SYNTHESIS OF 1,2-EPOXY-3-ALKANOLS VIA MITSUNOBU REACTION ON UNPROTECTED ENANTIOPURE ACYCLIC 1,2,3-TRIOLS

被引：4

作者：

GRAVIERPELLETIER, C

LEMERRER, Y

DEPEZAY, JC

机构：

[1] Université René Descartes, Laboratoire de Chimie et Biochimie Pharmacologiques et Toxicologiques, 75270 Paris Cedex 06, associé au CNRS, 45, rue des Saints-Pères

来源：

SYNTHETIC COMMUNICATIONS | 1994年 / 24卷 / 20期

关键词：

D O I：

10.1080/00397919408010604

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Mitsunobu reaction directly carried out on unprotected enantiopure acyclic 1,2,3-triols gave the corresponding chiral 1,2-epoxy-3-alkanols. Higher yields are obtained with relative threo configuration than with relative erythro configuration.

引用

页码：2843 / 2850

页数：8

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