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meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group

Over the last few decades C–H olefination has received significant interest, due to the importance and usefulness of aryl olefins both as synthetic targets and intermediates. While a wide range of ortho-olefination protocols have been developed, only a small number of meta-olefinations are currently...

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Autores principales: Spencer, Andrew R. A., Korde, Rishi, Font, Marc, Larrosa, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152615/
https://www.ncbi.nlm.nih.gov/pubmed/34122883
http://dx.doi.org/10.1039/d0sc01138j
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author Spencer, Andrew R. A.
Korde, Rishi
Font, Marc
Larrosa, Igor
author_facet Spencer, Andrew R. A.
Korde, Rishi
Font, Marc
Larrosa, Igor
author_sort Spencer, Andrew R. A.
collection PubMed
description Over the last few decades C–H olefination has received significant interest, due to the importance and usefulness of aryl olefins both as synthetic targets and intermediates. While a wide range of ortho-olefination protocols have been developed, only a small number of meta-olefinations are currently available. Importantly, the most common approach to meta-olefination, using a large meta-directing template, is not suitable for substrates such as fluorobenzenes, which cannot be derivatised. We report that the meta-selective olefination of fluoroarenes can be achieved via the use of CO(2) as a traceless directing group, which can be easily installed and removed in a one-pot process. Furthermore, this approach avoids the use of stoichiometric Ag(i)-salts, commonly used in C–H olefinations, and affords complete meta- over ortho/para-regioselectivity.
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spelling pubmed-81526152021-06-11 meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group Spencer, Andrew R. A. Korde, Rishi Font, Marc Larrosa, Igor Chem Sci Chemistry Over the last few decades C–H olefination has received significant interest, due to the importance and usefulness of aryl olefins both as synthetic targets and intermediates. While a wide range of ortho-olefination protocols have been developed, only a small number of meta-olefinations are currently available. Importantly, the most common approach to meta-olefination, using a large meta-directing template, is not suitable for substrates such as fluorobenzenes, which cannot be derivatised. We report that the meta-selective olefination of fluoroarenes can be achieved via the use of CO(2) as a traceless directing group, which can be easily installed and removed in a one-pot process. Furthermore, this approach avoids the use of stoichiometric Ag(i)-salts, commonly used in C–H olefinations, and affords complete meta- over ortho/para-regioselectivity. The Royal Society of Chemistry 2020-03-31 /pmc/articles/PMC8152615/ /pubmed/34122883 http://dx.doi.org/10.1039/d0sc01138j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Spencer, Andrew R. A.
Korde, Rishi
Font, Marc
Larrosa, Igor
meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group
title meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group
title_full meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group
title_fullStr meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group
title_full_unstemmed meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group
title_short meta-Selective olefination of fluoroarenes with alkynes using CO(2) as a traceless directing group
title_sort meta-selective olefination of fluoroarenes with alkynes using co(2) as a traceless directing group
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152615/
https://www.ncbi.nlm.nih.gov/pubmed/34122883
http://dx.doi.org/10.1039/d0sc01138j
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