Show simple item record

dc.contributor.authorParvatkar, P.T.
dc.contributor.authorParameswaran, P.S.
dc.contributor.authorTilve, S.G.
dc.date.accessioned2009-12-18T09:03:18Z
dc.date.available2009-12-18T09:03:18Z
dc.date.issued2009
dc.identifier.citationThe Journal of Organic Chemistry, vol.74(21); 8369-8372
dc.identifier.urihttp://drs.nio.org/drs/handle/2264/3474
dc.description.abstractA 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)
dc.language.isoen
dc.publisherAmerican Chemical Society
dc.rightsCopyright [2009]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subjectcryptotackieine
dc.subjectpolycyclic structures
dc.subjectindole-3-carboxyaldehyde
dc.subjectaryl amines
dc.titleAn expeditious I sub(2)-catalyzed entry into 6H-indolo[2,3-b]quinoline system of cryptotackieine
dc.typeJournal Article


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record