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Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes
The oxidation of iodoarenes is central to the field of hypervalent iodine chemistry. It was found that the metathetical redox reaction between (diacetoxyiodo)arenes and iodoarenes is possible in the presence of a catalytic amount of Lewis acid. This discovery opens a new strategy to access (diacetox...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332457/ https://www.ncbi.nlm.nih.gov/pubmed/26694343 http://dx.doi.org/10.3390/molecules201219874 |
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author | Jobin-Des Lauriers, Antoine Legault, Claude Y. |
author_facet | Jobin-Des Lauriers, Antoine Legault, Claude Y. |
author_sort | Jobin-Des Lauriers, Antoine |
collection | PubMed |
description | The oxidation of iodoarenes is central to the field of hypervalent iodine chemistry. It was found that the metathetical redox reaction between (diacetoxyiodo)arenes and iodoarenes is possible in the presence of a catalytic amount of Lewis acid. This discovery opens a new strategy to access (diacetoxyiodo)arenes. A computational study is provided to rationalize the results observed. |
format | Online Article Text |
id | pubmed-6332457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63324572019-01-24 Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes Jobin-Des Lauriers, Antoine Legault, Claude Y. Molecules Article The oxidation of iodoarenes is central to the field of hypervalent iodine chemistry. It was found that the metathetical redox reaction between (diacetoxyiodo)arenes and iodoarenes is possible in the presence of a catalytic amount of Lewis acid. This discovery opens a new strategy to access (diacetoxyiodo)arenes. A computational study is provided to rationalize the results observed. MDPI 2015-12-17 /pmc/articles/PMC6332457/ /pubmed/26694343 http://dx.doi.org/10.3390/molecules201219874 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jobin-Des Lauriers, Antoine Legault, Claude Y. Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes |
title | Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes |
title_full | Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes |
title_fullStr | Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes |
title_full_unstemmed | Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes |
title_short | Metathetical Redox Reaction of (Diacetoxyiodo)arenes and Iodoarenes |
title_sort | metathetical redox reaction of (diacetoxyiodo)arenes and iodoarenes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332457/ https://www.ncbi.nlm.nih.gov/pubmed/26694343 http://dx.doi.org/10.3390/molecules201219874 |
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