Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides

Palladium-catalyzed alkynylation has emerged as one of the most reliable methods for the synthesis of alkynes which are often used in natural product syntheses and material science. An efficient method for coupling alkynyltrifluoroborates with various aryl bromides in the presence of a palladium cat...

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Detalles Bibliográficos
Autores principales: Coltuclu, Vitali, Dadush, Eric, Naravane, Abhijit, Kabalka, George W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270459/
https://www.ncbi.nlm.nih.gov/pubmed/23434861
http://dx.doi.org/10.3390/molecules18021755
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author Coltuclu, Vitali
Dadush, Eric
Naravane, Abhijit
Kabalka, George W.
author_facet Coltuclu, Vitali
Dadush, Eric
Naravane, Abhijit
Kabalka, George W.
author_sort Coltuclu, Vitali
collection PubMed
description Palladium-catalyzed alkynylation has emerged as one of the most reliable methods for the synthesis of alkynes which are often used in natural product syntheses and material science. An efficient method for coupling alkynyltrifluoroborates with various aryl bromides in the presence of a palladium catalyst has been developed using microwave irradiation. The microwave reactions are rapid and efficient.
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spelling pubmed-62704592018-12-14 Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides Coltuclu, Vitali Dadush, Eric Naravane, Abhijit Kabalka, George W. Molecules Article Palladium-catalyzed alkynylation has emerged as one of the most reliable methods for the synthesis of alkynes which are often used in natural product syntheses and material science. An efficient method for coupling alkynyltrifluoroborates with various aryl bromides in the presence of a palladium catalyst has been developed using microwave irradiation. The microwave reactions are rapid and efficient. MDPI 2013-01-29 /pmc/articles/PMC6270459/ /pubmed/23434861 http://dx.doi.org/10.3390/molecules18021755 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Coltuclu, Vitali
Dadush, Eric
Naravane, Abhijit
Kabalka, George W.
Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
title Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
title_full Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
title_fullStr Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
title_full_unstemmed Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
title_short Microwave-Enhanced Cross-Coupling Reactions Involving Alkynyltrifluoroborates with Aryl Bromides
title_sort microwave-enhanced cross-coupling reactions involving alkynyltrifluoroborates with aryl bromides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270459/
https://www.ncbi.nlm.nih.gov/pubmed/23434861
http://dx.doi.org/10.3390/molecules18021755
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AT naravaneabhijit microwaveenhancedcrosscouplingreactionsinvolvingalkynyltrifluoroborateswitharylbromides
AT kabalkageorgew microwaveenhancedcrosscouplingreactionsinvolvingalkynyltrifluoroborateswitharylbromides

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