1,2-ethanedisulfenyl chloride as a reagent for the preparation of ethylenedithio substituted aromatics.

被引：3

作者：

Allared, F ^{[1
]}

Blid, J ^{[1
]}

Hellberg, J ^{[1
]}

Remonen, T ^{[1
]}

Svensson, M ^{[1
]}

机构：

[1] Royal Inst Technol, S-10044 Stockholm, Sweden

来源：

SYNTHETIC METALS | 2001年 / 120卷 / 1-3期

关键词：

heterocycle synthesis; ethylenedithio substitution; sulfenyl chlorides;

D O I：

10.1016/S0379-6779(00)01227-3

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

1,2-ethanedisulfenyl chloride 1 has been utilized as a electrophilic reagent for the preparation of dihydro-1,4-dithiino substituted aromatics. The title reagent reacts with activated aromatics to give several new heterocyclic systems in modest yields.

引用

页码：1061 / 1062

页数：2

共 9 条

[1] Regioselective synthesis of mixed indole 2,3-bis(sulfides). A study of the mechanism of the second sulfenylation of indole [J].