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Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway
We have successfully developed a novel cathodic cross-coupling reaction of aryl halides with arenes. Utilization of the cathodic single electron transfer (SET) mechanism for activation of aryl halides enables the cross-coupling reaction to proceed without the need for any transition metal catalysts...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155275/ https://www.ncbi.nlm.nih.gov/pubmed/28272364 http://dx.doi.org/10.3390/molecules22030413 |
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author | Qu, Yang Tateno, Hiroyuki Matsumura, Yoshimasa Kashiwagi, Tsuneo Atobe, Mahito |
author_facet | Qu, Yang Tateno, Hiroyuki Matsumura, Yoshimasa Kashiwagi, Tsuneo Atobe, Mahito |
author_sort | Qu, Yang |
collection | PubMed |
description | We have successfully developed a novel cathodic cross-coupling reaction of aryl halides with arenes. Utilization of the cathodic single electron transfer (SET) mechanism for activation of aryl halides enables the cross-coupling reaction to proceed without the need for any transition metal catalysts or single electron donors in a mild condition. The SET from a cathode to an aryl halide initiates a radical chain by giving an anion radical of the aryl halide. The following propagation cycle also consists entirely of anion radical intermediates. |
format | Online Article Text |
id | pubmed-6155275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61552752018-11-13 Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway Qu, Yang Tateno, Hiroyuki Matsumura, Yoshimasa Kashiwagi, Tsuneo Atobe, Mahito Molecules Article We have successfully developed a novel cathodic cross-coupling reaction of aryl halides with arenes. Utilization of the cathodic single electron transfer (SET) mechanism for activation of aryl halides enables the cross-coupling reaction to proceed without the need for any transition metal catalysts or single electron donors in a mild condition. The SET from a cathode to an aryl halide initiates a radical chain by giving an anion radical of the aryl halide. The following propagation cycle also consists entirely of anion radical intermediates. MDPI 2017-03-07 /pmc/articles/PMC6155275/ /pubmed/28272364 http://dx.doi.org/10.3390/molecules22030413 Text en © 2017 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 Qu, Yang Tateno, Hiroyuki Matsumura, Yoshimasa Kashiwagi, Tsuneo Atobe, Mahito Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway |
title | Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway |
title_full | Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway |
title_fullStr | Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway |
title_full_unstemmed | Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway |
title_short | Cathodic Aromatic C,C Cross-Coupling Reaction via Single Electron Transfer Pathway |
title_sort | cathodic aromatic c,c cross-coupling reaction via single electron transfer pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155275/ https://www.ncbi.nlm.nih.gov/pubmed/28272364 http://dx.doi.org/10.3390/molecules22030413 |
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