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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp012z10ws57q
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dc.contributor.advisorSorensen, Erik J.-
dc.contributor.authorWilson, Jessica Laura-
dc.date.accessioned2015-07-27T18:40:30Z-
dc.date.available2015-07-27T18:40:30Z-
dc.date.created2015-04-20-
dc.date.issued2015-07-27-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp012z10ws57q-
dc.description.abstractPisiferol is an abietane diterpene with antitumor, antifungal and antibiotic activities. It features a complex tricyclic core structure with a trans-ring junction and an axial methanolic group. I discuss different approaches to render the synthesis asymmetric within the context of previous work done by the Sorensen laboratory. Because the key steps in the synthesis pathway have already been validated using racemic material, if successful, these efforts would render the asymmetric total synthesis of pisiferol complete.en_US
dc.format.extent101 pagesen_US
dc.language.isoen_USen_US
dc.titleProgress Towards the Total Synthesis of Pisiferolen_US
dc.typePrinceton University Senior Theses-
pu.date.classyear2015en_US
pu.departmentChemistryen_US
pu.pdf.coverpageSeniorThesisCoverPage-
Appears in Collections:Chemistry, 1926-2023

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