Allyltrichlorostannane additions to chiral dipeptide aldehydes

被引：18

作者：

Dias, LC ^{[1
]}

Ferreira, E ^{[1
]}

机构：

[1] Univ Estadual Campinas, Inst Quim, BR-13083970 Campinas, SP, Brazil

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 41期

基金：

巴西圣保罗研究基金会;

关键词：

D O I：

10.1016/S0040-4039(01)01502-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The first examples of successful allylsilane additions to chiral dipeptide aldehydes are described. Treatment of allylsilanes with tin tetrachloride at room temperature affords allyltrichlorostarnnane intermediates that reacts with dipeptide aldehydes to give 1,2-syn-homoallylic alcohols, potential intermediates for the synthesis of hydroxyethylene dipeptide isosteres. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：7159 / 7162

页数：4

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