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|Author||Mahoney, Kaitlyn M.|
|Date of Issue||2010-05-10T14:50:04Z|
|Description||Advisor: Gholam A. Mirafzal||en_US|
|Description||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|
|Sponsorship||Drake University, Department of Chemistry||en_US|
|Part of Series||DUCURS 2010;16|
|Title||Oxidation of Alkenes Using Dioxirane of 1,3-Dichloroacetone||en_US|
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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.