Total synthesis of 7-N-Acetyldemethyllavendamycin Piperazine amide : an honors thesis (HONRS 499)

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dc.contributor.advisor Behforouz, Mohammad en_US
dc.contributor.author York, Jeremy S. en_US
dc.date.accessioned 2011-06-06T19:33:02Z
dc.date.available 2011-06-06T19:33:02Z
dc.date.created 1999 en_US
dc.date.issued 1999
dc.identifier.other A-226 en_US
dc.identifier.uri http://cardinalscholar.bsu.edu/handle/handle/193236
dc.description.abstract This thesis is part of ongoing research in the structure-activity relationship studies of various lavendamycin analogs as possible chemotherapeutic agents. Lavendamycin and its analogs have proven to be active anti-tumor and anti-cancer compounds in preliminary studies. The specific work contained in this thesis focuses on the synthesis of a new analog of the lavendamycin molecule. This analog was synthesized in hopes of gaining a better understanding of the effects of structure on the activity of the compound and on the solubility of the compound. This in turn will lead to analogs of lavendamycin that have a high selective toxicity and a high level of solubility in physiological solvents.
dc.description.sponsorship Honors College
dc.format.extent 1 v. : ill. ; 29 cm. en_US
dc.source Virtual Press en_US
dc.subject.lcsh Chemistry. en_US
dc.title Total synthesis of 7-N-Acetyldemethyllavendamycin Piperazine amide : an honors thesis (HONRS 499) en_US
dc.type Undergraduate senior honors thesis.
dc.description.degree Thesis (B.?.)
dc.identifier.cardcat-url http://liblink.bsu.edu/catkey/1242384 en_US


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  • Undergraduate Honors Theses [5772]
    Honors theses submitted to the Honors College by Ball State University undergraduate students in partial fulfillment of degree requirements.

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