Flow Rhodaelectro-Catalyzed Alkyne Annulations by Versatile C-H Activation: Mechanistic Support for Rhodium(III/IV)

被引:121
作者
Kong, Wei-Jun [1 ]
Finger, Lars H. [1 ]
Messinis, Antonis M. [1 ]
Kuniyil, Rositha [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
LIGHT PHOTOREDOX CATALYSIS; FUNCTIONALIZATION; ELECTROSYNTHESIS; STRATEGIES; BATCH; RH;
D O I
10.1021/jacs.9b07763
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A flow-metallaelectro-catalyzed C-H activation was realized in terms of robust rhodaelectro-catalyzed alkyne annulations. To this end, a modular electro-flow cell with a porous graphite felt anode was designed to ensure efficient turnover. Thereby, a variety of C-H/N-H functionalizations proved amenable for alkyne annulations with high levels of regioselectivity and functional group tolerance, viable in both an inter- or intramolecular manner. The electro-flow C-H activation allowed easy scale up, while in-operando kinetic analysis was accomplished by online flow-NMR spectroscopy. Mechanistic studies suggest an oxidatively induced reductive elimination pathway on rhodium(III) in an electrocatalytic regime.
引用
收藏
页码:17198 / 17206
页数:9
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