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A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide
We describe the development of a new palladium-catalyzed method to generate ketones via the oxidative coupling of two arenes and CO. This transformation is catalyzed by simple palladium salts, and is postulated to proceed via the conversion of arenes into high energy aroyl triflate electrophiles. Ex...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157493/ https://www.ncbi.nlm.nih.gov/pubmed/34122815 http://dx.doi.org/10.1039/d0sc00085j |
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author | Levesque, Taleah M. Kinney, R. Garrison Arndtsen, Bruce A. |
author_facet | Levesque, Taleah M. Kinney, R. Garrison Arndtsen, Bruce A. |
author_sort | Levesque, Taleah M. |
collection | PubMed |
description | We describe the development of a new palladium-catalyzed method to generate ketones via the oxidative coupling of two arenes and CO. This transformation is catalyzed by simple palladium salts, and is postulated to proceed via the conversion of arenes into high energy aroyl triflate electrophiles. Exploiting the latter can also allow the synthesis of unsymmetrical ketones from two different arenes. |
format | Online Article Text |
id | pubmed-8157493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81574932021-06-11 A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide Levesque, Taleah M. Kinney, R. Garrison Arndtsen, Bruce A. Chem Sci Chemistry We describe the development of a new palladium-catalyzed method to generate ketones via the oxidative coupling of two arenes and CO. This transformation is catalyzed by simple palladium salts, and is postulated to proceed via the conversion of arenes into high energy aroyl triflate electrophiles. Exploiting the latter can also allow the synthesis of unsymmetrical ketones from two different arenes. The Royal Society of Chemistry 2020-02-20 /pmc/articles/PMC8157493/ /pubmed/34122815 http://dx.doi.org/10.1039/d0sc00085j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Levesque, Taleah M. Kinney, R. Garrison Arndtsen, Bruce A. A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
title | A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
title_full | A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
title_fullStr | A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
title_full_unstemmed | A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
title_short | A palladium-catalyzed C–H functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
title_sort | palladium-catalyzed c–h functionalization route to ketones via the oxidative coupling of arenes with carbon monoxide |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157493/ https://www.ncbi.nlm.nih.gov/pubmed/34122815 http://dx.doi.org/10.1039/d0sc00085j |
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