Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4990
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dc.contributor.authorBasawaraj R
dc.contributor.authorParameshwarappa G
dc.contributor.authorSangapure S.S.
dc.date.accessioned2020-06-12T15:05:54Z-
dc.date.available2020-06-12T15:05:54Z-
dc.date.issued2007
dc.identifier.citationIndian Drugs , Vol. 44 , 1 , p. 8 - 12en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4990-
dc.description.abstract5-Chloro-3-methyl-2-benzofuran carbohydrazide (4) upon treatment with potassium isothiocynate in presence of hydrochloric acid in water gave 5-chloro-3-methylbenzofuran-2-carbo-N-thiosemicarbazide (5). The cyclisation of 5-chloro-3-methylbenzofuran-2-carbo-N-thiosemicarbazide (5) under different reaction conditions offered 1,3,4-oxadiazole, 1,3,4-thiadiazole, 1,2,4-triazole, thiazolidinone and thiopyrimidinone. The structures of these compounds were established on the basis of spectral data. Some of these compounds exhibited good antimicrobial activity.en_US
dc.publisherIndian Drug Manufacturers' Association
dc.subjectAntibacterial and antifungal activity
dc.subjectBenzofuran derivatives
dc.titleSynthesis and biological evaluation of some new benzofuran derivativesen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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