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Cobalt-catalyzed chemoselective dehydrogenation through radical translocation under visible light.


ABSTRACT: The transformations that allow the direct removal of hydrogen from their corresponding saturated counterparts by the dehydrogenative strategy are a dream reaction that has remained largely underexplored. In this report, a straightforward and robust cobaloxime-catalyzed photochemical dehydrogenation strategy via intramolecular HAT is described for the first time. The reaction proceeds through an intramolecular radical translocation followed by the cobalt assisted dehydrogenation without needing any other external photosensitizers, noble-metals or oxidants. With this approach, a series of valuable unsaturated compounds such as α,β-unsaturated amides, enamides and allylic and homoallylic sulfonamides were obtained in moderate to excellent yields with good chemo- and regioselectivities, and the synthetic versatility was demonstrated by a range of transformations. And mechanistic studies of the method are discussed.

SUBMITTER: Yu WL 

PROVIDER: S-EPMC9258329 | biostudies-literature | 2022 Jul

REPOSITORIES: biostudies-literature

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Cobalt-catalyzed chemoselective dehydrogenation through radical translocation under visible light.

Yu Wan-Lei WL   Ren Zi-Gang ZG   Ma Ke-Xing KX   Yang Hui-Qing HQ   Yang Jun-Jie JJ   Zheng Haixue H   Wu Wangsuo W   Xu Peng-Fei PF  

Chemical science 20220615 26


The transformations that allow the direct removal of hydrogen from their corresponding saturated counterparts by the dehydrogenative strategy are a dream reaction that has remained largely underexplored. In this report, a straightforward and robust cobaloxime-catalyzed photochemical dehydrogenation strategy <i>via</i> intramolecular HAT is described for the first time. The reaction proceeds through an intramolecular radical translocation followed by the cobalt assisted dehydrogenation without ne  ...[more]

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