Electrochemically Facilitated Oxidative Coupling of Quinoxalin‐2(1 H )‐Ones with Diarylphosphine Oxides and Pyrroles: A Green Protocol for C−P, C−C( sp   2  ) Bond Formation | Zendy

Hu Chen | Zendy; Hong Gang | Zendy; Zhou Chen | Zendy; Tang ZhiCong | Zendy; Han JianWei | Zendy; Wang LiMin | Zendy

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Electrochemically Facilitated Oxidative Coupling of Quinoxalin‐2(1 H )‐Ones with Diarylphosphine Oxides and Pyrroles: A Green Protocol for C−P, C−C( sp 2 ) Bond Formation

Author(s) -

Hu Chen,

Hong Gang,

Zhou Chen,

Tang ZhiCong,

Han JianWei,

Wang LiMin

Publication year - 2019

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.201900484

Subject(s) - chemistry , dehydrogenation , oxidative phosphorylation , electrochemistry , oxidative coupling of methane , coupling (piping) , metal , combinatorial chemistry , medicinal chemistry , organic chemistry , catalysis , electrode , biochemistry , metallurgy , materials science

A metal‐free and oxidant‐free protocol for oxidative coupling of quinoxalin‐2(1 H )‐ones with diarylphosphine oxides and pyrroles via electrochemical dehydrogenation has been reported. A broad range of C3‐functionalized products were obtained in good to excellent yields.

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