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Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light

An efficient synthesis of imides using metal-free photoredox-catalyzed direct α-oxygenation of N,N′-disubstituted anilines in the presence of 9-mesityl-10-methylacridinium [Acr(+)-Mes]BF(4) as a photoredox catalyst and molecular oxygen as a green oxidant under visible light was developed. This photo...

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Detalles Bibliográficos
Autores principales: Neerathilingam, Nalladhambi, Anandhan, Ramasamy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984950/
https://www.ncbi.nlm.nih.gov/pubmed/35424823
http://dx.doi.org/10.1039/d2ra00585a
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author Neerathilingam, Nalladhambi
Anandhan, Ramasamy
author_facet Neerathilingam, Nalladhambi
Anandhan, Ramasamy
author_sort Neerathilingam, Nalladhambi
collection PubMed
description An efficient synthesis of imides using metal-free photoredox-catalyzed direct α-oxygenation of N,N′-disubstituted anilines in the presence of 9-mesityl-10-methylacridinium [Acr(+)-Mes]BF(4) as a photoredox catalyst and molecular oxygen as a green oxidant under visible light was developed. This photochemical approach offered operational simplicity, high atom economy with a low E-factor, and functional group tolerance under mild reaction conditions. Control and quenching experiments confirmed the occurrence of a radical pathway and superoxide radical anion α-oxygenation reactions, and also provided strong evidence for the reductive quenching of [Acr(+)-Mes]BF(4) based on a Stern–Volmer plot, which led to the proposed mechanism of this reaction.
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spelling pubmed-89849502022-04-13 Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light Neerathilingam, Nalladhambi Anandhan, Ramasamy RSC Adv Chemistry An efficient synthesis of imides using metal-free photoredox-catalyzed direct α-oxygenation of N,N′-disubstituted anilines in the presence of 9-mesityl-10-methylacridinium [Acr(+)-Mes]BF(4) as a photoredox catalyst and molecular oxygen as a green oxidant under visible light was developed. This photochemical approach offered operational simplicity, high atom economy with a low E-factor, and functional group tolerance under mild reaction conditions. Control and quenching experiments confirmed the occurrence of a radical pathway and superoxide radical anion α-oxygenation reactions, and also provided strong evidence for the reductive quenching of [Acr(+)-Mes]BF(4) based on a Stern–Volmer plot, which led to the proposed mechanism of this reaction. The Royal Society of Chemistry 2022-03-15 /pmc/articles/PMC8984950/ /pubmed/35424823 http://dx.doi.org/10.1039/d2ra00585a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Neerathilingam, Nalladhambi
Anandhan, Ramasamy
Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light
title Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light
title_full Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light
title_fullStr Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light
title_full_unstemmed Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light
title_short Metal-free photoredox-catalyzed direct α-oxygenation of N,N-dibenzylanilines to imides under visible light
title_sort metal-free photoredox-catalyzed direct α-oxygenation of n,n-dibenzylanilines to imides under visible light
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984950/
https://www.ncbi.nlm.nih.gov/pubmed/35424823
http://dx.doi.org/10.1039/d2ra00585a
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