A new entry to Phenanthridine ring systems via sequential application of Suzuki and the Modified Pictet-Spengler Reactions

Mandadapu, A K; Saifuddin, Mohammad; Agarwal, P K; Kundu, Bijoy

dc.contributor.author	Mandadapu, A K
dc.contributor.author	Saifuddin, Mohammad
dc.contributor.author	Agarwal, P K
dc.contributor.author	Kundu, Bijoy
dc.date.accessioned	2012-05-24T04:52:18Z
dc.date.available	2012-05-24T04:52:18Z
dc.date.issued	2009
dc.identifier.citation	Organic & Biomolecular Chemistry, 2009, 7, 2796-2803	en
dc.identifier.uri	http://hdl.handle.net/123456789/771
dc.description.abstract	A mild, efficient and versatile method has been developed for the two step synthesis of phenanthridine ring systems using the Suzuki and the modified Pictet-Spengler strategy. The strategy involves synthesis of a substrate in which an aryl amine is tethered to an activated arene ring at the carbon ortho to the activated carbon nucleophile so as to facilitate the formation of phenanthridine ring via -cyclization.	en
dc.format.extent	803513 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CDRI Communication No. 7748	en
dc.subject	phenanthridine	en
dc.subject	nucleophile	en
dc.title	A new entry to Phenanthridine ring systems via sequential application of Suzuki and the Modified Pictet-Spengler Reactions	en
dc.type	Article	en