Reaction of aryl di-, tri-, or tetrabromides with arylboronic acids or alkenes in the presence of a palladium-tetraphosphine catalyst

被引:42
作者
Berthiol, F
Kondolff, I
Doucet, H
Santelli, M
机构
[1] Fac Sci & Tech St Jerome, CNRS, UMR 6180, Synth Organ Lab, F-13397 Marseille 20, France
[2] Univ Aix Marseille 3, Fac Sci St Jerome, F-13397 Marseille 20, France
关键词
tetraphosphine; palladium; Suzuki-coupling; Heck-vinylation; arylboronic acids; alkenes; aryl bromides;
D O I
10.1016/j.jorganchem.2004.06.007
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 and Heck reactions of aryl di-, tri-, or tetrabromides with a range of arylboronic acids or alkenes with moderate to high ratio substrate/catalyst in good yields. Aryl polybromides such as dibromobenzenes, 1,3,5-tribromobenzene, 1,2,4,5-tetrabromobenzene, dibromopyridines or a dibromothiophene have been successfully used. Convenient synthesis of a variety of di- and triarylated or vinylated compounds and even a 1,2,4,5-tetraarylated compound were prepared by use of this reaction. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:2786 / 2798
页数:13
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