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dc.contributor.advisorMagnus, Philip D.
dc.creatorRivera, Heriberto
dc.date.accessioned2012-01-27T21:25:35Z
dc.date.available2012-01-27T21:25:35Z
dc.date.created2011-12
dc.date.issued2012-01-27
dc.date.submittedDecember 2011
dc.identifier.urihttp://hdl.handle.net/2152/ETD-UT-2011-12-4421
dc.descriptiontext
dc.description.abstractHerein we describe the synthesis of (±) platensimycin, a potent antibiotic against gram-positive bacteria. The first chapter reviews (±) platensimycin’s isolation, biological profile and previously reported studies relevant to the area. The second chapter describes our initial efforts to synthesize (±) platensimycin. The third chapter accounts our second generation synthesis and its completion. The fourth chapter entails the experimental details of the important compounds in our synthesis.
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.subjectPlatensimycin
dc.subjectSynthesis
dc.subjectAntibiotic
dc.titleA direct, concise and stereoselective formal synthesis of platensimycin
dc.date.updated2012-01-27T21:25:48Z
dc.identifier.slug2152/ETD-UT-2011-12-4421
dc.description.departmentChemistry
dc.type.genrethesis*
thesis.degree.departmentChemistry
thesis.degree.disciplineChemistry
thesis.degree.grantorUniversity of Texas at Austin
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy


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