Tandem C-2 Functionalization-Intramolecular Azide-Alkyne 1,3-dipolar Cycloaddition Reaction: A Convenient Route to Highly Diversified 9H-benzo[b]pyrrolo [1,2-g][1,2,3]triazolo[1,5-d][1,4] diazepines

Hussain, M K; Ansari, M I; Kant, Ruchir; Hajela, Kanchan

dc.contributor.author	Hussain, M K
dc.contributor.author	Ansari, M I
dc.contributor.author	Kant, Ruchir
dc.contributor.author	Hajela, Kanchan
dc.date.accessioned	2014-08-01T10:16:33Z
dc.date.available	2014-08-01T10:16:33Z
dc.date.issued	2014
dc.identifier.citation	Organic Letters, 2014, 16 (2), 560–563	en
dc.identifier.uri	http://hdl.handle.net/123456789/1333
dc.description.abstract	An eﬃcient diversity oriented synthetic approach to annulated 9H-benzo[b]pyrrolo[1,2-g][1,2,3]triazolo[1,5-d][1,4] diazepines has been developed using a Sc(OTf)3 catalyzed two component tandem C-2 functionalization-intramolecular azide-alkyne 1,3-dipolar cycloaddition reaction. The reaction shows high substrate tolerance and provides a library of fused heterocycles that may lead to novel biologically active compounds or drug lead molecules.	en
dc.format.extent	211950 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CSIR –CDRI Communication No. 8584	en
dc.subject	Tandem C-2 Functionalization	en
dc.subject	Cycloaddition Reaction	en
dc.subject	Convenient Route	en
dc.subject	Highly Diversified	en
dc.subject	Diazepines	en
dc.title	Tandem C-2 Functionalization-Intramolecular Azide-Alkyne 1,3-dipolar Cycloaddition Reaction: A Convenient Route to Highly Diversified 9H-benzo[b]pyrrolo [1,2-g][1,2,3]triazolo[1,5-d][1,4] diazepines	en
dc.type	Article	en