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dc.contributor.advisorDeardorff, Don
dc.contributor.authorCannon, Jeffrey
dc.contributor.authorPapazian, Jason
dc.date.accessioned2020-08-13T14:55:52Z
dc.date.available2020-08-13T14:55:52Z
dc.date.issued2005-01-01 0:00
dc.identifier.urihttps://scholar.oxy.edu/handle/20.500.12711/580
dc.description.abstractStereochemistry and enantiopurity are important aspects of biologically active molecules. Our research uses synthetic methods that create and expand upon enantiopurity. Using an enzyme to produce a chiral starting material, we are able to manipulate the molecule towards a synthetic goal while preserving the stereochemistry. The enzymatically derived starting material is elaborated upon using a novel synthesis involving palladium(0) and Grubbs catalysts. Using these methods we are able to synthesize a natural product that showcases the power of our methodology and the stereoselectivity of our procedures.
dc.description.sponsorshipNorris Scholars Program and C. David West Fellowship
dc.titleEnantioselective Synthesis of a Natural Product: Coniine Jeffrey Cannon and Jason Papazian
dc.typearticle
dc.abstract.formathtml
dc.description.departmentchem
dc.source.issueurc_student
dc.source.issueurc_student
dc.identifier.legacyhttps://scholar.oxy.edu/urc_student/321
dc.source.statuspublished


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