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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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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. |
format | Online Article Text |
id | pubmed-9070767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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