SIMPLE AND EFFICIENT ACCESS TO THE LEFT-HAND SEGMENT OF AZINOMYCINS

被引：26
|
作者：
SHISHIDO, K
OMODANI, T
SHIBUYA, M
机构：
[1] Faculty of Pharmaceutical Sciences, University of Tokushima, Tokushima 770
来源：
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1992年 / 16期
关键词：
D O I：
10.1039/p19920002053
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A practical synthesis of the epoxy carboxylic acid 4, the left-hand segment of azinomycins, and its conversion into the naturally occurring amide 3 have been achieved enantioselectively.
引用
收藏
页码：2053 / 2054
页数：2
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