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dc.contributor.authorMahoney, Kaitlyn M.
dc.date.accessioned2010-05-10T14:50:04Z
dc.date.available2010-05-10T14:50:04Z
dc.date.issued2010-05-10T14:50:04Z
dc.identifier.urihttp://hdl.handle.net/2092/1367
dc.descriptionAdvisor: Gholam A. Mirafzalen_US
dc.description.abstractOxidation of alkenes using dioxirane system generated from 1,3-dichloroacetone and oxone produces good to excellent yields of epoxide products. The reaction system is facile, mild, efficient and safe. Our experimental results of 1:1 competitive epoxidation reactions involving styrene substrate and its derivatives will be presented to demonstrate sensitivity of the dioxirane epoxidation system to the polarity & ionizability of the pi bonds in the substrates.en_US
dc.description.sponsorshipDrake University, Department of Chemistryen_US
dc.language.isoenen_US
dc.relation.ispartofseriesDUCURS 2010;16
dc.subjectAlkenesen_US
dc.subjectOxidationen_US
dc.titleOxidation of Alkenes Using Dioxirane of 1,3-Dichloroacetoneen_US
dc.typePresentationen_US


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  • DUCURS [196]
    Poster sessions and presentation from the Drake University Conference on Undergraduate Research in the Sciences held each April at Olmsted Center on the Drake campus.

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