Tandem approaches for the synthesis of functionalized pyrrolidones: Efficient routes toward allokainic acid and kainic acid

Bhat, C.; Tilve, S.G.

dc.contributor.author	Bhat, C.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T03:40:31Z
dc.date.available	2015-06-04T03:40:31Z
dc.date.issued	2013
dc.identifier.citation	Tetrahedron Letters. 54(3); 2013; 245-248.	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2012.11.007
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2868
dc.description.abstract	Tandem approaches for the synthesis of pyrrolidone precursor of allokainic acid and kainic acid are described. The synthesis of pyrrolidone intermediate of allokainic acid is achieved by tandem Wittig-Michael reaction and tandem amidation-Michael reaction while one pot amidation-Ene-esterification is employed for the synthesis of Ganem intermediate (2:1) of kainic acid.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	Tandem approaches for the synthesis of functionalized pyrrolidones: Efficient routes toward allokainic acid and kainic acid	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y