Total Synthesis of (-)- and (+)-Tedanalactam

Majik, M.S.; Parameswaran, P.S.; Tilve, S.G.

dc.contributor.author	Majik, M.S.
dc.contributor.author	Parameswaran, P.S.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-03T10:12:30Z
dc.date.available	2015-06-03T10:12:30Z
dc.date.issued	2009
dc.identifier.citation	Journal of Organic Chemistry. 74(16); 2009; 6378-6381.	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/jo901143b
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2261
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.	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Chemistry	en_US
dc.title	Total Synthesis of (-)- and (+)-Tedanalactam	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y