Reactions of p-toluenesulfenyl chloride with enol acetates. The synthetic potential of the resulting adducts

被引：0

作者：

W. A. Smit

E. A. Yagodkin

G.V. Zatonsky

机构：

[1] Russian Academy of Sciences,N. D. Zelinsky Institute of Organic Chemistry

来源：

Russian Chemical Bulletin | 2005年 / 54卷

关键词：

enol acetates; arenesulfenyl chlorides; electrophilic addition; C-nucleophiles; β-arylthioalkylation;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Reactions of vinyl and propen-2-yl acetates with p-toluenesulfenyl chloride afforded the corresponding α-chloro-β-(p-tolyl)thioalkyl acetates in nearly quantitative yields.These adducts reacted with some C-nucleophiles in the presence of Lewis acids to give the corresponding alkylation products.

引用

页码：743 / 747

页数：4

共 26 条

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