Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Henderson, Scott H., West, Ryan A., Ward, Simon E., Honey, Mark A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2018
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
_version_ 1783337123877748736
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
work_keys_str_mv AT hendersonscotth metalfreeselectivemonohalodecarboxylationofheteroarenesundermildconditions
AT westryana metalfreeselectivemonohalodecarboxylationofheteroarenesundermildconditions
AT wardsimone metalfreeselectivemonohalodecarboxylationofheteroarenesundermildconditions
AT honeymarka metalfreeselectivemonohalodecarboxylationofheteroarenesundermildconditions