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An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold
In the field of drug discovery, isoxazole is a five-membered heterocyclic moiety commonly found in many commercially available drugs. In view of their enormous significance, it is always imperative to unleash new eco-friendly synthetic strategies. Among various novel synthetic techniques in use for...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042182/ https://www.ncbi.nlm.nih.gov/pubmed/35493554 http://dx.doi.org/10.1039/d1ra04624a |
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author | Das, Soumyadip Chanda, Kaushik |
author_facet | Das, Soumyadip Chanda, Kaushik |
author_sort | Das, Soumyadip |
collection | PubMed |
description | In the field of drug discovery, isoxazole is a five-membered heterocyclic moiety commonly found in many commercially available drugs. In view of their enormous significance, it is always imperative to unleash new eco-friendly synthetic strategies. Among various novel synthetic techniques in use for isoxazole synthesis, most synthetic methods employ Cu(i) or Ru(ii) as catalysts for (3 + 2) cycloaddition reaction. The particular disadvantages associated with metal-catalyzed reactions are high costs, low abundance, toxicity, a significant generation of waste, and difficulty to separate from the reaction mixtures. In view of these drawbacks, it is always imperative to develop alternate metal-free synthetic routes. This review article highlights a comprehensive overview on the potential application of metal-free synthetic routes for the synthesis of isoxazoles with significant biological interests. |
format | Online Article Text |
id | pubmed-9042182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90421822022-04-28 An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold Das, Soumyadip Chanda, Kaushik RSC Adv Chemistry In the field of drug discovery, isoxazole is a five-membered heterocyclic moiety commonly found in many commercially available drugs. In view of their enormous significance, it is always imperative to unleash new eco-friendly synthetic strategies. Among various novel synthetic techniques in use for isoxazole synthesis, most synthetic methods employ Cu(i) or Ru(ii) as catalysts for (3 + 2) cycloaddition reaction. The particular disadvantages associated with metal-catalyzed reactions are high costs, low abundance, toxicity, a significant generation of waste, and difficulty to separate from the reaction mixtures. In view of these drawbacks, it is always imperative to develop alternate metal-free synthetic routes. This review article highlights a comprehensive overview on the potential application of metal-free synthetic routes for the synthesis of isoxazoles with significant biological interests. The Royal Society of Chemistry 2021-10-06 /pmc/articles/PMC9042182/ /pubmed/35493554 http://dx.doi.org/10.1039/d1ra04624a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Das, Soumyadip Chanda, Kaushik An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
title | An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
title_full | An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
title_fullStr | An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
title_full_unstemmed | An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
title_short | An overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
title_sort | overview of metal-free synthetic routes to isoxazoles: the privileged scaffold |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9042182/ https://www.ncbi.nlm.nih.gov/pubmed/35493554 http://dx.doi.org/10.1039/d1ra04624a |
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