REACTIONS OF ALPHA-SUBSTITUTED GLYCINE DERIVATIVES WITH STANNANES

被引：5

作者：

EASTON, CJ

PETERS, SC

机构：

[1] Department of Organic Chemistry, University of Adelaide, Adelaide, SA 5001

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 38期

关键词：

D O I：

10.1016/S0040-4039(00)61151-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Alpha-benzoyloxy- and alpha-methoxy-substituted glycine derivatives are more stable than the corresponding bromides, yet they undergo analogous reactions with stannanes. Their reactions with mixtures of hexabutylditin and dialkyl disulphides give alpha-alkylthio-substituted glycine derivatives, a procedure that is applicable to the synthesis of cross-linked amino acid derivatives.

引用

页码：5581 / 5584

页数：4

共 18 条

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