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
收藏
页码：2581 / 2586
页数：6
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