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Challenges and Breakthroughs in Selective Amide Activation
In contrast to ketones and carboxylic esters, amides are classically seen as comparatively unreactive members of the carbonyl family, owing to their unique structural and electronic features. However, recent decades have seen the emergence of research programmes focused on the selective activation o...
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/PMC10092240/ https://www.ncbi.nlm.nih.gov/pubmed/36124856 http://dx.doi.org/10.1002/anie.202212213 |
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author | Feng, Minghao Zhang, Haoqi Maulide, Nuno |
author_facet | Feng, Minghao Zhang, Haoqi Maulide, Nuno |
author_sort | Feng, Minghao |
collection | PubMed |
description | In contrast to ketones and carboxylic esters, amides are classically seen as comparatively unreactive members of the carbonyl family, owing to their unique structural and electronic features. However, recent decades have seen the emergence of research programmes focused on the selective activation of amides under mild conditions. In the past four years, this area has continued to rapidly develop, with new advances coming in at a fast pace. Several novel activation strategies have been demonstrated as effective tools for selective amide activation, enabling transformations that are at once synthetically useful and mechanistically intriguing. This Minireview comprises recent advances in the field, highlighting new trends and breakthroughs in what could be called a new age of amide activation. |
format | Online Article Text |
id | pubmed-10092240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100922402023-04-13 Challenges and Breakthroughs in Selective Amide Activation Feng, Minghao Zhang, Haoqi Maulide, Nuno Angew Chem Int Ed Engl Minireviews In contrast to ketones and carboxylic esters, amides are classically seen as comparatively unreactive members of the carbonyl family, owing to their unique structural and electronic features. However, recent decades have seen the emergence of research programmes focused on the selective activation of amides under mild conditions. In the past four years, this area has continued to rapidly develop, with new advances coming in at a fast pace. Several novel activation strategies have been demonstrated as effective tools for selective amide activation, enabling transformations that are at once synthetically useful and mechanistically intriguing. This Minireview comprises recent advances in the field, highlighting new trends and breakthroughs in what could be called a new age of amide activation. John Wiley and Sons Inc. 2022-11-02 2022-12-05 /pmc/articles/PMC10092240/ /pubmed/36124856 http://dx.doi.org/10.1002/anie.202212213 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 | Minireviews Feng, Minghao Zhang, Haoqi Maulide, Nuno Challenges and Breakthroughs in Selective Amide Activation |
title | Challenges and Breakthroughs in Selective Amide Activation |
title_full | Challenges and Breakthroughs in Selective Amide Activation |
title_fullStr | Challenges and Breakthroughs in Selective Amide Activation |
title_full_unstemmed | Challenges and Breakthroughs in Selective Amide Activation |
title_short | Challenges and Breakthroughs in Selective Amide Activation |
title_sort | challenges and breakthroughs in selective amide activation |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10092240/ https://www.ncbi.nlm.nih.gov/pubmed/36124856 http://dx.doi.org/10.1002/anie.202212213 |
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