Facile stereoselective syntheses of (E)- and (Z)-α-substituted cinnamates by stereoselective dehydration reaction with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC)

被引：17
|
作者：
Sai, H [1 ]
Ohmizu, H [1 ]
机构：
[1] Tanabe Seiyaku Co Ltd, Discovery Res Lab, Osaka 5328505, Japan
来源：
TETRAHEDRON LETTERS | 1999年 / 40卷 / 27期
关键词：
D O I：
10.1016/S0040-4039(99)00923-5
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Highly stereoselective syntheses of (E)- and (Z)-alpha-substituted cinnamates have been achieved by dehydration reaction of anti- and syn-alpha-substituted-beta-hydroxyphenylpropionates with EDC in good yields. This facile method has been applied to the stereoselective syntheses of (E)- and (Z)-alpha-alkylidene-gamma-butyrolactones. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码：5019 / 5022
页数：4
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