Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation

A facile and high-yielding protocol for diverse benzotriazoles through intramolecular N-arylation of different o-chloro-1,2,3-benzotriazenes using CuI/Cs(2)CO(3) has been developed.

Detalles Bibliográficos
Autores principales: Kale, Raju R., Prasad, Virendra, Hussain, H.A., Tiwari, Vinod K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2010
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111836/
https://www.ncbi.nlm.nih.gov/pubmed/32287442
http://dx.doi.org/10.1016/j.tetlet.2010.08.083
_version_ 1783513367461232640
author Kale, Raju R.
Prasad, Virendra
Hussain, H.A.
Tiwari, Vinod K.
author_facet Kale, Raju R.
Prasad, Virendra
Hussain, H.A.
Tiwari, Vinod K.
author_sort Kale, Raju R.
collection PubMed
description A facile and high-yielding protocol for diverse benzotriazoles through intramolecular N-arylation of different o-chloro-1,2,3-benzotriazenes using CuI/Cs(2)CO(3) has been developed.
format Online
Article
Text
id pubmed-7111836
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Elsevier Ltd.
record_format MEDLINE/PubMed
spelling pubmed-71118362020-04-02 Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation Kale, Raju R. Prasad, Virendra Hussain, H.A. Tiwari, Vinod K. Tetrahedron Lett Article A facile and high-yielding protocol for diverse benzotriazoles through intramolecular N-arylation of different o-chloro-1,2,3-benzotriazenes using CuI/Cs(2)CO(3) has been developed. Elsevier Ltd. 2010-10-27 2010-09-01 /pmc/articles/PMC7111836/ /pubmed/32287442 http://dx.doi.org/10.1016/j.tetlet.2010.08.083 Text en Copyright © 2010 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Kale, Raju R.
Prasad, Virendra
Hussain, H.A.
Tiwari, Vinod K.
Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation
title Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation
title_full Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation
title_fullStr Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation
title_full_unstemmed Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation
title_short Facile route for N(1)-aryl benzotriazoles from diazoamino arynes via CuI-mediated intramolecular N-arylation
title_sort facile route for n(1)-aryl benzotriazoles from diazoamino arynes via cui-mediated intramolecular n-arylation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111836/
https://www.ncbi.nlm.nih.gov/pubmed/32287442
http://dx.doi.org/10.1016/j.tetlet.2010.08.083
work_keys_str_mv AT kalerajur facilerouteforn1arylbenzotriazolesfromdiazoaminoarynesviacuimediatedintramolecularnarylation
AT prasadvirendra facilerouteforn1arylbenzotriazolesfromdiazoaminoarynesviacuimediatedintramolecularnarylation
AT hussainha facilerouteforn1arylbenzotriazolesfromdiazoaminoarynesviacuimediatedintramolecularnarylation
AT tiwarivinodk facilerouteforn1arylbenzotriazolesfromdiazoaminoarynesviacuimediatedintramolecularnarylation

Ejemplares similares