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Recent Advances in Visible-Light-Mediated Amide Synthesis

Visible-light photoredox catalysis has attracted tremendous interest within the synthetic community. As such, the activation mode potentially provides a more sustainable and efficient platform for the activation of organic molecules, enabling the invention of many controlled radical-involved reactio...

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Detalles Bibliográficos
Autores principales: Lu, Bin, Xiao, Wen-Jing, Chen, Jia-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781888/
https://www.ncbi.nlm.nih.gov/pubmed/35056829
http://dx.doi.org/10.3390/molecules27020517
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author Lu, Bin
Xiao, Wen-Jing
Chen, Jia-Rong
author_facet Lu, Bin
Xiao, Wen-Jing
Chen, Jia-Rong
author_sort Lu, Bin
collection PubMed
description Visible-light photoredox catalysis has attracted tremendous interest within the synthetic community. As such, the activation mode potentially provides a more sustainable and efficient platform for the activation of organic molecules, enabling the invention of many controlled radical-involved reactions under mild conditions. In this context, amide synthesis via the strategy of photoredox catalysis has received growing interest due to the ubiquitous presence of this structural motif in numerous natural products, pharmaceuticals and functionalized materials. Employing this strategy, a wide variety of amides can be prepared effectively from halides, arenes and even alkanes under irradiation of visible light. These methods provide a robust alternative to well-established strategies for amide synthesis that involve condensation between a carboxylic acid and amine mediated by a stoichiometric activating agent. In this review, the representative progresses made on the synthesis of amides through visible light-mediated radical reactions are summarized.
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spelling pubmed-87818882022-01-22 Recent Advances in Visible-Light-Mediated Amide Synthesis Lu, Bin Xiao, Wen-Jing Chen, Jia-Rong Molecules Review Visible-light photoredox catalysis has attracted tremendous interest within the synthetic community. As such, the activation mode potentially provides a more sustainable and efficient platform for the activation of organic molecules, enabling the invention of many controlled radical-involved reactions under mild conditions. In this context, amide synthesis via the strategy of photoredox catalysis has received growing interest due to the ubiquitous presence of this structural motif in numerous natural products, pharmaceuticals and functionalized materials. Employing this strategy, a wide variety of amides can be prepared effectively from halides, arenes and even alkanes under irradiation of visible light. These methods provide a robust alternative to well-established strategies for amide synthesis that involve condensation between a carboxylic acid and amine mediated by a stoichiometric activating agent. In this review, the representative progresses made on the synthesis of amides through visible light-mediated radical reactions are summarized. MDPI 2022-01-14 /pmc/articles/PMC8781888/ /pubmed/35056829 http://dx.doi.org/10.3390/molecules27020517 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lu, Bin
Xiao, Wen-Jing
Chen, Jia-Rong
Recent Advances in Visible-Light-Mediated Amide Synthesis
title Recent Advances in Visible-Light-Mediated Amide Synthesis
title_full Recent Advances in Visible-Light-Mediated Amide Synthesis
title_fullStr Recent Advances in Visible-Light-Mediated Amide Synthesis
title_full_unstemmed Recent Advances in Visible-Light-Mediated Amide Synthesis
title_short Recent Advances in Visible-Light-Mediated Amide Synthesis
title_sort recent advances in visible-light-mediated amide synthesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781888/
https://www.ncbi.nlm.nih.gov/pubmed/35056829
http://dx.doi.org/10.3390/molecules27020517
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