Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/24971
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dc.contributor.authorMuhammad Waqas-
dc.date.accessioned2023-04-20T03:39:23Z-
dc.date.available2023-04-20T03:39:23Z-
dc.date.issued2011-
dc.identifier.urihttp://hdl.handle.net/123456789/24971-
dc.description.abstractA new series of thiazolo[3,2 -b][l,2,4]triazoles was synthesized by intramolecular dehydrative cyclization of aryl-2-(4H-l,2,4-triazol-3- ylthio )ethanones by refluxing them in phosphorus oxychloride. The ethanones were prepared from 5-substituted l,2,4-triazole-3-thiols and phenacylbromides by a nucleophilic substitution bimolecular reaction. The structures of newly synthesized thiazolo[3,2-b][l,2,4]triazoles were characterized by IR, 1" NMR and 13C NMR.en_US
dc.language.isoenen_US
dc.publisherQuaid I Azam Universityen_US
dc.subjectChemistryen_US
dc.titleSynthesis and Characterization of Some New Thiazolo[3,2 -b j [1,2,4]triazolesen_US
dc.typeThesisen_US
Appears in Collections:M.Phil

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