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Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow
Herein, we report a photocatalytic procedure that enables the acylation/arylation of unfunctionalized alkyl derivatives in flow. The method exploits the ability of the decatungstate anion to act as a hydrogen atom abstractor and produce nucleophilic carbon‐centered radicals that are intercepted by a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518495/ https://www.ncbi.nlm.nih.gov/pubmed/34329531 http://dx.doi.org/10.1002/anie.202108987 |
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author | Mazzarella, Daniele Pulcinella, Antonio Bovy, Loïc Broersma, Rémy Noël, Timothy |
author_facet | Mazzarella, Daniele Pulcinella, Antonio Bovy, Loïc Broersma, Rémy Noël, Timothy |
author_sort | Mazzarella, Daniele |
collection | PubMed |
description | Herein, we report a photocatalytic procedure that enables the acylation/arylation of unfunctionalized alkyl derivatives in flow. The method exploits the ability of the decatungstate anion to act as a hydrogen atom abstractor and produce nucleophilic carbon‐centered radicals that are intercepted by a nickel catalyst to ultimately forge C(sp(3))−C(sp(2)) bonds. Owing to the intensified conditions in flow, the reaction time can be reduced from 12–48 hours to only 5–15 minutes. Finally, kinetic measurements highlight how the intensified conditions do not change the reaction mechanism but reliably speed up the overall process. |
format | Online Article Text |
id | pubmed-8518495 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85184952021-10-21 Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow Mazzarella, Daniele Pulcinella, Antonio Bovy, Loïc Broersma, Rémy Noël, Timothy Angew Chem Int Ed Engl Communications Herein, we report a photocatalytic procedure that enables the acylation/arylation of unfunctionalized alkyl derivatives in flow. The method exploits the ability of the decatungstate anion to act as a hydrogen atom abstractor and produce nucleophilic carbon‐centered radicals that are intercepted by a nickel catalyst to ultimately forge C(sp(3))−C(sp(2)) bonds. Owing to the intensified conditions in flow, the reaction time can be reduced from 12–48 hours to only 5–15 minutes. Finally, kinetic measurements highlight how the intensified conditions do not change the reaction mechanism but reliably speed up the overall process. John Wiley and Sons Inc. 2021-08-20 2021-09-20 /pmc/articles/PMC8518495/ /pubmed/34329531 http://dx.doi.org/10.1002/anie.202108987 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Mazzarella, Daniele Pulcinella, Antonio Bovy, Loïc Broersma, Rémy Noël, Timothy Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow |
title | Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow |
title_full | Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow |
title_fullStr | Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow |
title_full_unstemmed | Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow |
title_short | Rapid and Direct Photocatalytic C(sp(3))−H Acylation and Arylation in Flow |
title_sort | rapid and direct photocatalytic c(sp(3))−h acylation and arylation in flow |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518495/ https://www.ncbi.nlm.nih.gov/pubmed/34329531 http://dx.doi.org/10.1002/anie.202108987 |
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