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Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups

We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity...

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Autores principales: Röckl, Johannes L., Schollmeyer, Dieter, Franke, Robert, Waldvogel, Siegfried R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973026/
https://www.ncbi.nlm.nih.gov/pubmed/31498544
http://dx.doi.org/10.1002/anie.201910077
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author Röckl, Johannes L.
Schollmeyer, Dieter
Franke, Robert
Waldvogel, Siegfried R.
author_facet Röckl, Johannes L.
Schollmeyer, Dieter
Franke, Robert
Waldvogel, Siegfried R.
author_sort Röckl, Johannes L.
collection PubMed
description We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans.
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spelling pubmed-69730262020-01-27 Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups Röckl, Johannes L. Schollmeyer, Dieter Franke, Robert Waldvogel, Siegfried R. Angew Chem Int Ed Engl Communications We herein present a metal‐free, electrosynthetic method that enables the direct dehydrogenative coupling reactions of phenols carrying electron‐withdrawing groups for the first time. The reactions are easy to conduct and scalable, as they are carried out in undivided cells and obviate the necessity for additional supporting electrolyte. As such, this conversion is efficient, practical, and thereby environmentally friendly, as production of waste is minimized. The method features a broad substrate scope, and a variety of functional groups are tolerated, providing easy access to precursors for novel polydentate ligands and even heterocycles such as dibenzofurans. John Wiley and Sons Inc. 2019-11-19 2020-01-02 /pmc/articles/PMC6973026/ /pubmed/31498544 http://dx.doi.org/10.1002/anie.201910077 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Communications
Röckl, Johannes L.
Schollmeyer, Dieter
Franke, Robert
Waldvogel, Siegfried R.
Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
title Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
title_full Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
title_fullStr Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
title_full_unstemmed Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
title_short Dehydrogenative Anodic C−C Coupling of Phenols Bearing Electron‐Withdrawing Groups
title_sort dehydrogenative anodic c−c coupling of phenols bearing electron‐withdrawing groups
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973026/
https://www.ncbi.nlm.nih.gov/pubmed/31498544
http://dx.doi.org/10.1002/anie.201910077
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