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Allylic Oxidation of Steroidal Compounds Using Vanadyl Acetylacetonate and Tert-butyl Hydroperoxide


Metadata FieldValueLanguage
dc.contributor.advisorParish, Edwarden_US
dc.contributor.authorGrainger, Wendellen_US
dc.date.accessioned2015-07-29T14:17:56Z
dc.date.available2015-07-29T14:17:56Z
dc.date.issued2015-07-29
dc.identifier.urihttp://hdl.handle.net/10415/4800
dc.description.abstractAllylic oxidation is an important reaction in steroid chemistry. Previously reported methods have various limits which do not apply when using vanadyl acetylacetonate and tert-butyl hydroperoxide. These limits include costs, need for inert environments, short half-lives of catalysts, over-oxidation, need for protection groups, and low yields. Vanadyl acetylacetonate is inexpensive and shelf stable. Here, we describe the novel use of vanadyl acetylacetonate for oxidation of a variety of ∆5 steroidal olefins, without protection groups, in ambient atmosphere and at room temperature.en_US
dc.rightsEMBARGO_GLOBALen_US
dc.subjectChemistry and Biochemistryen_US
dc.titleAllylic Oxidation of Steroidal Compounds Using Vanadyl Acetylacetonate and Tert-butyl Hydroperoxideen_US
dc.typeDissertationen_US
dc.embargo.lengthMONTHS_WITHHELD:6en_US
dc.embargo.statusEMBARGOEDen_US
dc.embargo.enddate2016-01-01en_US

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