@article { ISI:000272133800017,
	title = {Concise enantioselective synthesis of (+)-lentiginosine},
	journal = {Tetrahedron-Asymmetry},
	volume = {20},
	number = {19},
	year = {2009},
	month = {OCT},
	pages = {2287-2292},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A high yielding enantioselective synthesis of the indolizidine alkaloid, (+)-lentiginosine, has been described based on asymmetric oza-Cope rearrangement and the L-proline catalyzed alpha-aminooxylation of aldehydes. The strategy also makes use of ring-closing metathesis for the construction of piperidine core. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2009.08.027},
	author = {Shaikh, Tanveer Mahamadali and Sudalai, Arumugam}
}
