Stereoselective synthesis of the C9-C19 lactone-dipropionate fragment of calyculin C

被引：6

作者：

Karisalmi, K ^{[1
]}

Koskinen, AMP ^{[1
]}

机构：

[1] Helsinki Univ Technol, Organ Chem Lab, FIN-02015 Helsinki, Finland

来源：

TETRAHEDRON LETTERS | 2004年 / 45卷 / 44期

基金：

芬兰科学院;

关键词：

aldol reactions; crotylation; diastereoselectivity; natural products; stereoselective synthesis;

D O I：

10.1016/j.tetlet.2004.09.012

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A highly diastereoselective synthesis of the title fragment of calyculin C has been developed based on an internal asymmetric induction between a chiral aldehyde and Z-crotyl trifluorosilane. (C) 2004 Elsevier Ltd. All rights reserved.

引用

页码：8245 / 8248

页数：4

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