dc.contributor.author | Majik, M.S. | |
dc.contributor.author | Parameswaran, P.S. | |
dc.contributor.author | Tilve, S.G. | |
dc.date.accessioned | 2009-12-18T09:04:24Z | |
dc.date.available | 2009-12-18T09:04:24Z | |
dc.date.issued | 2009 | |
dc.identifier.citation | The Journal of Organic Chemistry, vol.74(16); 6378-6381 | |
dc.identifier.uri | http://drs.nio.org/drs/handle/2264/3477 | |
dc.description.abstract | The 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.iso | en | |
dc.publisher | American Chemical Society | |
dc.rights | Copyright 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.subject | tedanalactam | |
dc.subject | enantiomers | |
dc.subject | piperidone | |
dc.subject | oxidation-Wittig reaction | |
dc.title | Total synthesis of (-)- and (+)-tedanalactam | |
dc.type | Journal Article | |