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Green methodologies for the synthesis of 2-aminothiophene

Pollution and the rising energy demand have prompted the design of new synthetic reactions that meet the principles of green chemistry. In particular, alternative synthesis of 2-aminothiophene have recently focused interest because 2-aminothiophene is a unique 5-membered S-heterocycle and a pharmaco...

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Detalles Bibliográficos
Autores principales: Duvauchelle, Valentin, Meffre, Patrick, Benfodda, Zohra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421116/
https://www.ncbi.nlm.nih.gov/pubmed/36060495
http://dx.doi.org/10.1007/s10311-022-01482-1
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author Duvauchelle, Valentin
Meffre, Patrick
Benfodda, Zohra
author_facet Duvauchelle, Valentin
Meffre, Patrick
Benfodda, Zohra
author_sort Duvauchelle, Valentin
collection PubMed
description Pollution and the rising energy demand have prompted the design of new synthetic reactions that meet the principles of green chemistry. In particular, alternative synthesis of 2-aminothiophene have recently focused interest because 2-aminothiophene is a unique 5-membered S-heterocycle and a pharmacophore providing antiprotozoal, antiproliferative, antiviral, antibacterial or antifungal properties. Here, we review new synthetic routes to 2-aminothiophenes, including multicomponent reactions, homogeneously- or heterogeneously-catalyzed reactions, with focus on green pathways.
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spelling pubmed-94211162022-08-30 Green methodologies for the synthesis of 2-aminothiophene Duvauchelle, Valentin Meffre, Patrick Benfodda, Zohra Environ Chem Lett Review Pollution and the rising energy demand have prompted the design of new synthetic reactions that meet the principles of green chemistry. In particular, alternative synthesis of 2-aminothiophene have recently focused interest because 2-aminothiophene is a unique 5-membered S-heterocycle and a pharmacophore providing antiprotozoal, antiproliferative, antiviral, antibacterial or antifungal properties. Here, we review new synthetic routes to 2-aminothiophenes, including multicomponent reactions, homogeneously- or heterogeneously-catalyzed reactions, with focus on green pathways. Springer International Publishing 2022-08-29 2023 /pmc/articles/PMC9421116/ /pubmed/36060495 http://dx.doi.org/10.1007/s10311-022-01482-1 Text en © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review
Duvauchelle, Valentin
Meffre, Patrick
Benfodda, Zohra
Green methodologies for the synthesis of 2-aminothiophene
title Green methodologies for the synthesis of 2-aminothiophene
title_full Green methodologies for the synthesis of 2-aminothiophene
title_fullStr Green methodologies for the synthesis of 2-aminothiophene
title_full_unstemmed Green methodologies for the synthesis of 2-aminothiophene
title_short Green methodologies for the synthesis of 2-aminothiophene
title_sort green methodologies for the synthesis of 2-aminothiophene
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9421116/
https://www.ncbi.nlm.nih.gov/pubmed/36060495
http://dx.doi.org/10.1007/s10311-022-01482-1
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