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Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity

Starting from N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides, a series of new functionalized 1,3,4-thiadiazoles were prepared. The structures of the compounds prepared were confirmed by both elemental and spectral analyses as well as by alternate synthesis. The mechanisms of the studied reacti...

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Autores principales: Abdelhamid, Abdou O., Gomha, Sobhi M., Shawali, Ahmad S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642155/
https://www.ncbi.nlm.nih.gov/pubmed/26644926
http://dx.doi.org/10.1016/j.jare.2014.08.007
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author Abdelhamid, Abdou O.
Gomha, Sobhi M.
Shawali, Ahmad S.
author_facet Abdelhamid, Abdou O.
Gomha, Sobhi M.
Shawali, Ahmad S.
author_sort Abdelhamid, Abdou O.
collection PubMed
description Starting from N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides, a series of new functionalized 1,3,4-thiadiazoles were prepared. The structures of the compounds prepared were confirmed by both elemental and spectral analyses as well as by alternate synthesis. The mechanisms of the studied reactions are outlined. The antimicrobial activities of the compounds prepared were screened and the results showed that most of such compounds exhibit considerable activities.
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spelling pubmed-46421552015-12-07 Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity Abdelhamid, Abdou O. Gomha, Sobhi M. Shawali, Ahmad S. J Adv Res Original Article Starting from N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides, a series of new functionalized 1,3,4-thiadiazoles were prepared. The structures of the compounds prepared were confirmed by both elemental and spectral analyses as well as by alternate synthesis. The mechanisms of the studied reactions are outlined. The antimicrobial activities of the compounds prepared were screened and the results showed that most of such compounds exhibit considerable activities. Elsevier 2015-11 2014-08-23 /pmc/articles/PMC4642155/ /pubmed/26644926 http://dx.doi.org/10.1016/j.jare.2014.08.007 Text en © 2014 Production and hosting by Elsevier B.V. on behalf of Cairo University. 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 Original Article
Abdelhamid, Abdou O.
Gomha, Sobhi M.
Shawali, Ahmad S.
Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
title Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
title_full Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
title_fullStr Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
title_full_unstemmed Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
title_short Utility of N-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
title_sort utility of n-aryl 2-aroylhydrazono-propanehydrazonoyl chlorides as precursors for synthesis of new functionalized 1,3,4-thiadiazoles with potential antimicrobial activity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642155/
https://www.ncbi.nlm.nih.gov/pubmed/26644926
http://dx.doi.org/10.1016/j.jare.2014.08.007
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