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Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds

A metal-free cross-dehydrogenative coupling of quinones with toluene derivatives has been established. A series of quinones were subjected to reaction with toluene derivatives in the presence of di-tertbutyl peroxide (DTBP) for direct synthesis of benzylquinones. The method exhibits good functional...

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Detalles Bibliográficos
Autores principales: Dong, Yu, Yang, Jian, He, Shuai, Shi, Zhi-Chuan, Wang, Yu, Zhang, Xiao-Mei, Wang, Ji-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070767/
https://www.ncbi.nlm.nih.gov/pubmed/35529195
http://dx.doi.org/10.1039/c9ra05678e
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author Dong, Yu
Yang, Jian
He, Shuai
Shi, Zhi-Chuan
Wang, Yu
Zhang, Xiao-Mei
Wang, Ji-Yu
author_facet Dong, Yu
Yang, Jian
He, Shuai
Shi, Zhi-Chuan
Wang, Yu
Zhang, Xiao-Mei
Wang, Ji-Yu
author_sort Dong, Yu
collection PubMed
description A metal-free cross-dehydrogenative coupling of quinones with toluene derivatives has been established. A series of quinones were subjected to reaction with toluene derivatives in the presence of di-tertbutyl peroxide (DTBP) for direct synthesis of benzylquinones. The method exhibits good functional group tolerance, and desired products were obtained in moderate to good yields. Meanwhile, a radical pathway was proposed to describe the cross-dehydrogenative coupling of quinones with toluene derivatives.
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spelling pubmed-90707672022-05-06 Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds Dong, Yu Yang, Jian He, Shuai Shi, Zhi-Chuan Wang, Yu Zhang, Xiao-Mei Wang, Ji-Yu RSC Adv Chemistry A metal-free cross-dehydrogenative coupling of quinones with toluene derivatives has been established. A series of quinones were subjected to reaction with toluene derivatives in the presence of di-tertbutyl peroxide (DTBP) for direct synthesis of benzylquinones. The method exhibits good functional group tolerance, and desired products were obtained in moderate to good yields. Meanwhile, a radical pathway was proposed to describe the cross-dehydrogenative coupling of quinones with toluene derivatives. The Royal Society of Chemistry 2019-09-02 /pmc/articles/PMC9070767/ /pubmed/35529195 http://dx.doi.org/10.1039/c9ra05678e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Dong, Yu
Yang, Jian
He, Shuai
Shi, Zhi-Chuan
Wang, Yu
Zhang, Xiao-Mei
Wang, Ji-Yu
Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds
title Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds
title_full Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds
title_fullStr Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds
title_full_unstemmed Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds
title_short Metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic C(sp(3))–H bonds
title_sort metal-free oxidative cross-dehydrogenative coupling of quinones with benzylic c(sp(3))–h bonds
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070767/
https://www.ncbi.nlm.nih.gov/pubmed/35529195
http://dx.doi.org/10.1039/c9ra05678e
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