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Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines
New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions.
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263357/ https://www.ncbi.nlm.nih.gov/pubmed/20657457 http://dx.doi.org/10.3390/molecules15052949 |
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author | Kabri, Youssef Verhaeghe, Pierre Gellis, Armand Vanelle, Patrice |
author_facet | Kabri, Youssef Verhaeghe, Pierre Gellis, Armand Vanelle, Patrice |
author_sort | Kabri, Youssef |
collection | PubMed |
description | New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions. |
format | Online Article Text |
id | pubmed-6263357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62633572019-01-02 Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines Kabri, Youssef Verhaeghe, Pierre Gellis, Armand Vanelle, Patrice Molecules Article New diarylquinazolines displaying pharmaceutical potential were synthesized in high yields from 4,7-dichloro-2-(2-methylprop-1-enyl)-6-nitroquinazoline by using microwave-promoted regioselective Suzuki-Miyaura cross-coupling reactions. MDPI 2010-04-27 /pmc/articles/PMC6263357/ /pubmed/20657457 http://dx.doi.org/10.3390/molecules15052949 Text en © 2010 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 Kabri, Youssef Verhaeghe, Pierre Gellis, Armand Vanelle, Patrice Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines |
title | Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines |
title_full | Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines |
title_fullStr | Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines |
title_full_unstemmed | Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines |
title_short | Regioselective Suzuki-Miyaura Reaction: Application to the Microwave-promoted Synthesis of 4,7-Diarylquinazolines |
title_sort | regioselective suzuki-miyaura reaction: application to the microwave-promoted synthesis of 4,7-diarylquinazolines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263357/ https://www.ncbi.nlm.nih.gov/pubmed/20657457 http://dx.doi.org/10.3390/molecules15052949 |
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