期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 51, 页码 18452-18455出版社
AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b11025
关键词
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资金
- CaSuS PhD Program
- CSC
- DFG
Electrochemical cobalt-catalyzed C-H functionalizations were achieved in terms of C-H oxygenation under mild conditions at 23 degrees C. The robust electrochemical C-H functionalization was characterized by ample substrate scope, whereas mechanistic studies provided support for a facile C-H cleavage. The electrochemical cobalt-catalyzed C-H oxygenation proved viable on arenes and alkenes with excellent levels of positional and diastereo-selectivity, avoiding the use of stoichiometric silver(I) oxidants under ambient conditions.
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