A direct, concise and stereoselective formal synthesis of platensimycin
dc.contributor.advisor | Magnus, Philip D. | en |
dc.contributor.committeeMember | Krische, Michael J. | en |
dc.contributor.committeeMember | Jones, Richard M. | en |
dc.contributor.committeeMember | Siegel, Dionicio R. | en |
dc.contributor.committeeMember | Kerwin, Sean M. | en |
dc.creator | Rivera, Heriberto | en |
dc.date.accessioned | 2012-01-27T21:25:35Z | en |
dc.date.accessioned | 2017-05-11T22:23:54Z | |
dc.date.available | 2012-01-27T21:25:35Z | en |
dc.date.available | 2017-05-11T22:23:54Z | |
dc.date.issued | 2011-12 | en |
dc.date.submitted | December 2011 | en |
dc.date.updated | 2012-01-27T21:25:48Z | en |
dc.description | text | en |
dc.description.abstract | Herein 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. | en |
dc.description.department | Chemistry | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.slug | 2152/ETD-UT-2011-12-4421 | en |
dc.identifier.uri | http://hdl.handle.net/2152/ETD-UT-2011-12-4421 | en |
dc.language.iso | eng | en |
dc.subject | Platensimycin | en |
dc.subject | Synthesis | en |
dc.subject | Antibiotic | en |
dc.title | A direct, concise and stereoselective formal synthesis of platensimycin | en |
dc.type.genre | thesis | en |