O(2)-Mediated Dehydrogenative Phenoxazination of Phenols

[Image: see text] Phenoxazines, in particular N-arylated phenoxazines, represent an increasingly important scaffold in the material sciences. Moreover, the oxygen-gas-mediated dehydrogenative phenochalcogenazination concept of phenols has been developed and exemplified for X = sulfur and recently fo...

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Autores principales: Benchouaia, Rajaa, Nandi, Shiny, Maurer, Clemens, Patureau, Frederic W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981320/
https://www.ncbi.nlm.nih.gov/pubmed/35276045
http://dx.doi.org/10.1021/acs.joc.1c02827
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author Benchouaia, Rajaa
Nandi, Shiny
Maurer, Clemens
Patureau, Frederic W.
author_facet Benchouaia, Rajaa
Nandi, Shiny
Maurer, Clemens
Patureau, Frederic W.
author_sort Benchouaia, Rajaa
collection PubMed
description [Image: see text] Phenoxazines, in particular N-arylated phenoxazines, represent an increasingly important scaffold in the material sciences. Moreover, the oxygen-gas-mediated dehydrogenative phenochalcogenazination concept of phenols has been developed and exemplified for X = sulfur and recently for X = selenium and tellurium. The smallest chalcogen, X = oxygen, is herein exemplified with various functional groups under a likewise trivial oxygen atmosphere.
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spelling pubmed-89813202022-04-06 O(2)-Mediated Dehydrogenative Phenoxazination of Phenols Benchouaia, Rajaa Nandi, Shiny Maurer, Clemens Patureau, Frederic W. J Org Chem [Image: see text] Phenoxazines, in particular N-arylated phenoxazines, represent an increasingly important scaffold in the material sciences. Moreover, the oxygen-gas-mediated dehydrogenative phenochalcogenazination concept of phenols has been developed and exemplified for X = sulfur and recently for X = selenium and tellurium. The smallest chalcogen, X = oxygen, is herein exemplified with various functional groups under a likewise trivial oxygen atmosphere. American Chemical Society 2022-03-11 2022-04-01 /pmc/articles/PMC8981320/ /pubmed/35276045 http://dx.doi.org/10.1021/acs.joc.1c02827 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Benchouaia, Rajaa
Nandi, Shiny
Maurer, Clemens
Patureau, Frederic W.
O(2)-Mediated Dehydrogenative Phenoxazination of Phenols
title O(2)-Mediated Dehydrogenative Phenoxazination of Phenols
title_full O(2)-Mediated Dehydrogenative Phenoxazination of Phenols
title_fullStr O(2)-Mediated Dehydrogenative Phenoxazination of Phenols
title_full_unstemmed O(2)-Mediated Dehydrogenative Phenoxazination of Phenols
title_short O(2)-Mediated Dehydrogenative Phenoxazination of Phenols
title_sort o(2)-mediated dehydrogenative phenoxazination of phenols
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981320/
https://www.ncbi.nlm.nih.gov/pubmed/35276045
http://dx.doi.org/10.1021/acs.joc.1c02827
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