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meta-C–H arylation of fluoroarenes via traceless directing group relay strategy

While several methods for the ortho selective arylation of fluoroarenes, meta-functionalisation has never been achieved. We report a new methodology, based on the traceless directing group relay concept, leading to the first meta-selective (hetero)arylation of fluoroarenes. In this strategy, CO(2) i...

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Detalles Bibliográficos
Autores principales: Font, Marc, Spencer, Andrew R. A., Larrosa, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137440/
https://www.ncbi.nlm.nih.gov/pubmed/30310635
http://dx.doi.org/10.1039/c8sc02417k
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author Font, Marc
Spencer, Andrew R. A.
Larrosa, Igor
author_facet Font, Marc
Spencer, Andrew R. A.
Larrosa, Igor
author_sort Font, Marc
collection PubMed
description While several methods for the ortho selective arylation of fluoroarenes, meta-functionalisation has never been achieved. We report a new methodology, based on the traceless directing group relay concept, leading to the first meta-selective (hetero)arylation of fluoroarenes. In this strategy, CO(2) is introduced as a transient directing group, to control a Pd-catalysed arylation meta to the fluoro functionality, prior to its release in a sequential, one-pot fashion. This method has shown compatibility with a number of functional groups and substitution patterns in both the fluoroarene core and aryl iodide coupling partners, and proceeds with complete meta-selectivity and mono vs. bis-arylation selectivity.
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spelling pubmed-61374402018-10-11 meta-C–H arylation of fluoroarenes via traceless directing group relay strategy Font, Marc Spencer, Andrew R. A. Larrosa, Igor Chem Sci Chemistry While several methods for the ortho selective arylation of fluoroarenes, meta-functionalisation has never been achieved. We report a new methodology, based on the traceless directing group relay concept, leading to the first meta-selective (hetero)arylation of fluoroarenes. In this strategy, CO(2) is introduced as a transient directing group, to control a Pd-catalysed arylation meta to the fluoro functionality, prior to its release in a sequential, one-pot fashion. This method has shown compatibility with a number of functional groups and substitution patterns in both the fluoroarene core and aryl iodide coupling partners, and proceeds with complete meta-selectivity and mono vs. bis-arylation selectivity. Royal Society of Chemistry 2018-07-25 /pmc/articles/PMC6137440/ /pubmed/30310635 http://dx.doi.org/10.1039/c8sc02417k Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Font, Marc
Spencer, Andrew R. A.
Larrosa, Igor
meta-C–H arylation of fluoroarenes via traceless directing group relay strategy
title meta-C–H arylation of fluoroarenes via traceless directing group relay strategy
title_full meta-C–H arylation of fluoroarenes via traceless directing group relay strategy
title_fullStr meta-C–H arylation of fluoroarenes via traceless directing group relay strategy
title_full_unstemmed meta-C–H arylation of fluoroarenes via traceless directing group relay strategy
title_short meta-C–H arylation of fluoroarenes via traceless directing group relay strategy
title_sort meta-c–h arylation of fluoroarenes via traceless directing group relay strategy
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137440/
https://www.ncbi.nlm.nih.gov/pubmed/30310635
http://dx.doi.org/10.1039/c8sc02417k
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AT larrosaigor metacharylationoffluoroarenesviatracelessdirectinggrouprelaystrategy