Tandem Wittig-Ene Reaction Approach to Kainic Acid

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(9); 2009; 3591-3594.	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/jo900196t
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2260
dc.description.abstract	The first example of a tandem Wittig-intramolecular ene reaction approach and its application toward the synthesis of kainic acid is reported. The synthetic pathway involves conversion of prenyl bromide into phosphorane 3, followed by one-pot Wittig olefination and an ene reaction with glyoxalic acid to give the cis fused pyrrolidine skeleton of kainic acid.	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Chemistry	en_US
dc.title	Tandem Wittig-Ene Reaction Approach to Kainic Acid	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y