Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Mazzarella, Daniele, Pulcinella, Antonio, Bovy, Loïc, Broersma, Rémy, Noël, Timothy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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
_version_ 1784584237118128128
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
work_keys_str_mv AT mazzarelladaniele rapidanddirectphotocatalyticcsp3hacylationandarylationinflow
AT pulcinellaantonio rapidanddirectphotocatalyticcsp3hacylationandarylationinflow
AT bovyloic rapidanddirectphotocatalyticcsp3hacylationandarylationinflow
AT broersmaremy rapidanddirectphotocatalyticcsp3hacylationandarylationinflow
AT noeltimothy rapidanddirectphotocatalyticcsp3hacylationandarylationinflow