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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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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. |
format | Online Article Text |
id | pubmed-8984950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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