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dc.contributor.authorPatil S.G
dc.contributor.authorGirisha M
dc.contributor.authorBadiger J
dc.contributor.authorKudari S.M
dc.contributor.authorPurohit M.G.
dc.date.accessioned2020-06-12T15:05:54Z-
dc.date.available2020-06-12T15:05:54Z-
dc.date.issued2007
dc.identifier.citationIndian Journal of Heterocyclic Chemistry , Vol. 17 , 1 , p. 37 - 40en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4988-
dc.description.abstractCyclization of sebacic acid dihydrazide (1) with substituted carboxylic acids (2a-e) using phosphorus oxychloride as cyclizing agent yielded 1,8-bis (5-aryl substituted-1,3,4-oxadiazol-2-yl) octanes (3a-e). These were then reacted with hydrazine hydrate/phenyl hydrazine in ethanol to yield 1,8-bis (5-aryl substituted-4-amino-1,2,4-triazol-3-yl) octanes (4a-e) and 1,8-bis (5-aryl substituted-4-anilino-1,2,4-triazol-3-yl) octanes (5a-e) respectively. The structures of the newly synthesized compounds were confirmed by IR, 1H NMR, MS and analytical data. These compounds were screened for anticonvulsant and antimicrobial activity.en_US
dc.titleSynthesis and anticonvulsant, antimicrobial activity of some bis-1,3,4-oxadiazole and bis-1,2,4-triazole derivatives from sebacic aciden_US
dc.typeArticle
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