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Intramolecular dehydrogenative amination of alkenes via dual organic photoredox and cobalt catalysis without a hydrogen acceptor

Direct C–H/N–H dehydrogenative coupling is a promising yet thermodynamically unfavorable transformation in the absence of a sacrificial hydrogen acceptor. Herein, a conceptually novel oxidant-free dehydrogenative amination of alkenes through a synergistic photoredox and cobalt catalysis with H 2 evo...

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Published in:Green chemistry : an international journal and green chemistry resource : GC 2022-08, Vol.24 (16), p.6131-6137
Main Authors: Yu, Wan-Lei, Ren, Zi-Gang, Ma, Wei, Zheng, Haixue, Wu, Wangsuo, Xu, Peng-Fei
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description Direct C–H/N–H dehydrogenative coupling is a promising yet thermodynamically unfavorable transformation in the absence of a sacrificial hydrogen acceptor. Herein, a conceptually novel oxidant-free dehydrogenative amination of alkenes through a synergistic photoredox and cobalt catalysis with H 2 evolution has been achieved. With this approach, a wide range of five-membered N-heterocycles were synthesized with excellent atom-economy. The green system will address the challenges that are sensitive to traditionally oxidative conditions. Furthermore, the scope and mechanistic details of the method are discussed.
doi_str_mv 10.1039/D2GC02084J
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source Royal Society of Chemistry
subjects Alkenes
Amination
Atom economy
Catalysis
Cobalt
Dehydrogenation
Green chemistry
Hydrogen evolution
Oxidants
Oxidizing agents
title Intramolecular dehydrogenative amination of alkenes via dual organic photoredox and cobalt catalysis without a hydrogen acceptor
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