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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-6137440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT fontmarc metacharylationoffluoroarenesviatracelessdirectinggrouprelaystrategy AT spencerandrewra metacharylationoffluoroarenesviatracelessdirectinggrouprelaystrategy AT larrosaigor metacharylationoffluoroarenesviatracelessdirectinggrouprelaystrategy |