@article { ISI:000264650100005,
	title = {Concise enantioselective synthesis of (+)-febrifugine},
	journal = {Tetrahedron-Asymmetry},
	volume = {20},
	number = {1},
	year = {2009},
	month = {JAN},
	pages = {84-88},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short enantioselective synthesis of (+)-febrifugine, a potent antimalarial alkaloid, has been described based on the regioselective asymmetric dihydroxylation of a 1,4-dienic ester as the key step. The strategy also involves chemoselective [3,3]-sigmatropic rearrangement of 1,5-hexadiene-3-ol and intramolecular lactamization of azidolactone for the construction of piperidine core. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2008.11.024},
	author = {Emmanuvel, Lourdusamy and Kamble, Dayanand A. and Sudalai, Arumugam}
}
