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Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions
An efficient solvent-free protocol for regioselective bromination of substituted coumarins has been developed by using dioxane dibromide as the solid brominating agent. The efficacy of the solvent-free protocol has been established. The effects of the electronic nature and location of the substituen...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302096/ https://www.ncbi.nlm.nih.gov/pubmed/22423301 http://dx.doi.org/10.3762/bjoc.8.35 |
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author | Chaudhuri, Subrata Kumar Roy, Sanchita Bhar, Sanjay |
author_facet | Chaudhuri, Subrata Kumar Roy, Sanchita Bhar, Sanjay |
author_sort | Chaudhuri, Subrata Kumar |
collection | PubMed |
description | An efficient solvent-free protocol for regioselective bromination of substituted coumarins has been developed by using dioxane dibromide as the solid brominating agent. The efficacy of the solvent-free protocol has been established. The effects of the electronic nature and location of the substituents on the outcome of the reaction have been rationalized with a proposed mechanism. |
format | Online Article Text |
id | pubmed-3302096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-33020962012-03-15 Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions Chaudhuri, Subrata Kumar Roy, Sanchita Bhar, Sanjay Beilstein J Org Chem Full Research Paper An efficient solvent-free protocol for regioselective bromination of substituted coumarins has been developed by using dioxane dibromide as the solid brominating agent. The efficacy of the solvent-free protocol has been established. The effects of the electronic nature and location of the substituents on the outcome of the reaction have been rationalized with a proposed mechanism. Beilstein-Institut 2012-02-29 /pmc/articles/PMC3302096/ /pubmed/22423301 http://dx.doi.org/10.3762/bjoc.8.35 Text en Copyright © 2012, Chaudhuri 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 Chaudhuri, Subrata Kumar Roy, Sanchita Bhar, Sanjay Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
title | Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
title_full | Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
title_fullStr | Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
title_full_unstemmed | Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
title_short | Dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
title_sort | dioxane dibromide mediated bromination of substituted coumarins under solvent-free conditions |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302096/ https://www.ncbi.nlm.nih.gov/pubmed/22423301 http://dx.doi.org/10.3762/bjoc.8.35 |
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