)C(=0)OCH₂

G13-359 2-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G 13-360 2-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G13-361 2-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G 13-362 2-CF₃Ph (2-CNPh)C(=0)OCH₂

G 13-363 2-CF₃Ph (3-CNPh)C(=0)OCH₂

G 13-364 2-CF₃Ph (4-CNPh)C(=0)OCH₂

G 13-365 2-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G 13-366 2-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G 13-367 2-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G 13-368 2-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G 13-369 2-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G13-412 3-CF₃Ph (3-CH₃OPh)OCH₂

G13-413 3-CF₃Ph (4-CH₃OPh)OCH₂

G13-414 3-CF₃Ph (2-FPh)OCH₂

G13-415 3-CF₃Ph (3-FPh)OCH₂

G13-416 3-CF₃Ph (4-FPh)OCH₂

G13-417 3-CF₃Ph (2-CIPh)OCH₂

G13-418 3-CF₃Ph (3-CIPh)OCH₂

G13-419 3-CF₃Ph (4-CIPh)OCH₂

G 13-420 3-CF₃Ph (2-BrPh)OCH₂

G 13-421 3-CF₃Ph (3-BrPh)OCH₂

G 13-422 3-CF₃Ph (4-BrPh)OCH₂

G 13-423 3-CF₃Ph (2-CF₃OPh)OCH₂

G 13-424 3-CF₃Ph (3-CF₃OPh)OCH₂

G 13-425 3-CF₃Ph (4-CF₃OPh)OCH₂

G 13-426 3-CF₃Ph (2-CNPh)OCH₂

G 13-427 3-CF₃Ph (3-CNPh)OCH₂

G 13-428 3-CF₃Ph (4-CNPh)OCH₂

G 13-429 3-CF₃Ph (2-N0₂Ph)OCH₂

G 13-430 3-CF₃Ph (3-N0₂Ph)OCH₂

G13-431 3-CF₃Ph (4-N0₂Ph)OCH₂

G 13-432 3-CF₃Ph (2-CF₃Ph)OCH₂

G 13-433 3-CF₃Ph (3-CF₃Ph)OCH₂

G 13-434 3-CF₃Ph (4-CF₃Ph)OCH₂

G 13-435 3-CF₃Ph PhCH₂OCH₂

G 13-436 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 13-437 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G 13-438 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G 13-439 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 13-440 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G 13-441 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 13-442 3-CF₃Ph (2-FPh)CH₂OCH₂

G 13-443 3-CF₃Ph (3-FPh)CH₂OCH₂

G 13-444 3-CF₃Ph (4-FPh)CH₂OCH₂

G 13-445 3-CF₃Ph (2-CIPh)CH₂OCH₂

G 13-446 3-CF₃Ph (3-CIPh)CH₂OCH₂

G 13-447 3-CF₃Ph (4-CIPh)CH₂OCH₂

G 13-448 3-CF₃Ph (2-BrPh)CH₂OCH₂

G 13-449 3-CF₃Ph (3-BrPh)CH₂OCH₂

G 13-450 3-CF₃Ph (4-BrPh)CH₂OCH₂

G13-451 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 13-452 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 13-453 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 13-454 3-CF₃Ph (2-CNPh)CH₂OCH₂

G 13-455 3-CF₃Ph (3-CNPh)CH₂OCH₂

G 13-456 3-CF₃Ph (4-CNPh)CH₂OCH₂

G 13-457 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 13-458 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G 13-459 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G13-550 4-CF₃Ph (3-BrPh)OCH₂

G13-551 4-CF₃Ph (4-BrPh)OCH₂

G 13-552 4-CF₃Ph (2-CF₃OPh)OCH₂

G13-553 4-CF₃Ph (3-CF₃OPh)OCH₂

G 13-554 4-CF₃Ph (4-CF₃OPh)OCH₂

G13-555 4-CF₃Ph (2-CNPh)OCH₂

G 13-556 4-CF₃Ph (3-CNPh)OCH₂

G13-557 4-CF₃Ph (4-CNPh)OCH₂

G13-558 4-CF₃Ph (2-N0₂Ph)OCH₂

G13-559 4-CF₃Ph (3-N0₂Ph)OCH₂

G 13-560 4-CF₃Ph (4-N0₂Ph)OCH₂

G13-561 4-CF₃Ph (2-CF₃Ph)OCH₂

G 13-562 4-CF₃Ph (3-CF₃Ph)OCH₂

G 13-563 4-CF₃Ph (4-CF₃Ph)OCH₂

G 13-564 4-CF₃Ph PhCH₂OCH₂

G 13-565 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 13-566 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G 13-567 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G 13-568 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 13-569 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G13-570 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G13-571 4-CF₃Ph (2-FPh)CH₂OCH₂

G 13-572 4-CF₃Ph (3-FPh)CH₂OCH₂

G13-573 4-CF₃Ph (4-FPh)CH₂OCH₂

G 13-574 4-CF₃Ph (2-CIPh)CH₂OCH₂

G13-575 4-CF₃Ph (3-CIPh)CH₂OCH₂

G 13-576 4-CF₃Ph (4-CIPh)CH₂OCH₂

G13-577 4-CF₃Ph (2-BrPh)CH₂OCH₂

G13-578 4-CF₃Ph (3-BrPh)CH₂OCH₂

G13-579 4-CF₃Ph (4-BrPh)CH₂OCH₂

G13-580 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G13-581 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 13-582 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G13-583 4-CF₃Ph (2-CNPh)CH₂OCH₂

G 13-584 4-CF₃Ph (3-CNPh)CH₂OCH₂

G13-585 4-CF₃Ph (4-CNPh)CH₂OCH₂

G 13-586 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G13-587 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G13-588 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G13-589 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G13-590 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G13-591 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G 13-592 4-CF₃Ph CH₃C(=0)OCH₂

G13-593 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G 13-594 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G13-595 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G 13-596 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G13-597 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂ G13-598 4-CF₃Ph CF₃C(=0)OCH₂

G13-599 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G 13-600 4-CF₃Ph (c-hex)C(=0)OCH₂

G13-601 4-CF₃Ph PhC(=0)OCH₂

G 13-602 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 13-603 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 13-604 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 13-605 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 13-606 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G 13-607 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G 13-608 4-CF₃Ph (2-FPh)C(=0)OCH₂

G 13-609 4-CF₃Ph (3-FPh)C(=0)OCH₂

G13-610 4-CF₃Ph (4-FPh)C(=0)OCH₂

G13-611 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G13-612 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G13-613 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G13-614 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G13-615 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G13-616 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G13-617 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G13-618 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G13-619 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G 13-620 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G 13-621 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G 13-622 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G 13-623 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G 13-624 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G 13-625 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G 13-626 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G 13-627 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G 13-628 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂

G 13-629 3,5-(CF₃)₂Ph CH₃

G 13-630 3,5-(CF₃)₂Ph CH3CH2

G13-631 3,5-(CF₃)₂Ph CH3CH2CH2

G 13-632 3,5-(CF₃)₂Ph (CH₃)₂CH

G 13-633 3,5-(CF₃)₂Ph CH₃C(=0)

G 13-634 3,5-(CF₃)₂Ph CH₃CH₂C(=0)

G 13-635 3,5-(CF₃)₂Ph (CH₃)₂CHC(=0)

G 13-636 3,5-(CF₃)₂Ph (CH₃)₃CC(=0)

G 13-637 3,5-(CF₃)₂Ph (CH₃)₃CCH₂C(=0)

G 13-638 3,5-(CF₃)₂Ph CH₃CH₂CH(CH₃)C(=0)

G 13-639 3,5-(CF₃)₂Ph (CH₃)₂CHCH₂C(=0)

G 13-640 3,5-(CF₃)₂Ph (CH₃)₃CCH₂CH₂C(=0)

G 13-641 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)

G 13-642 3,5-(CF₃)₂Ph (c-hex)C(=0)

G 13-643 3,5-(CF₃)₂Ph (c-pen)C(=0)

G 13-644 3,5-(CF₃)₂Ph (c-hep)C(=0)

G 13-645 3,5-(CF₃)₂Ph (c-pro)C(=0)

G 13-688 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G 13-689 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G 13-690 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G13-691 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G 13-692 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G 13-693 3,5-(CF₃)₂Ph PhCH₂OCH₂

G 13-694 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G 13-695 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G 13-696 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G 13-697 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G 13-698 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G 13-699 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G13-700 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G13-701 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G 13-702 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G13-703 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G 13-704 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G13-705 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G 13-706 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G13-707 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G13-708 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G13-709 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G13-710 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G13-711 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G13-712 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G13-713 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G13-714 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G13-715 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G13-716 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G13-717 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G13-718 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G13-719 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G 13-720 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G13-721 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G 13-722 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G 13-723 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G 13-724 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G 13-725 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G 13-726 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 13-727 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G 13-728 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G 13-729 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G13-730 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G13-731 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G 13-732 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G13-733 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G 13-734 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G13-735 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂ G 13-736 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G13-737 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G13-738 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G13-739 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G 13-740 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G13-741 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G 13-742 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G 13-743 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G 13-744 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G 13-745 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G 13-746 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G 13-747 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G 13-748 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G 13-749 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G13-750 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G13-751 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G 13-752 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G13-753 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G 13-754 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G13-755 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G 13-756 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G13-757 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0304] Table 9b

G14-61 4-CIPh H CH₃

G 14-62 2-CF₃Ph H CH₃

G 14-63 3-CF₃Ph H CH₃

G 14-64 4-CF₃Ph H CH₃

G 14-65 2-CF₃CF₂Ph H CH₃

G 14-66 3-CF₃CF₂Ph H CH₃

G 14-67 4-CF₃CF₂Ph H CH₃

G 14-68 2-CF₃OPh H CH₃

G 14-69 3-CF₃OPh H CH₃

G14-70 4-CF₃OPh H CH₃

G14-71 2-CF₃CH₂OPh H CH₃

G 14-72 3-CF₃CH₂OPh H CH₃

G14-73 4-CF₃CH₂OPh H CH₃

G 14-74 2-CF₃-3-F-Ph H CH₃

G14-75 2-CF₃-4-F-Ph H CH₃

G 14-76 2-CF₃-5-F-Ph H CH₃

G14-77 2-CF₃-6-F-Ph H CH₃

G14-78 2-CF₃-3-CI-Ph H CH₃

G14-79 2-CF₃-4-CI-Ph H CH₃

G14-80 2-CF₃-5-CI-Ph H CH₃

G14-81 2-CF₃-6-CI-Ph H CH₃

G 14-82 2-CF₃-3-CH₃-Ph H CH₃

G14-83 2-CF₃-4-CH₃-Ph H CH₃

G 14-84 2-CF₃-5-CH₃-Ph H CH₃

G14-85 2-CF₃-6-CH₃-Ph H CH₃

G 14-86 2,3-(CF₃)₂Ph H CH₃

G14-87 2,4-(CF₃)₂Ph H CH₃

G14-88 2,6-(CF₃)₂Ph H CH₃

G14-89 3,5-(CF₃)₂Ph H CH₃

G14-90 2-CF₃-3-CN-Ph H CH₃

G14-91 2-CF₃-4-CNPh H CH₃

G 14-92 2-CF₃-5-CN-Ph H CH₃

G14-93 2-CF₃-6-CN-Ph H CH₃

G 14-94 2-Pyridyl H CH₃

G14-95 3-Pyridyl H CH₃

G 14-96 4-Pyridyl H CH₃

G14-97 CF₃ H Ph

G14-98 CF₃ H 2-F-Ph

G14-99 CF₃ H 3-F-Ph

G14-100 CF₃ H 4-F-Ph

G14-101 CF₃ H 2-CI-Ph

G14-102 CF₃ H 3-CI-Ph

G14-103 CF₃ H 4-CI-Ph

G14-104 CF₃ H 2-CF₃-Ph

G14-105 CF₃ H 3-CF₃-Ph

G14-106 CF₃ H 4-CF₃-Ph

G14-107 CF₃ H 2-CF₃Q-Ph

G14-150 CF₃ (2-CH₃OPh)OCH₂ 2-CI-Ph

G14-151 CF₃ (3-CH₃OPh)OCH₂ 2-CI-Ph

G14-152 CF₃ (4-CH₃OPh)OCH₂ 2-CI-Ph

G14-153 CF₃ (2-FPh)OCH₂ 2-CI-Ph

G14-154 CF₃ (3-FPh)OCH₂ 2-CI-Ph

G14-155 CF₃ (4-FPh)OCH₂ 2-CI-Ph

G14-156 CF₃ (2-CIPh)OCH₂ 2-CI-Ph

G14-157 CF₃ (3-CIPh)OCH₂ 2-CI-Ph

G14-158 CF₃ (4-CIPh)OCH₂ 2-CI-Ph

G14-159 CF₃ (2-BrPh)OCH₂ 2-CI-Ph

G14-160 CF₃ (3-BrPh)OCH₂ 2-CI-Ph

G14-161 CF₃ (4-BrPh)OCH₂ 2-CI-Ph

G14-162 CF₃ (2-CF₃OPh)OCH₂ 2-CI-Ph

G14-163 CF₃ (3-CF₃OPh)OCH₂ 2-CI-Ph

G14-164 CF₃ (4-CF₃OPh)OCH₂ 2-CI-Ph

G14-165 CF₃ (2-CNPh)OCH₂ 2-CI-Ph

G14-166 CF₃ (3-CNPh)OCH₂ 2-CI-Ph

G14-167 CF₃ (4-CNPh)OCH₂ 2-CI-Ph

G14-168 CF₃ (2-N0₂Ph)OCH₂ 2-CI-Ph

G14-169 CF₃ (3-N0₂Ph)OCH₂ 2-CI-Ph

G14-170 CF₃ (4-N0₂Ph)OCH₂ 2-CI-Ph

G14-171 CF₃ (2-CF₃Ph)OCH₂ 2-CI-Ph

G14-172 CF₃ (3-CF₃Ph)OCH₂ 2-CI-Ph

G14-173 CF₃ (4-CF₃Ph)OCH₂ 2-CI-Ph

G14-174 CF₃ PhCH₂OCH₂ 2-CI-Ph

G14-175 CF₃ (2-CH₃Ph)CH₂OCH₂ 2-CI-Ph

G14-176 CF₃ (3-CH₃Ph)CH₂OCH₂ 2-CI-Ph

G14-177 CF₃ (4-CH₃Ph)CH₂OCH₂ 2-CI-Ph

G14-178 CF₃ (2-CH₃OPh)CH₂OCH₂ 2-CI-Ph

G14-179 CF₃ (3-CH₃OPh)CH₂OCH₂ 2-CI-Ph

G14-180 CF₃ (4-CH₃OPh)CH₂OCH₂ 2-CI-Ph

G14-181 CF₃ (2-FPh)CH₂OCH₂ 2-CI-Ph

G14-182 CF₃ (3-FPh)CH₂OCH₂ 2-CI-Ph

G14-183 CF₃ (4-FPh)CH₂OCH₂ 2-CI-Ph

G14-184 CF₃ (2-CIPh)CH₂OCH₂ 2-CI-Ph

G14-185 CF₃ (3-CIPh)CH₂OCH₂ 2-CI-Ph

G14-186 CF₃ (4-CIPh)CH₂OCH₂ 2-CI-Ph

G14-187 CF₃ (2-BrPh)CH₂OCH₂ 2-CI-Ph

G14-188 CF₃ (3-BrPh)CH₂OCH₂ 2-CI-Ph

G14-189 CF₃ (4-BrPh)CH₂OCH₂ 2-CI-Ph

G14-190 CF₃ (2-CF₃OPh)CH₂OCH₂ 2-CI-Ph

G14-191 CF₃ (3-CF₃OPh)CH₂OCH₂ 2-CI-Ph

G14-192 CF₃ (4-CF₃OPh)CH₂OCH₂ 2-CI-Ph

G14-193 CF₃ (2-CNPh)CH₂OCH₂ 2-CI-Ph

G14-194 CF₃ (3-CNPh)CH₂OCH₂ 2-CI-Ph

G14-195 CF₃ (4-CNPh)CH₂OCH₂ 2-CI-Ph

G14-196 CF₃ (2-N0₂Ph)CH₂OCH₂ 2-CI-Ph

G14-197 CF₃ (3-N0₂Ph)CH₂OCH₂ 2-CI-Ph G14-198 CF₃ (4-N0₂Ph)CH₂OCH₂ 2-CI-Ph

G14-199 CF₃ (2-CF₃Ph)CH₂OCH₂ 2-CI-Ph

G 14-200 CF₃ (3-CF₃Ph)CH₂OCH₂ 2-CI-Ph

G14-201 CF₃ (4-CF₃Ph)CH₂OCH₂ 2-CI-Ph

G 14-202 CF₃ CH₃C(=0)OCH₂ 2-CI-Ph

G 14-203 CF₃ CH₃CH₂C(=0)OCH₂ 2-CI-Ph

G 14-204 CF₃ CH(CH₃)₂C(=0)OCH₂ 2-CI-Ph

G 14-205 CF₃ (CH₃)₃C(=0)OCH₂ 2-CI-Ph

G 14-206 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 2-CI-Ph

G 14-207 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 2-CI-Ph

G 14-208 CF₃ CF₃C(=0)OCH₂ 2-CI-Ph

G 14-209 CF₃ CF₃CF₂C(=0)OCH₂ 2-CI-Ph

G14-210 CF₃ (c-hex)C(=0)OCH₂ 2-CI-Ph

G14-211 CF₃ PhC(=0)OCH₂ 2-CI-Ph

G14-212 CF₃ (2-CH₃Ph)C(=0)OCH₂ 2-CI-Ph

G14-213 CF₃ (3-CH₃Ph)C(=0)OCH₂ 2-CI-Ph

G14-214 CF₃ (4-CH₃Ph)C(=0)OCH₂ 2-CI-Ph

G14-215 CF₃ (2-CH₃OPh)C(=0)OCH₂ 2-CI-Ph

G14-216 CF₃ (3-CH₃OPh)C(=0)OCH₂ 2-CI-Ph

G14-217 CF₃ (4-CH₃OPh)C(=0)OCH₂ 2-CI-Ph

G14-218 CF₃ (2-FPh)C(=0)OCH₂ 2-CI-Ph

G14-219 CF₃ (3-FPh)C(=0)OCH₂ 2-CI-Ph

G 14-220 CF₃ (4-FPh)C(=0)OCH₂ 2-CI-Ph

G 14-221 CF₃ (2-CIPh)C(=0)OCH₂ 2-CI-Ph

G 14-222 CF₃ (3-CIPh)C(=0)OCH₂ 2-CI-Ph

G 14-223 CF₃ (4-CIPh)C(=0)OCH₂ 2-CI-Ph

G 14-224 CF₃ (2-BrPh)C(=0)OCH₂ 2-CI-Ph

G 14-225 CF₃ (3-BrPh)C(=0)OCH₂ 2-CI-Ph

G 14-226 CF₃ (4-BrPh)C(=0)OCH₂ 2-CI-Ph

G 14-227 CF₃ (2-CF₃OPh)C(=0)OCH₂ 2-CI-Ph

G 14-228 CF₃ (3-CF₃OPh)C(=0)OCH₂ 2-CI-Ph

G 14-229 CF₃ (4-CF₃OPh)C(=0)OCH₂ 2-CI-Ph

G 14-230 CF₃ (2-CNPh)C(=0)OCH₂ 2-CI-Ph

G14-231 CF₃ (3-CNPh)C(=0)OCH₂ 2-CI-Ph

G 14-232 CF₃ (4-CNPh)C(=0)OCH₂ 2-CI-Ph

G 14-233 CF₃ (2-N0₂Ph)C(=0)OCH₂ 2-CI-Ph

G 14-234 CF₃ (3-N0₂Ph)C(=0)OCH₂ 2-CI-Ph

G 14-235 CF₃ (4-N0₂Ph)C(=0)OCH₂ 2-CI-Ph

G 14-236 CF₃ (2-CF₃Ph)C(=0)OCH₂ 2-CI-Ph

G 14-237 CF₃ (3-CF₃Ph)C(=0)OCH₂ 2-CI-Ph

G 14-238 CF₃ (4-CF₃Ph)C(=0)OCH₂ 2-CI-Ph

G 14-239 CF₃ CH₃ 3-CI-Ph

G 14-240 CF₃ CH3CH2 3-CI-Ph

G 14-241 CF₃ CH3CH2CH2 3-CI-Ph

G 14-242 CF₃ (CH₃)₂CH 3-CI-Ph

G 14-243 CF₃ CH₃C(=0) 3-CI-Ph

G 14-244 CF₃ CH₃CH₂C(=0) 3-CI-Ph

G 14-245 CF₃ (CH₃)₂CHC(=0) 3-CI-Ph

G 14-288 CF₃ (2-BrPh)OCH₂ 3-CI-Ph

G 14-289 CF₃ (3-BrPh)OCH₂ 3-CI-Ph

G 14-290 CF₃ (4-BrPh)OCH₂ 3-CI-Ph

G14-291 CF₃ (2-CF₃OPh)OCH₂ 3-CI-Ph

G 14-292 CF₃ (3-CF₃OPh)OCH₂ 3-CI-Ph

G 14-293 CF₃ (4-CF₃OPh)OCH₂ 3-CI-Ph

G 14-294 CF₃ (2-CNPh)OCH₂ 3-CI-Ph

G 14-295 CF₃ (3-CNPh)OCH₂ 3-CI-Ph

G 14-296 CF₃ (4-CNPh)OCH₂ 3-CI-Ph

G 14-297 CF₃ (2-N0₂Ph)OCH₂ 3-CI-Ph

G 14-298 CF₃ (3-N0₂Ph)OCH₂ 3-CI-Ph

G 14-299 CF₃ (4-N0₂Ph)OCH₂ 3-CI-Ph

G14-300 CF₃ (2-CF₃Ph)OCH₂ 3-CI-Ph

G14-301 CF₃ (3-CF₃Ph)OCH₂ 3-CI-Ph

G 14-302 CF₃ (4-CF₃Ph)OCH₂ 3-CI-Ph

G14-303 CF₃ PhCH₂OCH₂ 3-CI-Ph

G 14-304 CF₃ (2-CH₃Ph)CH₂OCH₂ 3-CI-Ph

G14-305 CF₃ (3-CH₃Ph)CH₂OCH₂ 3-CI-Ph

G 14-306 CF₃ (4-CH₃Ph)CH₂OCH₂ 3-CI-Ph

G14-307 CF₃ (2-CH₃OPh)CH₂OCH₂ 3-CI-Ph

G14-308 CF₃ (3-CH₃OPh)CH₂OCH₂ 3-CI-Ph

G14-309 CF₃ (4-CH₃OPh)CH₂OCH₂ 3-CI-Ph

G14-310 CF₃ (2-FPh)CH₂OCH₂ 3-CI-Ph

G14-311 CF₃ (3-FPh)CH₂OCH₂ 3-CI-Ph

G14-312 CF₃ (4-FPh)CH₂OCH₂ 3-CI-Ph

G14-313 CF₃ (2-CIPh)CH₂OCH₂ 3-CI-Ph

G14-314 CF₃ (3-CIPh)CH₂OCH₂ 3-CI-Ph

G14-315 CF₃ (4-CIPh)CH₂OCH₂ 3-CI-Ph

G14-316 CF₃ (2-BrPh)CH₂OCH₂ 3-CI-Ph

G14-317 CF₃ (3-BrPh)CH₂OCH₂ 3-CI-Ph

G14-318 CF₃ (4-BrPh)CH₂OCH₂ 3-CI-Ph

G14-319 CF₃ (2-CF₃OPh)CH₂OCH₂ 3-CI-Ph

G 14-320 CF₃ (3-CF₃OPh)CH₂OCH₂ 3-CI-Ph

G14-321 CF₃ (4-CF₃OPh)CH₂OCH₂ 3-CI-Ph

G 14-322 CF₃ (2-CNPh)CH₂OCH₂ 3-CI-Ph

G 14-323 CF₃ (3-CNPh)CH₂OCH₂ 3-CI-Ph

G 14-324 CF₃ (4-CNPh)CH₂OCH₂ 3-CI-Ph

G 14-325 CF₃ (2-N0₂Ph)CH₂OCH₂ 3-CI-Ph

G 14-326 CF₃ (3-N0₂Ph)CH₂OCH₂ 3-CI-Ph

G 14-327 CF₃ (4-N0₂Ph)CH₂OCH₂ 3-CI-Ph

G 14-328 CF₃ (2-CF₃Ph)CH₂OCH₂ 3-CI-Ph

G 14-329 CF₃ (3-CF₃Ph)CH₂OCH₂ 3-CI-Ph

G14-330 CF₃ (4-CF₃Ph)CH₂OCH₂ 3-CI-Ph

G14-331 CF₃ CH₃C(=0)OCH₂ 3-CI-Ph

G 14-332 CF₃ CH₃CH₂C(=0)OCH₂ 3-CI-Ph

G14-333 CF₃ CH(CH₃)₂C(=0)OCH₂ 3-CI-Ph

G 14-334 CF₃ (CH₃)₃C(=0)OCH₂ 3-CI-Ph

G14-335 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 3-CI-Ph G 14-336 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 3-CI-Ph

G14-337 CF₃ CF₃C(=0)OCH₂ 3-CI-Ph

G14-338 CF₃ CF₃CF₂C(=0)OCH₂ 3-CI-Ph

G14-339 CF₃ (c-hex)C(=0)OCH₂ 3-CI-Ph

G 14-340 CF₃ PhC(=0)OCH₂ 3-CI-Ph

G14-341 CF₃ (2-CH₃Ph)C(=0)OCH₂ 3-CI-Ph

G 14-342 CF₃ (3-CH₃Ph)C(=0)OCH₂ 3-CI-Ph

G 14-343 CF₃ (4-CH₃Ph)C(=0)OCH₂ 3-CI-Ph

G 14-344 CF₃ (2-CH₃OPh)C(=0)OCH₂ 3-CI-Ph

G 14-345 CF₃ (3-CH₃OPh)C(=0)OCH₂ 3-CI-Ph

G 14-346 CF₃ (4-CH₃OPh)C(=0)OCH₂ 3-CI-Ph

G 14-347 CF₃ (2-FPh)C(=0)OCH₂ 3-CI-Ph

G 14-348 CF₃ (3-FPh)C(=0)OCH₂ 3-CI-Ph

G 14-349 CF₃ (4-FPh)C(=0)OCH₂ 3-CI-Ph

G14-350 CF₃ (2-CIPh)C(=0)OCH₂ 3-CI-Ph

G14-351 CF₃ (3-CIPh)C(=0)OCH₂ 3-CI-Ph

G 14-352 CF₃ (4-CIPh)C(=0)OCH₂ 3-CI-Ph

G14-353 CF₃ (2-BrPh)C(=0)OCH₂ 3-CI-Ph

G 14-354 CF₃ (3-BrPh)C(=0)OCH₂ 3-CI-Ph

G14-355 CF₃ (4-BrPh)C(=0)OCH₂ 3-CI-Ph

G 14-356 CF₃ (2-CF₃OPh)C(=0)OCH₂ 3-CI-Ph

G14-357 CF₃ (3-CF₃OPh)C(=0)OCH₂ 3-CI-Ph

G14-358 CF₃ (4-CF₃OPh)C(=0)OCH₂ 3-CI-Ph

G14-359 CF₃ (2-CNPh)C(=0)OCH₂ 3-CI-Ph

G 14-360 CF₃ (3-CNPh)C(=0)OCH₂ 3-CI-Ph

G14-361 CF₃ (4-CNPh)C(=0)OCH₂ 3-CI-Ph

G 14-362 CF₃ (2-N0₂Ph)C(=0)OCH₂ 3-CI-Ph

G 14-363 CF₃ (3-N0₂Ph)C(=0)OCH₂ 3-CI-Ph

G 14-364 CF₃ (4-N0₂Ph)C(=0)OCH₂ 3-CI-Ph

G 14-365 CF₃ (2-CF₃Ph)C(=0)OCH₂ 3-CI-Ph

G 14-366 CF₃ (3-CF₃Ph)C(=0)OCH₂ 3-CI-Ph

G 14-367 CF₃ (4-CF₃Ph)C(=0)OCH₂ 3-CI-Ph

G 14-368 CF₃ CH₃ 4-CI-Ph

G 14-369 CF₃ CH3CH2 4-CI-Ph

G14-370 CF₃ CH3CH2CH2 4-CI-Ph

G14-371 CF₃ (CH₃)₂CH 4-CI-Ph

G 14-372 CF₃ CH₃C(=0) 4-CI-Ph

G14-373 CF₃ CH₃CH₂C(=0) 4-CI-Ph

G 14-374 CF₃ (CH₃)₂CHC(=0) 4-CI-Ph

G14-375 CF₃ (CH₃)₃CC(=0) 4-CI-Ph

G 14-376 CF₃ (CH₃)₃CCH₂C(=0) 4-CI-Ph

G14-377 CF₃ CH₃CH₂CH(CH₃)C(=0) 4-CI-Ph

G14-378 CF₃ (CH₃)₂CHCH₂C(=0) 4-CI-Ph

G14-379 CF₃ (CH₃)₃CCH₂CH₂C(=0) 4-CI-Ph

G14-380 CF₃ CH₃CH₂C(CH₃)₂C(=0) 4-CI-Ph

G14-381 CF₃ (c-hex)C(=0) 4-CI-Ph

G 14-382 CF₃ (c-pen)C(=0) 4-CI-Ph

G14-383 CF₃ (c-hep)C(=Q) 4-CI-Ph

G 14-426 CF₃ (2-N0₂Ph)OCH₂ 4-CI-Ph

G 14-427 CF₃ (3-N0₂Ph)OCH₂ 4-CI-Ph

G 14-428 CF₃ (4-N0₂Ph)OCH₂ 4-CI-Ph

G 14-429 CF₃ (2-CF₃Ph)OCH₂ 4-CI-Ph

G 14-430 CF₃ (3-CF₃Ph)OCH₂ 4-CI-Ph

G14-431 CF₃ (4-CF₃Ph)OCH₂ 4-CI-Ph

G 14-432 CF₃ PhCH₂OCH₂ 4-CI-Ph

G 14-433 CF₃ (2-CH₃Ph)CH₂OCH₂ 4-CI-Ph

G 14-434 CF₃ (3-CH₃Ph)CH₂OCH₂ 4-CI-Ph

G 14-435 CF₃ (4-CH₃Ph)CH₂OCH₂ 4-CI-Ph

G 14-436 CF₃ (2-CH₃OPh)CH₂OCH₂ 4-CI-Ph

G 14-437 CF₃ (3-CH₃OPh)CH₂OCH₂ 4-CI-Ph

G 14-438 CF₃ (4-CH₃OPh)CH₂OCH₂ 4-CI-Ph

G 14-439 CF₃ (2-FPh)CH₂OCH₂ 4-CI-Ph

G 14-440 CF₃ (3-FPh)CH₂OCH₂ 4-CI-Ph

G 14-441 CF₃ (4-FPh)CH₂OCH₂ 4-CI-Ph

G 14-442 CF₃ (2-CIPh)CH₂OCH₂ 4-CI-Ph

G 14-443 CF₃ (3-CIPh)CH₂OCH₂ 4-CI-Ph

G 14-444 CF₃ (4-CIPh)CH₂OCH₂ 4-CI-Ph

G 14-445 CF₃ (2-BrPh)CH₂OCH₂ 4-CI-Ph

G 14-446 CF₃ (3-BrPh)CH₂OCH₂ 4-CI-Ph

G 14-447 CF₃ (4-BrPh)CH₂OCH₂ 4-CI-Ph

G 14-448 CF₃ (2-CF₃OPh)CH₂OCH₂ 4-CI-Ph

G 14-449 CF₃ (3-CF₃OPh)CH₂OCH₂ 4-CI-Ph

G 14-450 CF₃ (4-CF₃OPh)CH₂OCH₂ 4-CI-Ph

G14-451 CF₃ (2-CNPh)CH₂OCH₂ 4-CI-Ph

G 14-452 CF₃ (3-CNPh)CH₂OCH₂ 4-CI-Ph

G 14-453 CF₃ (4-CNPh)CH₂OCH₂ 4-CI-Ph

G 14-454 CF₃ (2-N0₂Ph)CH₂OCH₂ 4-CI-Ph

G 14-455 CF₃ (3-N0₂Ph)CH₂OCH₂ 4-CI-Ph

G 14-456 CF₃ (4-N0₂Ph)CH₂OCH₂ 4-CI-Ph

G 14-457 CF₃ (2-CF₃Ph)CH₂OCH₂ 4-CI-Ph

G 14-458 CF₃ (3-CF₃Ph)CH₂OCH₂ 4-CI-Ph

G 14-459 CF₃ (4-CF₃Ph)CH₂OCH₂ 4-CI-Ph

G 14-460 CF₃ CH₃C(=0)OCH₂ 4-CI-Ph

G 14-461 CF₃ CH₃CH₂C(=0)OCH₂ 4-CI-Ph

G 14-462 CF₃ CH(CH₃)₂C(=0)OCH₂ 4-CI-Ph

G 14-463 CF₃ (CH₃)₃C(=0)OCH₂ 4-CI-Ph

G 14-464 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 4-CI-Ph

G 14-465 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 4-CI-Ph

G 14-466 CF₃ CF₃C(=0)OCH₂ 4-CI-Ph

G 14-467 CF₃ CF₃CF₂C(=0)OCH₂ 4-CI-Ph

G 14-468 CF₃ (c-hex)C(=0)OCH₂ 4-CI-Ph

G 14-469 CF₃ PhC(=0)OCH₂ 4-CI-Ph

G 14-470 CF₃ (2-CH₃Ph)C(=0)OCH₂ 4-CI-Ph

G14-471 CF₃ (3-CH₃Ph)C(=0)OCH₂ 4-CI-Ph

G 14-472 CF₃ (4-CH₃Ph)C(=0)OCH₂ 4-CI-Ph

G 14-473 CF₃ (2-CH₃OPh)C(=0)OCH₂ 4-CI-Ph G 14-474 CF₃ (3-CH₃OPh)C(=0)OCH₂ 4-CI-Ph

G 14-475 CF₃ (4-CH₃OPh)C(=0)OCH₂ 4-CI-Ph

G 14-476 CF₃ (2-FPh)C(=0)OCH₂ 4-CI-Ph

G 14-477 CF₃ (3-FPh)C(=0)OCH₂ 4-CI-Ph

G 14-478 CF₃ (4-FPh)C(=0)OCH₂ 4-CI-Ph

G 14-479 CF₃ (2-CIPh)C(=0)OCH₂ 4-CI-Ph

G 14-480 CF₃ (3-CIPh)C(=0)OCH₂ 4-CI-Ph

G14-481 CF₃ (4-CIPh)C(=0)OCH₂ 4-CI-Ph

G 14-482 CF₃ (2-BrPh)C(=0)OCH₂ 4-CI-Ph

G 14-483 CF₃ (3-BrPh)C(=0)OCH₂ 4-CI-Ph

G 14-484 CF₃ (4-BrPh)C(=0)OCH₂ 4-CI-Ph

G 14-485 CF₃ (2-CF₃OPh)C(=0)OCH₂ 4-CI-Ph

G 14-486 CF₃ (3-CF₃OPh)C(=0)OCH₂ 4-CI-Ph

G 14-487 CF₃ (4-CF₃OPh)C(=0)OCH₂ 4-CI-Ph

G 14-488 CF₃ (2-CNPh)C(=0)OCH₂ 4-CI-Ph

G 14-489 CF₃ (3-CNPh)C(=0)OCH₂ 4-CI-Ph

G 14-490 CF₃ (4-CNPh)C(=0)OCH₂ 4-CI-Ph

G14-491 CF₃ (2-N0₂Ph)C(=0)OCH₂ 4-CI-Ph

G 14-492 CF₃ (3-N0₂Ph)C(=0)OCH₂ 4-CI-Ph

G 14-493 CF₃ (4-N0₂Ph)C(=0)OCH₂ 4-CI-Ph

G 14-494 CF₃ (2-CF₃Ph)C(=0)OCH₂ 4-CI-Ph

G 14-495 CF₃ (3-CF₃Ph)C(=0)OCH₂ 4-CI-Ph

G 14-496 CF₃ (4-CF₃Ph)C(=0)OCH₂ 4-CI-Ph

G 14-497 CF₃ CH₃ 2-CF₃-Ph

G 14-498 CF₃ CH3CH2 2-CF₃-Ph

G 14-499 CF₃ CH3CH2CH2 2-CF₃-Ph

G14-500 CF₃ (CH₃)₂CH 2-CF₃-Ph

G14-501 CF₃ CH₃C(=0) 2-CF₃-Ph

G 14-502 CF₃ CH₃CH₂C(=0) 2-CF₃-Ph

G14-503 CF₃ (CH₃)₂CHC(=0) 2-CF₃-Ph

G 14-504 CF₃ (CH₃)₃CC(=0) 2-CF₃-Ph

G14-505 CF₃ (CH₃)₃CCH₂C(=0) 2-CF₃-Ph

G 14-506 CF₃ CH₃CH₂CH(CH₃)C(=0) 2-CF₃-Ph

G14-507 CF₃ (CH₃)₂CHCH₂C(=0) 2-CF₃-Ph

G14-508 CF₃ (CH₃)₃CCH₂CH₂C(=0) 2-CF₃-Ph

G14-509 CF₃ CH₃CH₂C(CH₃)₂C(=0) 2-CF₃-Ph

G14-510 CF₃ (c-hex)C(=0) 2-CF₃-Ph

G14-511 CF₃ (c-pen)C(=0) 2-CF₃-Ph

G14-512 CF₃ (c-hep)C(=0) 2-CF₃-Ph

G14-513 CF₃ (c-pro)C(=0) 2-CF₃-Ph

G14-514 CF₃ CF₃C(=0) 2-CF₃-Ph

G14-515 CF₃ (CH₃)₂NC(=0) 2-CF₃-Ph

G14-516 CF₃ (CH₃CH₂)₂NC(=0) 2-CF₃-Ph

G14-517 CF₃ (CH₃CH₂CH₂)₂NC(=0) 2-CF₃-Ph

G14-518 CF₃ CH₃CH₂N(CH₃)C(=0) 2-CF₃-Ph

G14-519 CF₃ [(CH₃)₂CHCH₂]₂NC(=0) 2-CF₃-Ph

G 14-520 CF₃ CH₃ON(CH₃)C(=0) 2-CF₃-Ph

G14-521 CF₃ (CH₂=CHCH₂)₂N C(=0) 2-CF₃-Ph

G 14-564 CF₃ (4-CH₃Ph)CH₂OCH₂ 2-CF₃-Ph

G 14-565 CF₃ (2-CH₃OPh)CH₂OCH₂ 2-CF₃-Ph

G 14-566 CF₃ (3-CH₃OPh)CH₂OCH₂ 2-CF₃-Ph

G 14-567 CF₃ (4-CH₃OPh)CH₂OCH₂ 2-CF₃-Ph

G 14-568 CF₃ (2-FPh)CH₂OCH₂ 2-CF₃-Ph

G 14-569 CF₃ (3-FPh)CH₂OCH₂ 2-CF₃-Ph

G14-570 CF₃ (4-FPh)CH₂OCH₂ 2-CF₃-Ph

G14-571 CF₃ (2-CIPh)CH₂OCH₂ 2-CF₃-Ph

G 14-572 CF₃ (3-CIPh)CH₂OCH₂ 2-CF₃-Ph

G14-573 CF₃ (4-CIPh)CH₂OCH₂ 2-CF₃-Ph

G 14-574 CF₃ (2-BrPh)CH₂OCH₂ 2-CF₃-Ph

G14-575 CF₃ (3-BrPh)CH₂OCH₂ 2-CF₃-Ph

G 14-576 CF₃ (4-BrPh)CH₂OCH₂ 2-CF₃-Ph

G14-577 CF₃ (2-CF₃OPh)CH₂OCH₂ 2-CF₃-Ph

G14-578 CF₃ (3-CF₃OPh)CH₂OCH₂ 2-CF₃-Ph

G14-579 CF₃ (4-CF₃OPh)CH₂OCH₂ 2-CF₃-Ph

G14-580 CF₃ (2-CNPh)CH₂OCH₂ 2-CF₃-Ph

G14-581 CF₃ (3-CNPh)CH₂OCH₂ 2-CF₃-Ph

G 14-582 CF₃ (4-CNPh)CH₂OCH₂ 2-CF₃-Ph

G14-583 CF₃ (2-N0₂Ph)CH₂OCH₂ 2-CF₃-Ph

G 14-584 CF₃ (3-N0₂Ph)CH₂OCH₂ 2-CF₃-Ph

G14-585 CF₃ (4-N0₂Ph)CH₂OCH₂ 2-CF₃-Ph

G 14-586 CF₃ (2-CF₃Ph)CH₂OCH₂ 2-CF₃-Ph

G14-587 CF₃ (3-CF₃Ph)CH₂OCH₂ 2-CF₃-Ph

G14-588 CF₃ (4-CF₃Ph)CH₂OCH₂ 2-CF₃-Ph

G14-589 CF₃ CH₃C(=0)OCH₂ 2-CF₃-Ph

G14-590 CF₃ CH₃CH₂C(=0)OCH₂ 2-CF₃-Ph

G14-591 CF₃ CH(CH₃)₂C(=0)OCH₂ 2-CF₃-Ph

G 14-592 CF₃ (CH₃)₃C(=0)OCH₂ 2-CF₃-Ph

G14-593 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 2-CF₃-Ph

G 14-594 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 2-CF₃-Ph

G14-595 CF₃ CF₃C(=0)OCH₂ 2-CF₃-Ph

G 14-596 CF₃ CF₃CF₂C(=0)OCH₂ 2-CF₃-Ph

G14-597 CF₃ (c-hex)C(=0)OCH₂ 2-CF₃-Ph

G14-598 CF₃ PhC(=0)OCH₂ 2-CF₃-Ph

G14-599 CF₃ (2-CH₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 14-600 CF₃ (3-CH₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G14-601 CF₃ (4-CH₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 14-602 CF₃ (2-CH₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-603 CF₃ (3-CH₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-604 CF₃ (4-CH₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-605 CF₃ (2-FPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-606 CF₃ (3-FPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-607 CF₃ (4-FPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-608 CF₃ (2-CIPh)C(=0)OCH₂ 2-CF₃-Ph

G 14-609 CF₃ (3-CIPh)C(=0)OCH₂ 2-CF₃-Ph

G14-610 CF₃ (4-CIPh)C(=0)OCH₂ 2-CF₃-Ph

G14-611 CF₃ (2-BrPh)C(=0)OCH₂ 2-CF₃-Ph

G14-700 CF₃ (2-CIPh)CH₂OCH₂ 3-CF₃-Ph

G14-701 CF₃ (3-CIPh)CH₂OCH₂ 3-CF₃-Ph

G 14-702 CF₃ (4-CIPh)CH₂OCH₂ 3-CF₃-Ph

G14-703 CF₃ (2-BrPh)CH₂OCH₂ 3-CF₃-Ph

G 14-704 CF₃ (3-BrPh)CH₂OCH₂ 3-CF₃-Ph

G14-705 CF₃ (4-BrPh)CH₂OCH₂ 3-CF₃-Ph

G 14-706 CF₃ (2-CF₃OPh)CH₂OCH₂ 3-CF₃-Ph

G14-707 CF₃ (3-CF₃OPh)CH₂OCH₂ 3-CF₃-Ph

G14-708 CF₃ (4-CF₃OPh)CH₂OCH₂ 3-CF₃-Ph

G14-709 CF₃ (2-CNPh)CH₂OCH₂ 3-CF₃-Ph

G14-710 CF₃ (3-CNPh)CH₂OCH₂ 3-CF₃-Ph

G14-711 CF₃ (4-CNPh)CH₂OCH₂ 3-CF₃-Ph

G14-712 CF₃ (2-N0₂Ph)CH₂OCH₂ 3-CF₃-Ph

G14-713 CF₃ (3-N0₂Ph)CH₂OCH₂ 3-CF₃-Ph

G14-714 CF₃ (4-N0₂Ph)CH₂OCH₂ 3-CF₃-Ph

G14-715 CF₃ (2-CF₃Ph)CH₂OCH₂ 3-CF₃-Ph

G14-716 CF₃ (3-CF₃Ph)CH₂OCH₂ 3-CF₃-Ph

G14-717 CF₃ (4-CF₃Ph)CH₂OCH₂ 3-CF₃-Ph

G14-718 CF₃ CH₃C(=0)OCH₂ 3-CF₃-Ph

G14-719 CF₃ CH₃CH₂C(=0)OCH₂ 3-CF₃-Ph

G 14-720 CF₃ CH(CH₃)₂C(=0)OCH₂ 3-CF₃-Ph

G14-721 CF₃ (CH₃)₃C(=0)OCH₂ 3-CF₃-Ph

G 14-722 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 3-CF₃-Ph

G 14-723 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 3-CF₃-Ph

G 14-724 CF₃ CF₃C(=0)OCH₂ 3-CF₃-Ph

G 14-725 CF₃ CF₃CF₂C(=0)OCH₂ 3-CF₃-Ph

G 14-726 CF₃ (c-hex)C(=0)OCH₂ 3-CF₃-Ph

G 14-727 CF₃ PhC(=0)OCH₂ 3-CF₃-Ph

G 14-728 CF₃ (2-CH₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G 14-729 CF₃ (3-CH₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G14-730 CF₃ (4-CH₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G14-731 CF₃ (2-CH₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-732 CF₃ (3-CH₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G14-733 CF₃ (4-CH₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-734 CF₃ (2-FPh)C(=0)OCH₂ 3-CF₃-Ph

G14-735 CF₃ (3-FPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-736 CF₃ (4-FPh)C(=0)OCH₂ 3-CF₃-Ph

G14-737 CF₃ (2-CIPh)C(=0)OCH₂ 3-CF₃-Ph

G14-738 CF₃ (3-CIPh)C(=0)OCH₂ 3-CF₃-Ph

G14-739 CF₃ (4-CIPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-740 CF₃ (2-BrPh)C(=0)OCH₂ 3-CF₃-Ph

G14-741 CF₃ (3-BrPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-742 CF₃ (4-BrPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-743 CF₃ (2-CF₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-744 CF₃ (3-CF₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-745 CF₃ (4-CF₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-746 CF₃ (2-CNPh)C(=0)OCH₂ 3-CF₃-Ph

G 14-747 CF₃ (3-CNPh)C(=0)OCH₂ 3-CF₃-Ph

G14-790 CF₃ (c-hex)OCH₂ 4-CF₃-Ph

G14-791 CF₃ PhOCH₂ 4-CF₃-Ph

G 14-792 CF₃ (2-CH₃Ph)OCH₂ 4-CF₃-Ph

G14-793 CF₃ (3-CH₃Ph)OCH₂ 4-CF₃-Ph

G 14-794 CF₃ (4-CH₃Ph)OCH₂ 4-CF₃-Ph

G14-795 CF₃ (2-CH₃OPh)OCH₂ 4-CF₃-Ph

G 14-796 CF₃ (3-CH₃OPh)OCH₂ 4-CF₃-Ph

G14-797 CF₃ (4-CH₃OPh)OCH₂ 4-CF₃-Ph

G14-798 CF₃ (2-FPh)OCH₂ 4-CF₃-Ph

G14-799 CF₃ (3-FPh)OCH₂ 4-CF₃-Ph

G14-800 CF₃ (4-FPh)OCH₂ 4-CF₃-Ph

G14-801 CF₃ (2-CIPh)OCH₂ 4-CF₃-Ph

G 14-802 CF₃ (3-CIPh)OCH₂ 4-CF₃-Ph

G14-803 CF₃ (4-CIPh)OCH₂ 4-CF₃-Ph

G 14-804 CF₃ (2-BrPh)OCH₂ 4-CF₃-Ph

G14-805 CF₃ (3-BrPh)OCH₂ 4-CF₃-Ph

G 14-806 CF₃ (4-BrPh)OCH₂ 4-CF₃-Ph

G14-807 CF₃ (2-CF₃OPh)OCH₂ 4-CF₃-Ph

G14-808 CF₃ (3-CF₃OPh)OCH₂ 4-CF₃-Ph

G14-809 CF₃ (4-CF₃OPh)OCH₂ 4-CF₃-Ph

G14-810 CF₃ (2-CNPh)OCH₂ 4-CF₃-Ph

G14-811 CF₃ (3-CNPh)OCH₂ 4-CF₃-Ph

G14-812 CF₃ (4-CNPh)OCH₂ 4-CF₃-Ph

G14-813 CF₃ (2-N0₂Ph)OCH₂ 4-CF₃-Ph

G14-814 CF₃ (3-N0₂Ph)OCH₂ 4-CF₃-Ph

G14-815 CF₃ (4-N0₂Ph)OCH₂ 4-CF₃-Ph

G14-816 CF₃ (2-CF₃Ph)OCH₂ 4-CF₃-Ph

G14-817 CF₃ (3-CF₃Ph)OCH₂ 4-CF₃-Ph

G14-818 CF₃ (4-CF₃Ph)OCH₂ 4-CF₃-Ph

G14-819 CF₃ PhCH₂OCH₂ 4-CF₃-Ph

G 14-820 CF₃ (2-CH₃Ph)CH₂OCH₂ 4-CF₃-Ph

G14-821 CF₃ (3-CH₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-822 CF₃ (4-CH₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-823 CF₃ (2-CH₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 14-824 CF₃ (3-CH₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 14-825 CF₃ (4-CH₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 14-826 CF₃ (2-FPh)CH₂OCH₂ 4-CF₃-Ph

G 14-827 CF₃ (3-FPh)CH₂OCH₂ 4-CF₃-Ph

G 14-828 CF₃ (4-FPh)CH₂OCH₂ 4-CF₃-Ph

G 14-829 CF₃ (2-CIPh)CH₂OCH₂ 4-CF₃-Ph

G14-830 CF₃ (3-CIPh)CH₂OCH₂ 4-CF₃-Ph

G14-831 CF₃ (4-CIPh)CH₂OCH₂ 4-CF₃-Ph

G 14-832 CF₃ (2-BrPh)CH₂OCH₂ 4-CF₃-Ph

G14-833 CF₃ (3-BrPh)CH₂OCH₂ 4-CF₃-Ph

G 14-834 CF₃ (4-BrPh)CH₂OCH₂ 4-CF₃-Ph

G14-835 CF₃ (2-CF₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 14-836 CF₃ (3-CF₃OPh)CH₂OCH₂ 4-CF₃-Ph

G14-837 CF₃ (4-CF₃OPh)CH₂OCH₂ 4-CF₃-Ph G14-838 CF₃ (2-CNPh)CH₂OCH₂ 4-CF₃-Ph

G14-839 CF₃ (3-CNPh)CH₂OCH₂ 4-CF₃-Ph

G 14-840 CF₃ (4-CNPh)CH₂OCH₂ 4-CF₃-Ph

G14-841 CF₃ (2-N0₂Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-842 CF₃ (3-N0₂Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-843 CF₃ (4-N0₂Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-844 CF₃ (2-CF₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-845 CF₃ (3-CF₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-846 CF₃ (4-CF₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 14-847 CF₃ CH₃C(=0)OCH₂ 4-CF₃-Ph

G 14-848 CF₃ CH₃CH₂C(=0)OCH₂ 4-CF₃-Ph

G 14-849 CF₃ CH(CH₃)₂C(=0)OCH₂ 4-CF₃-Ph

G14-850 CF₃ (CH₃)₃C(=0)OCH₂ 4-CF₃-Ph

G14-851 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 4-CF₃-Ph

G 14-852 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 4-CF₃-Ph

G14-853 CF₃ CF₃C(=0)OCH₂ 4-CF₃-Ph

G 14-854 CF₃ CF₃CF₂C(=0)OCH₂ 4-CF₃-Ph

G14-855 CF₃ (c-hex)C(=0)OCH₂ 4-CF₃-Ph

G 14-856 CF₃ PhC(=0)OCH₂ 4-CF₃-Ph

G14-857 CF₃ (2-CH₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G14-858 CF₃ (3-CH₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G14-859 CF₃ (4-CH₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G 14-860 CF₃ (2-CH₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G14-861 CF₃ (3-CH₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-862 CF₃ (4-CH₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-863 CF₃ (2-FPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-864 CF₃ (3-FPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-865 CF₃ (4-FPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-866 CF₃ (2-CIPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-867 CF₃ (3-CIPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-868 CF₃ (4-CIPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-869 CF₃ (2-BrPh)C(=0)OCH₂ 4-CF₃-Ph

G14-870 CF₃ (3-BrPh)C(=0)OCH₂ 4-CF₃-Ph

G14-871 CF₃ (4-BrPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-872 CF₃ (2-CF₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G14-873 CF₃ (3-CF₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-874 CF₃ (4-CF₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G14-875 CF₃ (2-CNPh)C(=0)OCH₂ 4-CF₃-Ph

G 14-876 CF₃ (3-CNPh)C(=0)OCH₂ 4-CF₃-Ph

G14-877 CF₃ (4-CNPh)C(=0)OCH₂ 4-CF₃-Ph

G14-878 CF₃ (2-N0₂Ph)C(=0)OCH₂ 4-CF₃-Ph

G14-879 CF₃ (3-N0₂Ph)C(=0)OCH₂ 4-CF₃-Ph

G14-880 CF₃ (4-N0₂Ph)C(=0)OCH₂ 4-CF₃-Ph

G14-881 CF₃ (2-CF₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G 14-882 CF₃ (3-CF₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G14-883 CF₃ (4-CF₃Ph)C(=0)OCH₂ 4-CF₃-Ph

[0305] Table 9c

G 15-86 2,3-(CF₃)₂Ph H CH₃

G15-87 2,4-(CF₃)₂Ph H CH₃

G15-88 2,6-(CF₃)₂Ph H CH₃

G15-89 3,5-(CF₃)₂Ph H CH₃

G15-90 2-CF₃-3-CN-Ph H CH₃

G15-91 2-CF₃-4-CNPh H CH₃

G 15-92 2-CF₃-5-CN-Ph H CH₃

G15-93 2-CF₃-6-CN-Ph H CH₃

G 15-94 2-Pyridyl H CH₃

G15-95 3-Pyridyl H CH₃

G 15-96 4-Pyridyl H CH₃

G15-97 CF₃ H Ph

G15-98 CF₃ H 2-F-Ph

G15-99 CF₃ H 3-F-Ph

G15-100 CF₃ H 4-F-Ph

G15-101 CF₃ H 2-CI-Ph

G15-102 CF₃ H 3-CI-Ph

G15-103 CF₃ H 4-CI-Ph

G15-104 CF₃ H 2-CF₃-Ph

G15-105 CF₃ H 3-CF₃-Ph

G15-106 CF₃ H 4-CF₃-Ph

G15-107 CF₃ H 2-CF₃0-Ph

G15-108 CF₃ H 3-CF₃0-Ph

G15-109 CF₃ H 4-CF₃0-Ph

G15-110 CF₃ CH₃ 2-CI-Ph

G15-111 CF₃ CH3CH2 2-CI-Ph

G15-112 CF₃ CH3CH2CH2 2-CI-Ph

G15-113 CF₃ (CH₃)₂CH 2-CI-Ph

G15-114 CF₃ CH₃C(=0) 2-CI-Ph

G15-115 CF₃ CH₃CH₂C(=0) 2-CI-Ph

G15-116 CF₃ (CH₃)₂CHC(=0) 2-CI-Ph

G15-117 CF₃ (CH₃)₃CC(=0) 2-CI-Ph

G15-118 CF₃ (CH₃)₃CCH₂C(=0) 2-CI-Ph

G15-119 CF₃ CH₃CH₂CH(CH₃)C(=0) 2-CI-Ph

G15-120 CF₃ (CH₃)₂CHCH₂C(=0) 2-CI-Ph

G15-121 CF₃ (CH₃)₃CCH₂CH₂C(=0) 2-CI-Ph

G15-122 CF₃ CH₃CH₂C(CH₃)₂C(=0) 2-CI-Ph

G15-123 CF₃ (c-hex)C(=0) 2-CI-Ph

G15-124 CF₃ (c-pen)C(=0) 2-CI-Ph

G15-125 CF₃ (c-hep)C(=0) 2-CI-Ph

G15-126 CF₃ (c-pro)C(=0) 2-CI-Ph

G15-127 CF₃ CF₃C(=0) 2-CI-Ph

G15-128 CF₃ (CH₃)₂NC(=0) 2-CI-Ph

G15-129 CF₃ (CH₃CH₂)₂NC(=0) 2-CI-Ph

G15-130 CF₃ (CH₃CH₂CH₂)₂NC(=0) 2-CI-Ph

G15-131 CF₃ CH₃CH₂N(CH₃)C(=0) 2-CI-Ph

G15-132 CF₃ [(CH₃)₂CHCH₂]₂NC(=0) 2-CI-Ph

G15-133 CF₃ CH₃ON(CH₃)C(=0) 2-CI-Ph

G15-176 CF₃ (3-CH₃Ph)CH₂OCH₂ 2-CI-Ph

G15-177 CF₃ (4-CH₃Ph)CH₂OCH₂ 2-CI-Ph

G15-178 CF₃ (2-CH₃OPh)CH₂OCH₂ 2-CI-Ph

G15-179 CF₃ (3-CH₃OPh)CH₂OCH₂ 2-CI-Ph

G15-180 CF₃ (4-CH₃OPh)CH₂OCH₂ 2-CI-Ph

G15-181 CF₃ (2-FPh)CH₂OCH₂ 2-CI-Ph

G15-182 CF₃ (3-FPh)CH₂OCH₂ 2-CI-Ph

G15-183 CF₃ (4-FPh)CH₂OCH₂ 2-CI-Ph

G15-184 CF₃ (2-CIPh)CH₂OCH₂ 2-CI-Ph

G15-185 CF₃ (3-CIPh)CH₂OCH₂ 2-CI-Ph

G15-186 CF₃ (4-CIPh)CH₂OCH₂ 2-CI-Ph

G15-187 CF₃ (2-BrPh)CH₂OCH₂ 2-CI-Ph

G15-188 CF₃ (3-BrPh)CH₂OCH₂ 2-CI-Ph

G15-189 CF₃ (4-BrPh)CH₂OCH₂ 2-CI-Ph

G15-190 CF₃ (2-CF₃OPh)CH₂OCH₂ 2-CI-Ph

G15-191 CF₃ (3-CF₃OPh)CH₂OCH₂ 2-CI-Ph

G15-192 CF₃ (4-CF₃OPh)CH₂OCH₂ 2-CI-Ph

G15-193 CF₃ (2-CNPh)CH₂OCH₂ 2-CI-Ph

G15-194 CF₃ (3-CNPh)CH₂OCH₂ 2-CI-Ph

G15-195 CF₃ (4-CNPh)CH₂OCH₂ 2-CI-Ph

G15-196 CF₃ (2-N0₂Ph)CH₂OCH₂ 2-CI-Ph

G15-197 CF₃ (3-N0₂Ph)CH₂OCH₂ 2-CI-Ph

G15-198 CF₃ (4-N0₂Ph)CH₂OCH₂ 2-CI-Ph

G15-199 CF₃ (2-CF₃Ph)CH₂OCH₂ 2-CI-Ph

G 15-200 CF₃ (3-CF₃Ph)CH₂OCH₂ 2-CI-Ph

G15-201 CF₃ (4-CF₃Ph)CH₂OCH₂ 2-CI-Ph

G 15-202 CF₃ CH₃C(=0)OCH₂ 2-CI-Ph

G 15-203 CF₃ CH₃CH₂C(=0)OCH₂ 2-CI-Ph

G 15-204 CF₃ CH(CH₃)₂C(=0)OCH₂ 2-CI-Ph

G 15-205 CF₃ (CH₃)₃C(=0)OCH₂ 2-CI-Ph

G 15-206 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 2-CI-Ph

G 15-207 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 2-CI-Ph

G 15-208 CF₃ CF₃C(=0)OCH₂ 2-CI-Ph

G 15-209 CF₃ CF₃CF₂C(=0)OCH₂ 2-CI-Ph

G15-210 CF₃ (c-hex)C(=0)OCH₂ 2-CI-Ph

G15-211 CF₃ PhC(=0)OCH₂ 2-CI-Ph

G15-212 CF₃ (2-CH₃Ph)C(=0)OCH₂ 2-CI-Ph

G15-213 CF₃ (3-CH₃Ph)C(=0)OCH₂ 2-CI-Ph

G15-214 CF₃ (4-CH₃Ph)C(=0)OCH₂ 2-CI-Ph

G15-215 CF₃ (2-CH₃OPh)C(=0)OCH₂ 2-CI-Ph

G15-216 CF₃ (3-CH₃OPh)C(=0)OCH₂ 2-CI-Ph

G15-217 CF₃ (4-CH₃OPh)C(=0)OCH₂ 2-CI-Ph

G15-218 CF₃ (2-FPh)C(=0)OCH₂ 2-CI-Ph

G15-219 CF₃ (3-FPh)C(=0)OCH₂ 2-CI-Ph

G 15-220 CF₃ (4-FPh)C(=0)OCH₂ 2-CI-Ph

G 15-221 CF₃ (2-CIPh)C(=0)OCH₂ 2-CI-Ph

G 15-222 CF₃ (3-CIPh)C(=0)OCH₂ 2-CI-Ph

G 15-223 CF₃ (4-CIPh)C(=0)OCH₂ 2-CI-Ph G 15-224 CF₃ (2-BrPh)C(=0)OCH₂ 2-CI-Ph

G 15-225 CF₃ (3-BrPh)C(=0)OCH₂ 2-CI-Ph

G 15-226 CF₃ (4-BrPh)C(=0)OCH₂ 2-CI-Ph

G 15-227 CF₃ (2-CF₃OPh)C(=0)OCH₂ 2-CI-Ph

G 15-228 CF₃ (3-CF₃OPh)C(=0)OCH₂ 2-CI-Ph

G 15-229 CF₃ (4-CF₃OPh)C(=0)OCH₂ 2-CI-Ph

G 15-230 CF₃ (2-CNPh)C(=0)OCH₂ 2-CI-Ph

G15-231 CF₃ (3-CNPh)C(=0)OCH₂ 2-CI-Ph

G 15-232 CF₃ (4-CNPh)C(=0)OCH₂ 2-CI-Ph

G 15-233 CF₃ (2-N0₂Ph)C(=0)OCH₂ 2-CI-Ph

G 15-234 CF₃ (3-N0₂Ph)C(=0)OCH₂ 2-CI-Ph

G 15-235 CF₃ (4-N0₂Ph)C(=0)OCH₂ 2-CI-Ph

G 15-236 CF₃ (2-CF₃Ph)C(=0)OCH₂ 2-CI-Ph

G 15-237 CF₃ (3-CF₃Ph)C(=0)OCH₂ 2-CI-Ph

G 15-238 CF₃ (4-CF₃Ph)C(=0)OCH₂ 2-CI-Ph

G 15-239 CF₃ CH₃ 3-CI-Ph

G 15-240 CF₃ CH3CH2 3-CI-Ph

G 15-241 CF₃ CH3CH2CH2 3-CI-Ph

G 15-242 CF₃ (CH₃)₂CH 3-CI-Ph

G 15-243 CF₃ CH₃C(=0) 3-CI-Ph

G 15-244 CF₃ CH₃CH₂C(=0) 3-CI-Ph

G 15-245 CF₃ (CH₃)₂CHC(=0) 3-CI-Ph

G 15-246 CF₃ (CH₃)₃CC(=0) 3-CI-Ph

G 15-247 CF₃ (CH₃)₃CCH₂C(=0) 3-CI-Ph

G 15-248 CF₃ CH₃CH₂CH(CH₃)C(=0) 3-CI-Ph

G 15-249 CF₃ (CH₃)₂CHCH₂C(=0) 3-CI-Ph

G 15-250 CF₃ (CH₃)₃CCH₂CH₂C(=0) 3-CI-Ph

G15-251 CF₃ CH₃CH₂C(CH₃)₂C(=0) 3-CI-Ph

G 15-252 CF₃ (c-hex)C(=0) 3-CI-Ph

G 15-253 CF₃ (c-pen)C(=0) 3-CI-Ph

G 15-254 CF₃ (c-hep)C(=0) 3-CI-Ph

G 15-255 CF₃ (c-pro)C(=0) 3-CI-Ph

G 15-256 CF₃ CF₃C(=0) 3-CI-Ph

G 15-257 CF₃ (CH₃)₂NC(=0) 3-CI-Ph

G 15-258 CF₃ (CH₃CH₂)₂NC(=0) 3-CI-Ph

G 15-259 CF₃ (CH₃CH₂CH₂)₂NC(=0) 3-CI-Ph

G 15-260 CF₃ CH₃CH₂N(CH₃)C(=0) 3-CI-Ph

G 15-261 CF₃ [(CH₃)₂CHCH₂]₂NC(=0) 3-CI-Ph

G 15-262 CF₃ CH₃ON(CH₃)C(=0) 3-CI-Ph

G 15-263 CF₃ (CH₂=CHCH₂)₂N C(=0) 3-CI-Ph

G 15-264 CF₃ (CHCCH₂)₂NC(=0) 3-CI-Ph

G 15-265 CF₃ 3-CI-Ph

G 15-266 CF₃ O 3-CI-Ph

G15-313 CF₃ (2-CIPh)CH₂OCH₂ 3-CI-Ph

G15-314 CF₃ (3-CIPh)CH₂OCH₂ 3-CI-Ph

G15-315 CF₃ (4-CIPh)CH₂OCH₂ 3-CI-Ph

G15-316 CF₃ (2-BrPh)CH₂OCH₂ 3-CI-Ph

G15-317 CF₃ (3-BrPh)CH₂OCH₂ 3-CI-Ph

G15-318 CF₃ (4-BrPh)CH₂OCH₂ 3-CI-Ph

G15-319 CF₃ (2-CF₃OPh)CH₂OCH₂ 3-CI-Ph

G 15-320 CF₃ (3-CF₃OPh)CH₂OCH₂ 3-CI-Ph

G15-321 CF₃ (4-CF₃OPh)CH₂OCH₂ 3-CI-Ph

G 15-322 CF₃ (2-CNPh)CH₂OCH₂ 3-CI-Ph

G 15-323 CF₃ (3-CNPh)CH₂OCH₂ 3-CI-Ph

G 15-324 CF₃ (4-CNPh)CH₂OCH₂ 3-CI-Ph

G 15-325 CF₃ (2-N0₂Ph)CH₂OCH₂ 3-CI-Ph

G 15-326 CF₃ (3-N0₂Ph)CH₂OCH₂ 3-CI-Ph

G 15-327 CF₃ (4-N0₂Ph)CH₂OCH₂ 3-CI-Ph

G 15-328 CF₃ (2-CF₃Ph)CH₂OCH₂ 3-CI-Ph

G 15-329 CF₃ (3-CF₃Ph)CH₂OCH₂ 3-CI-Ph

G15-330 CF₃ (4-CF₃Ph)CH₂OCH₂ 3-CI-Ph

G15-331 CF₃ CH₃C(=0)OCH₂ 3-CI-Ph

G 15-332 CF₃ CH₃CH₂C(=0)OCH₂ 3-CI-Ph

G15-333 CF₃ CH(CH₃)₂C(=0)OCH₂ 3-CI-Ph

G 15-334 CF₃ (CH₃)₃C(=0)OCH₂ 3-CI-Ph

G15-335 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 3-CI-Ph

G 15-336 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 3-CI-Ph

G15-337 CF₃ CF₃C(=0)OCH₂ 3-CI-Ph

G15-338 CF₃ CF₃CF₂C(=0)OCH₂ 3-CI-Ph

G15-339 CF₃ (c-hex)C(=0)OCH₂ 3-CI-Ph

G 15-340 CF₃ PhC(=0)OCH₂ 3-CI-Ph

G15-341 CF₃ (2-CH₃Ph)C(=0)OCH₂ 3-CI-Ph

G 15-342 CF₃ (3-CH₃Ph)C(=0)OCH₂ 3-CI-Ph

G 15-343 CF₃ (4-CH₃Ph)C(=0)OCH₂ 3-CI-Ph

G 15-344 CF₃ (2-CH₃OPh)C(=0)OCH₂ 3-CI-Ph

G 15-345 CF₃ (3-CH₃OPh)C(=0)OCH₂ 3-CI-Ph

G 15-346 CF₃ (4-CH₃OPh)C(=0)OCH₂ 3-CI-Ph

G 15-347 CF₃ (2-FPh)C(=0)OCH₂ 3-CI-Ph

G 15-348 CF₃ (3-FPh)C(=0)OCH₂ 3-CI-Ph

G 15-349 CF₃ (4-FPh)C(=0)OCH₂ 3-CI-Ph

G15-350 CF₃ (2-CIPh)C(=0)OCH₂ 3-CI-Ph

G15-351 CF₃ (3-CIPh)C(=0)OCH₂ 3-CI-Ph

G 15-352 CF₃ (4-CIPh)C(=0)OCH₂ 3-CI-Ph

G15-353 CF₃ (2-BrPh)C(=0)OCH₂ 3-CI-Ph

G 15-354 CF₃ (3-BrPh)C(=0)OCH₂ 3-CI-Ph

G15-355 CF₃ (4-BrPh)C(=0)OCH₂ 3-CI-Ph

G 15-356 CF₃ (2-CF₃OPh)C(=0)OCH₂ 3-CI-Ph

G15-357 CF₃ (3-CF₃OPh)C(=0)OCH₂ 3-CI-Ph

G15-358 CF₃ (4-CF₃OPh)C(=0)OCH₂ 3-CI-Ph

G15-359 CF₃ (2-CNPh)C(=0)OCH₂ 3-CI-Ph

G 15-360 CF₃ (3-CNPh)C(=0)OCH₂ 3-CI-Ph

G 15-403 CF₃ (c-hex)OCH₂ 4-CI-Ph

G 15-404 CF₃ PhOCH₂ 4-CI-Ph

G 15-405 CF₃ (2-CH₃Ph)OCH₂ 4-CI-Ph

G 15-406 CF₃ (3-CH₃Ph)OCH₂ 4-CI-Ph

G 15-407 CF₃ (4-CH₃Ph)OCH₂ 4-CI-Ph

G 15-408 CF₃ (2-CH₃OPh)OCH₂ 4-CI-Ph

G 15-409 CF₃ (3-CH₃OPh)OCH₂ 4-CI-Ph

G15-410 CF₃ (4-CH₃OPh)OCH₂ 4-CI-Ph

G15-41 1 CF₃ (2-FPh)OCH₂ 4-CI-Ph

G15-412 CF₃ (3-FPh)OCH₂ 4-CI-Ph

G15-413 CF₃ (4-FPh)OCH₂ 4-CI-Ph

G15-414 CF₃ (2-CIPh)OCH₂ 4-CI-Ph

G15-415 CF₃ (3-CIPh)OCH₂ 4-CI-Ph

G15-416 CF₃ (4-CIPh)OCH₂ 4-CI-Ph

G15-417 CF₃ (2-BrPh)OCH₂ 4-CI-Ph

G15-418 CF₃ (3-BrPh)OCH₂ 4-CI-Ph

G15-419 CF₃ (4-BrPh)OCH₂ 4-CI-Ph

G 15-420 CF₃ (2-CF₃OPh)OCH₂ 4-CI-Ph

G 15-421 CF₃ (3-CF₃OPh)OCH₂ 4-CI-Ph

G 15-422 CF₃ (4-CF₃OPh)OCH₂ 4-CI-Ph

G 15-423 CF₃ (2-CNPh)OCH₂ 4-CI-Ph

G 15-424 CF₃ (3-CNPh)OCH₂ 4-CI-Ph

G 15-425 CF₃ (4-CNPh)OCH₂ 4-CI-Ph

G 15-426 CF₃ (2-N0₂Ph)OCH₂ 4-CI-Ph

G 15-427 CF₃ (3-N0₂Ph)OCH₂ 4-CI-Ph

G 15-428 CF₃ (4-N0₂Ph)OCH₂ 4-CI-Ph

G 15-429 CF₃ (2-CF₃Ph)OCH₂ 4-CI-Ph

G 15-430 CF₃ (3-CF₃Ph)OCH₂ 4-CI-Ph

G15-431 CF₃ (4-CF₃Ph)OCH₂ 4-CI-Ph

G 15-432 CF₃ PhCH₂OCH₂ 4-CI-Ph

G 15-433 CF₃ (2-CH₃Ph)CH₂OCH₂ 4-CI-Ph

G 15-434 CF₃ (3-CH₃Ph)CH₂OCH₂ 4-CI-Ph

G 15-435 CF₃ (4-CH₃Ph)CH₂OCH₂ 4-CI-Ph

G 15-436 CF₃ (2-CH₃OPh)CH₂OCH₂ 4-CI-Ph

G 15-437 CF₃ (3-CH₃OPh)CH₂OCH₂ 4-CI-Ph

G 15-438 CF₃ (4-CH₃OPh)CH₂OCH₂ 4-CI-Ph

G 15-439 CF₃ (2-FPh)CH₂OCH₂ 4-CI-Ph

G 15-440 CF₃ (3-FPh)CH₂OCH₂ 4-CI-Ph

G 15-441 CF₃ (4-FPh)CH₂OCH₂ 4-CI-Ph

G 15-442 CF₃ (2-CIPh)CH₂OCH₂ 4-CI-Ph

G 15-443 CF₃ (3-CIPh)CH₂OCH₂ 4-CI-Ph

G 15-444 CF₃ (4-CIPh)CH₂OCH₂ 4-CI-Ph

G 15-445 CF₃ (2-BrPh)CH₂OCH₂ 4-CI-Ph

G 15-446 CF₃ (3-BrPh)CH₂OCH₂ 4-CI-Ph

G 15-447 CF₃ (4-BrPh)CH₂OCH₂ 4-CI-Ph

G 15-448 CF₃ (2-CF₃OPh)CH₂OCH₂ 4-CI-Ph

G 15-449 CF₃ (3-CF₃OPh)CH₂OCH₂ 4-CI-Ph

G 15-450 CF₃ (4-CF₃OPh)CH₂OCH₂ 4-CI-Ph G15-451 CF₃ (2-CNPh)CH₂OCH₂ 4-CI-Ph

G 15-452 CF₃ (3-CNPh)CH₂OCH₂ 4-CI-Ph

G 15-453 CF₃ (4-CNPh)CH₂OCH₂ 4-CI-Ph

G 15-454 CF₃ (2-N0₂Ph)CH₂OCH₂ 4-CI-Ph

G 15-455 CF₃ (3-N0₂Ph)CH₂OCH₂ 4-CI-Ph

G 15-456 CF₃ (4-N0₂Ph)CH₂OCH₂ 4-CI-Ph

G 15-457 CF₃ (2-CF₃Ph)CH₂OCH₂ 4-CI-Ph

G 15-458 CF₃ (3-CF₃Ph)CH₂OCH₂ 4-CI-Ph

G 15-459 CF₃ (4-CF₃Ph)CH₂OCH₂ 4-CI-Ph

G 15-460 CF₃ CH₃C(=0)OCH₂ 4-CI-Ph

G 15-461 CF₃ CH₃CH₂C(=0)OCH₂ 4-CI-Ph

G 15-462 CF₃ CH(CH₃)₂C(=0)OCH₂ 4-CI-Ph

G 15-463 CF₃ (CH₃)₃C(=0)OCH₂ 4-CI-Ph

G 15-464 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 4-CI-Ph

G 15-465 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 4-CI-Ph

G 15-466 CF₃ CF₃C(=0)OCH₂ 4-CI-Ph

G 15-467 CF₃ CF₃CF₂C(=0)OCH₂ 4-CI-Ph

G 15-468 CF₃ (c-hex)C(=0)OCH₂ 4-CI-Ph

G 15-469 CF₃ PhC(=0)OCH₂ 4-CI-Ph

G 15-470 CF₃ (2-CH₃Ph)C(=0)OCH₂ 4-CI-Ph

G15-471 CF₃ (3-CH₃Ph)C(=0)OCH₂ 4-CI-Ph

G 15-472 CF₃ (4-CH₃Ph)C(=0)OCH₂ 4-CI-Ph

G 15-473 CF₃ (2-CH₃OPh)C(=0)OCH₂ 4-CI-Ph

G 15-474 CF₃ (3-CH₃OPh)C(=0)OCH₂ 4-CI-Ph

G 15-475 CF₃ (4-CH₃OPh)C(=0)OCH₂ 4-CI-Ph

G 15-476 CF₃ (2-FPh)C(=0)OCH₂ 4-CI-Ph

G 15-477 CF₃ (3-FPh)C(=0)OCH₂ 4-CI-Ph

G 15-478 CF₃ (4-FPh)C(=0)OCH₂ 4-CI-Ph

G 15-479 CF₃ (2-CIPh)C(=0)OCH₂ 4-CI-Ph

G 15-480 CF₃ (3-CIPh)C(=0)OCH₂ 4-CI-Ph

G15-481 CF₃ (4-CIPh)C(=0)OCH₂ 4-CI-Ph

G 15-482 CF₃ (2-BrPh)C(=0)OCH₂ 4-CI-Ph

G 15-483 CF₃ (3-BrPh)C(=0)OCH₂ 4-CI-Ph

G 15-484 CF₃ (4-BrPh)C(=0)OCH₂ 4-CI-Ph

G 15-485 CF₃ (2-CF₃OPh)C(=0)OCH₂ 4-CI-Ph

G 15-486 CF₃ (3-CF₃OPh)C(=0)OCH₂ 4-CI-Ph

G 15-487 CF₃ (4-CF₃OPh)C(=0)OCH₂ 4-CI-Ph

G 15-488 CF₃ (2-CNPh)C(=0)OCH₂ 4-CI-Ph

G 15-489 CF₃ (3-CNPh)C(=0)OCH₂ 4-CI-Ph

G 15-490 CF₃ (4-CNPh)C(=0)OCH₂ 4-CI-Ph

G15-491 CF₃ (2-N0₂Ph)C(=0)OCH₂ 4-CI-Ph

G 15-492 CF₃ (3-N0₂Ph)C(=0)OCH₂ 4-CI-Ph

G 15-493 CF₃ (4-N0₂Ph)C(=0)OCH₂ 4-CI-Ph

G 15-494 CF₃ (2-CF₃Ph)C(=0)OCH₂ 4-CI-Ph

G 15-495 CF₃ (3-CF₃Ph)C(=0)OCH₂ 4-CI-Ph

G 15-496 CF₃ (4-CF₃Ph)C(=0)OCH₂ 4-CI-Ph

G 15-497 CF₃ CH₃ 2-CF₃-Ph

G 15-498 CF₃ CH3CH2 2-CF₃-Ph

G15-541 CF₃ (3-FPh)OCH₂ 2-CF₃-Ph

G 15-542 CF₃ (4-FPh)OCH₂ 2-CF₃-Ph

G 15-543 CF₃ (2-CIPh)OCH₂ 2-CF₃-Ph

G 15-544 CF₃ (3-CIPh)OCH₂ 2-CF₃-Ph

G 15-545 CF₃ (4-CIPh)OCH₂ 2-CF₃-Ph

G 15-546 CF₃ (2-BrPh)OCH₂ 2-CF₃-Ph

G 15-547 CF₃ (3-BrPh)OCH₂ 2-CF₃-Ph

G 15-548 CF₃ (4-BrPh)OCH₂ 2-CF₃-Ph

G 15-549 CF₃ (2-CF₃OPh)OCH₂ 2-CF₃-Ph

G15-550 CF₃ (3-CF₃OPh)OCH₂ 2-CF₃-Ph

G15-551 CF₃ (4-CF₃OPh)OCH₂ 2-CF₃-Ph

G 15-552 CF₃ (2-CNPh)OCH₂ 2-CF₃-Ph

G15-553 CF₃ (3-CNPh)OCH₂ 2-CF₃-Ph

G 15-554 CF₃ (4-CNPh)OCH₂ 2-CF₃-Ph

G15-555 CF₃ (2-N0₂Ph)OCH₂ 2-CF₃-Ph

G 15-556 CF₃ (3-N0₂Ph)OCH₂ 2-CF₃-Ph

G15-557 CF₃ (4-N0₂Ph)OCH₂ 2-CF₃-Ph

G15-558 CF₃ (2-CF₃Ph)OCH₂ 2-CF₃-Ph

G15-559 CF₃ (3-CF₃Ph)OCH₂ 2-CF₃-Ph

G 15-560 CF₃ (4-CF₃Ph)OCH₂ 2-CF₃-Ph

G15-561 CF₃ PhCH₂OCH₂ 2-CF₃-Ph

G 15-562 CF₃ (2-CH₃Ph)CH₂OCH₂ 2-CF₃-Ph

G 15-563 CF₃ (3-CH₃Ph)CH₂OCH₂ 2-CF₃-Ph

G 15-564 CF₃ (4-CH₃Ph)CH₂OCH₂ 2-CF₃-Ph

G 15-565 CF₃ (2-CH₃OPh)CH₂OCH₂ 2-CF₃-Ph

G 15-566 CF₃ (3-CH₃OPh)CH₂OCH₂ 2-CF₃-Ph

G 15-567 CF₃ (4-CH₃OPh)CH₂OCH₂ 2-CF₃-Ph

G 15-568 CF₃ (2-FPh)CH₂OCH₂ 2-CF₃-Ph

G 15-569 CF₃ (3-FPh)CH₂OCH₂ 2-CF₃-Ph

G15-570 CF₃ (4-FPh)CH₂OCH₂ 2-CF₃-Ph

G15-571 CF₃ (2-CIPh)CH₂OCH₂ 2-CF₃-Ph

G 15-572 CF₃ (3-CIPh)CH₂OCH₂ 2-CF₃-Ph

G15-573 CF₃ (4-CIPh)CH₂OCH₂ 2-CF₃-Ph

G 15-574 CF₃ (2-BrPh)CH₂OCH₂ 2-CF₃-Ph

G15-575 CF₃ (3-BrPh)CH₂OCH₂ 2-CF₃-Ph

G 15-576 CF₃ (4-BrPh)CH₂OCH₂ 2-CF₃-Ph

G15-577 CF₃ (2-CF₃OPh)CH₂OCH₂ 2-CF₃-Ph

G15-578 CF₃ (3-CF₃OPh)CH₂OCH₂ 2-CF₃-Ph

G15-579 CF₃ (4-CF₃OPh)CH₂OCH₂ 2-CF₃-Ph

G15-580 CF₃ (2-CNPh)CH₂OCH₂ 2-CF₃-Ph

G15-581 CF₃ (3-CNPh)CH₂OCH₂ 2-CF₃-Ph

G 15-582 CF₃ (4-CNPh)CH₂OCH₂ 2-CF₃-Ph

G15-583 CF₃ (2-N0₂Ph)CH₂OCH₂ 2-CF₃-Ph

G 15-584 CF₃ (3-N0₂Ph)CH₂OCH₂ 2-CF₃-Ph

G15-585 CF₃ (4-N0₂Ph)CH₂OCH₂ 2-CF₃-Ph

G 15-586 CF₃ (2-CF₃Ph)CH₂OCH₂ 2-CF₃-Ph

G15-587 CF₃ (3-CF₃Ph)CH₂OCH₂ 2-CF₃-Ph

G15-588 CF₃ (4-CF₃Ph)CH₂OCH₂ 2-CF₃-Ph G15-589 CF₃ CH₃C(=0)OCH₂ 2-CF₃-Ph

G15-590 CF₃ CH₃CH₂C(=0)OCH₂ 2-CF₃-Ph

G15-591 CF₃ CH(CH₃)₂C(=0)OCH₂ 2-CF₃-Ph

G 15-592 CF₃ (CH₃)₃C(=0)OCH₂ 2-CF₃-Ph

G15-593 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 2-CF₃-Ph

G 15-594 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 2-CF₃-Ph

G15-595 CF₃ CF₃C(=0)OCH₂ 2-CF₃-Ph

G 15-596 CF₃ CF₃CF₂C(=0)OCH₂ 2-CF₃-Ph

G15-597 CF₃ (c-hex)C(=0)OCH₂ 2-CF₃-Ph

G15-598 CF₃ PhC(=0)OCH₂ 2-CF₃-Ph

G15-599 CF₃ (2-CH₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-600 CF₃ (3-CH₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G15-601 CF₃ (4-CH₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-602 CF₃ (2-CH₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-603 CF₃ (3-CH₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-604 CF₃ (4-CH₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-605 CF₃ (2-FPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-606 CF₃ (3-FPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-607 CF₃ (4-FPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-608 CF₃ (2-CIPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-609 CF₃ (3-CIPh)C(=0)OCH₂ 2-CF₃-Ph

G15-610 CF₃ (4-CIPh)C(=0)OCH₂ 2-CF₃-Ph

G15-611 CF₃ (2-BrPh)C(=0)OCH₂ 2-CF₃-Ph

G15-612 CF₃ (3-BrPh)C(=0)OCH₂ 2-CF₃-Ph

G15-613 CF₃ (4-BrPh)C(=0)OCH₂ 2-CF₃-Ph

G15-614 CF₃ (2-CF₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G15-615 CF₃ (3-CF₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G15-616 CF₃ (4-CF₃OPh)C(=0)OCH₂ 2-CF₃-Ph

G15-617 CF₃ (2-CNPh)C(=0)OCH₂ 2-CF₃-Ph

G15-618 CF₃ (3-CNPh)C(=0)OCH₂ 2-CF₃-Ph

G15-619 CF₃ (4-CNPh)C(=0)OCH₂ 2-CF₃-Ph

G 15-620 CF₃ (2-N0₂Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-621 CF₃ (3-N0₂Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-622 CF₃ (4-N0₂Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-623 CF₃ (2-CF₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-624 CF₃ (3-CF₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-625 CF₃ (4-CF₃Ph)C(=0)OCH₂ 2-CF₃-Ph

G 15-626 CF₃ CH₃ 3-CF₃-Ph

G 15-627 CF₃ CH3CH2 3-CF₃-Ph

G 15-628 CF₃ CH3CH2CH2 3-CF₃-Ph

G 15-629 CF₃ (CH₃)₂CH 3-CF₃-Ph

G 15-630 CF₃ CH₃C(=0) 3-CF₃-Ph

G15-631 CF₃ CH₃CH₂C(=0) 3-CF₃-Ph

G 15-632 CF₃ (CH₃)₂CHC(=0) 3-CF₃-Ph

G 15-633 CF₃ (CH₃)₃CC(=0) 3-CF₃-Ph

G 15-634 CF₃ (CH₃)₃CCH₂C(=0) 3-CF₃-Ph

G 15-635 CF₃ CH₃CH₂CH(CH₃)C(=0) 3-CF₃-Ph

G 15-636 CF₃ (CH₃)₂CHCH₂C(=0) 3-CF₃-Ph

G 15-679 CF₃ (3-CF₃OPh)OCH₂ 3-CF₃-Ph

G 15-680 CF₃ (4-CF₃OPh)OCH₂ 3-CF₃-Ph

G15-681 CF₃ (2-CNPh)OCH₂ 3-CF₃-Ph

G 15-682 CF₃ (3-CNPh)OCH₂ 3-CF₃-Ph

G 15-683 CF₃ (4-CNPh)OCH₂ 3-CF₃-Ph

G 15-684 CF₃ (2-N0₂Ph)OCH₂ 3-CF₃-Ph

G 15-685 CF₃ (3-N0₂Ph)OCH₂ 3-CF₃-Ph

G 15-686 CF₃ (4-N0₂Ph)OCH₂ 3-CF₃-Ph

G 15-687 CF₃ (2-CF₃Ph)OCH₂ 3-CF₃-Ph

G 15-688 CF₃ (3-CF₃Ph)OCH₂ 3-CF₃-Ph

G 15-689 CF₃ (4-CF₃Ph)OCH₂ 3-CF₃-Ph

G 15-690 CF₃ PhCH₂OCH₂ 3-CF₃-Ph

G15-691 CF₃ (2-CH₃Ph)CH₂OCH₂ 3-CF₃-Ph

G 15-692 CF₃ (3-CH₃Ph)CH₂OCH₂ 3-CF₃-Ph

G 15-693 CF₃ (4-CH₃Ph)CH₂OCH₂ 3-CF₃-Ph

G 15-694 CF₃ (2-CH₃OPh)CH₂OCH₂ 3-CF₃-Ph

G 15-695 CF₃ (3-CH₃OPh)CH₂OCH₂ 3-CF₃-Ph

G 15-696 CF₃ (4-CH₃OPh)CH₂OCH₂ 3-CF₃-Ph

G 15-697 CF₃ (2-FPh)CH₂OCH₂ 3-CF₃-Ph

G 15-698 CF₃ (3-FPh)CH₂OCH₂ 3-CF₃-Ph

G 15-699 CF₃ (4-FPh)CH₂OCH₂ 3-CF₃-Ph

G15-700 CF₃ (2-CIPh)CH₂OCH₂ 3-CF₃-Ph

G15-701 CF₃ (3-CIPh)CH₂OCH₂ 3-CF₃-Ph

G 15-702 CF₃ (4-CIPh)CH₂OCH₂ 3-CF₃-Ph

G15-703 CF₃ (2-BrPh)CH₂OCH₂ 3-CF₃-Ph

G 15-704 CF₃ (3-BrPh)CH₂OCH₂ 3-CF₃-Ph

G15-705 CF₃ (4-BrPh)CH₂OCH₂ 3-CF₃-Ph

G 15-706 CF₃ (2-CF₃OPh)CH₂OCH₂ 3-CF₃-Ph

G15-707 CF₃ (3-CF₃OPh)CH₂OCH₂ 3-CF₃-Ph

G15-708 CF₃ (4-CF₃OPh)CH₂OCH₂ 3-CF₃-Ph

G15-709 CF₃ (2-CNPh)CH₂OCH₂ 3-CF₃-Ph

G15-710 CF₃ (3-CNPh)CH₂OCH₂ 3-CF₃-Ph

G15-711 CF₃ (4-CNPh)CH₂OCH₂ 3-CF₃-Ph

G15-712 CF₃ (2-N0₂Ph)CH₂OCH₂ 3-CF₃-Ph

G15-713 CF₃ (3-N0₂Ph)CH₂OCH₂ 3-CF₃-Ph

G15-714 CF₃ (4-N0₂Ph)CH₂OCH₂ 3-CF₃-Ph

G15-715 CF₃ (2-CF₃Ph)CH₂OCH₂ 3-CF₃-Ph

G15-716 CF₃ (3-CF₃Ph)CH₂OCH₂ 3-CF₃-Ph

G15-717 CF₃ (4-CF₃Ph)CH₂OCH₂ 3-CF₃-Ph

G15-718 CF₃ CH₃C(=0)OCH₂ 3-CF₃-Ph

G15-719 CF₃ CH₃CH₂C(=0)OCH₂ 3-CF₃-Ph

G 15-720 CF₃ CH(CH₃)₂C(=0)OCH₂ 3-CF₃-Ph

G15-721 CF₃ (CH₃)₃C(=0)OCH₂ 3-CF₃-Ph

G 15-722 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 3-CF₃-Ph

G 15-723 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 3-CF₃-Ph

G 15-724 CF₃ CF₃C(=0)OCH₂ 3-CF₃-Ph

G 15-725 CF₃ CF₃CF₂C(=0)OCH₂ 3-CF₃-Ph

G 15-726 CF₃ (c-hex)C(=0)OCH₂ 3-CF₃-Ph G 15-727 CF₃ PhC(=0)OCH₂ 3-CF₃-Ph

G 15-728 CF₃ (2-CH₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G 15-729 CF₃ (3-CH₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G15-730 CF₃ (4-CH₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G15-731 CF₃ (2-CH₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-732 CF₃ (3-CH₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G15-733 CF₃ (4-CH₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-734 CF₃ (2-FPh)C(=0)OCH₂ 3-CF₃-Ph

G15-735 CF₃ (3-FPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-736 CF₃ (4-FPh)C(=0)OCH₂ 3-CF₃-Ph

G15-737 CF₃ (2-CIPh)C(=0)OCH₂ 3-CF₃-Ph

G15-738 CF₃ (3-CIPh)C(=0)OCH₂ 3-CF₃-Ph

G15-739 CF₃ (4-CIPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-740 CF₃ (2-BrPh)C(=0)OCH₂ 3-CF₃-Ph

G15-741 CF₃ (3-BrPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-742 CF₃ (4-BrPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-743 CF₃ (2-CF₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-744 CF₃ (3-CF₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-745 CF₃ (4-CF₃OPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-746 CF₃ (2-CNPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-747 CF₃ (3-CNPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-748 CF₃ (4-CNPh)C(=0)OCH₂ 3-CF₃-Ph

G 15-749 CF₃ (2-N0₂Ph)C(=0)OCH₂ 3-CF₃-Ph

G15-750 CF₃ (3-N0₂Ph)C(=0)OCH₂ 3-CF₃-Ph

G15-751 CF₃ (4-N0₂Ph)C(=0)OCH₂ 3-CF₃-Ph

G 15-752 CF₃ (2-CF₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G15-753 CF₃ (3-CF₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G 15-754 CF₃ (4-CF₃Ph)C(=0)OCH₂ 3-CF₃-Ph

G15-755 CF₃ CH₃ 4-CF₃-Ph

G 15-756 CF₃ CH3CH2 4-CF₃-Ph

G15-757 CF₃ CH3CH2CH2 4-CF₃-Ph

G15-758 CF₃ (CH₃)₂CH 4-CF₃-Ph

G15-759 CF₃ CH₃C(=0) 4-CF₃-Ph

G 15-760 CF₃ CH₃CH₂C(=0) 4-CF₃-Ph

G15-761 CF₃ (CH₃)₂CHC(=0) 4-CF₃-Ph

G 15-762 CF₃ (CH₃)₃CC(=0) 4-CF₃-Ph

G 15-763 CF₃ (CH₃)₃CCH₂C(=0) 4-CF₃-Ph

G 15-764 CF₃ CH₃CH₂CH(CH₃)C(=0) 4-CF₃-Ph

G 15-765 CF₃ (CH₃)₂CHCH₂C(=0) 4-CF₃-Ph

G 15-766 CF₃ (CH₃)₃CCH₂CH₂C(=0) 4-CF₃-Ph

G 15-767 CF₃ CH₃CH₂C(CH₃)₂C(=0) 4-CF₃-Ph

G 15-768 CF₃ (c-hex)C(=0) 4-CF₃-Ph

G 15-769 CF₃ (c-pen)C(=0) 4-CF₃-Ph

G15-770 CF₃ (c-hep)C(=0) 4-CF₃-Ph

G15-771 CF₃ (c-pro)C(=0) 4-CF₃-Ph

G 15-772 CF₃ CF₃C(=0) 4-CF₃-Ph

G15-773 CF₃ (CH₃)₂NC(=0) 4-CF₃-Ph

G 15-774 CF₃ (CH₃CH₂)₂NC(=0) 4-CF₃-Ph

G15-817 CF₃ (3-CF₃Ph)OCH₂ 4-CF₃-Ph

G15-818 CF₃ (4-CF₃Ph)OCH₂ 4-CF₃-Ph

G15-819 CF₃ PhCH₂OCH₂ 4-CF₃-Ph

G 15-820 CF₃ (2-CH₃Ph)CH₂OCH₂ 4-CF₃-Ph

G15-821 CF₃ (3-CH₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-822 CF₃ (4-CH₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-823 CF₃ (2-CH₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 15-824 CF₃ (3-CH₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 15-825 CF₃ (4-CH₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 15-826 CF₃ (2-FPh)CH₂OCH₂ 4-CF₃-Ph

G 15-827 CF₃ (3-FPh)CH₂OCH₂ 4-CF₃-Ph

G 15-828 CF₃ (4-FPh)CH₂OCH₂ 4-CF₃-Ph

G 15-829 CF₃ (2-CIPh)CH₂OCH₂ 4-CF₃-Ph

G15-830 CF₃ (3-CIPh)CH₂OCH₂ 4-CF₃-Ph

G15-831 CF₃ (4-CIPh)CH₂OCH₂ 4-CF₃-Ph

G 15-832 CF₃ (2-BrPh)CH₂OCH₂ 4-CF₃-Ph

G15-833 CF₃ (3-BrPh)CH₂OCH₂ 4-CF₃-Ph

G 15-834 CF₃ (4-BrPh)CH₂OCH₂ 4-CF₃-Ph

G15-835 CF₃ (2-CF₃OPh)CH₂OCH₂ 4-CF₃-Ph

G 15-836 CF₃ (3-CF₃OPh)CH₂OCH₂ 4-CF₃-Ph

G15-837 CF₃ (4-CF₃OPh)CH₂OCH₂ 4-CF₃-Ph

G15-838 CF₃ (2-CNPh)CH₂OCH₂ 4-CF₃-Ph

G15-839 CF₃ (3-CNPh)CH₂OCH₂ 4-CF₃-Ph

G 15-840 CF₃ (4-CNPh)CH₂OCH₂ 4-CF₃-Ph

G15-841 CF₃ (2-N0₂Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-842 CF₃ (3-N0₂Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-843 CF₃ (4-N0₂Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-844 CF₃ (2-CF₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-845 CF₃ (3-CF₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-846 CF₃ (4-CF₃Ph)CH₂OCH₂ 4-CF₃-Ph

G 15-847 CF₃ CH₃C(=0)OCH₂ 4-CF₃-Ph

G 15-848 CF₃ CH₃CH₂C(=0)OCH₂ 4-CF₃-Ph

G 15-849 CF₃ CH(CH₃)₂C(=0)OCH₂ 4-CF₃-Ph

G15-850 CF₃ (CH₃)₃C(=0)OCH₂ 4-CF₃-Ph

G15-851 CF₃ (CH₃)₃CCH₂(=0)OCH₂ 4-CF₃-Ph

G 15-852 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂ 4-CF₃-Ph

G15-853 CF₃ CF₃C(=0)OCH₂ 4-CF₃-Ph

G 15-854 CF₃ CF₃CF₂C(=0)OCH₂ 4-CF₃-Ph

G15-855 CF₃ (c-hex)C(=0)OCH₂ 4-CF₃-Ph

G 15-856 CF₃ PhC(=0)OCH₂ 4-CF₃-Ph

G15-857 CF₃ (2-CH₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G15-858 CF₃ (3-CH₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G15-859 CF₃ (4-CH₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G 15-860 CF₃ (2-CH₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G15-861 CF₃ (3-CH₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-862 CF₃ (4-CH₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-863 CF₃ (2-FPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-864 CF₃ (3-FPh)C(=0)OCH₂ 4-CF₃-Ph G 15-865 CF₃ (4-FPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-866 CF₃ (2-CIPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-867 CF₃ (3-CIPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-868 CF₃ (4-CIPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-869 CF₃ (2-BrPh)C(=0)OCH₂ 4-CF₃-Ph

G15-870 CF₃ (3-BrPh)C(=0)OCH₂ 4-CF₃-Ph

G15-871 CF₃ (4-BrPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-872 CF₃ (2-CF₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G15-873 CF₃ (3-CF₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-874 CF₃ (4-CF₃OPh)C(=0)OCH₂ 4-CF₃-Ph

G15-875 CF₃ (2-CNPh)C(=0)OCH₂ 4-CF₃-Ph

G 15-876 CF₃ (3-CNPh)C(=0)OCH₂ 4-CF₃-Ph

G15-877 CF₃ (4-CNPh)C(=0)OCH₂ 4-CF₃-Ph

G15-878 CF₃ (2-N0₂Ph)C(=0)OCH₂ 4-CF₃-Ph

G15-879 CF₃ (3-N0₂Ph)C(=0)OCH₂ 4-CF₃-Ph

G15-880 CF₃ (4-N0₂Ph)C(=0)OCH₂ 4-CF₃-Ph

G15-881 CF₃ (2-CF₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G 15-882 CF₃ (3-CF₃Ph)C(=0)OCH₂ 4-CF₃-Ph

G15-883 CF₃ (4-CF₃Ph)C(=0)OCH₂ 4-CF₃-Ph

[0306] Table 9 d

G16-155 CF₃ (4-CH₃Ph)OCH₂

G16-156 CF₃ (2-CH₃OPh)OCH₂

G16-157 CF₃ (3-CH₃OPh)OCH₂

G16-158 CF₃ (4-CH₃OPh)OCH₂

G16-159 CF₃ (2-FPh)OCH₂

G16-160 CF₃ (3-FPh)OCH₂

G16-161 CF₃ (4-FPh)OCH₂

G16-162 CF₃ (2-CIPh)OCH₂

G16-163 CF₃ (3-CIPh)OCH₂

G16-164 CF₃ (4-CIPh)OCH₂

G16-165 CF₃ (2-BrPh)OCH₂

G16-166 CF₃ (3-BrPh)OCH₂

G16-167 CF₃ (4-BrPh)OCH₂

G16-168 CF₃ (2-CF₃OPh)OCH₂

G16-169 CF₃ (3-CF₃OPh)OCH₂

G16-170 CF₃ (4-CF₃OPh)OCH₂

G16-171 CF₃ (2-CNPh)OCH₂

G16-172 CF₃ (3-CNPh)OCH₂

G16-173 CF₃ (4-CNPh)OCH₂

G16-174 CF₃ (2-N0₂Ph)OCH₂

G16-175 CF₃ (3-N0₂Ph)OCH₂

G16-176 CF₃ (4-N0₂Ph)OCH₂

G16-177 CF₃ (2-CF₃Ph)OCH₂

G16-178 CF₃ (3-CF₃Ph)OCH₂

G16-179 CF₃ (4-CF₃Ph)OCH₂

G16-180 CF₃ PhCH₂OCH₂

G16-181 CF₃ (2-CH₃Ph)CH₂OCH₂

G16-182 CF₃ (3-CH₃Ph)CH₂OCH₂

G16-183 CF₃ (4-CH₃Ph)CH₂OCH₂

G16-184 CF₃ (2-CH₃OPh)CH₂OCH₂

G16-185 CF₃ (3-CH₃OPh)CH₂OCH₂

G16-186 CF₃ (4-CH₃OPh)CH₂OCH₂

G16-187 CF₃ (2-FPh)CH₂OCH₂

G16-188 CF₃ (3-FPh)CH₂OCH₂

G16-189 CF₃ (4-FPh)CH₂OCH₂

G16-190 CF₃ (2-CIPh)CH₂OCH₂

G16-191 CF₃ (3-CIPh)CH₂OCH₂

G16-192 CF₃ (4-CIPh)CH₂OCH₂

G16-193 CF₃ (2-BrPh)CH₂OCH₂

G16-194 CF₃ (3-BrPh)CH₂OCH₂

G16-195 CF₃ (4-BrPh)CH₂OCH₂

G16-196 CF₃ (2-CF₃OPh)CH₂OCH₂

G16-197 CF₃ (3-CF₃OPh)CH₂OCH₂

G16-198 CF₃ (4-CF₃OPh)CH₂OCH₂

G16-199 CF₃ (2-CNPh)CH₂OCH₂

G 16-200 CF₃ (3-CNPh)CH₂OCH₂

G16-201 CF₃ (4-CNPh)CH₂OCH₂

G 16-202 CF₃ (2-N0₂Ph)CH₂OCH₂

G 16-293 2-CF₃Ph (4-CIPh)OCH₂

G 16-294 2-CF₃Ph (2-BrPh)OCH₂

G 16-295 2-CF₃Ph (3-BrPh)OCH₂

G 16-296 2-CF₃Ph (4-BrPh)OCH₂

G 16-297 2-CF₃Ph (2-CF₃OPh)OCH₂

G 16-298 2-CF₃Ph (3-CF₃OPh)OCH₂

G 16-299 2-CF₃Ph (4-CF₃OPh)OCH₂

G16-300 2-CF₃Ph (2-CNPh)OCH₂

G16-301 2-CF₃Ph (3-CNPh)OCH₂

G 16-302 2-CF₃Ph (4-CNPh)OCH₂

G16-303 2-CF₃Ph (2-N0₂Ph)OCH₂

G 16-304 2-CF₃Ph (3-N0₂Ph)OCH₂

G16-305 2-CF₃Ph (4-N0₂Ph)OCH₂

G 16-306 2-CF₃Ph (2-CF₃Ph)OCH₂

G16-307 2-CF₃Ph (3-CF₃Ph)OCH₂

G16-308 2-CF₃Ph (4-CF₃Ph)OCH₂

G16-309 2-CF₃Ph PhCH₂OCH₂

G16-310 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G16-311 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G16-312 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G16-313 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G16-314 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G16-315 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G16-316 2-CF₃Ph (2-FPh)CH₂OCH₂

G16-317 2-CF₃Ph (3-FPh)CH₂OCH₂

G16-318 2-CF₃Ph (4-FPh)CH₂OCH₂

G16-319 2-CF₃Ph (2-CIPh)CH₂OCH₂

G 16-320 2-CF₃Ph (3-CIPh)CH₂OCH₂

G16-321 2-CF₃Ph (4-CIPh)CH₂OCH₂

G 16-322 2-CF₃Ph (2-BrPh)CH₂OCH₂

G 16-323 2-CF₃Ph (3-BrPh)CH₂OCH₂

G 16-324 2-CF₃Ph (4-BrPh)CH₂OCH₂

G 16-325 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 16-326 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 16-327 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 16-328 2-CF₃Ph (2-CNPh)CH₂OCH₂

G 16-329 2-CF₃Ph (3-CNPh)CH₂OCH₂

G16-330 2-CF₃Ph (4-CNPh)CH₂OCH₂

G16-331 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 16-332 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G16-333 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 16-334 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G16-335 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 16-336 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G16-337 2-CF₃Ph CH₃C(=0)OCH₂

G16-338 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G16-339 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 16-340 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G16-431 3-CF₃Ph (4-CNPh)OCH₂

G 16-432 3-CF₃Ph (2-N0₂Ph)OCH₂

G 16-433 3-CF₃Ph (3-N0₂Ph)OCH₂

G 16-434 3-CF₃Ph (4-N0₂Ph)OCH₂

G 16-435 3-CF₃Ph (2-CF₃Ph)OCH₂

G 16-436 3-CF₃Ph (3-CF₃Ph)OCH₂

G 16-437 3-CF₃Ph (4-CF₃Ph)OCH₂

G 16-438 3-CF₃Ph PhCH₂OCH₂

G 16-439 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 16-440 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G 16-441 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G 16-442 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 16-443 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G 16-444 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 16-445 3-CF₃Ph (2-FPh)CH₂OCH₂

G 16-446 3-CF₃Ph (3-FPh)CH₂OCH₂

G 16-447 3-CF₃Ph (4-FPh)CH₂OCH₂

G 16-448 3-CF₃Ph (2-CIPh)CH₂OCH₂

G 16-449 3-CF₃Ph (3-CIPh)CH₂OCH₂

G 16-450 3-CF₃Ph (4-CIPh)CH₂OCH₂

G16-451 3-CF₃Ph (2-BrPh)CH₂OCH₂

G 16-452 3-CF₃Ph (3-BrPh)CH₂OCH₂

G 16-453 3-CF₃Ph (4-BrPh)CH₂OCH₂

G 16-454 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 16-455 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 16-456 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 16-457 3-CF₃Ph (2-CNPh)CH₂OCH₂

G 16-458 3-CF₃Ph (3-CNPh)CH₂OCH₂

G 16-459 3-CF₃Ph (4-CNPh)CH₂OCH₂

G 16-460 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 16-461 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G 16-462 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 16-463 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G 16-464 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 16-465 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G 16-466 3-CF₃Ph CH₃C(=0)OCH₂

G 16-467 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G 16-468 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 16-469 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G 16-470 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G16-471 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 16-472 3-CF₃Ph CF₃C(=0)OCH₂

G 16-473 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G 16-474 3-CF₃Ph (c-hex)C(=0)OCH₂

G 16-475 3-CF₃Ph PhC(=0)OCH₂

G 16-476 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 16-477 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 16-478 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 16-569 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G16-570 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G16-571 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 16-572 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G16-573 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 16-574 4-CF₃Ph (2-FPh)CH₂OCH₂

G16-575 4-CF₃Ph (3-FPh)CH₂OCH₂

G 16-576 4-CF₃Ph (4-FPh)CH₂OCH₂

G16-577 4-CF₃Ph (2-CIPh)CH₂OCH₂

G16-578 4-CF₃Ph (3-CIPh)CH₂OCH₂

G16-579 4-CF₃Ph (4-CIPh)CH₂OCH₂

G16-580 4-CF₃Ph (2-BrPh)CH₂OCH₂

G16-581 4-CF₃Ph (3-BrPh)CH₂OCH₂

G 16-582 4-CF₃Ph (4-BrPh)CH₂OCH₂

G16-583 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 16-584 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G16-585 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 16-586 4-CF₃Ph (2-CNPh)CH₂OCH₂

G16-587 4-CF₃Ph (3-CNPh)CH₂OCH₂

G16-588 4-CF₃Ph (4-CNPh)CH₂OCH₂

G16-589 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G16-590 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G16-591 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 16-592 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G16-593 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 16-594 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G16-595 4-CF₃Ph CH₃C(=0)OCH₂

G 16-596 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G16-597 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G16-598 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G16-599 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G 16-600 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G16-601 4-CF₃Ph CF₃C(=0)OCH₂

G 16-602 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G 16-603 4-CF₃Ph (c-hex)C(=0)OCH₂

G 16-604 4-CF₃Ph PhC(=0)OCH₂

G 16-605 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 16-606 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 16-607 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 16-608 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 16-609 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G16-610 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G16-611 4-CF₃Ph (2-FPh)C(=0)OCH₂

G16-612 4-CF₃Ph (3-FPh)C(=0)OCH₂

G16-613 4-CF₃Ph (4-FPh)C(=0)OCH₂

G16-614 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G16-615 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G16-616 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G 16-706 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G16-707 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G16-708 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G16-709 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G16-710 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G16-711 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G16-712 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G16-713 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G16-714 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G16-715 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G16-716 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G16-717 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G16-718 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G16-719 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G 16-720 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G16-721 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G 16-722 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G 16-723 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G 16-724 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G 16-725 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G 16-726 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G 16-727 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G 16-728 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G 16-729 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G16-730 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G16-731 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G 16-732 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G16-733 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G 16-734 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G16-735 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G 16-736 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G16-737 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G16-738 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G16-739 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G 16-740 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G16-741 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G 16-742 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G 16-743 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G 16-744 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G 16-745 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G 16-746 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G 16-747 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G 16-748 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G 16-749 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G16-750 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G16-751 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G 16-752 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G16-753 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂ G 16-754 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G16-755 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G 16-756 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G16-757 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G16-758 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G16-759 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G 16-760 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0307] Table 9 e

G17-167 CF₃ (4-BrPh)OCH₂

G17-168 CF₃ (2-CF₃OPh)OCH₂

G17-169 CF₃ (3-CF₃OPh)OCH₂

G17-170 CF₃ (4-CF₃OPh)OCH₂

G17-171 CF₃ (2-CNPh)OCH₂

G17-172 CF₃ (3-CNPh)OCH₂

G17-173 CF₃ (4-CNPh)OCH₂

G17-174 CF₃ (2-N0₂Ph)OCH₂

G17-175 CF₃ (3-N0₂Ph)OCH₂

G17-176 CF₃ (4-N0₂Ph)OCH₂

G17-177 CF₃ (2-CF₃Ph)OCH₂

G17-178 CF₃ (3-CF₃Ph)OCH₂

G17-179 CF₃ (4-CF₃Ph)OCH₂

G17-180 CF₃ PhCH₂OCH₂

G17-181 CF₃ (2-CH₃Ph)CH₂OCH₂

G17-182 CF₃ (3-CH₃Ph)CH₂OCH₂

G17-183 CF₃ (4-CH₃Ph)CH₂OCH₂

G17-184 CF₃ (2-CH₃OPh)CH₂OCH₂

G17-185 CF₃ (3-CH₃OPh)CH₂OCH₂

G17-186 CF₃ (4-CH₃OPh)CH₂OCH₂

G17-187 CF₃ (2-FPh)CH₂OCH₂

G17-188 CF₃ (3-FPh)CH₂OCH₂

G17-189 CF₃ (4-FPh)CH₂OCH₂

G17-190 CF₃ (2-CIPh)CH₂OCH₂

G17-191 CF₃ (3-CIPh)CH₂OCH₂

G17-192 CF₃ (4-CIPh)CH₂OCH₂

G17-193 CF₃ (2-BrPh)CH₂OCH₂

G17-194 CF₃ (3-BrPh)CH₂OCH₂

G17-195 CF₃ (4-BrPh)CH₂OCH₂

G17-196 CF₃ (2-CF₃OPh)CH₂OCH₂

G17-197 CF₃ (3-CF₃OPh)CH₂OCH₂

G17-198 CF₃ (4-CF₃OPh)CH₂OCH₂

G17-199 CF₃ (2-CNPh)CH₂OCH₂

G 17-200 CF₃ (3-CNPh)CH₂OCH₂

G17-201 CF₃ (4-CNPh)CH₂OCH₂

G 17-202 CF₃ (2-N0₂Ph)CH₂OCH₂

G 17-203 CF₃ (3-N0₂Ph)CH₂OCH₂

G 17-204 CF₃ (4-N0₂Ph)CH₂OCH₂

G 17-205 CF₃ (2-CF₃Ph)CH₂OCH₂

G 17-206 CF₃ (3-CF₃Ph)CH₂OCH₂

G 17-207 CF₃ (4-CF₃Ph)CH₂OCH₂

G 17-208 CF₃ CH₃C(=0)OCH₂

G 17-209 CF₃ CH₃CH₂C(=0)OCH₂

G17-210 CF₃ CH(CH₃)₂C(=0)OCH₂

G17-211 CF₃ (CH₃)₃C(=0)OCH₂

G17-212 CF₃ (CH₃)₃CCH₂(=0)OCH₂

G17-213 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂

G17-214 CF₃ CF₃C(=0)OCH₂

G17-305 2-CF₃Ph (4-N0₂Ph)OCH₂

G 17-306 2-CF₃Ph (2-CF₃Ph)OCH₂

G17-307 2-CF₃Ph (3-CF₃Ph)OCH₂

G17-308 2-CF₃Ph (4-CF₃Ph)OCH₂

G17-309 2-CF₃Ph PhCH₂OCH₂

G17-310 2-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G17-311 2-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G17-312 2-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G17-313 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G17-314 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G17-315 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G17-316 2-CF₃Ph (2-FPh)CH₂OCH₂

G17-317 2-CF₃Ph (3-FPh)CH₂OCH₂

G17-318 2-CF₃Ph (4-FPh)CH₂OCH₂

G17-319 2-CF₃Ph (2-CIPh)CH₂OCH₂

G 17-320 2-CF₃Ph (3-CIPh)CH₂OCH₂

G17-321 2-CF₃Ph (4-CIPh)CH₂OCH₂

G 17-322 2-CF₃Ph (2-BrPh)CH₂OCH₂

G 17-323 2-CF₃Ph (3-BrPh)CH₂OCH₂

G 17-324 2-CF₃Ph (4-BrPh)CH₂OCH₂

G 17-325 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 17-326 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 17-327 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 17-328 2-CF₃Ph (2-CNPh)CH₂OCH₂

G 17-329 2-CF₃Ph (3-CNPh)CH₂OCH₂

G17-330 2-CF₃Ph (4-CNPh)CH₂OCH₂

G17-331 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 17-332 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G17-333 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 17-334 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G17-335 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 17-336 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G17-337 2-CF₃Ph CH₃C(=0)OCH₂

G17-338 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G17-339 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 17-340 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G17-341 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G 17-342 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 17-343 2-CF₃Ph CF₃C(=0)OCH₂

G 17-344 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G 17-345 2-CF₃Ph (c-hex)C(=0)OCH₂

G 17-346 2-CF₃Ph PhC(=0)OCH₂

G 17-347 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 17-348 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 17-349 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G17-350 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G17-351 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G 17-352 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G 17-442 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 17-443 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G 17-444 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 17-445 3-CF₃Ph (2-FPh)CH₂OCH₂

G 17-446 3-CF₃Ph (3-FPh)CH₂OCH₂

G 17-447 3-CF₃Ph (4-FPh)CH₂OCH₂

G 17-448 3-CF₃Ph (2-CIPh)CH₂OCH₂

G 17-449 3-CF₃Ph (3-CIPh)CH₂OCH₂

G 17-450 3-CF₃Ph (4-CIPh)CH₂OCH₂

G17-451 3-CF₃Ph (2-BrPh)CH₂OCH₂

G 17-452 3-CF₃Ph (3-BrPh)CH₂OCH₂

G 17-453 3-CF₃Ph (4-BrPh)CH₂OCH₂

G 17-454 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 17-455 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 17-456 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 17-457 3-CF₃Ph (2-CNPh)CH₂OCH₂

G 17-458 3-CF₃Ph (3-CNPh)CH₂OCH₂

G 17-459 3-CF₃Ph (4-CNPh)CH₂OCH₂

G 17-460 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 17-461 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G 17-462 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 17-463 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G 17-464 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 17-465 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G 17-466 3-CF₃Ph CH₃C(=0)OCH₂

G 17-467 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G 17-468 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 17-469 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G 17-470 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G17-471 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 17-472 3-CF₃Ph CF₃C(=0)OCH₂

G 17-473 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G 17-474 3-CF₃Ph (c-hex)C(=0)OCH₂

G 17-475 3-CF₃Ph PhC(=0)OCH₂

G 17-476 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 17-477 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 17-478 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 17-479 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 17-480 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G17-481 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G 17-482 3-CF₃Ph (2-FPh)C(=0)OCH₂

G 17-483 3-CF₃Ph (3-FPh)C(=0)OCH₂

G 17-484 3-CF₃Ph (4-FPh)C(=0)OCH₂

G 17-485 3-CF₃Ph (2-CIPh)C(=0)OCH₂

G 17-486 3-CF₃Ph (3-CIPh)C(=0)OCH₂

G 17-487 3-CF₃Ph (4-CIPh)C(=0)OCH₂

G 17-488 3-CF₃Ph (2-BrPh)C(=0)OCH₂

G 17-489 3-CF₃Ph (3-BrPh)C(=0)OCH₂

G 17-532 4-CF₃Ph CH₃OCH₂

G17-533 4-CF₃Ph CH₃CH₂OCH₂

G 17-534 4-CF₃Ph (CH₃)₂CHOCH₂

G17-535 4-CF₃Ph (CH₃)₃COCH₂

G 17-536 4-CF₃Ph (CH₃)₃CCH₂0CH₂

G17-537 4-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂

G17-538 4-CF₃Ph (c-hex)OCH₂

G17-539 4-CF₃Ph PhOCH₂

G 17-540 4-CF₃Ph (2-CH₃Ph)OCH₂

G17-541 4-CF₃Ph (3-CH₃Ph)OCH₂

G 17-542 4-CF₃Ph (4-CH₃Ph)OCH₂

G 17-543 4-CF₃Ph (2-CH₃OPh)OCH₂

G 17-544 4-CF₃Ph (3-CH₃OPh)OCH₂

G 17-545 4-CF₃Ph (4-CH₃OPh)OCH₂

G 17-546 4-CF₃Ph (2-FPh)OCH₂

G 17-547 4-CF₃Ph (3-FPh)OCH₂

G 17-548 4-CF₃Ph (4-FPh)OCH₂

G 17-549 4-CF₃Ph (2-CIPh)OCH₂

G17-550 4-CF₃Ph (3-CIPh)OCH₂

G17-551 4-CF₃Ph (4-CIPh)OCH₂

G 17-552 4-CF₃Ph (2-BrPh)OCH₂

G17-553 4-CF₃Ph (3-BrPh)OCH₂

G 17-554 4-CF₃Ph (4-BrPh)OCH₂

G17-555 4-CF₃Ph (2-CF₃OPh)OCH₂

G 17-556 4-CF₃Ph (3-CF₃OPh)OCH₂

G17-557 4-CF₃Ph (4-CF₃OPh)OCH₂

G17-558 4-CF₃Ph (2-CNPh)OCH₂

G17-559 4-CF₃Ph (3-CNPh)OCH₂

G 17-560 4-CF₃Ph (4-CNPh)OCH₂

G17-561 4-CF₃Ph (2-N0₂Ph)OCH₂

G 17-562 4-CF₃Ph (3-N0₂Ph)OCH₂

G 17-563 4-CF₃Ph (4-N0₂Ph)OCH₂

G 17-564 4-CF₃Ph (2-CF₃Ph)OCH₂

G 17-565 4-CF₃Ph (3-CF₃Ph)OCH₂

G 17-566 4-CF₃Ph (4-CF₃Ph)OCH₂

G 17-567 4-CF₃Ph PhCH₂OCH₂

G 17-568 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 17-569 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G17-570 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G17-571 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 17-572 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G17-573 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 17-574 4-CF₃Ph (2-FPh)CH₂OCH₂

G17-575 4-CF₃Ph (3-FPh)CH₂OCH₂

G 17-576 4-CF₃Ph (4-FPh)CH₂OCH₂

G17-577 4-CF₃Ph (2-CIPh)CH₂OCH₂

G17-578 4-CF₃Ph (3-CIPh)CH₂OCH₂

G17-579 4-CF₃Ph (4-CIPh)CH₂OCH₂ G17-580 4-CF₃Ph (2-BrPh)CH₂OCH₂

G17-581 4-CF₃Ph (3-BrPh)CH₂OCH₂

G 17-582 4-CF₃Ph (4-BrPh)CH₂OCH₂

G17-583 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 17-584 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G17-585 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 17-586 4-CF₃Ph (2-CNPh)CH₂OCH₂

G17-587 4-CF₃Ph (3-CNPh)CH₂OCH₂

G17-588 4-CF₃Ph (4-CNPh)CH₂OCH₂

G17-589 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G17-590 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G17-591 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 17-592 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G17-593 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 17-594 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G17-595 4-CF₃Ph CH₃C(=0)OCH₂

G 17-596 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G17-597 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G17-598 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G17-599 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G 17-600 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G17-601 4-CF₃Ph CF₃C(=0)OCH₂

G 17-602 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G 17-603 4-CF₃Ph (c-hex)C(=0)OCH₂

G 17-604 4-CF₃Ph PhC(=0)OCH₂

G 17-605 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 17-606 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 17-607 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 17-608 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 17-609 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G17-610 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G17-611 4-CF₃Ph (2-FPh)C(=0)OCH₂

G17-612 4-CF₃Ph (3-FPh)C(=0)OCH₂

G17-613 4-CF₃Ph (4-FPh)C(=0)OCH₂

G17-614 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G17-615 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G17-616 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G17-617 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G17-618 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G17-619 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G 17-620 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G 17-621 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G 17-622 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G 17-623 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G 17-624 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G 17-625 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G 17-626 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G 17-627 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G 17-670 3,5-(CF₃)₂Ph (3-CH₃Ph)OCH₂

G17-671 3,5-(CF₃)₂Ph (4-CH₃Ph)OCH₂

G 17-672 3,5-(CF₃)₂Ph (2-CH₃OPh)OCH₂

G 17-673 3,5-(CF₃)₂Ph (3-CH₃OPh)OCH₂

G 17-674 3,5-(CF₃)₂Ph (4-CH₃OPh)OCH₂

G 17-675 3,5-(CF₃)₂Ph (2-FPh)OCH₂

G 17-676 3,5-(CF₃)₂Ph (3-FPh)OCH₂

G 17-677 3,5-(CF₃)₂Ph (4-FPh)OCH₂

G 17-678 3,5-(CF₃)₂Ph (2-CIPh)OCH₂

G 17-679 3,5-(CF₃)₂Ph (3-CIPh)OCH₂

G 17-680 3,5-(CF₃)₂Ph (4-CIPh)OCH₂

G17-681 3,5-(CF₃)₂Ph (2-BrPh)OCH₂

G 17-682 3,5-(CF₃)₂Ph (3-BrPh)OCH₂

G 17-683 3,5-(CF₃)₂Ph (4-BrPh)OCH₂

G 17-684 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂

G 17-685 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂

G 17-686 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂

G 17-687 3,5-(CF₃)₂Ph (2-CNPh)OCH₂

G 17-688 3,5-(CF₃)₂Ph (3-CNPh)OCH₂

G 17-689 3,5-(CF₃)₂Ph (4-CNPh)OCH₂

G 17-690 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂

G17-691 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G 17-692 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G 17-693 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G 17-694 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G 17-695 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G 17-696 3,5-(CF₃)₂Ph PhCH₂OCH₂

G 17-697 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G 17-698 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G 17-699 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G17-700 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G17-701 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G 17-702 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G17-703 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G 17-704 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G17-705 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G 17-706 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G17-707 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G17-708 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G17-709 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G17-710 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G17-711 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G17-712 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G17-713 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G17-714 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G17-715 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G17-716 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G17-717 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂ G17-718 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G17-719 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G 17-720 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G17-721 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G 17-722 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G 17-723 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G 17-724 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G 17-725 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G 17-726 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂

G 17-727 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G 17-728 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G 17-729 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G17-730 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G17-731 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G 17-732 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G17-733 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G 17-734 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G17-735 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G 17-736 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G17-737 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G17-738 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G17-739 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G 17-740 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G17-741 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G 17-742 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G 17-743 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G 17-744 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G 17-745 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G 17-746 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G 17-747 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G 17-748 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G 17-749 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G17-750 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G17-751 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G 17-752 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G17-753 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G 17-754 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G17-755 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G 17-756 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G17-757 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G17-758 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G17-759 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G 17-760 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0308] Table 9 f

G18-177 CF₃ (2-CF₃Ph)OCH₂

G18-178 CF₃ (3-CF₃Ph)OCH₂

G18-179 CF₃ (4-CF₃Ph)OCH₂

G18-180 CF₃ PhCH₂OCH₂

G18-181 CF₃ (2-CH₃Ph)CH₂OCH₂

G18-182 CF₃ (3-CH₃Ph)CH₂OCH₂

G18-183 CF₃ (4-CH₃Ph)CH₂OCH₂

G18-184 CF₃ (2-CH₃OPh)CH₂OCH₂

G18-185 CF₃ (3-CH₃OPh)CH₂OCH₂

G18-186 CF₃ (4-CH₃OPh)CH₂OCH₂

G18-187 CF₃ (2-FPh)CH₂OCH₂

G18-188 CF₃ (3-FPh)CH₂OCH₂

G18-189 CF₃ (4-FPh)CH₂OCH₂

G18-190 CF₃ (2-CIPh)CH₂OCH₂

G18-191 CF₃ (3-CIPh)CH₂OCH₂

G18-192 CF₃ (4-CIPh)CH₂OCH₂

G18-193 CF₃ (2-BrPh)CH₂OCH₂

G18-194 CF₃ (3-BrPh)CH₂OCH₂

G18-195 CF₃ (4-BrPh)CH₂OCH₂

G18-196 CF₃ (2-CF₃OPh)CH₂OCH₂

G18-197 CF₃ (3-CF₃OPh)CH₂OCH₂

G18-198 CF₃ (4-CF₃OPh)CH₂OCH₂

G18-199 CF₃ (2-CNPh)CH₂OCH₂

G 18-200 CF₃ (3-CNPh)CH₂OCH₂

G18-201 CF₃ (4-CNPh)CH₂OCH₂

G 18-202 CF₃ (2-N0₂Ph)CH₂OCH₂

G 18-203 CF₃ (3-N0₂Ph)CH₂OCH₂

G 18-204 CF₃ (4-N0₂Ph)CH₂OCH₂

G 18-205 CF₃ (2-CF₃Ph)CH₂OCH₂

G 18-206 CF₃ (3-CF₃Ph)CH₂OCH₂

G 18-207 CF₃ (4-CF₃Ph)CH₂OCH₂

G 18-208 CF₃ CH₃C(=0)OCH₂

G 18-209 CF₃ CH₃CH₂C(=0)OCH₂

G18-210 CF₃ CH(CH₃)₂C(=0)OCH₂

G18-211 CF₃ (CH₃)₃C(=0)OCH₂

G18-212 CF₃ (CH₃)₃CCH₂(=0)OCH₂

G18-213 CF₃ CH₃CH₂C(CH₃)₂C(=0)OCH₂

G18-214 CF₃ CF₃C(=0)OCH₂

G18-215 CF₃ CF₃CF₂C(=0)OCH₂

G18-216 CF₃ (c-hex)C(=0)OCH₂

G18-217 CF₃ PhC(=0)OCH₂

G18-218 CF₃ (2-CH₃Ph)C(=0)OCH₂

G18-219 CF₃ (3-CH₃Ph)C(=0)OCH₂

G 18-220 CF₃ (4-CH₃Ph)C(=0)OCH₂

G 18-221 CF₃ (2-CH₃OPh)C(=0)OCH₂

G 18-222 CF₃ (3-CH₃OPh)C(=0)OCH₂

G 18-223 CF₃ (4-CH₃OPh)C(=0)OCH₂

G 18-224 CF₃ (2-FPh)C(=0)OCH₂

G18-313 2-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G18-314 2-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G18-315 2-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G18-316 2-CF₃Ph (2-FPh)CH₂OCH₂

G18-317 2-CF₃Ph (3-FPh)CH₂OCH₂

G18-318 2-CF₃Ph (4-FPh)CH₂OCH₂

G18-319 2-CF₃Ph (2-CIPh)CH₂OCH₂

G 18-320 2-CF₃Ph (3-CIPh)CH₂OCH₂

G18-321 2-CF₃Ph (4-CIPh)CH₂OCH₂

G 18-322 2-CF₃Ph (2-BrPh)CH₂OCH₂

G 18-323 2-CF₃Ph (3-BrPh)CH₂OCH₂

G 18-324 2-CF₃Ph (4-BrPh)CH₂OCH₂

G 18-325 2-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 18-326 2-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 18-327 2-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 18-328 2-CF₃Ph (2-CNPh)CH₂OCH₂

G 18-329 2-CF₃Ph (3-CNPh)CH₂OCH₂

G18-330 2-CF₃Ph (4-CNPh)CH₂OCH₂

G18-331 2-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 18-332 2-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G18-333 2-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 18-334 2-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G18-335 2-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 18-336 2-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G18-337 2-CF₃Ph CH₃C(=0)OCH₂

G18-338 2-CF₃Ph CH₃CH₂C(=0)OCH₂

G18-339 2-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 18-340 2-CF₃Ph (CH₃)₃C(=0)OCH₂

G18-341 2-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G 18-342 2-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 18-343 2-CF₃Ph CF₃C(=0)OCH₂

G 18-344 2-CF₃Ph CF₃CF₂C(=0)OCH₂

G 18-345 2-CF₃Ph (c-hex)C(=0)OCH₂

G 18-346 2-CF₃Ph PhC(=0)OCH₂

G 18-347 2-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 18-348 2-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 18-349 2-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G18-350 2-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G18-351 2-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G 18-352 2-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G18-353 2-CF₃Ph (2-FPh)C(=0)OCH₂

G 18-354 2-CF₃Ph (3-FPh)C(=0)OCH₂

G18-355 2-CF₃Ph (4-FPh)C(=0)OCH₂

G 18-356 2-CF₃Ph (2-CIPh)C(=0)OCH₂

G18-357 2-CF₃Ph (3-CIPh)C(=0)OCH₂

G18-358 2-CF₃Ph (4-CIPh)C(=0)OCH₂

G18-359 2-CF₃Ph (2-BrPh)C(=0)OCH₂

G 18-360 2-CF₃Ph (3-BrPh)C(=0)OCH₂

G 18-403 3-CF₃Ph CH₃OCH₂

G 18-404 3-CF₃Ph CH₃CH₂OCH₂

G 18-405 3-CF₃Ph (CH₃)₂CHOCH₂

G 18-406 3-CF₃Ph (CH₃)₃COCH₂

G 18-407 3-CF₃Ph (CH₃)₃CCH₂0CH₂

G 18-408 3-CF₃Ph CH₃CH₂C(CH₃)₂OCH₂

G 18-409 3-CF₃Ph (c-hex)OCH₂

G18-410 3-CF₃Ph PhOCH₂

G18-41 1 3-CF₃Ph (2-CH₃Ph)OCH₂

G18-412 3-CF₃Ph (3-CH₃Ph)OCH₂

G18-413 3-CF₃Ph (4-CH₃Ph)OCH₂

G18-414 3-CF₃Ph (2-CH₃OPh)OCH₂

G18-415 3-CF₃Ph (3-CH₃OPh)OCH₂

G18-416 3-CF₃Ph (4-CH₃OPh)OCH₂

G18-417 3-CF₃Ph (2-FPh)OCH₂

G18-418 3-CF₃Ph (3-FPh)OCH₂

G18-419 3-CF₃Ph (4-FPh)OCH₂

G 18-420 3-CF₃Ph (2-CIPh)OCH₂

G 18-421 3-CF₃Ph (3-CIPh)OCH₂

G 18-422 3-CF₃Ph (4-CIPh)OCH₂

G 18-423 3-CF₃Ph (2-BrPh)OCH₂

G 18-424 3-CF₃Ph (3-BrPh)OCH₂

G 18-425 3-CF₃Ph (4-BrPh)OCH₂

G 18-426 3-CF₃Ph (2-CF₃OPh)OCH₂

G 18-427 3-CF₃Ph (3-CF₃OPh)OCH₂

G 18-428 3-CF₃Ph (4-CF₃OPh)OCH₂

G 18-429 3-CF₃Ph (2-CNPh)OCH₂

G 18-430 3-CF₃Ph (3-CNPh)OCH₂

G18-431 3-CF₃Ph (4-CNPh)OCH₂

G 18-432 3-CF₃Ph (2-N0₂Ph)OCH₂

G 18-433 3-CF₃Ph (3-N0₂Ph)OCH₂

G 18-434 3-CF₃Ph (4-N0₂Ph)OCH₂

G 18-435 3-CF₃Ph (2-CF₃Ph)OCH₂

G 18-436 3-CF₃Ph (3-CF₃Ph)OCH₂

G 18-437 3-CF₃Ph (4-CF₃Ph)OCH₂

G 18-438 3-CF₃Ph PhCH₂OCH₂

G 18-439 3-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 18-440 3-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G 18-441 3-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G 18-442 3-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 18-443 3-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G 18-444 3-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 18-445 3-CF₃Ph (2-FPh)CH₂OCH₂

G 18-446 3-CF₃Ph (3-FPh)CH₂OCH₂

G 18-447 3-CF₃Ph (4-FPh)CH₂OCH₂

G 18-448 3-CF₃Ph (2-CIPh)CH₂OCH₂

G 18-449 3-CF₃Ph (3-CIPh)CH₂OCH₂

G 18-450 3-CF₃Ph (4-CIPh)CH₂OCH₂ G18-451 3-CF₃Ph (2-BrPh)CH₂OCH₂

G 18-452 3-CF₃Ph (3-BrPh)CH₂OCH₂

G 18-453 3-CF₃Ph (4-BrPh)CH₂OCH₂

G 18-454 3-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 18-455 3-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G 18-456 3-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 18-457 3-CF₃Ph (2-CNPh)CH₂OCH₂

G 18-458 3-CF₃Ph (3-CNPh)CH₂OCH₂

G 18-459 3-CF₃Ph (4-CNPh)CH₂OCH₂

G 18-460 3-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G 18-461 3-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G 18-462 3-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 18-463 3-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G 18-464 3-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 18-465 3-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G 18-466 3-CF₃Ph CH₃C(=0)OCH₂

G 18-467 3-CF₃Ph CH₃CH₂C(=0)OCH₂

G 18-468 3-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G 18-469 3-CF₃Ph (CH₃)₃C(=0)OCH₂

G 18-470 3-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G18-471 3-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G 18-472 3-CF₃Ph CF₃C(=0)OCH₂

G 18-473 3-CF₃Ph CF₃CF₂C(=0)OCH₂

G 18-474 3-CF₃Ph (c-hex)C(=0)OCH₂

G 18-475 3-CF₃Ph PhC(=0)OCH₂

G 18-476 3-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 18-477 3-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 18-478 3-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 18-479 3-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 18-480 3-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G18-481 3-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G 18-482 3-CF₃Ph (2-FPh)C(=0)OCH₂

G 18-483 3-CF₃Ph (3-FPh)C(=0)OCH₂

G 18-484 3-CF₃Ph (4-FPh)C(=0)OCH₂

G 18-485 3-CF₃Ph (2-CIPh)C(=0)OCH₂

G 18-486 3-CF₃Ph (3-CIPh)C(=0)OCH₂

G 18-487 3-CF₃Ph (4-CIPh)C(=0)OCH₂

G 18-488 3-CF₃Ph (2-BrPh)C(=0)OCH₂

G 18-489 3-CF₃Ph (3-BrPh)C(=0)OCH₂

G 18-490 3-CF₃Ph (4-BrPh)C(=0)OCH₂

G18-491 3-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G 18-492 3-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G 18-493 3-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G 18-494 3-CF₃Ph (2-CNPh)C(=0)OCH₂

G 18-495 3-CF₃Ph (3-CNPh)C(=0)OCH₂

G 18-496 3-CF₃Ph (4-CNPh)C(=0)OCH₂

G 18-497 3-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G 18-498 3-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G18-541 4-CF₃Ph (3-CH₃Ph)OCH₂

G 18-542 4-CF₃Ph (4-CH₃Ph)OCH₂

G 18-543 4-CF₃Ph (2-CH₃OPh)OCH₂

G 18-544 4-CF₃Ph (3-CH₃OPh)OCH₂

G 18-545 4-CF₃Ph (4-CH₃OPh)OCH₂

G 18-546 4-CF₃Ph (2-FPh)OCH₂

G 18-547 4-CF₃Ph (3-FPh)OCH₂

G 18-548 4-CF₃Ph (4-FPh)OCH₂

G 18-549 4-CF₃Ph (2-CIPh)OCH₂

G18-550 4-CF₃Ph (3-CIPh)OCH₂

G18-551 4-CF₃Ph (4-CIPh)OCH₂

G 18-552 4-CF₃Ph (2-BrPh)OCH₂

G18-553 4-CF₃Ph (3-BrPh)OCH₂

G 18-554 4-CF₃Ph (4-BrPh)OCH₂

G18-555 4-CF₃Ph (2-CF₃OPh)OCH₂

G 18-556 4-CF₃Ph (3-CF₃OPh)OCH₂

G18-557 4-CF₃Ph (4-CF₃OPh)OCH₂

G18-558 4-CF₃Ph (2-CNPh)OCH₂

G18-559 4-CF₃Ph (3-CNPh)OCH₂

G 18-560 4-CF₃Ph (4-CNPh)OCH₂

G18-561 4-CF₃Ph (2-N0₂Ph)OCH₂

G 18-562 4-CF₃Ph (3-N0₂Ph)OCH₂

G 18-563 4-CF₃Ph (4-N0₂Ph)OCH₂

G 18-564 4-CF₃Ph (2-CF₃Ph)OCH₂

G 18-565 4-CF₃Ph (3-CF₃Ph)OCH₂

G 18-566 4-CF₃Ph (4-CF₃Ph)OCH₂

G 18-567 4-CF₃Ph PhCH₂OCH₂

G 18-568 4-CF₃Ph (2-CH₃Ph)CH₂OCH₂

G 18-569 4-CF₃Ph (3-CH₃Ph)CH₂OCH₂

G18-570 4-CF₃Ph (4-CH₃Ph)CH₂OCH₂

G18-571 4-CF₃Ph (2-CH₃OPh)CH₂OCH₂

G 18-572 4-CF₃Ph (3-CH₃OPh)CH₂OCH₂

G18-573 4-CF₃Ph (4-CH₃OPh)CH₂OCH₂

G 18-574 4-CF₃Ph (2-FPh)CH₂OCH₂

G18-575 4-CF₃Ph (3-FPh)CH₂OCH₂

G 18-576 4-CF₃Ph (4-FPh)CH₂OCH₂

G18-577 4-CF₃Ph (2-CIPh)CH₂OCH₂

G18-578 4-CF₃Ph (3-CIPh)CH₂OCH₂

G18-579 4-CF₃Ph (4-CIPh)CH₂OCH₂

G18-580 4-CF₃Ph (2-BrPh)CH₂OCH₂

G18-581 4-CF₃Ph (3-BrPh)CH₂OCH₂

G 18-582 4-CF₃Ph (4-BrPh)CH₂OCH₂

G18-583 4-CF₃Ph (2-CF₃OPh)CH₂OCH₂

G 18-584 4-CF₃Ph (3-CF₃OPh)CH₂OCH₂

G18-585 4-CF₃Ph (4-CF₃OPh)CH₂OCH₂

G 18-586 4-CF₃Ph (2-CNPh)CH₂OCH₂

G18-587 4-CF₃Ph (3-CNPh)CH₂OCH₂

G18-588 4-CF₃Ph (4-CNPh)CH₂OCH₂ G18-589 4-CF₃Ph (2-N0₂Ph)CH₂OCH₂

G18-590 4-CF₃Ph (3-N0₂Ph)CH₂OCH₂

G18-591 4-CF₃Ph (4-N0₂Ph)CH₂OCH₂

G 18-592 4-CF₃Ph (2-CF₃Ph)CH₂OCH₂

G18-593 4-CF₃Ph (3-CF₃Ph)CH₂OCH₂

G 18-594 4-CF₃Ph (4-CF₃Ph)CH₂OCH₂

G18-595 4-CF₃Ph CH₃C(=0)OCH₂

G 18-596 4-CF₃Ph CH₃CH₂C(=0)OCH₂

G18-597 4-CF₃Ph CH(CH₃)₂C(=0)OCH₂

G18-598 4-CF₃Ph (CH₃)₃C(=0)OCH₂

G18-599 4-CF₃Ph (CH₃)₃CCH₂(=0)OCH₂

G 18-600 4-CF₃Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G18-601 4-CF₃Ph CF₃C(=0)OCH₂

G 18-602 4-CF₃Ph CF₃CF₂C(=0)OCH₂

G 18-603 4-CF₃Ph (c-hex)C(=0)OCH₂

G 18-604 4-CF₃Ph PhC(=0)OCH₂

G 18-605 4-CF₃Ph (2-CH₃Ph)C(=0)OCH₂

G 18-606 4-CF₃Ph (3-CH₃Ph)C(=0)OCH₂

G 18-607 4-CF₃Ph (4-CH₃Ph)C(=0)OCH₂

G 18-608 4-CF₃Ph (2-CH₃OPh)C(=0)OCH₂

G 18-609 4-CF₃Ph (3-CH₃OPh)C(=0)OCH₂

G18-610 4-CF₃Ph (4-CH₃OPh)C(=0)OCH₂

G18-611 4-CF₃Ph (2-FPh)C(=0)OCH₂

G18-612 4-CF₃Ph (3-FPh)C(=0)OCH₂

G18-613 4-CF₃Ph (4-FPh)C(=0)OCH₂

G18-614 4-CF₃Ph (2-CIPh)C(=0)OCH₂

G18-615 4-CF₃Ph (3-CIPh)C(=0)OCH₂

G18-616 4-CF₃Ph (4-CIPh)C(=0)OCH₂

G18-617 4-CF₃Ph (2-BrPh)C(=0)OCH₂

G18-618 4-CF₃Ph (3-BrPh)C(=0)OCH₂

G18-619 4-CF₃Ph (4-BrPh)C(=0)OCH₂

G 18-620 4-CF₃Ph (2-CF₃OPh)C(=0)OCH₂

G 18-621 4-CF₃Ph (3-CF₃OPh)C(=0)OCH₂

G 18-622 4-CF₃Ph (4-CF₃OPh)C(=0)OCH₂

G 18-623 4-CF₃Ph (2-CNPh)C(=0)OCH₂

G 18-624 4-CF₃Ph (3-CNPh)C(=0)OCH₂

G 18-625 4-CF₃Ph (4-CNPh)C(=0)OCH₂

G 18-626 4-CF₃Ph (2-N0₂Ph)C(=0)OCH₂

G 18-627 4-CF₃Ph (3-N0₂Ph)C(=0)OCH₂

G 18-628 4-CF₃Ph (4-N0₂Ph)C(=0)OCH₂

G 18-629 4-CF₃Ph (2-CF₃Ph)C(=0)OCH₂

G 18-630 4-CF₃Ph (3-CF₃Ph)C(=0)OCH₂

G18-631 4-CF₃Ph (4-CF₃Ph)C(=0)OCH₂

G 18-632 3,5-(CF₃)₂Ph CH₃

G 18-633 3,5-(CF₃)₂Ph CH3CH2

G 18-634 3,5-(CF₃)₂Ph CH3CH2CH2

G 18-635 3,5-(CF₃)₂Ph (CH₃)₂CH

G 18-636 3,5-(CF₃)₂Ph CH₃C(=0)

G 18-679 3,5-(CF₃)₂Ph (3-CIPh)OCH₂

G 18-680 3,5-(CF₃)₂Ph (4-CIPh)OCH₂

G18-681 3,5-(CF₃)₂Ph (2-BrPh)OCH₂

G 18-682 3,5-(CF₃)₂Ph (3-BrPh)OCH₂

G 18-683 3,5-(CF₃)₂Ph (4-BrPh)OCH₂

G 18-684 3,5-(CF₃)₂Ph (2-CF₃OPh)OCH₂

G 18-685 3,5-(CF₃)₂Ph (3-CF₃OPh)OCH₂

G 18-686 3,5-(CF₃)₂Ph (4-CF₃OPh)OCH₂

G 18-687 3,5-(CF₃)₂Ph (2-CNPh)OCH₂

G 18-688 3,5-(CF₃)₂Ph (3-CNPh)OCH₂

G 18-689 3,5-(CF₃)₂Ph (4-CNPh)OCH₂

G 18-690 3,5-(CF₃)₂Ph (2-N0₂Ph)OCH₂

G18-691 3,5-(CF₃)₂Ph (3-N0₂Ph)OCH₂

G 18-692 3,5-(CF₃)₂Ph (4-N0₂Ph)OCH₂

G 18-693 3,5-(CF₃)₂Ph (2-CF₃Ph)OCH₂

G 18-694 3,5-(CF₃)₂Ph (3-CF₃Ph)OCH₂

G 18-695 3,5-(CF₃)₂Ph (4-CF₃Ph)OCH₂

G 18-696 3,5-(CF₃)₂Ph PhCH₂OCH₂

G 18-697 3,5-(CF₃)₂Ph (2-CH₃Ph)CH₂OCH₂

G 18-698 3,5-(CF₃)₂Ph (3-CH₃Ph)CH₂OCH₂

G 18-699 3,5-(CF₃)₂Ph (4-CH₃Ph)CH₂OCH₂

G18-700 3,5-(CF₃)₂Ph (2-CH₃OPh)CH₂OCH₂

G18-701 3,5-(CF₃)₂Ph (3-CH₃OPh)CH₂OCH₂

G 18-702 3,5-(CF₃)₂Ph (4-CH₃OPh)CH₂OCH₂

G18-703 3,5-(CF₃)₂Ph (2-FPh)CH₂OCH₂

G 18-704 3,5-(CF₃)₂Ph (3-FPh)CH₂OCH₂

G18-705 3,5-(CF₃)₂Ph (4-FPh)CH₂OCH₂

G 18-706 3,5-(CF₃)₂Ph (2-CIPh)CH₂OCH₂

G18-707 3,5-(CF₃)₂Ph (3-CIPh)CH₂OCH₂

G18-708 3,5-(CF₃)₂Ph (4-CIPh)CH₂OCH₂

G18-709 3,5-(CF₃)₂Ph (2-BrPh)CH₂OCH₂

G18-710 3,5-(CF₃)₂Ph (3-BrPh)CH₂OCH₂

G18-711 3,5-(CF₃)₂Ph (4-BrPh)CH₂OCH₂

G18-712 3,5-(CF₃)₂Ph (2-CF₃OPh)CH₂OCH₂

G18-713 3,5-(CF₃)₂Ph (3-CF₃OPh)CH₂OCH₂

G18-714 3,5-(CF₃)₂Ph (4-CF₃OPh)CH₂OCH₂

G18-715 3,5-(CF₃)₂Ph (2-CNPh)CH₂OCH₂

G18-716 3,5-(CF₃)₂Ph (3-CNPh)CH₂OCH₂

G18-717 3,5-(CF₃)₂Ph (4-CNPh)CH₂OCH₂

G18-718 3,5-(CF₃)₂Ph (2-N0₂Ph)CH₂OCH₂

G18-719 3,5-(CF₃)₂Ph (3-N0₂Ph)CH₂OCH₂

G 18-720 3,5-(CF₃)₂Ph (4-N0₂Ph)CH₂OCH₂

G18-721 3,5-(CF₃)₂Ph (2-CF₃Ph)CH₂OCH₂

G 18-722 3,5-(CF₃)₂Ph (3-CF₃Ph)CH₂OCH₂

G 18-723 3,5-(CF₃)₂Ph (4-CF₃Ph)CH₂OCH₂

G 18-724 3,5-(CF₃)₂Ph CH₃C(=0)OCH₂

G 18-725 3,5-(CF₃)₂Ph CH₃CH₂C(=0)OCH₂

G 18-726 3,5-(CF₃)₂Ph CH(CH₃)₂C(=0)OCH₂ G 18-727 3,5-(CF₃)₂Ph (CH₃)₃C(=0)OCH₂

G 18-728 3,5-(CF₃)₂Ph (CH₃)₃CCH₂(=0)OCH₂

G 18-729 3,5-(CF₃)₂Ph CH₃CH₂C(CH₃)₂C(=0)OCH₂

G18-730 3,5-(CF₃)₂Ph CF₃C(=0)OCH₂

G18-731 3,5-(CF₃)₂Ph CF₃CF₂C(=0)OCH₂

G 18-732 3,5-(CF₃)₂Ph (c-hex)C(=0)OCH₂

G18-733 3,5-(CF₃)₂Ph PhC(=0)OCH₂

G 18-734 3,5-(CF₃)₂Ph (2-CH₃Ph)C(=0)OCH₂

G18-735 3,5-(CF₃)₂Ph (3-CH₃Ph)C(=0)OCH₂

G 18-736 3,5-(CF₃)₂Ph (4-CH₃Ph)C(=0)OCH₂

G18-737 3,5-(CF₃)₂Ph (2-CH₃OPh)C(=0)OCH₂

G18-738 3,5-(CF₃)₂Ph (3-CH₃OPh)C(=0)OCH₂

G18-739 3,5-(CF₃)₂Ph (4-CH₃OPh)C(=0)OCH₂

G 18-740 3,5-(CF₃)₂Ph (2-FPh)C(=0)OCH₂

G18-741 3,5-(CF₃)₂Ph (3-FPh)C(=0)OCH₂

G 18-742 3,5-(CF₃)₂Ph (4-FPh)C(=0)OCH₂

G 18-743 3,5-(CF₃)₂Ph (2-CIPh)C(=0)OCH₂

G 18-744 3,5-(CF₃)₂Ph (3-CIPh)C(=0)OCH₂

G 18-745 3,5-(CF₃)₂Ph (4-CIPh)C(=0)OCH₂

G 18-746 3,5-(CF₃)₂Ph (2-BrPh)C(=0)OCH₂

G 18-747 3,5-(CF₃)₂Ph (3-BrPh)C(=0)OCH₂

G 18-748 3,5-(CF₃)₂Ph (4-BrPh)C(=0)OCH₂

G 18-749 3,5-(CF₃)₂Ph (2-CF₃OPh)C(=0)OCH₂

G18-750 3,5-(CF₃)₂Ph (3-CF₃OPh)C(=0)OCH₂

G18-751 3,5-(CF₃)₂Ph (4-CF₃OPh)C(=0)OCH₂

G 18-752 3,5-(CF₃)₂Ph (2-CNPh)C(=0)OCH₂

G18-753 3,5-(CF₃)₂Ph (3-CNPh)C(=0)OCH₂

G 18-754 3,5-(CF₃)₂Ph (4-CNPh)C(=0)OCH₂

G18-755 3,5-(CF₃)₂Ph (2-N0₂Ph)C(=0)OCH₂

G 18-756 3,5-(CF₃)₂Ph (3-N0₂Ph)C(=0)OCH₂

G18-757 3,5-(CF₃)₂Ph (4-N0₂Ph)C(=0)OCH₂

G18-758 3,5-(CF₃)₂Ph (2-CF₃Ph)C(=0)OCH₂

G18-759 3,5-(CF₃)₂Ph (3-CF₃Ph)C(=0)OCH₂

G 18-760 3,5-(CF₃)₂Ph (4-CF₃Ph)C(=0)OCH₂

[0309] Table 10

G 13-20 H-NMR (DMSO-d₆) δ: 9.61 (1 H, s), 9.20 (1 H, s), 8.63 (2H, d), 7.96 (2H, d)

G16-1 H-NMR (DMSO-d₆) δ: 8.78 (1 H, s)

G18-1 H-NMR (DMSO-d₆) δ: 8.88 (1 H, s)

[0310] A novel insecticidal oxadiazolinone derivative of the present invention usually has high activity and exhibits safety. Furthermore, the oxadiazolinone derivative of the present invention is highly environmentally safe because of being degraded in the natural world and is exceedingly useful as an insecticide and the like.

Claims

Claims

1. An oxadiazolinone derivative represented by the formula (I):

wherein

G represents a 5- or 6-membered heterocyclic ring containing at least one of oxygen, nitrogen and sulfur atoms, and the heterocyclic ring may be substituted by R³, with the proviso that when G represents a pyridine ring substituted by R³ and when the nitrogen atom in the pyridine ring is at an ortho position relative to the carbon atom bonded to the oxadiazolinone ring, the positions of the carbon atom bonded to R¹ and the carbon atom bonded to R³ are each limited to any position selected from the ortho and meta positions relative to this nitrogen atom;

R³ represents hydrogen, halogen, nitro, cyano, C_M2 alkyl, C_M2 haloalkyi, C_M2 alkoxy, Ci-₁₂ haloalkoxy, C_M2 alkylsulfenyl, C_M2 alkylsulfinyl, C_M2 alkylsulfonyl, C_M2 haloalkylsulfenyl, Ci-₁₂ haloalkylsulfinyl, C_M2 haloalkylsulfonyl, hydroxy, mercapto or C₃.₈ cycloalkyl;

X represents an oxygen or sulfur atom;

R¹ represents C_M2 haloalkyi, C_M2 haloalkoxy, C_M2 alkoxy, phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylsulfinyl, phenylsulfonyl, phenylamino, (phenyl)(Ci_i₂ alkyl)amino, phenyl- Ci-₁₂ alkoxy, phenyl-Ci_i₂ alkylsulfenyl, phenyl-Ci_i₂ alkylsulfinyl, phenyl-Ci_i₂ alkylsulfonyl, phenyl-Ci_i₂ alkylamino, C_M2 alkylsulfenyl, C_M2 alkylsulfinyl, C_M2 alkylsulfonyl, C_{M 2}

haloalkylsulfenyl, C_M2 haloalkylsulfinyl, C_M2 haloalkylsulfonyl, C_M2 alkylsulfinyl-Ci-i₂ alkyl, Ci. 12 alkylsulfonyl-Ci-12 alkyl, CM₂ haloalkylsulfenyl-Ci-i₂ alkyl, CM₂ haloalkylsulfinyl-Ci-i₂ alkyl, Ci- 12 haloalkylsulfonyl-Ci-i2 alkyl, C2-12 alkenyloxy, C2-12 haloalkenyloxy, C2-12 alkynyloxy, C2-12 haloalkynyloxy, (C_M2 alkyl)₃ silyloxy or hydroxy, and these substituents can be optionally substituted by a substituent(s) selected from halogen, cyano, amino, mercapto, C_M2 alkyl, Ci- 12 haloalkyi, C_M2 haloalkoxy, C2-12 alkenyloxy, C2-12 haloalkenyloxy, C2-12 alkynyloxy, C2-12 haloalkynyloxy, C_M2 alkylsulfenyl-Ci-12 alkyl and hydroxy; and

R² represents hydrogen, -CH₂CN, C_M2 alkyl, C_M2 haloalkyi, C₃.₈ cycloalkyl which may be optionally substituted by a substituent(s) selected from halogen, C_M2 alkyl and C_{M 2} haloalkyi, benzyl which may be optionally substituted by a substituent selected from halogen, cyano, nitro, Ci_₃ alkyl, Ci_₃ haloalkyl and Ci_₃ alkoxy or a substituent represented by one selected from the following formulas Q1 , Q2, Q3, Q4, and Q5:

wherein, in each of the formulas Q1 to Q5,

a bond marked with * represents a bond with the nitrogen atom bonded to R² in the formula (I);

R²¹ represents hydrogen, CM₂ alkyl, CM₂ haloalkyl or C₃.₈ cycloalkyl;

R²² and R²³ individually represent hydrogen, CM₂ alkyl, CM₂ haloalkyl, CM₂ alkoxy, C₃.₈ cycloalkyl, C₂_i₂ alkenyloxy or C₂_i₂ alkynyloxy, or R²² and R²³ form a 3- to 8-membered heterocyclic ring together with the nitrogen atom bonded thereto, and the heterocyclic ring may be substituted by a substituent(s) selected from halogen, CM₂ alkyl, CM₂ haloalkyl, nitro, CM₂ alkoxy, cyano, CM₂ haloalkoxy, CM₂ alkylsulfenyl, CM₂ alkylsulfinyl, CM₂ alkylsulfonyl, CM₂ haloalkylsulfenyl, CM₂ haloalkylsulfinyl, CM₂ haloalkylsulfonyl, hydroxy and mercapto;

R²⁴ and R²⁵ individually represent a substituent selected from CM₂ alkyl, CM₂ haloalkyl, C₃-8 cycloalkyl, phenyl and phenyl-Ci_₃ alkyl, and these substituents can be optionally substituted by a substituent(s) selected from halogen, CM₂ alkyl, CM₂ haloalkyl, nitro, CM₂ alkoxy, cyano, CM₂ haloalkoxy, CM₂ alkylsulfenyl, CM₂ alkylsulfinyl, CM₂ alkylsulfonyl, CM₂ haloalkylsulfenyl, CM₂ haloalkylsulfinyl, CM₂ haloalkylsulfonyl, hydroxy and mercapto; and

R²⁶ represents a hydrogen atom or CM₂ alkyl.

2. The oxadiazolinone derivative according to claim 1 , wherein when the heterocyclic ring constituting G is substituted by R³,

R³ represents hydrogen, halogen, nitro, cyano, Ci_₆ alkyl, Ci_₆ haloalkyl, Ci_₆ alkoxy, Ci_₆ haloalkoxy, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, hydroxy, mercapto or C₃.₇ cycloalkyl;

X represents an oxygen or sulfur atom;

R¹ represents Ci_₆ haloalkyl, Ci_₆ haloalkoxy, Ci_₆ alkoxy, phenyl, phenoxy, pyridyl, phenylsulfenyl, phenylsulfinyl, phenylsulfonyl, phenylamino, (phenyl)(Ci_₆ alkyl)amino, phenyl- Ci-3 alkoxy, phenyl-Ci_₃ alkylsulfenyl, phenyl-Ci_₃ alkylsulfinyl, phenyl-Ci_₃ alkylsulfonyl, phenyl- Ci-3 alkylamino, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, Ci_₆ alkylsulfinyl-Ci_-3 alkyl, Ci_₆ alkylsulfonyl-Ci_₃ alkyl, Ci-6 haloalkylsulfenyl-Ci_₃ alkyl, Ci_₆ haloalkylsulfinyl-Ci_-3 alkyl, Ci_₆ haloalkylsulfonyl-Ci_₃ alkyl, C₂-6 alkenyloxy, C₂-6 haloalkenyloxy, C₂-6 alkynyloxy, C₂-6 haloalkynyloxy, (Ci_₆ alkyl)₃ silyloxy or hydroxy, and these substituents can be optionally substituted by a substituent(s) selected from halogen, cyano, amino, mercapto, Ci_₆ alkyl, Ci_₆ haloalkyl, Ci_₆ haloalkoxy, C₂-6 alkenyloxy, C₂. 6 haloalkenyloxy, C₂.₆ alkynyloxy, C₂.₆ haloalkynyloxy, Ci_₆ alkylsulfenyl-Ci.₃ alkyl and hydroxy; and

R² represents hydrogen, -CH₂CN, Ci_₆ alkyl, Ci_₆ haloalkyl, C₃.₆ cycloalkyl optionally substituted by a substituent selected from halogen, Ci_₆ alkyl and Ci_₆ haloalkyl, benzyl optionally substituted by a substituent selected from halogen, cyano, nitro, Ci_₆ alkyl, Ci_₆ haloalkyl and Ci_₆ alkoxy or a substituent represented by one selected from the following formulas Q1 , Q2, Q3, Q4, and Q5:

Q 1 Q 2 Q 3 Q 4 Q 5

wherein, in each of the formulas Q1 to Q5,

a bond marked with * represents a bond with the nitrogen atom bonded to R² in the formula (I);

R²¹ represents hydrogen, Ci_₆ alkyl, Ci_₆ haloalkyl or C₃.₆ cycloalkyl;

R²² and R²³ individually represent hydrogen, Ci_₆ alkyl, Ci_₆ haloalkyl, Ci_₆ alkoxy, C₃.₇ cycloalkyl, C₂.₆ alkenyloxy or C₂.₆ alkynyloxy, or R²² and R²³ form a 3- to 8-membered heterocyclic ring together with the nitrogen atom bonded thereto, and the heterocyclic ring can be optionally substituted by a substituent selected from halogen, Ci_₆ alkyl, Ci_₆ haloalkyl, nitro, C1-6 alkoxy, cyano, Ci_₆ haloalkoxy, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, hydroxy and mercapto;

R²⁴ and R²⁵ individually represent a substituent selected from Ci_₆ alkyl, Ci_₆ haloalkyl, C₃.₇ cycloalkyl, phenyl and phenyl-Ci_₃ alkyl, and these substituents can be optionally substituted by a substituent(s) selected from halogen, Ci_₆ alkyl, Ci_₆ haloalkyl, nitro, Ci_₆ alkoxy, cyano, Ci_₆ haloalkoxy, Ci_₆ alkylsulfenyl, Ci_₆ alkylsulfinyl, Ci_₆ alkylsulfonyl, Ci_₆ haloalkylsulfenyl, Ci_₆ haloalkylsulfinyl, Ci_₆ haloalkylsulfonyl, hydroxy and mercapto; and

R²⁶ represents a hydrogen atom or Ci_₆ alkyl.

3. An insecticide containing the oxadiazolinone derivative according to claim 1 or 2 as an active ingredient.

4. An animal parasite control agent containing the oxadiazolinone derivative according to claim 1 or 2 as an active ingredient.

5. Use of an oxadiazolinone derivative according to claim 1 or 2 as an insecticide.

6. Use of an oxadiazolinone derivative according to claim 1 or 2 for combating aphids and/or mites.

7. A seed coated with an oxadiazolinone derivative according to claim 1 or 2.