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1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review
This review article presents a survey of the utility of a new synthetic strategy for 1,3,4-thiadiazole derivatives based on reactions of nitrilimines with various functionalized sulfur dipolarophiles which proceed via tandem in situ 1,3-dipolar cycloaddition and β-elimination of simple molecule from...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Elsevier
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294724/ https://www.ncbi.nlm.nih.gov/pubmed/25685467 http://dx.doi.org/10.1016/j.jare.2013.01.004 |
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author | Shawali, Ahmad S. |
author_facet | Shawali, Ahmad S. |
author_sort | Shawali, Ahmad S. |
collection | PubMed |
description | This review article presents a survey of the utility of a new synthetic strategy for 1,3,4-thiadiazole derivatives based on reactions of nitrilimines with various functionalized sulfur dipolarophiles which proceed via tandem in situ 1,3-dipolar cycloaddition and β-elimination of simple molecule from the initially formed cycloadduct. The biological activities of some of the compounds prepared by such a strategy are pointed out. Only the literature reports within the period from 2000 to mid 2012 are covered. |
format | Online Article Text |
id | pubmed-4294724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-42947242015-02-14 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review Shawali, Ahmad S. J Adv Res Review This review article presents a survey of the utility of a new synthetic strategy for 1,3,4-thiadiazole derivatives based on reactions of nitrilimines with various functionalized sulfur dipolarophiles which proceed via tandem in situ 1,3-dipolar cycloaddition and β-elimination of simple molecule from the initially formed cycloadduct. The biological activities of some of the compounds prepared by such a strategy are pointed out. Only the literature reports within the period from 2000 to mid 2012 are covered. Elsevier 2014-01 2013-04-06 /pmc/articles/PMC4294724/ /pubmed/25685467 http://dx.doi.org/10.1016/j.jare.2013.01.004 Text en © 2014 Cairo University. Production and hosting by Elsevier B.V. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/). |
spellingShingle | Review Shawali, Ahmad S. 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review |
title | 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review |
title_full | 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review |
title_fullStr | 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review |
title_full_unstemmed | 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review |
title_short | 1,3,4-Thiadiazoles of pharmacological interest: Recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: Review |
title_sort | 1,3,4-thiadiazoles of pharmacological interest: recent trends in their synthesis via tandem 1,3-dipolar cycloaddition: review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4294724/ https://www.ncbi.nlm.nih.gov/pubmed/25685467 http://dx.doi.org/10.1016/j.jare.2013.01.004 |
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