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Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis
Chlorine gas or electropositive chlorine reagents are used to prepare chlorinated aromatic compounds, which are found in pharmaceuticals, agrochemicals, and polymers, and serve as synthetic precursors for metal‐catalyzed cross‐couplings. Nature chlorinates with chloride anions, FAD‐dependent halogen...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069574/ https://www.ncbi.nlm.nih.gov/pubmed/26991557 http://dx.doi.org/10.1002/anie.201600783 |
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author | Hering, Thea Mühldorf, Bernd Wolf, Robert König, Burkhard |
author_facet | Hering, Thea Mühldorf, Bernd Wolf, Robert König, Burkhard |
author_sort | Hering, Thea |
collection | PubMed |
description | Chlorine gas or electropositive chlorine reagents are used to prepare chlorinated aromatic compounds, which are found in pharmaceuticals, agrochemicals, and polymers, and serve as synthetic precursors for metal‐catalyzed cross‐couplings. Nature chlorinates with chloride anions, FAD‐dependent halogenases, and O(2) as the oxidant. A photocatalytic oxidative chlorination is described based on the organic dye riboflavin tetraacetate mimicking the enzymatic process. The chemical process allows within the suitable arene redox potential window a broader substrate scope compared to the specific activation in the enzymatic binding pocket. |
format | Online Article Text |
id | pubmed-5069574 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50695742016-11-01 Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis Hering, Thea Mühldorf, Bernd Wolf, Robert König, Burkhard Angew Chem Int Ed Engl Communications Chlorine gas or electropositive chlorine reagents are used to prepare chlorinated aromatic compounds, which are found in pharmaceuticals, agrochemicals, and polymers, and serve as synthetic precursors for metal‐catalyzed cross‐couplings. Nature chlorinates with chloride anions, FAD‐dependent halogenases, and O(2) as the oxidant. A photocatalytic oxidative chlorination is described based on the organic dye riboflavin tetraacetate mimicking the enzymatic process. The chemical process allows within the suitable arene redox potential window a broader substrate scope compared to the specific activation in the enzymatic binding pocket. John Wiley and Sons Inc. 2016-03-17 2016-04-18 /pmc/articles/PMC5069574/ /pubmed/26991557 http://dx.doi.org/10.1002/anie.201600783 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Communications Hering, Thea Mühldorf, Bernd Wolf, Robert König, Burkhard Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis |
title | Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis |
title_full | Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis |
title_fullStr | Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis |
title_full_unstemmed | Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis |
title_short | Halogenase‐Inspired Oxidative Chlorination Using Flavin Photocatalysis |
title_sort | halogenase‐inspired oxidative chlorination using flavin photocatalysis |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069574/ https://www.ncbi.nlm.nih.gov/pubmed/26991557 http://dx.doi.org/10.1002/anie.201600783 |
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