CONCISE SYNTHESIS OF NEW HOMOAZASUGARS - FULLY SUBSTITUTED, FUNCTIONALLY DIVERSE PYRROLIDINES

被引：12

作者：

CAMPANINI, L ^{[1
]}

DUREAULT, A ^{[1
]}

DEPEZAY, JC ^{[1
]}

机构：

[1] UNIV PARIS 05,CHIM & BIOCHIM PHARMACOL & TOXICOL LAB,CNRS,F-75270 PARIS 06,FRANCE

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 44期

关键词：

D O I：

10.1016/0040-4039(95)01674-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Five-membered deoxyazosugars of D-gluco configuration, bearing an aminomethyl, a bromomethyl or a thiomethyl group at the pseudo anomeric position, were prepared by nucleophilic opening of C-2 symmetric bis-aziridines followed by chemoselective transformations of the nucleophile. The 1-bromo-2,5-imino-D-glucitol 4 could be converted into attractive bicyclic compounds.

引用

页码：8015 / 8018

页数：4

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