Palladium-Catalyzed Suzuki-Miyaura Type Coupling Reaction of Aryl Halides with Triphenylborane-Pyridine

被引：1

作者：

Yang Minghua ^{[1
]}

Gu Yongbing ^{[1
]}

Wang Yan ^{[1
]}

Zhao Xiyu ^{[1
]}

Yan Guobing ^{[1
]}

机构：

[1] Lishui Univ, Dept Chem, Lishui 323000, Zhejiang, Peoples R China

来源：

CHINESE JOURNAL OF CHEMISTRY | 2012年 / 30卷 / 10期

关键词：

triphenylbroane-pyridine; Suzuki-Miyaura coupling; aryl halides; palladium catalysts; BORONIC ACIDS; CONVENIENT; COMPLEXES; COMBINATION; ARENES;

D O I：

10.1002/cjoc.201200775

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The Suzuki-Miyaura type coupling reaction of aryl halides with triphenylborane-pyridine was described. The reaction can be catalyzed by Pd(OAc)2 (5 mol%) in presence of Cs2CO3 at 50 degrees C or 80 degrees C, and functionalized biaryls were obtained in good to excellent yields. This protocol is general and can tolerate a wide range of functional groups.

引用

页码：2581 / 2586

页数：6

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