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Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond

A C(sp(2))–C(sp(2)) reaction between aromatic hydrazines and quinoxalines has been developed through a photocatalytic system. The protocol is established for C(sp(2))–N bond cleavage and direct C(sp(2))–H functionalization for the coupling of C(sp(2))–C(sp(2)) via photocatalysis under mild and ideal...

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Autores principales: Wu, Mei, Lian, Nancheng, Wu, Cuimin, Wu, Xinyao, Chen, Houzheng, Lin, Chen, Zhou, Sunying, Ke, Fang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274563/
https://www.ncbi.nlm.nih.gov/pubmed/37333794
http://dx.doi.org/10.1039/d3ra03479h
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author Wu, Mei
Lian, Nancheng
Wu, Cuimin
Wu, Xinyao
Chen, Houzheng
Lin, Chen
Zhou, Sunying
Ke, Fang
author_facet Wu, Mei
Lian, Nancheng
Wu, Cuimin
Wu, Xinyao
Chen, Houzheng
Lin, Chen
Zhou, Sunying
Ke, Fang
author_sort Wu, Mei
collection PubMed
description A C(sp(2))–C(sp(2)) reaction between aromatic hydrazines and quinoxalines has been developed through a photocatalytic system. The protocol is established for C(sp(2))–N bond cleavage and direct C(sp(2))–H functionalization for the coupling of C(sp(2))–C(sp(2)) via photocatalysis under mild and ideal air conditions without the presence of a strong base and metal. The mechanistic studies reveal that the generation of a benzene radical via the oxidative cleavage of aromatic hydrazines for the cross-coupling of C(sp(2))–C(sp(2)) with the assistance of a photocatalyst is essential. The process exhibits excellent compatibility with functional groups and provides convenient access to various 3-arylquinoxalin-2(1H)-ones in good to excellent yields.
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spelling pubmed-102745632023-06-17 Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond Wu, Mei Lian, Nancheng Wu, Cuimin Wu, Xinyao Chen, Houzheng Lin, Chen Zhou, Sunying Ke, Fang RSC Adv Chemistry A C(sp(2))–C(sp(2)) reaction between aromatic hydrazines and quinoxalines has been developed through a photocatalytic system. The protocol is established for C(sp(2))–N bond cleavage and direct C(sp(2))–H functionalization for the coupling of C(sp(2))–C(sp(2)) via photocatalysis under mild and ideal air conditions without the presence of a strong base and metal. The mechanistic studies reveal that the generation of a benzene radical via the oxidative cleavage of aromatic hydrazines for the cross-coupling of C(sp(2))–C(sp(2)) with the assistance of a photocatalyst is essential. The process exhibits excellent compatibility with functional groups and provides convenient access to various 3-arylquinoxalin-2(1H)-ones in good to excellent yields. The Royal Society of Chemistry 2023-06-16 /pmc/articles/PMC10274563/ /pubmed/37333794 http://dx.doi.org/10.1039/d3ra03479h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wu, Mei
Lian, Nancheng
Wu, Cuimin
Wu, Xinyao
Chen, Houzheng
Lin, Chen
Zhou, Sunying
Ke, Fang
Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond
title Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond
title_full Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond
title_fullStr Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond
title_full_unstemmed Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond
title_short Metal-free visible-induced C(sp(2))–C(sp(2)) coupling of quinoxalin-2(H)-ones via oxidative cleavage of the C–N bond
title_sort metal-free visible-induced c(sp(2))–c(sp(2)) coupling of quinoxalin-2(h)-ones via oxidative cleavage of the c–n bond
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10274563/
https://www.ncbi.nlm.nih.gov/pubmed/37333794
http://dx.doi.org/10.1039/d3ra03479h
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