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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9314079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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