Oxidation of Alkenes Using Dioxirane of 1,3-Dichloroacetone

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 [190]
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.