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Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives

Conditions allowing the one pot 2,5-diheteroarylation of 2,5-dibromothiophene derivatives in the presence of palladium catalysts are reported. Using KOAc as the base, DMA as the solvent and only 0.5–2 mol % palladium catalysts, the target 2,5-diheteroarylated thiophenes were obtained in moderate to...

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Autores principales: Belkessam, Fatma, Mohand, Aidene, Soulé, Jean-François, Elias, Abdelhamid, Doucet, Henri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273267/
https://www.ncbi.nlm.nih.gov/pubmed/25550758
http://dx.doi.org/10.3762/bjoc.10.309
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author Belkessam, Fatma
Mohand, Aidene
Soulé, Jean-François
Elias, Abdelhamid
Doucet, Henri
author_facet Belkessam, Fatma
Mohand, Aidene
Soulé, Jean-François
Elias, Abdelhamid
Doucet, Henri
author_sort Belkessam, Fatma
collection PubMed
description Conditions allowing the one pot 2,5-diheteroarylation of 2,5-dibromothiophene derivatives in the presence of palladium catalysts are reported. Using KOAc as the base, DMA as the solvent and only 0.5–2 mol % palladium catalysts, the target 2,5-diheteroarylated thiophenes were obtained in moderate to good yields and with a wide variety of heteroarenes such as thiazoles, thiophenes, furans, pyrroles, pyrazoles or isoxazoles. Moreover, sequential heteroarylation reactions allow the access to 2,5-diheteroarylated thiophenes bearing two different heteroaryl units.
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spelling pubmed-42732672014-12-30 Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives Belkessam, Fatma Mohand, Aidene Soulé, Jean-François Elias, Abdelhamid Doucet, Henri Beilstein J Org Chem Full Research Paper Conditions allowing the one pot 2,5-diheteroarylation of 2,5-dibromothiophene derivatives in the presence of palladium catalysts are reported. Using KOAc as the base, DMA as the solvent and only 0.5–2 mol % palladium catalysts, the target 2,5-diheteroarylated thiophenes were obtained in moderate to good yields and with a wide variety of heteroarenes such as thiazoles, thiophenes, furans, pyrroles, pyrazoles or isoxazoles. Moreover, sequential heteroarylation reactions allow the access to 2,5-diheteroarylated thiophenes bearing two different heteroaryl units. Beilstein-Institut 2014-12-09 /pmc/articles/PMC4273267/ /pubmed/25550758 http://dx.doi.org/10.3762/bjoc.10.309 Text en Copyright © 2014, Belkessam 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 Full Research Paper
Belkessam, Fatma
Mohand, Aidene
Soulé, Jean-François
Elias, Abdelhamid
Doucet, Henri
Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
title Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
title_full Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
title_fullStr Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
title_full_unstemmed Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
title_short Palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
title_sort palladium-catalyzed 2,5-diheteroarylation of 2,5-dibromothiophene derivatives
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273267/
https://www.ncbi.nlm.nih.gov/pubmed/25550758
http://dx.doi.org/10.3762/bjoc.10.309
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