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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2014
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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. |
format | Online Article Text |
id | pubmed-4273267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
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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