PhI(OAc)2-BF3-OEt2 Mediated Domino Imine Activation, Intramolecular C-C Bond Formation and β-Elimination: New Approach for the synthesis of Fluorenones, Xanthones and Phenanthridines

Sarkar, Satinath; Tadigoppula, Narender

dc.contributor.author	Sarkar, Satinath
dc.contributor.author	Tadigoppula, Narender
dc.date.accessioned	2016-06-13T10:00:04Z
dc.date.available	2016-06-13T10:00:04Z
dc.date.issued	2014
dc.identifier.citation	RSC Advances, 2014, 4, 40964–40968	en
dc.identifier.uri	http://hdl.handle.net/123456789/1640
dc.description.abstract	PhI(OAc)2-BF3-OEt2 mediated domino synthesis of biologically important fluorenones, xanthones and phenanthridines has been developed. The reaction proceeds through imine activation, intramolecular C-C bond formation and β-elimination.	en
dc.format.extent	193861 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	The CSIR-CDRI communication no 8764	en
dc.subject	Fluorenones	en
dc.subject	Xanthones	en
dc.subject	Phenanthridines	en
dc.subject	Carbon–carbon bond	en
dc.title	PhI(OAc)2-BF3-OEt2 Mediated Domino Imine Activation, Intramolecular C-C Bond Formation and β-Elimination: New Approach for the synthesis of Fluorenones, Xanthones and Phenanthridines	en
dc.type	Article	en