α-sulfenylation of acylsilanes and aldehydes with N-(phenylthio)succinimide

被引：23

作者：

Huang, CH ^{[1
]}

Liao, KS ^{[1
]}

De, SK ^{[1
]}

Tsai, YM ^{[1
]}

机构：

[1] Natl Taiwan Univ, Dept Chem, Taipei 106, Taiwan

来源：

TETRAHEDRON LETTERS | 2000年 / 41卷 / 20期

关键词：

imides; silicon and compounds; sulfides;

D O I：

10.1016/S0040-4039(00)00515-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reactions of acylsilanes with N-(phenylthio)succinimide in the presence of p-toluenesulfonic acid in acetonitrile give alpha-sulfenylated acylsilanes in good yields. Aldehydes with alpha-alkyl substituent afford moderate yields of alpha-sulfenylated products under the same conditions. (C) 2000 Elsevier Science Ltd. All rights reserved.

引用

页码：3911 / 3914

页数：4

共 19 条

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