Efficient coupling of heteroaryl halides with arylboronic acids in the presence of a palladium-tetraphosphine catalyst

被引：71
|
作者：
Feuerstein, M [1 ]
Doucet, H [1 ]
Santelli, M [1 ]
机构：
[1] Fac Sci & Tech St Jerome, CNRS, Organ Synth Lab, F-13397 Marseille, France
来源：
JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2003年 / 687卷 / 02期
关键词：
tetraphosphine; palladium; suzuki-coupling; arylboronic acids; heteroaryl halides;
D O I：
10.1016/j.jorganchem.2003.07.005
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
Cis,cis,cis-1,2,3,4-tetrakis(diphenylphosphinomethyl)cyclopentane: 1/2[PdCl(C3H5)](2) system catalyses the Suzuki cross-coupling of heteroaryl halides with a range of arylboronic acids with very high ratio substrate/catalyst in good yields. Substrates such as pyridines, quinolines, thiophenes, an indole, pyrimidines or a furane have been used successfully. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码：327 / 336
页数：10
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