Double reductive cyclization: A facile synthesis of the indoloquinoline alkaloid cryptotackieine

Parvatkar, P.T.; Parameswaran, P.S.; Tilve, S.G.

dc.contributor.author	Parvatkar, P.T.
dc.contributor.author	Parameswaran, P.S.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-03T09:34:35Z
dc.date.available	2015-06-03T09:34:35Z
dc.date.issued	2007
dc.identifier.citation	Tetrahedron Letters. 48(44); 2007; 7870-7872.	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2007.08.126
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/1978
dc.description.abstract	A new synthesis of the indoloquinoline alkaloid cryptotackieine, isolated from Cryptolepis sanguinolenta, is described which involves a Perkin reaction, a tandem double reduction-double cyclization reaction followed by regioselective methylation at the quinoline nitrogen.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	Double reductive cyclization: A facile synthesis of the indoloquinoline alkaloid cryptotackieine	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y