Selective epoxidation of olefines using dioxirane system

dc.contributor.author	Rosebraugh, Matthew
dc.contributor.author	Cole, Erin
dc.contributor.author	Mirafzal, Gholam A.
dc.date.accessioned	2007-05-31T20:04:54Z
dc.date.available	2007-05-31T20:04:54Z
dc.date.issued	2007-05-31T20:04:54Z
dc.identifier.uri	http://hdl.handle.net/2092/565
dc.description.abstract	Oxidation of alkenes using 1,3-dichloromethyldioxirane produces good to excellent yield of epoxide products. The reaction system is facile, mild, efficient and safe. Our results involving epoxidation of various alkene substrates with different degree of ionizibilities, along with our studies involving selectivity experiments in 1:1 competitive alkenes epoxidation reactions will be presented.	en
dc.format.extent	2481762 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en_US
dc.relation.ispartofseries	DUCURS 2006;19
dc.subject	Organic chemistry	en
dc.subject	Epoxy compounds	en
dc.subject	Epoxide	en
dc.subject	Oxone	en
dc.subject	Dioxirane	en
dc.title	Selective epoxidation of olefines using dioxirane system	en
dc.type	Presentation	en

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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.