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Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles

Herein, we describe a one-pot protocol for the synthesis of a novel series of polycyclic triazole derivatives. Transition metal-catalyzed decarboxylative CuAAC and dehydrogenative cross coupling reactions are combined in a single flask and achieved good yields of the respective triazoles (up to 97%...

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Autores principales: Bharathimohan, Kuppusamy, Ponpandian, Thanasekaran, Ahamed, A Jafar, Bhuvanesh, Nattamai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311670/
https://www.ncbi.nlm.nih.gov/pubmed/25670973
http://dx.doi.org/10.3762/bjoc.10.321
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author Bharathimohan, Kuppusamy
Ponpandian, Thanasekaran
Ahamed, A Jafar
Bhuvanesh, Nattamai
author_facet Bharathimohan, Kuppusamy
Ponpandian, Thanasekaran
Ahamed, A Jafar
Bhuvanesh, Nattamai
author_sort Bharathimohan, Kuppusamy
collection PubMed
description Herein, we describe a one-pot protocol for the synthesis of a novel series of polycyclic triazole derivatives. Transition metal-catalyzed decarboxylative CuAAC and dehydrogenative cross coupling reactions are combined in a single flask and achieved good yields of the respective triazoles (up to 97% yield). This methodology is more convenient to produce the complex polycyclic molecules in a simple way.
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spelling pubmed-43116702015-02-10 Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles Bharathimohan, Kuppusamy Ponpandian, Thanasekaran Ahamed, A Jafar Bhuvanesh, Nattamai Beilstein J Org Chem Letter Herein, we describe a one-pot protocol for the synthesis of a novel series of polycyclic triazole derivatives. Transition metal-catalyzed decarboxylative CuAAC and dehydrogenative cross coupling reactions are combined in a single flask and achieved good yields of the respective triazoles (up to 97% yield). This methodology is more convenient to produce the complex polycyclic molecules in a simple way. Beilstein-Institut 2014-12-17 /pmc/articles/PMC4311670/ /pubmed/25670973 http://dx.doi.org/10.3762/bjoc.10.321 Text en Copyright © 2014, Bharathimohan 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 Letter
Bharathimohan, Kuppusamy
Ponpandian, Thanasekaran
Ahamed, A Jafar
Bhuvanesh, Nattamai
Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
title Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
title_full Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
title_fullStr Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
title_full_unstemmed Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
title_short Sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
title_sort sequential decarboxylative azide–alkyne cycloaddition and dehydrogenative coupling reactions: one-pot synthesis of polycyclic fused triazoles
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311670/
https://www.ncbi.nlm.nih.gov/pubmed/25670973
http://dx.doi.org/10.3762/bjoc.10.321
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