ENANTIOSELECTIVE REFORMATSKY REACTION WITH KETONES - ASYMMETRIC-SYNTHESIS OF BETA-(TERT-HYDROXY)ESTERS

被引：36

作者：

SOAI, K

OSHIO, A

SAITO, T

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1993年 / 09期

关键词：

D O I：

10.1039/c39930000811

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Optically active beta-(tert-hydroxy)esters with good enantiomeric excesses (up to 75% e.e.) are synthesised via enantioselective Reformatsky reaction with ketones in the presence of chiral N,N-dialkylnorephedrine.

引用

页码：811 / 812

页数：2

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