Total synthesis of demethyllavendamycin amides : an honors thesis (HONRS 499)

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dc.contributor.advisor Behforouz, Mohammad en_US Lucas, Jennifer S. en_US 2011-06-06T19:07:54Z 2011-06-06T19:07:54Z 2000 en_US 2000
dc.identifier.other A-233 en_US
dc.description.abstract This thesis involves the total synthesis of three analogs of lavendamycin, a chemotherapeutic agent: 7-N-chloroacetyldemethyllavendamycin Amide, 7-Nchloroacetyldemethyllavendamycin Amide of Pyrrolidine, and 7-Nbu ldemethyllavendamycin Amide of Piperazine. This research is part of an ongoing project involving synthesis and structure-activity relationship studies of various analogs of lavendamycin. These analogs contain the amide functional group in the C-2' position. The C-2' amides have proved to be very active anticancer agents.
dc.description.sponsorship Honors College
dc.format.extent 30 leaves : ill. ; 29 cm. en_US
dc.source Virtual Press en_US
dc.subject.lcsh Chemistry. en_US
dc.title Total synthesis of demethyllavendamycin amides : an honors thesis (HONRS 499) en_US
dc.type Undergraduate senior honors thesis Thesis (B.?)
dc.identifier.cardcat-url en_US

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  • Undergraduate Honors Theses [5928]
    Honors theses submitted to the Honors College by Ball State University undergraduate students in partial fulfillment of degree requirements.

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