Facile synthesis of Dihydroquinoline-fused-Canthines via intramolecular

Hutait, Samiran; Singh, Virender; Batra, Sanjay

dc.contributor.author	Hutait, Samiran
dc.contributor.author	Singh, Virender
dc.contributor.author	Batra, Sanjay
dc.date.accessioned	2011-05-13T09:28:57Z
dc.date.available	2011-05-13T09:28:57Z
dc.date.issued	2010
dc.identifier.citation	Eur J Org Chem,2010, 6269-6276	en
dc.identifier.uri	http://hdl.handle.net/123456789/673
dc.description.abstract	The synthesis of dihydroquinoline-fused-canthines via intramolecular aza-Diels-Alder reaction between N-prenylated-1-formyl-9H--carbolines and substituted anilines in the presence of Lewis acid followed by oxidation is described. Additionally it has been found that the N-protected aldehyde in the presence of suitable catalyst (ZnBr2 or Yb (OTf)3) undergoes intramolecular carbonyl- ene reaction in diastereoselective fashion to afford syn- or anti-isomer of a new canthine derivative.	en
dc.format.extent	201717 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CDRI Communication No 7949	en
dc.subject	Canthine	en
dc.subject	Carbonyl-ene	en
dc.subject	Aza-Diels-Alder	en
dc.subject	Yb (OTf) 3	en
dc.subject	Lewis acid	en
dc.title	Facile synthesis of Dihydroquinoline-fused-Canthines via intramolecular	en
dc.type	Article	en