Chiral sulfoxides in asymmetric synthesis: Enantioselective synthesis of (-)-(5S,7R)-tarchonanthuslactone

被引:45
作者
Solladie, G
GressotKempf, L
机构
[1] Univ. Louis Pasteur (ECPM), Lab. de Stereochimie Associe au CNRS, 67008 - Strasbourg
关键词
D O I
10.1016/0957-4166(96)00292-3
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The enantioselective synthesis of (-)-(5S, 7R)-Tarchonanthuslactone, a substituted delta-lactone isolated from a compositae, is described. The main feature of this short synthesis is the stereoselective reduction of a beta,delta-diketosulfoxide affording in 6 steps the chiral central part of the molecule, a syn-1,3-diol unit. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:2371 / 2379
页数:9
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