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Direct Dehydrogenative Access to Unsymmetrical Phenones

The first non‐directed dehydrogenative phenone coupling method of methylarenes with aromatic C−H bonds, displaying a large substrate scope, is herein reported. This reaction represents a far more direct atom‐ and step‐efficient alternative to the classical Friedel–Crafts or Suzuki–Miyaura derived ac...

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Detalles Bibliográficos
Autores principales: Yu, Congjun, Huang, Raolin, Patureau, Frederic W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314079/
https://www.ncbi.nlm.nih.gov/pubmed/35128810
http://dx.doi.org/10.1002/anie.202201142
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author Yu, Congjun
Huang, Raolin
Patureau, Frederic W.
author_facet Yu, Congjun
Huang, Raolin
Patureau, Frederic W.
author_sort Yu, Congjun
collection PubMed
description The first non‐directed dehydrogenative phenone coupling method of methylarenes with aromatic C−H bonds, displaying a large substrate scope, is herein reported. This reaction represents a far more direct atom‐ and step‐efficient alternative to the classical Friedel–Crafts or Suzuki–Miyaura derived acylation reactions. The method can be carried out on a gram scale and was successfully applied to the synthesis of several Ketoprofen drug analogues.
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spelling pubmed-93140792022-07-30 Direct Dehydrogenative Access to Unsymmetrical Phenones Yu, Congjun Huang, Raolin Patureau, Frederic W. Angew Chem Int Ed Engl Communications The first non‐directed dehydrogenative phenone coupling method of methylarenes with aromatic C−H bonds, displaying a large substrate scope, is herein reported. This reaction represents a far more direct atom‐ and step‐efficient alternative to the classical Friedel–Crafts or Suzuki–Miyaura derived acylation reactions. The method can be carried out on a gram scale and was successfully applied to the synthesis of several Ketoprofen drug analogues. John Wiley and Sons Inc. 2022-03-19 2022-05-09 /pmc/articles/PMC9314079/ /pubmed/35128810 http://dx.doi.org/10.1002/anie.202201142 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Yu, Congjun
Huang, Raolin
Patureau, Frederic W.
Direct Dehydrogenative Access to Unsymmetrical Phenones
title Direct Dehydrogenative Access to Unsymmetrical Phenones
title_full Direct Dehydrogenative Access to Unsymmetrical Phenones
title_fullStr Direct Dehydrogenative Access to Unsymmetrical Phenones
title_full_unstemmed Direct Dehydrogenative Access to Unsymmetrical Phenones
title_short Direct Dehydrogenative Access to Unsymmetrical Phenones
title_sort direct dehydrogenative access to unsymmetrical phenones
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9314079/
https://www.ncbi.nlm.nih.gov/pubmed/35128810
http://dx.doi.org/10.1002/anie.202201142
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