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α-Aminoazoles/azines: key reaction partners for multicomponent reactions
Aromatic α-aminoazaheterocycles are the focus of significant investigations and exploration by researchers owing to their key role in diverse biological and physiological processes. The existence of their derivatives in numerous drugs and alkaloids is due to their heterocyclic nitrogenous nature. Th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695948/ https://www.ncbi.nlm.nih.gov/pubmed/35423648 http://dx.doi.org/10.1039/d1ra00392e |
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author | Imtiaz, Shah Ahmad war, Jahangir Banoo, Syqa khan, Sarfaraz |
author_facet | Imtiaz, Shah Ahmad war, Jahangir Banoo, Syqa khan, Sarfaraz |
author_sort | Imtiaz, Shah |
collection | PubMed |
description | Aromatic α-aminoazaheterocycles are the focus of significant investigations and exploration by researchers owing to their key role in diverse biological and physiological processes. The existence of their derivatives in numerous drugs and alkaloids is due to their heterocyclic nitrogenous nature. Therefore, the synthesis of a structurally diverse range of their derivatives through simple and convenient methods represents a vital field of synthetic organic chemistry. Multicomponent reactions (MCRs) provide a platform to introduce desirable structure diversity and complexity into a molecule in a single operation with a significant reduction in the use of harmful organic waste, and hence have attracted particular attention as an excellent tool to access these derivatives. This review covers the advances made from 2010 to the beginning of 2020 in terms of the utilization of α-aminoazaheterocycles as synthetic precursors in MCRs. |
format | Online Article Text |
id | pubmed-8695948 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86959482022-04-13 α-Aminoazoles/azines: key reaction partners for multicomponent reactions Imtiaz, Shah Ahmad war, Jahangir Banoo, Syqa khan, Sarfaraz RSC Adv Chemistry Aromatic α-aminoazaheterocycles are the focus of significant investigations and exploration by researchers owing to their key role in diverse biological and physiological processes. The existence of their derivatives in numerous drugs and alkaloids is due to their heterocyclic nitrogenous nature. Therefore, the synthesis of a structurally diverse range of their derivatives through simple and convenient methods represents a vital field of synthetic organic chemistry. Multicomponent reactions (MCRs) provide a platform to introduce desirable structure diversity and complexity into a molecule in a single operation with a significant reduction in the use of harmful organic waste, and hence have attracted particular attention as an excellent tool to access these derivatives. This review covers the advances made from 2010 to the beginning of 2020 in terms of the utilization of α-aminoazaheterocycles as synthetic precursors in MCRs. The Royal Society of Chemistry 2021-03-16 /pmc/articles/PMC8695948/ /pubmed/35423648 http://dx.doi.org/10.1039/d1ra00392e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Imtiaz, Shah Ahmad war, Jahangir Banoo, Syqa khan, Sarfaraz α-Aminoazoles/azines: key reaction partners for multicomponent reactions |
title | α-Aminoazoles/azines: key reaction partners for multicomponent reactions |
title_full | α-Aminoazoles/azines: key reaction partners for multicomponent reactions |
title_fullStr | α-Aminoazoles/azines: key reaction partners for multicomponent reactions |
title_full_unstemmed | α-Aminoazoles/azines: key reaction partners for multicomponent reactions |
title_short | α-Aminoazoles/azines: key reaction partners for multicomponent reactions |
title_sort | α-aminoazoles/azines: key reaction partners for multicomponent reactions |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695948/ https://www.ncbi.nlm.nih.gov/pubmed/35423648 http://dx.doi.org/10.1039/d1ra00392e |
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