Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5214
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dc.contributor.authorSangapure S.S
dc.contributor.authorBasawaraj R.
dc.date.accessioned2020-06-12T15:06:32Z-
dc.date.available2020-06-12T15:06:32Z-
dc.date.issued2004
dc.identifier.citationIndian Journal of Pharmaceutical Sciences , Vol. 66 , 2 , p. 221 - 225en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/5214-
dc.description.abstractThe condensation of 5-chloro-3-methyl-2-benzofuran carbohydrazide (4) with phenylisothiocynate gave 5-chloro-3-methylbenzofuran-2-carbo-N- phenylthiosemicarbazide (5). The cyclisation of 5 under different reaction conditions furnished 1,3,4-oxadiazole, 1,3,4-thiadiazole, 1,2,4-triazole, thiadiazolidinone and thiopyrimidone. Their chemical structures have been assigned by IR, 1HNMR, Mass and elemental analyses. All the compounds synthesized were evaluated for antibacterial and antifungal activity.en_US
dc.titleSynthesis and biological activities of some 1,3,4-oxadiazoles, thiadiazoles, triazoles and related compounds possessing benzofuran moietyen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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