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Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions
Hydrodeaminated and monodeuterated aromatics were obtained via a visible-light driven reaction of arylazo sulfones. Deuteration occurs efficiently in deuterated media such as isopropanol-d(8) or in THF-d(8)/water mixtures and exhibits a high tolerance to the nature and the position of the aromatic s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601019/ https://www.ncbi.nlm.nih.gov/pubmed/31181774 http://dx.doi.org/10.3390/molecules24112164 |
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author | Amin, Hawraz I. M. Raviola, Carlotta Amin, Ahmed A. Mannucci, Barbara Protti, Stefano Fagnoni, Maurizio |
author_facet | Amin, Hawraz I. M. Raviola, Carlotta Amin, Ahmed A. Mannucci, Barbara Protti, Stefano Fagnoni, Maurizio |
author_sort | Amin, Hawraz I. M. |
collection | PubMed |
description | Hydrodeaminated and monodeuterated aromatics were obtained via a visible-light driven reaction of arylazo sulfones. Deuteration occurs efficiently in deuterated media such as isopropanol-d(8) or in THF-d(8)/water mixtures and exhibits a high tolerance to the nature and the position of the aromatic substituents. |
format | Online Article Text |
id | pubmed-6601019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66010192019-07-18 Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions Amin, Hawraz I. M. Raviola, Carlotta Amin, Ahmed A. Mannucci, Barbara Protti, Stefano Fagnoni, Maurizio Molecules Article Hydrodeaminated and monodeuterated aromatics were obtained via a visible-light driven reaction of arylazo sulfones. Deuteration occurs efficiently in deuterated media such as isopropanol-d(8) or in THF-d(8)/water mixtures and exhibits a high tolerance to the nature and the position of the aromatic substituents. MDPI 2019-06-08 /pmc/articles/PMC6601019/ /pubmed/31181774 http://dx.doi.org/10.3390/molecules24112164 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Amin, Hawraz I. M. Raviola, Carlotta Amin, Ahmed A. Mannucci, Barbara Protti, Stefano Fagnoni, Maurizio Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions |
title | Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions |
title_full | Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions |
title_fullStr | Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions |
title_full_unstemmed | Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions |
title_short | Hydro/Deutero Deamination of Arylazo Sulfones under Metal- and (Photo)Catalyst-Free Conditions |
title_sort | hydro/deutero deamination of arylazo sulfones under metal- and (photo)catalyst-free conditions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6601019/ https://www.ncbi.nlm.nih.gov/pubmed/31181774 http://dx.doi.org/10.3390/molecules24112164 |
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