SYNTHESIS OF OPTICALLY-ACTIVE ALPHA-HYDROXY LACTONES BY SHARPLESS ASYMMETRIC DIHYDROXYLATIONS OF KETENE ACETALS, ENOL ETHERS, AND ENE LACTONES

被引：36
|
作者：
CURRAN, DP
KO, SB
机构：
[1] Department of Chemistry, University of Pittsburgh, Pittsburgh
来源：
JOURNAL OF ORGANIC CHEMISTRY | 1994年 / 59卷 / 21期
关键词：
D O I：
10.1021/jo00100a005
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
Three different AD routes to optically active alpha-hydroxy lactones of good to excellent optical purity are reported. The substrates for the AD reaction are endocyclic ketene acetals, endocyclic enol ethers, and exocyclic alpha,beta-unsaturated lactones.
引用
收藏
页码：6139 / 6141
页数：3
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