Stereoselective synthesis of macrolactin A analogues .2. The C-1-C-14 fragment

被引：20

作者：

Benvegnu, TJ ^{[1
]}

Gree, RL ^{[1
]}

机构：

[1] ECOLE NATL SUPER CHIM RENNES,CNRS URA 1467,LAB SYNTH & ACTIVAT BIOMOL,F-35700 RENNES,FRANCE

来源：

TETRAHEDRON | 1996年 / 52卷 / 36期

关键词：

D O I：

10.1016/0040-4020(96)00667-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A synthetic approach to the C-1-C-14 part of Macrolactin A analogues is presented. The sequence involving hydroboration-Pd degrees coupling reaction was found to be the most efficient in term of chemio- and stereo-selectivity to prepare the sensitive and functionalized E,Z diene unit. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：11821 / 11826

页数：6

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