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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 |
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container_end_page | 6137 |
container_issue | 16 |
container_start_page | 6131 |
container_title | Green chemistry : an international journal and green chemistry resource : GC |
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creator | Yu, Wan-Lei Ren, Zi-Gang Ma, Wei Zheng, Haixue Wu, Wangsuo Xu, Peng-Fei |
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 |
format | article |
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2
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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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