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dc.contributor.authorRosebraugh, Matthew
dc.contributor.authorCole, Erin
dc.contributor.authorMirafzal, Gholam A.
dc.date.accessioned2007-05-31T20:04:54Z
dc.date.available2007-05-31T20:04:54Z
dc.date.issued2007-05-31T20:04:54Z
dc.identifier.urihttp://hdl.handle.net/2092/565
dc.description.abstractOxidation 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.extent2481762 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.relation.ispartofseriesDUCURS 2006;19
dc.subjectOrganic chemistryen
dc.subjectEpoxy compoundsen
dc.subjectEpoxideen
dc.subjectOxoneen
dc.subjectDioxiraneen
dc.titleSelective epoxidation of olefines using dioxirane systemen
dc.typePresentationen


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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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