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Studies on The Synthesis of B-Ring 6-Azasteroids


Metadata FieldValueLanguage
dc.contributor.advisorParish, Edward
dc.contributor.advisorDuin, Evert C.en_US
dc.contributor.advisorNeely, William C.en_US
dc.contributor.authorGandikota, Jyothien_US
dc.date.accessioned2008-09-09T21:16:42Z
dc.date.available2008-09-09T21:16:42Z
dc.date.issued2006-08-15en_US
dc.identifier.urihttp://hdl.handle.net/10415/340
dc.description.abstractAzasteroids, which carry a nitrogen in the C-6 position of the steroid nucleus are still mysterious and very few synthesized, were found to possess antimicrobial and antifungal properties apart from their pharmacodynamic actions. The literature reports for synthesizing these compounds is also very limited. We developed different approaches and modified, streamlined procedures for the synthesis of these compounds. The target molecules had different side chains (R= H, Me, Et) at the 6th position and were synthesized using ozone and other oxidizing agents. The oxidative cleavage of the B-ring was the key step to insert a nitrogen atom.en_US
dc.language.isoen_USen_US
dc.subjectChemistry and Biochemistryen_US
dc.titleStudies on The Synthesis of B-Ring 6-Azasteroidsen_US
dc.typeThesisen_US
dc.embargo.lengthNO_RESTRICTIONen_US
dc.embargo.statusNOT_EMBARGOEDen_US

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