Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2950
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dc.contributor.authorGreeshma, G-
dc.contributor.authorDhanya, B P-
dc.contributor.authorSaranya, J-
dc.contributor.authorReshmitha, T R-
dc.contributor.authorBaiju, T V-
dc.contributor.authorMeenu, M T-
dc.contributor.authorMangalam S Nair-
dc.contributor.authorNisha, P-
dc.contributor.authorRadhakrishnan, K V-
dc.date.accessioned2017-10-23T11:51:51Z-
dc.date.available2017-10-23T11:51:51Z-
dc.date.issued2017-06-08-
dc.identifier.citationEuropean Journal of Organic Chemistry, (21):3072-3077en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2950-
dc.description.abstractHerein, we describe a metal-free, iodosobenzene diacetate mediated trans-aziridination of zerumbone by the direct use of sulfonamides. Preliminary in vitro screening showed that the synthesized compounds had better antiproliferative and antidiabetic activities than the parent compound zerumbone.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectZerumboneen_US
dc.subjectHypervalent compoundsen_US
dc.subjectNitrogen heterocyclesen_US
dc.subjectSmall ring systemsen_US
dc.subjectSulfonamidesen_US
dc.titleMetal-Free Trans-Aziridination of Zerumbone: Synthesis and Biological Evaluation of Aziridine Derivatives of Zerumboneen_US
dc.typeArticleen_US
Appears in Collections:2017



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