Decarboxylative coupling reactions: a modern strategy for C-C-bond formation

被引:1267
作者
Rodriguez, Nuria [1 ]
Goossen, Lukas J. [1 ]
机构
[1] TU Kaiserslautern, FB Chem Organ Chem, D-67663 Kaiserslautern, Germany
关键词
AROMATIC CARBOXYLIC-ACIDS; PALLADIUM-CATALYZED DECARBOXYLATION; AB-INITIO PSEUDOPOTENTIALS; ALPHA-OXOCARBOXYLIC ACIDS; SUBSTITUTED BENZOIC-ACIDS; ACTIVATED IN-SITU; ARYL HALIDES; OXIDATIVE DECARBOXYLATION; BIARYL SYNTHESIS; ARENECARBOXYLIC ACIDS;
D O I
10.1039/c1cs15093f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This critical review examines transition metal-catalyzed decarboxylative couplings that have emerged within recent years as a powerful strategy to form carbon-carbon or carbon-heteroatom bonds starting from carboxylic acids. In these reactions, C-C bonds to carboxylate groups are cleaved, and in their place, new carbon-carbon bonds are formed. Decarboxylative cross-couplings constitute advantageous alternatives to traditional cross-coupling or addition reactions involving preformed organometallic reagents. Decarboxylative reaction variants are also known for Heck reactions, direct arylation processes, and carbon-heteroatom bond forming reactions.
引用
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页码:5030 / 5048
页数:19
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