Electro-Oxidative C-C Alkenylation by Rhodium(III) Catalysis

被引:107
作者
Qiu, Youai [1 ]
Scheremetjew, Alexej [1 ]
Ackermann, Lutz [1 ]
机构
[1] Georg August Univ Gottingen, Inst Organ & Biomol Chem, Tammannstr 2, D-37077 Gottingen, Germany
关键词
CARBON-CARBON BONDS; H FUNCTIONALIZATION; ACTIVATION; METAL; CLEAVAGE; ARYL; CYCLOBUTANONES; STRATEGIES; MECHANISM; EXCHANGE;
D O I
10.1021/jacs.8b13692
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical C-C activations were accomplished by expedient oxidative rhodium(III) catalysis. Thus, oxidative C-C alkenylations proved viable with the aid of electricity, avoiding the use of toxic and/or expensive transition-metal oxidants. The chelation-assisted C-C functionalizations proceeded with ample scope and excellent levels of chemo- and position selectivities within an organometallic C-C activation manifold. Detailed mechanistic studies provided support for a kinetically relevant C-C scission, and a well-defined organometallic rhodium(III) complex was identified as a catalytically competent intermediate. The electrochemical C-C functionalization was devoid of additional electrolytes, could be conducted on a gram scale, and provided position-selective access to densely 1,2,3-substituted arenes, which are not viable by C-H activation.
引用
收藏
页码:2731 / 2738
页数:8
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