Selective epoxidation of olefines using dioxirane system

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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 [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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