Electrochemical Cobalt-Catalyzed C-H Activation

被引:111
|
作者
Sauermann, Nicolas [1 ]
Meyer, Tjark H. [1 ]
Ackermann, Lutz [1 ,2 ]
机构
[1] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany
[2] Univ Pavia, Dept Chem, Viale Tamarelli 10, I-27100 Pavia, Italy
关键词
C-H activation; cobalt; electrochemistry; electrosynthesis; heterocycles; CROSS-COUPLING REACTIONS; GREEN CHEMISTRY; DIRECTED FUNCTIONALIZATION; ORGANIC ELECTROSYNTHESIS; BOND FUNCTIONALIZATION; SELECTIVE SYNTHESIS; AROMATIC AMIDES; ARYL HALIDES; PALLADIUM; ACCESS;
D O I
10.1002/chem.201802706
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon-heteroatom bonds represent omnipresent structural motifs of the vast majority of functionalized materials and bioactive compounds. C-H activation has emerged as arguably the most efficient strategy to construct C-Het bonds. Despite of major advances, these C-H transformations were largely dominated by precious transition metal catalysts, in combination with stoichiometric, toxic metal oxidants. Herein, we discuss the recent evolution of cobalt-catalyzed C-H activations that enable C-Het formations with electricity as the sole sustainable oxidant until May 2018.
引用
收藏
页码:16209 / 16217
页数:9
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