Studies on the Beckmann Rearrangement of 3beta-Acetoxycholest-5-En-7-One Oxime: Synthesis Of 3beta-Acetoxy-7a-AZA-B-Homocholest-5-En-7-One

dc.contributor.advisorTakemura, K. H.en_US
dc.contributor.authorHahn, Kwang J.en_US
dc.contributor.cuauthorHahn, Kwang J.en_US
dc.date.accessioned2017-02-13T22:54:56Z
dc.date.available2017-02-13T22:54:56Z
dc.date.issued1964en_US
dc.degree.disciplineChemistry (graduate program)en_US
dc.degree.grantorGraduate Schoolen_US
dc.degree.levelMS (Master of Science)en_US
dc.degree.nameM.S. in Chemistryen_US
dc.description.abstractThe synthetic modification of naturally occuring steroids has yielded an increasing number of biologically active and therapeutic agents. Modifications of known steroids (androgens, estrogens, progestogens, corticoids, and mineral corticoids) have produced compounds possessing new biological properties, and increased therapeutic value. | Among the modified steroids of interest are the nitrogen-containing azasteroids. The purpose of this investigation was to synthesize one such azasteroid, 3beta-acetoxy-7a-aza-B-homocholest-S-en-7-one via the Beckmann rearrangement of 3beta-acetoxycho-lest-5-en-7-one oxime.en_US
dc.description.noteProQuest Traditional Publishing Optionen_US
dc.identifier.urihttp://hdl.handle.net/10504/109575
dc.language.isoen_USen_US
dc.publisherCreighton Universityen_US
dc.publisher.locationOmaha, Nebraskaen_US
dc.rightsA non-exclusive distribution right is granted to Creighton University and to ProQuest following the publishing model selected above.en_US
dc.titleStudies on the Beckmann Rearrangement of 3beta-Acetoxycholest-5-En-7-One Oxime: Synthesis Of 3beta-Acetoxy-7a-AZA-B-Homocholest-5-En-7-Oneen_US
dc.typeThesis
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