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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...

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Detalles Bibliográficos
Autores principales: Hering, Thea, Mühldorf, Bernd, Wolf, Robert, König, Burkhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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