Ti(III)-Mediated Radical Cyclization of β-Aminoacrylate Containing Epoxy Alcohol Moieties: Synthesis of Highly Substituted Azacycles

Chakraborty, Tushar Kanti; Samanta, Rajarshi; Roy, Saumya; Balasubramanian, Sridhar

dc.contributor.author	Chakraborty, Tushar Kanti
dc.contributor.author	Samanta, Rajarshi
dc.contributor.author	Roy, Saumya
dc.contributor.author	Balasubramanian, Sridhar
dc.date.accessioned	2009-05-20T15:00:11Z
dc.date.available	2009-05-20T15:00:11Z
dc.date.issued	2009
dc.identifier.citation	Tetrahedron Letters,50,3306–3310 (2009)	en
dc.identifier.uri	http://hdl.handle.net/123456789/442
dc.description.abstract	Ti(III)-mediated radical cyclization of β-aminoacrylate containing 2,3-epoxy alcohol moieties led to the formation of highly substituted piperidine and pyrrolidine rings. The pyrrolidine ring system was then transformed into an indolizidine framework present in many natural products.	en
dc.format.extent	273805 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.relation.ispartofseries	CDRI Communication No.7694	en
dc.subject	Piperidine	en
dc.subject	pyrrolidine	en
dc.subject	indolizidine	en
dc.subject	Ti(III)-mediated epoxide opening	en
dc.subject	radical cyclization	en
dc.subject	β-aminoacrylates	en
dc.title	Ti(III)-Mediated Radical Cyclization of β-Aminoacrylate Containing Epoxy Alcohol Moieties: Synthesis of Highly Substituted Azacycles	en
dc.type	Article	en