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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...

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Detalles Bibliográficos
Autores principales: Feng, Minghao, Zhang, Haoqi, Maulide, Nuno
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/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.
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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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