A SHORT SYNTHETIC APPROACH TO ENANTIOMERICALLY PURE(-)-ANISOMYCIN

被引：16

作者：

YODA, H

NAKAJIMA, T

YAMAZAKI, H

TAKABE, K

机构：

[1] Department of Molecular Science, Faculty of Engineering, Shizuoka University, Hamamatsu

来源：

HETEROCYCLES | 1995年 / 41卷 / 11期

关键词：

D O I：

10.3987/COM-95-7214

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A convenient enantiomerically pure route to an antibiotic, natural (-)-anisomycin has been developed in a short number of steps by featuring the stereocontrolled elaboration of the functionalized homochiral lactam derived from 2,3,5-tri-O-benzyl-beta-L-arabinofuranose involving no separation of stereoisomers through the entire sequence.

引用

收藏

页码：2423 / 2426

页数：4

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