Review of electrochemical transition-metal-catalyzed C-H functionalization reactions

被引:15
作者
Changmai, Sumi [2 ,3 ]
Sultana, Sabera [4 ]
Saikia, Anil K. [1 ]
机构
[1] Indian Inst Technol Guwahati, Dept Chem, Gauhati 781039, Assam, India
[2] CSIR North East Inst Sci & Technol, Appl Organ Chem Chem Sci & Technol Div, Jorhat 785006, India
[3] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India
[4] Jubilant Biosys Ltd, Greater Noida 201306, India
来源
CHEMISTRYSELECT | 2023年 / 8卷 / 11期
关键词
metalla-electro-catalyzed; C-H activation; electrochemical cel; OXIDATIVE DIMERIZATION; 4+2 ANNULATION; PALLADIUM; BOND; ACTIVATION; ELECTROSYNTHESIS; ACETOXYLATION; 1-NAPHTHOLS; AZIDATION; DIOXYGEN;
D O I
10.1002/slct.202203530
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The combination of organometallic C-H activation and electro-catalysis has emerged as a potent synthetic technique for various molecular scaffolds since it avoids the use of harmful and expensive chemical oxidants in stoichiometric amounts. Moreover, the pre-functionalization of substrates is not required and newer ways to perform metal-catalyzed C-H activation reactions are possible. Here, we have discussed eletrochemically driven C-H acyloxylation, acetoxylation, oxygenation, acylation, amination, alkylation, halogenation, olefinations and C-H/N-H annulation reactions using various transition-metal-catalyst such as Ru, Rh, Pd, Co, Ni, Ir, Cu, Mn and Au by anodic oxidation, followed by reductive elimination to form the corresponding C-O, C-C, C-N and C-X (X=Cl, Br, S etc.) bonds. This review covers recent developments in transition-metal-catalyzed electrochemical C-H activation from 2007 until 2022.
引用
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页数:21
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