Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4881
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dc.contributor.authorBasavaraja, KM
dc.contributor.authorAgasimundin, YS
dc.date.accessioned2020-06-12T15:05:30Z-
dc.date.available2020-06-12T15:05:30Z-
dc.date.issued2008
dc.identifier.citationINDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY , Vol. 17 , 3 , p. 279 - 280en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4881-
dc.description.abstractThe treatment of 3-methoxy-2-(4'-aryl-3-mercapto-1',2,4'-triazol-5'-yl) benzofurans (1) with thionyl chloride produced the respective bis [2-(4'-aryl-1',2,4'-triazol-5'-yl)-3-methoxybenzofuran] sulphides (2a-c). 1 with ethanolic bromine at room temp gave bis[2-(4'-aryi-1',21,4'-triazol-5'-yl) -3-methoxybenzofuran] disulphides (3a-c). The structural assignment of these sulphides and disulphides was based on earlier observations and analytical and spectral data. The compounds synthesized were found to exhibit appreciable antibacterial activity.en_US
dc.publisherDR R S VARMA
dc.titleSynthesis of bis[2(4 '-aryl-1 ',2 ',4 '-triazol-5 '-yl)]-3-methoxybenzo-furansulfides and disulfides of biological interesten_US
dc.typeArticle
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