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Visible-Light-Driven Solventylation Strategy for Olefin Functionalization
[Image: see text] Amphiphilic aryl radicals generated upon visible light irradiation of arylazo sulfones have been exploited in the development of a solventylation strategy via hydrogen atom transfer (HAT). The present protocol succeeded in the versatile functionalization of various olefins with car...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798500/ https://www.ncbi.nlm.nih.gov/pubmed/36591128 http://dx.doi.org/10.1021/acsomega.2c07172 |
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author | Capurro, Pietro Ricciardiello, Valentina Lova, Paola Lambruschini, Chiara Protti, Stefano Basso, Andrea |
author_facet | Capurro, Pietro Ricciardiello, Valentina Lova, Paola Lambruschini, Chiara Protti, Stefano Basso, Andrea |
author_sort | Capurro, Pietro |
collection | PubMed |
description | [Image: see text] Amphiphilic aryl radicals generated upon visible light irradiation of arylazo sulfones have been exploited in the development of a solventylation strategy via hydrogen atom transfer (HAT). The present protocol succeeded in the versatile functionalization of various olefins with carbon-centered radicals deriving from acetone, acetonitrile, chloroform, methylene chloride, nitromethane, methyl acetate, and methyl formate under metal- and photocatalyst-free conditions. The direct addition of the aryl radicals onto the olefin substrates was suppressed under high dilution conditions. |
format | Online Article Text |
id | pubmed-9798500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97985002022-12-30 Visible-Light-Driven Solventylation Strategy for Olefin Functionalization Capurro, Pietro Ricciardiello, Valentina Lova, Paola Lambruschini, Chiara Protti, Stefano Basso, Andrea ACS Omega [Image: see text] Amphiphilic aryl radicals generated upon visible light irradiation of arylazo sulfones have been exploited in the development of a solventylation strategy via hydrogen atom transfer (HAT). The present protocol succeeded in the versatile functionalization of various olefins with carbon-centered radicals deriving from acetone, acetonitrile, chloroform, methylene chloride, nitromethane, methyl acetate, and methyl formate under metal- and photocatalyst-free conditions. The direct addition of the aryl radicals onto the olefin substrates was suppressed under high dilution conditions. American Chemical Society 2022-12-15 /pmc/articles/PMC9798500/ /pubmed/36591128 http://dx.doi.org/10.1021/acsomega.2c07172 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 | Capurro, Pietro Ricciardiello, Valentina Lova, Paola Lambruschini, Chiara Protti, Stefano Basso, Andrea Visible-Light-Driven Solventylation Strategy for Olefin Functionalization |
title | Visible-Light-Driven
Solventylation Strategy for Olefin
Functionalization |
title_full | Visible-Light-Driven
Solventylation Strategy for Olefin
Functionalization |
title_fullStr | Visible-Light-Driven
Solventylation Strategy for Olefin
Functionalization |
title_full_unstemmed | Visible-Light-Driven
Solventylation Strategy for Olefin
Functionalization |
title_short | Visible-Light-Driven
Solventylation Strategy for Olefin
Functionalization |
title_sort | visible-light-driven
solventylation strategy for olefin
functionalization |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798500/ https://www.ncbi.nlm.nih.gov/pubmed/36591128 http://dx.doi.org/10.1021/acsomega.2c07172 |
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