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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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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. |
format | Online Article Text |
id | pubmed-10026369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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