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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...

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Autores principales: Großmann, Luca Marius, Beier, Vera, Duttenhofer, Lea, Lennartz, Laura, Opatz, Till
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/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.
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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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