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Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions
The halodecarboxylation of heteroarene carboxylic acids by treatment with N-bromosuccinimide or N-chlorosuccinimide was performed. This procedure provides a convenient route to synthetically useful mono-halogenated heteroarene intermediates such as halo-indoles, -aza-indoles, -indazoles and -aza-ind...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030312/ https://www.ncbi.nlm.nih.gov/pubmed/30110478 http://dx.doi.org/10.1098/rsos.180333 |
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author | Henderson, Scott H. West, Ryan A. Ward, Simon E. Honey, Mark A. |
author_facet | Henderson, Scott H. West, Ryan A. Ward, Simon E. Honey, Mark A. |
author_sort | Henderson, Scott H. |
collection | PubMed |
description | The halodecarboxylation of heteroarene carboxylic acids by treatment with N-bromosuccinimide or N-chlorosuccinimide was performed. This procedure provides a convenient route to synthetically useful mono-halogenated heteroarene intermediates such as halo-indoles, -aza-indoles, -indazoles and -aza-indazoles. The mild conditions employed and simple protocol provides an advantage over traditional halodecarboxylation procedures that require expensive and toxic metal catalysts, basic conditions, time-consuming intermediate isolation and elevated reaction temperatures. |
format | Online Article Text |
id | pubmed-6030312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-60303122018-07-17 Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions Henderson, Scott H. West, Ryan A. Ward, Simon E. Honey, Mark A. R Soc Open Sci Chemistry The halodecarboxylation of heteroarene carboxylic acids by treatment with N-bromosuccinimide or N-chlorosuccinimide was performed. This procedure provides a convenient route to synthetically useful mono-halogenated heteroarene intermediates such as halo-indoles, -aza-indoles, -indazoles and -aza-indazoles. The mild conditions employed and simple protocol provides an advantage over traditional halodecarboxylation procedures that require expensive and toxic metal catalysts, basic conditions, time-consuming intermediate isolation and elevated reaction temperatures. The Royal Society Publishing 2018-06-20 /pmc/articles/PMC6030312/ /pubmed/30110478 http://dx.doi.org/10.1098/rsos.180333 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Chemistry Henderson, Scott H. West, Ryan A. Ward, Simon E. Honey, Mark A. Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
title | Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
title_full | Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
title_fullStr | Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
title_full_unstemmed | Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
title_short | Metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
title_sort | metal-free selective mono-halodecarboxylation of heteroarenes under mild conditions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6030312/ https://www.ncbi.nlm.nih.gov/pubmed/30110478 http://dx.doi.org/10.1098/rsos.180333 |
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