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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/442

Title: Ti(III)-Mediated Radical Cyclization of β-Aminoacrylate Containing Epoxy Alcohol Moieties: Synthesis of Highly Substituted Azacycles
Authors: Chakraborty, Tushar Kanti
Samanta, Rajarshi
Roy, Saumya
Balasubramanian, Sridhar
Keywords: Piperidine
pyrrolidine
indolizidine
Ti(III)-mediated epoxide opening
radical cyclization
β-aminoacrylates
Issue Date: 2009
Citation: Tetrahedron Letters,50,3306–3310 (2009)
Series/Report no.: CDRI Communication No.7694
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.
URI: http://hdl.handle.net/123456789/442
Appears in Collections:Medicinal and Process Chemistry

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