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An Iodide‐Mediated Anodic Amide Coupling
The ubiquity of amide bonds, present in natural products and common pharmaceuticals renders this functional group one of the most prevalent in organic chemistry. Despite its importance and a wide variety of existing methods for its formation, the latter still can be a challenge for classical activat...
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/PMC9804404/ https://www.ncbi.nlm.nih.gov/pubmed/35835720 http://dx.doi.org/10.1002/chem.202201768 |
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author | Großmann, Luca Marius Beier, Vera Duttenhofer, Lea Lennartz, Laura Opatz, Till |
author_facet | Großmann, Luca Marius Beier, Vera Duttenhofer, Lea Lennartz, Laura Opatz, Till |
author_sort | Großmann, Luca Marius |
collection | PubMed |
description | The ubiquity of amide bonds, present in natural products and common pharmaceuticals renders this functional group one of the most prevalent in organic chemistry. Despite its importance and a wide variety of existing methods for its formation, the latter still can be a challenge for classical activating reagents such as chloridating agents or carbodiimides. As the spent reagents often cannot be recycled, the development of more sustainable methods is highly desirable. Herein, we report an operationally simple and mild indirect electrochemical protocol to effect the condensation of carboxylic acids with amines, forming a wide variety of carboxamides. |
format | Online Article Text |
id | pubmed-9804404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98044042023-01-03 An Iodide‐Mediated Anodic Amide Coupling Großmann, Luca Marius Beier, Vera Duttenhofer, Lea Lennartz, Laura Opatz, Till Chemistry Research Articles The ubiquity of amide bonds, present in natural products and common pharmaceuticals renders this functional group one of the most prevalent in organic chemistry. Despite its importance and a wide variety of existing methods for its formation, the latter still can be a challenge for classical activating reagents such as chloridating agents or carbodiimides. As the spent reagents often cannot be recycled, the development of more sustainable methods is highly desirable. Herein, we report an operationally simple and mild indirect electrochemical protocol to effect the condensation of carboxylic acids with amines, forming a wide variety of carboxamides. John Wiley and Sons Inc. 2022-08-22 2022-09-27 /pmc/articles/PMC9804404/ /pubmed/35835720 http://dx.doi.org/10.1002/chem.202201768 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://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 | Research Articles Großmann, Luca Marius Beier, Vera Duttenhofer, Lea Lennartz, Laura Opatz, Till An Iodide‐Mediated Anodic Amide Coupling |
title | An Iodide‐Mediated Anodic Amide Coupling |
title_full | An Iodide‐Mediated Anodic Amide Coupling |
title_fullStr | An Iodide‐Mediated Anodic Amide Coupling |
title_full_unstemmed | An Iodide‐Mediated Anodic Amide Coupling |
title_short | An Iodide‐Mediated Anodic Amide Coupling |
title_sort | iodide‐mediated anodic amide coupling |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804404/ https://www.ncbi.nlm.nih.gov/pubmed/35835720 http://dx.doi.org/10.1002/chem.202201768 |
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