Palladium-catalyzed cross-coupling reactions of aryl mesylates

被引：261

作者：

So, Chau Ming

Kwong, Fuk Yee ^{[1
]}

机构：

[1] Hong Kong Polytech Univ, State Key Lab Chirosci, Kowloon, Hong Kong, Peoples R China

来源：

CHEMICAL SOCIETY REVIEWS | 2011年 / 40卷 / 10期

关键词：

SUZUKI-MIYAURA; TOSYLATES; AMINATION; METAL; ARENESULFONATES; HALIDES; CYANATION; BROMIDES; CARBONYLATION; ARYLAMINES;

D O I：

10.1039/c1cs15114b

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Palladium-catalyzed cross-coupling reactions are state-of-the art methods for synthesis of many important compounds. The development of the use of the phenol-derived sulfonated hydroxyl group in the coupling reactions is highly attractive as the hydroxyl group is commonly present in organic compounds and they are versatile alternatives to aryl halides in cross-coupling reactions. In this tutorial review, we summarize the current development of palladium-catalyzed cross-coupling reactions of aryl mesylates.

引用

页码：4963 / 4972

页数：10

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