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Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals

Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and functional materials. The method for reduction of aryl halides with ubiquitous distribution is highly sought after for late-stage construction of various aromatic compounds. The visible-light-driven re...

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Autores principales: Lan, Jihong, Chen, Rongxiang, Duo, Fangfang, Hu, Menghui, Lu, Xiaoyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458128/
https://www.ncbi.nlm.nih.gov/pubmed/36080129
http://dx.doi.org/10.3390/molecules27175364
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author Lan, Jihong
Chen, Rongxiang
Duo, Fangfang
Hu, Menghui
Lu, Xiaoyan
author_facet Lan, Jihong
Chen, Rongxiang
Duo, Fangfang
Hu, Menghui
Lu, Xiaoyan
author_sort Lan, Jihong
collection PubMed
description Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and functional materials. The method for reduction of aryl halides with ubiquitous distribution is highly sought after for late-stage construction of various aromatic compounds. The visible-light-driven reduction of aryl halides to aryl radicals by electron transfer provides an efficient, simple, and environmentally friendly method for the construction of aromatic compounds. This review summarizes the recent progress in the generation of aryl radicals by visible-light-driven reduction of aryl halides with metal complexes, organic compounds, semiconductors as catalysts, and alkali-assisted reaction system. The ability and mechanism of reduction of aromatic halides in various visible light induced systems are summarized, intending to illustrate a comprehensive introduction of this research topic to the readers.
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spelling pubmed-94581282022-09-09 Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals Lan, Jihong Chen, Rongxiang Duo, Fangfang Hu, Menghui Lu, Xiaoyan Molecules Review Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and functional materials. The method for reduction of aryl halides with ubiquitous distribution is highly sought after for late-stage construction of various aromatic compounds. The visible-light-driven reduction of aryl halides to aryl radicals by electron transfer provides an efficient, simple, and environmentally friendly method for the construction of aromatic compounds. This review summarizes the recent progress in the generation of aryl radicals by visible-light-driven reduction of aryl halides with metal complexes, organic compounds, semiconductors as catalysts, and alkali-assisted reaction system. The ability and mechanism of reduction of aromatic halides in various visible light induced systems are summarized, intending to illustrate a comprehensive introduction of this research topic to the readers. MDPI 2022-08-23 /pmc/articles/PMC9458128/ /pubmed/36080129 http://dx.doi.org/10.3390/molecules27175364 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lan, Jihong
Chen, Rongxiang
Duo, Fangfang
Hu, Menghui
Lu, Xiaoyan
Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals
title Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals
title_full Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals
title_fullStr Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals
title_full_unstemmed Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals
title_short Visible-Light Photocatalytic Reduction of Aryl Halides as a Source of Aryl Radicals
title_sort visible-light photocatalytic reduction of aryl halides as a source of aryl radicals
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458128/
https://www.ncbi.nlm.nih.gov/pubmed/36080129
http://dx.doi.org/10.3390/molecules27175364
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