A general palladium-catalyzed coupling of aryl bromides/triflates and thiols

被引：473

作者：

Itoh, T ^{[1
]}

Mase, T ^{[1
]}

机构：

[1] Banyu Pharmaceut Co Ltd, Proc Res, Proc R&D, Okazaki, Aichi 4440858, Japan

来源：

ORGANIC LETTERS | 2004年 / 6卷 / 24期

关键词：

D O I：

10.1021/ol047996t

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[GRAPHICS] We have developed an efficient palladium-catalyzed carbon-sulfur bond formation reaction of aryl bromides, triflates, and activated aryl chloride, Using this protocol, we have shown tolerance to a wide variety of aryl thiols and alkyl thiols that can also be used as sulfide equivalents.

引用

页码：4587 / 4590

页数：4

共 48 条

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