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dc.contributor.authorMajik, M.S.
dc.contributor.authorParameswaran, P.S.
dc.contributor.authorTilve, S.G.
dc.date.accessioned2009-12-18T09:04:24Z
dc.date.available2009-12-18T09:04:24Z
dc.date.issued2009
dc.identifier.citationThe Journal of Organic Chemistry, vol.74(16); 6378-6381
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/3477
dc.description.abstractThe first stereoselective route providing access to both enantiomers of tedanalactam, a naturally occurring piperidone, has been developed. The stereogenic centers were generated by the use of Sharpless asymmetric dihydroxylation. Tandem oxidation-Wittig reaction and one-pot deprotection, lactamization, and oxirane ring formation are the other key elements
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.rightsCopyright ACS [2009]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subjecttedanalactam
dc.subjectenantiomers
dc.subjectpiperidone
dc.subjectoxidation-Wittig reaction
dc.titleTotal synthesis of (-)- and (+)-tedanalactam
dc.typeJournal Article


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