Recent Progress in the C-N Bond Formation via High-Valent Group 9 Cp*M(III)-Catalyzed Directed sp2C-H Activation

被引:34
|
作者
Sk, Md Raja [1 ]
Bera, Sourav Sekhar [1 ]
Basuli, Suchand [1 ]
Metya, Abhisek [1 ]
Maji, Modhu Sudan [1 ]
机构
[1] Indian Inst Technol Kharagpur, Dept Chem, Kharagpur 721302, W Bengal, India
关键词
C-H activation; C-N bond formation; cobalt(III); rhodium(III); iridium(III); SITE-SELECTIVE AMIDATION; H AMIDATION; ORTHO-C(SP(2))-H AMIDATION; AMINATION; ARENES; ALDEHYDES; INDOLES; AZIDES; MILD; 2-AMINOBENZALDEHYDES;
D O I
10.1002/ajoc.202000367
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The presence of nitrogen atom in a wide variety of organic compounds called for the use of powerful C-H activation strategy in the C-N bond formation. Pentamethylcyclopentadienyl (Cp*) based, high-valent, group 9 transition-metal complexes have shown a great potential as catalysts in the C-H activation/functionalization over the years. This minireview summarizes recent progress made in the context of C-N bond formation via catalytic (sp(2))C-H activation with Cp*M(III) (M=Co, Rh and Ir) catalysts. A general plausible mechanism is briefly discussed at the beginning, and then results are arranged according to metal cobalt, rhodium and iridium, respectively.
引用
收藏
页码:1701 / 1717
页数:17
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