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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3046
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dc.contributor.authorKumar, Dalip-
dc.date.accessioned2021-10-27T04:20:36Z-
dc.date.available2021-10-27T04:20:36Z-
dc.date.issued2012-09-20-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cmdc.201200363-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3046-
dc.description.abstractA novel series of bis(indolyl)-1,3,4-oxadiazoles was prepared from the corresponding hydrazide-hydrazones via iodobenzene diacetate-promoted oxidative cyclization. Evaluation against a panel of human cancer cell lines revealed that some derivatives possess potent cytotoxicity with tunable selectivity for different cancer types.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectSynthesisen_US
dc.subjectNovel Bis-(indolyl)-1,3,4-oxadiazolesen_US
dc.subjectPotent Cytotoxic Agentsen_US
dc.titleA Facile Synthesis of Novel Bis-(indolyl)-1,3,4-oxadiazoles as Potent Cytotoxic Agentsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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