Electrochemical Cobalt-Catalyzed C–H Oxygenation at Room Temperature
Electrochemical cobalt-catalyzed C–H functionalizations were achieved in terms of C–H oxygenation under mild conditions at 23 °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 e...
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Published in: | Journal of the American Chemical Society Vol. 139; no. 51; pp. 18452 - 18455 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
American Chemical Society
27-12-2017
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Online Access: | Get full text |
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Summary: | Electrochemical cobalt-catalyzed C–H functionalizations were achieved in terms of C–H oxygenation under mild conditions at 23 °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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/jacs.7b11025 |