@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}
}
@article { ISI:000333089400003,
	title = {Co(III)(salen)-catalyzed phenolic kinetic resolution of two stereocentered benzyloxy and azido epoxides: its application in the synthesis of ICI-118,551, an anti-hypertensive agent},
	journal = {Organic \& Biomolecular Chemistry},
	volume = {12},
	number = {15},
	year = {2014},
	month = {FEB},
	pages = {2349-2355},
	publisher = {ROYAL SOC CHEMISTRY},
	type = {Article},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>The salen Co(III)-catalyzed phenolic kinetic resolution of racemic anti- or syn-azido and benzyloxy epoxides provides a practical route to a range of enantioenriched anti-or syn-1-aryloxy-3-azido or benzyloxy-2-alcohols in excellent yields and ees. The synthetic potential of this protocol is illustrated with an enantioselective synthesis of ICI-118,551, a beta-blocker, in a highly optically pure form (99\% ee).</p>},
	issn = {1477-0520},
	doi = {10.1039/c3ob42501k},
	author = {Karabal, Pratibha U. and Kamble, Dayanand A. and Sudalai, Arumugam}
}
