ENANTIOSELECTIVE SYNTHESIS OF BETA-HYDROXY ESTERS BY INDIUM-INDUCED REFORMATSKY REACTION

被引：48

作者：

JOHAR, PS ^{[1
]}

ARAKI, S ^{[1
]}

BUTSUGAN, Y ^{[1
]}

机构：

[1] NAGOYA INST TECHNOL,DEPT APPL CHEM,SHOWA KU,NAGOYA,AICHI 466,JAPAN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1992年 / 06期

关键词：

D O I：

10.1039/p19920000711

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Indium-induced Reformatsky reaction, with stoicheiometric amounts of chiral amino alcohols such as cinchonine and cinchonidine, gave optically active beta-hydroxy esters in 40-70% e.e.

引用

页码：711 / 713

页数：3

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