Iridium-Catalyzed Electrooxidative C-H Activation by Chemoselective Redox-Catalyst Cooperation

被引:116
作者
Qiu, Youai [1 ]
Stangier, Maximilian [1 ]
Meyer, Tjark H. [1 ]
Oliveira, Joao C. A. [1 ]
Ackermann, Lutz [1 ]
机构
[1] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany
关键词
C-H activation; electrochemistry; iridium catalysis; Redox catalysts; selectivity; DIRECTING GROUPS; OXIDASE CATALYSIS; DIRECT ARYLATION; BENZOIC-ACIDS; METAL; FUNCTIONALIZATION; ALKENYLATIONS; STRATEGIES; AMINATION; RHODIUM;
D O I
10.1002/anie.201809611
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Iridium-catalyzed electrochemical C-H activation was accomplished within a cooperative catalysis manifold, setting the stage for electrooxidative C-H alkenylations through weak O-coordination. The iridium-electrocatalyzed C-H activation featured high functional-group tolerance through assistance of a metal-free redox mediator through indirect electrolysis. Detailed mechanistic insights provided strong support for an organometallic C-H cleavage and a synergistic iridium(III/I)/redox catalyst regime, enabling the use of sustainable electricity as the terminal oxidant with improved selectivity features.
引用
收藏
页码:14179 / 14183
页数:5
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