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dc.contributor.authorKudari, SM
dc.contributor.authorBadiger, SE
dc.date.accessioned2020-06-12T15:08:00Z-
dc.date.available2020-06-12T15:08:00Z-
dc.date.issued1998
dc.identifier.citationASIAN JOURNAL OF CHEMISTRY , Vol. 10 , 3 , p. 462 - 466en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5429-
dc.description.abstractSebacic acid dihydrazide on refluxing with alcoholic potassium hydroxide and carbon disulphide afforded 1,8-bis-(1,3,4-oxadiazolyl 5-thione-2-yl) octane(II). Compound (II) on reacting with ethylchloroformate and ethylchloroacetate yielded the liquid esters (III and IV). The esters thus obtained on reacting with hydrazine hydrate afforded 1,8-bis-(5-thioformic/acetic acid hydrazide 1,3,4-oxadiazol-2-yl) octanes (V and VI). The compound (II) on reacting with various aromatic amines with formaldehyde yielded 1,8-bis-(4-aryl amino methyl 1,3,4-oxadiazol-5-thione-2-yl) octanes (VII a-1). The compound (II) on further reacting with chloroacetic acid afforded 1,8-bis-(5-thioacetic acid 1,3,4-oxadiazol-2-yl) octane (VIII).en_US
dc.publisherMRS PUSHPA AGARWAL
dc.titleSynthesis of new series of 1,8-bis-(4-aryl amino methyl 1,3,4-oxadiazolyl-5-thion-2-yl) octanes, 1,8-bis-(5-thio acetic/formic acid hydrazide/acetic acid 1,3,4-oxadiazol-2-yl) octanesen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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