JPS64374B2 - - Google Patents

Info

Publication number
JPS64374B2
JPS64374B2 JP57173967A JP17396782A JPS64374B2 JP S64374 B2 JPS64374 B2 JP S64374B2 JP 57173967 A JP57173967 A JP 57173967A JP 17396782 A JP17396782 A JP 17396782A JP S64374 B2 JPS64374 B2 JP S64374B2
Authority
JP
Japan
Prior art keywords
reaction
eugenol
formula
isomerization
derivatives
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP57173967A
Other languages
English (en)
Japanese (ja)
Other versions
JPS5965035A (ja
Inventor
Akemichi Furuhata
Keiichi Takagi
Kunio Kojo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
T Hasegawa Co Ltd
Original Assignee
T Hasegawa Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by T Hasegawa Co Ltd filed Critical T Hasegawa Co Ltd
Priority to JP57173967A priority Critical patent/JPS5965035A/ja
Publication of JPS5965035A publication Critical patent/JPS5965035A/ja
Publication of JPS64374B2 publication Critical patent/JPS64374B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
JP57173967A 1982-10-05 1982-10-05 トランス−イソオイゲノ−ルおよびその誘導体の製法 Granted JPS5965035A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57173967A JPS5965035A (ja) 1982-10-05 1982-10-05 トランス−イソオイゲノ−ルおよびその誘導体の製法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57173967A JPS5965035A (ja) 1982-10-05 1982-10-05 トランス−イソオイゲノ−ルおよびその誘導体の製法

Publications (2)

Publication Number Publication Date
JPS5965035A JPS5965035A (ja) 1984-04-13
JPS64374B2 true JPS64374B2 (enrdf_load_stackoverflow) 1989-01-06

Family

ID=15970349

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57173967A Granted JPS5965035A (ja) 1982-10-05 1982-10-05 トランス−イソオイゲノ−ルおよびその誘導体の製法

Country Status (1)

Country Link
JP (1) JPS5965035A (enrdf_load_stackoverflow)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107188788B (zh) * 2017-05-26 2020-05-29 浙江大学 一种丁香酚纯化方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5245697B2 (enrdf_load_stackoverflow) * 1974-07-31 1977-11-17

Also Published As

Publication number Publication date
JPS5965035A (ja) 1984-04-13

Similar Documents

Publication Publication Date Title
Takaya et al. Rhodium-catalyzed asymmetric 1, 4-addition of 2-alkenyl-1, 3, 2-benzodioxaboroles to α, β-unsaturated ketones
US4536347A (en) Selective hydrogenation of unsaturated carbonyl compounds
US4310709A (en) Manufacture of but-2-en-1-ol compounds by isomerizing the corresponding but-3-en-1-ol compounds
US4062898A (en) Conversion of acetals
JPS6097054A (ja) 選択的接触水素化方法
US4460786A (en) Process for the selective addition of a compound having an activated carbon atom onto a substituted conjugated diene
US4455442A (en) Preparation of unsaturated alcohols
US5410094A (en) Tertiary alkynols
Harada et al. A convenient synthesis of 2-deoxy-D-ribose
JPS64374B2 (enrdf_load_stackoverflow)
DE69520077T2 (de) Oxotitankomplexe verwendbar als Katalysatoren für assymetrische Reaktionen insbesondere zur Herstellung von beta-hydroxy-Ketonen oder alpha-hydroxy-Carbonsäureestern
US4355168A (en) Process for preparing aryl- or heteroarylhexadienoic acids
D'yakonov et al. A new stereoselective synthesis of biologically active di-and trienoic acids containing a (1Z, 5Z)-diene moiety
US4421922A (en) Process for the production of tetronic acid
JPS5941974B2 (ja) α，β−不飽和アルデヒド類の水素添加方法
JP3881288B2 (ja) ５−アリールペンタノールの製造法
Hashimoto et al. The trityl cation catalyzed Michael type reaction of stannylated nucleophiles with ethylthioketene dithioacetals
US3742063A (en) Dihydroxybutanones
US3185744A (en) Process for isomerizing the double bond of straight chain terminal monoolefins
JPH06166680A (ja) アルキル ３オクソ−２−ペンチル−１−シクロペンテンアセテートの製造法および並びに出発物質としてのエポキシ−エステル
Nokami et al. Reaction of propargyl bromide and trimethylsilylpropargyl iodide with metallic tin, aluminum, and aldehydes or ketones. Selective synthesis of β-acetylene, β-trimethylsilylacetylene, and α-trimethylsilylallene alcohols
SU634660A3 (ru) Способ получени 1,1,1-тригалоген4-метил-3-пентен-2-олов
JPS60184050A (ja) α−ケトエステル類を製造する方法
SU569552A1 (ru) Способ получени -этинилзамещенных третичных спиртов
EP1685089A1 (en) Process for the preparation of aliphatic primary alcohols and intermediates in such process