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TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides
A TBHP-mediated dehydrogenative cross-oxidative-coupling approach has been developed for the synthesis of N-arylbenzamides from methylarenes and acetanilides. This cross-coupling method is free of transition metal catalysts and ligands, and no extra organic solvents are required, which make it an us...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238673/ https://www.ncbi.nlm.nih.gov/pubmed/28144291 http://dx.doi.org/10.3762/bjoc.12.217 |
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author | Chen, Cui Liu, Weibing Zhou, Peng |
author_facet | Chen, Cui Liu, Weibing Zhou, Peng |
author_sort | Chen, Cui |
collection | PubMed |
description | A TBHP-mediated dehydrogenative cross-oxidative-coupling approach has been developed for the synthesis of N-arylbenzamides from methylarenes and acetanilides. This cross-coupling method is free of transition metal catalysts and ligands, and no extra organic solvents are required, which make it an useful and attractive strategy for the straightforward construction of C–N bonds. Besides, this conversion is an important complement to the conventional C–N forming strategies. |
format | Online Article Text |
id | pubmed-5238673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-52386732017-01-31 TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides Chen, Cui Liu, Weibing Zhou, Peng Beilstein J Org Chem Full Research Paper A TBHP-mediated dehydrogenative cross-oxidative-coupling approach has been developed for the synthesis of N-arylbenzamides from methylarenes and acetanilides. This cross-coupling method is free of transition metal catalysts and ligands, and no extra organic solvents are required, which make it an useful and attractive strategy for the straightforward construction of C–N bonds. Besides, this conversion is an important complement to the conventional C–N forming strategies. Beilstein-Institut 2016-10-25 /pmc/articles/PMC5238673/ /pubmed/28144291 http://dx.doi.org/10.3762/bjoc.12.217 Text en Copyright © 2016, Chen et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms) |
spellingShingle | Full Research Paper Chen, Cui Liu, Weibing Zhou, Peng TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
title | TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
title_full | TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
title_fullStr | TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
title_full_unstemmed | TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
title_short | TBHP-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
title_sort | tbhp-mediated highly efficient dehydrogenative cross-oxidative coupling of methylarenes with acetanilides |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238673/ https://www.ncbi.nlm.nih.gov/pubmed/28144291 http://dx.doi.org/10.3762/bjoc.12.217 |
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