An expeditious I-2-Catalyzed entry into 6H-Indolo[2,3-b]quinoline system of 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	2015-06-03T10:12:31Z
dc.date.available	2015-06-03T10:12:31Z
dc.date.issued	2009
dc.identifier.citation	Journal of Organic Chemistry. 74(21); 2009; 8369-8372.	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/jo901361x
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2268
dc.description.abstract	A synthesis of a series of novel 6H-indolo[2,3-b]-quinolines with different substituents on the quinoline ring is described. The method involves reaction of indole-3-carboxyaldehyde with aryl amines in the presence of a catalytic amount of iodine in refluxing diphenyl ether to yield indolo[2,3-b]quinolines in one-pot. The present approach provides a new route for the synthesis of polycyclic structures related to an alkaloid cryptotackieine (neocryptolepine).	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Chemistry	en_US
dc.title	An expeditious I-2-Catalyzed entry into 6H-Indolo[2,3-b]quinoline system of Cryptotackieine	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y