dc.contributor.author | Parvatkar, P.T. | |
dc.contributor.author | Parameswaran, P.S. | |
dc.contributor.author | Tilve, S.G. | |
dc.date.accessioned | 2009-12-18T09:03:18Z | |
dc.date.available | 2009-12-18T09:03:18Z | |
dc.date.issued | 2009 | |
dc.identifier.citation | The Journal of Organic Chemistry, vol.74(21); 8369-8372 | |
dc.identifier.uri | http://drs.nio.org/drs/handle/2264/3474 | |
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) | |
dc.language.iso | en | |
dc.publisher | American Chemical Society | |
dc.rights | Copyright [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.subject | cryptotackieine | |
dc.subject | polycyclic structures | |
dc.subject | indole-3-carboxyaldehyde | |
dc.subject | aryl amines | |
dc.title | An expeditious I sub(2)-catalyzed entry into 6H-indolo[2,3-b]quinoline system of cryptotackieine | |
dc.type | Journal Article | |