Recent Developments in the Suzuki-Miyaura Reaction: 2010-2014

被引:314
|
作者
Maluenda, Irene [1 ]
Navarro, Oscar [1 ]
机构
[1] Univ Sussex, Dept Chem, Brighton BN1 9QJ, E Sussex, England
来源
MOLECULES | 2015年 / 20卷 / 05期
关键词
Suzuki-Miyaura; palladium; nickel; N-heterocyclic carbene; phosphine; polymerization; CROSS-COUPLING REACTIONS; PALLADIUM COMPLEXES SYNTHESIS; CATALYZED LIGAND-FREE; ORTHO-SUBSTITUTED BIARYLS; HETEROARYL BORONIC ACIDS; CONCISE TOTAL-SYNTHESIS; HIGHLY-ACTIVE CATALYST; ARYL CHLORIDES; RECYCLABLE CATALYST; CONJUGATED POLYMERS;
D O I
10.3390/molecules20057528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Suzuki-Miyaura reaction (SMR), involving the coupling of an organoboron reagent and an organic halide or pseudo-halide in the presence of a palladium or nickel catalyst and a base, has arguably become one of most utilized tools for the construction of a C-C bond. This review intends to be general account of all types of catalytic systems, new coupling partners and applications, including the literature between September 2010 and December 2014.
引用
收藏
页码:7528 / 7557
页数:30
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