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Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions
An approach for the preparation of polysubstituted indole-2-carbonitriles through a cross-coupling reaction of compounds 1-(but-2-ynyl)-1H-indole-2-carbonitriles and 1-benzyl-3-iodo-1H-indole-2-carbonitriles is described. The reactivity of indole derivatives with iodine at position 3 was studied usi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434198/ https://www.ncbi.nlm.nih.gov/pubmed/34500719 http://dx.doi.org/10.3390/molecules26175287 |
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author | Hrizi, Asma Cailler, Manon Romdhani-Younes, Moufida Carcenac, Yvan Thibonnet, Jérôme |
author_facet | Hrizi, Asma Cailler, Manon Romdhani-Younes, Moufida Carcenac, Yvan Thibonnet, Jérôme |
author_sort | Hrizi, Asma |
collection | PubMed |
description | An approach for the preparation of polysubstituted indole-2-carbonitriles through a cross-coupling reaction of compounds 1-(but-2-ynyl)-1H-indole-2-carbonitriles and 1-benzyl-3-iodo-1H-indole-2-carbonitriles is described. The reactivity of indole derivatives with iodine at position 3 was studied using cross-coupling reactions. The Sonogashira, Suzuki–Miyaura, Stille and Heck cross-couplings afforded a variety of di-, tri- and tetra-substituted indole-2-carbonitriles. |
format | Online Article Text |
id | pubmed-8434198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84341982021-09-12 Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions Hrizi, Asma Cailler, Manon Romdhani-Younes, Moufida Carcenac, Yvan Thibonnet, Jérôme Molecules Article An approach for the preparation of polysubstituted indole-2-carbonitriles through a cross-coupling reaction of compounds 1-(but-2-ynyl)-1H-indole-2-carbonitriles and 1-benzyl-3-iodo-1H-indole-2-carbonitriles is described. The reactivity of indole derivatives with iodine at position 3 was studied using cross-coupling reactions. The Sonogashira, Suzuki–Miyaura, Stille and Heck cross-couplings afforded a variety of di-, tri- and tetra-substituted indole-2-carbonitriles. MDPI 2021-08-31 /pmc/articles/PMC8434198/ /pubmed/34500719 http://dx.doi.org/10.3390/molecules26175287 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Hrizi, Asma Cailler, Manon Romdhani-Younes, Moufida Carcenac, Yvan Thibonnet, Jérôme Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions |
title | Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions |
title_full | Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions |
title_fullStr | Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions |
title_full_unstemmed | Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions |
title_short | Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions |
title_sort | synthesis of new highly functionalized 1h-indole-2-carbonitriles via cross-coupling reactions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434198/ https://www.ncbi.nlm.nih.gov/pubmed/34500719 http://dx.doi.org/10.3390/molecules26175287 |
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