Oxidation of Alkenes Using Dioxirane of 1,3-Dichloroacetone

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dc.contributor.author Mahoney, Kaitlyn M.
dc.date.accessioned 2010-05-10T14:50:04Z
dc.date.available 2010-05-10T14:50:04Z
dc.date.issued 2010-05-10T14:50:04Z
dc.identifier.uri http://hdl.handle.net/2092/1367
dc.description Advisor: Gholam A. Mirafzal en_US
dc.description.abstract Oxidation 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.sponsorship Drake University, Department of Chemistry en_US
dc.language.iso en en_US
dc.relation.ispartofseries DUCURS 2010;16
dc.subject Alkenes en_US
dc.subject Oxidation en_US
dc.title Oxidation of Alkenes Using Dioxirane of 1,3-Dichloroacetone en_US
dc.type Presentation en_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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