Font Size: a A A

Total synthesis of (-)-acutumine

Posted on:2010-11-15Degree:Ph.DType:Thesis
University:Brigham Young UniversityCandidate:Li, FangFull Text:PDF
GTID:2441390002474840Subject:Chemistry
Abstract/Summary:
Acutumine is a tetracyclic alkaloid isolated from the Asian vine Menispermum dauricum with selective T-cell cytotoxicity and antiamnestic properties. We have developed a total synthetic route to this congested alkaloid, during which we also found a novel, stereoselective radical-crossover reaction that combines an intramolecular radical conjugate addition with a subsequent enolate hydroxylation. Key features of this synthesis also include a reagent-controlled diastereoselective ketone allylation, an anionic oxy-Cope rearrangement to form a congested quaternary sterocenter, a pyridine-mediated selective ozonolysis, and a Lewis acid promoted Michael-type cyclization.*;*Please refer to dissertation for diagrams.
Keywords/Search Tags:Selective
Related items