Oxidant-free oxidative gold catalysis: the new paradigm in cross-coupling reactions

被引:167
作者
Akram, Manjur O. [1 ]
Banerjee, Somsuvra [1 ]
Saswade, Sagar S. [2 ]
Bedi, Vaibhav [2 ]
Patil, Nitin T. [2 ]
机构
[1] Natl Chem Lab, Div Organ Chem, CSIR, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India
[2] Indian Inst Sci Educ & Res Bhopal, Dept Chem, Bhopal 462066, India
关键词
HYPERVALENT IODINE REAGENTS; VISIBLE-LIGHT PHOTOREDOX; C-H FUNCTIONALIZATION; I/AU-III CATALYSIS; DIRECT ALKYNYLATION; REDUCTIVE ELIMINATION; ARYLDIAZONIUM SALTS; DIAZONIUM SALTS; DUAL GOLD; BOND FORMATION;
D O I
10.1039/c8cc05601c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The construction of C-C and C-X (X = hetero atom) bonds is the core aspect for the assembly of molecules. In this regard, late transition-metal-catalyzed cross-coupling reactions have retained their dominance for decades. Lately, gold catalysts have been emerging as a reliable contender for such transformations owing to the recent findings that reveal gold's potential beyond carbophilic -Lewis acid. The newfound ability of gold to undergo redox transformations under certain circumstances has allowed us to explore gold catalysts as a viable alternative to other late transition-metals for efficient construction of cross-coupled products. This feature article critically presents an overview of all the redox neutral cross-coupling reactions enabled by gold catalysis, which we believe would stimulate further research activities in this promising area.
引用
收藏
页码:11069 / 11083
页数:15
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