Facile enantiospecific synthesis of (-)-muricatacin

被引：24

作者：

Prasad, Kavirayani R. ^{[1
]}

Gandi, Vasudevarao ^{[1
]}

机构：

[1] Indian Inst Sci, Dept Organ Chem, Bangalore 560012, Karnataka, India

来源：

TETRAHEDRON-ASYMMETRY | 2008年 / 19卷 / 22期

关键词：

D O I：

10.1016/j.tetasy.2008.11.004

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

A facile approach for the enantiospecific synthesis of the bioactive butanolide (-)-muricatacin frorn L-(+)-tartaric acid is presented. Pivotal reaction sequence includes the elaboration of gamma-hydroxy amide derived from tartaric acid and ring-closing metathesis. (C) 2008 Elsevier Ltd. All rights reserved.

引用

页码：2616 / 2619

页数：4

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