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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...

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Autores principales: Capurro, Pietro, Ricciardiello, Valentina, Lova, Paola, Lambruschini, Chiara, Protti, Stefano, Basso, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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.
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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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