N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system

The coupling of arylboroxines with a variety of amines, amides, imides and sulfonamides catalyzed by a copper salt/EtOH system has been developed. In the absence of a base or additive the corresponding N-arylation products were obtained in moderate to excellent yields.

Detalles Bibliográficos
Autores principales: Zheng, Zhang-Guo, Wen, Jun, Wang, Na, Wu, Bo, Yu, Xiao-Qi
Formato: Texto
Lenguaje:English
Publicado: Beilstein-Institut 2008
Materias:
Preliminary Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2587945/
https://www.ncbi.nlm.nih.gov/pubmed/19043624
http://dx.doi.org/10.3762/bjoc.4.40
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author Zheng, Zhang-Guo
Wen, Jun
Wang, Na
Wu, Bo
Yu, Xiao-Qi
author_facet Zheng, Zhang-Guo
Wen, Jun
Wang, Na
Wu, Bo
Yu, Xiao-Qi
author_sort Zheng, Zhang-Guo
collection PubMed
description The coupling of arylboroxines with a variety of amines, amides, imides and sulfonamides catalyzed by a copper salt/EtOH system has been developed. In the absence of a base or additive the corresponding N-arylation products were obtained in moderate to excellent yields.
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spelling pubmed-25879452008-11-28 N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system Zheng, Zhang-Guo Wen, Jun Wang, Na Wu, Bo Yu, Xiao-Qi Beilstein J Org Chem Preliminary Communication The coupling of arylboroxines with a variety of amines, amides, imides and sulfonamides catalyzed by a copper salt/EtOH system has been developed. In the absence of a base or additive the corresponding N-arylation products were obtained in moderate to excellent yields. Beilstein-Institut 2008-11-07 /pmc/articles/PMC2587945/ /pubmed/19043624 http://dx.doi.org/10.3762/bjoc.4.40 Text en Copyright © 2008, Zheng et al. https://creativecommons.org/licenses/by/2.0https://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/2.0), 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 Preliminary Communication
Zheng, Zhang-Guo
Wen, Jun
Wang, Na
Wu, Bo
Yu, Xiao-Qi
N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system
title N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system
title_full N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system
title_fullStr N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system
title_full_unstemmed N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system
title_short N-Arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/EtOH system
title_sort n-arylation of amines, amides, imides and sulfonamides with arylboroxines catalyzed by simple copper salt/etoh system
topic Preliminary Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2587945/
https://www.ncbi.nlm.nih.gov/pubmed/19043624
http://dx.doi.org/10.3762/bjoc.4.40
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