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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