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Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides

Direct C–H functionalisation methodologies represent an opportunity to improve the overall ‘green’ credentials of organic coupling reactions, improving atom economy and reducing overall step count. Despite this, these reactions frequently run under reaction conditions that leave room for improved su...

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Detalles Bibliográficos
Autores principales: Findlay, Michael T., Hogg, Ashley S., Douglas, James J., Larrosa, Igor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026369/
https://www.ncbi.nlm.nih.gov/pubmed/36960441
http://dx.doi.org/10.1039/d2gc03860a
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author Findlay, Michael T.
Hogg, Ashley S.
Douglas, James J.
Larrosa, Igor
author_facet Findlay, Michael T.
Hogg, Ashley S.
Douglas, James J.
Larrosa, Igor
author_sort Findlay, Michael T.
collection PubMed
description Direct C–H functionalisation methodologies represent an opportunity to improve the overall ‘green’ credentials of organic coupling reactions, improving atom economy and reducing overall step count. Despite this, these reactions frequently run under reaction conditions that leave room for improved sustainability. Herein, we describe a recent advance in our ruthenium-catalysed C–H arylation methodology that aims to address some of the environmental impacts associated with this procedure, including solvent choice, reaction temperature, reaction time, and loading of the ruthenium catalyst. We believe that our findings demonstrate a reaction with improved environmental credentials and showcase it on a multi-gram scale within an industrial setting.
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spelling pubmed-100263692023-03-21 Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides Findlay, Michael T. Hogg, Ashley S. Douglas, James J. Larrosa, Igor Green Chem Chemistry Direct C–H functionalisation methodologies represent an opportunity to improve the overall ‘green’ credentials of organic coupling reactions, improving atom economy and reducing overall step count. Despite this, these reactions frequently run under reaction conditions that leave room for improved sustainability. Herein, we describe a recent advance in our ruthenium-catalysed C–H arylation methodology that aims to address some of the environmental impacts associated with this procedure, including solvent choice, reaction temperature, reaction time, and loading of the ruthenium catalyst. We believe that our findings demonstrate a reaction with improved environmental credentials and showcase it on a multi-gram scale within an industrial setting. The Royal Society of Chemistry 2023-03-07 /pmc/articles/PMC10026369/ /pubmed/36960441 http://dx.doi.org/10.1039/d2gc03860a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Findlay, Michael T.
Hogg, Ashley S.
Douglas, James J.
Larrosa, Igor
Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides
title Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides
title_full Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides
title_fullStr Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides
title_full_unstemmed Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides
title_short Improving the sustainability of the ruthenium-catalysed N-directed C–H arylation of arenes with aryl halides
title_sort improving the sustainability of the ruthenium-catalysed n-directed c–h arylation of arenes with aryl halides
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10026369/
https://www.ncbi.nlm.nih.gov/pubmed/36960441
http://dx.doi.org/10.1039/d2gc03860a
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