@article { ISI:000278198200009,
	title = {Short enantioselective synthesis of guggultetrol, a naturally occurring lipid},
	journal = {Tetrahedron-Asymmetry},
	volume = {21},
	number = {5},
	year = {2010},
	month = {MAR},
	pages = {558-561},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An enantioselective synthesis of the naturally occurring lipid, guggultetrol, is described with an overall yield of 24\% starting from commercially available 1-pentadecanol in ten linear steps. The key chiral-inducing steps include a Sharpless asymmetric epoxidation of allylic alcohol and a dihydroxylation of an alpha,beta-unsaturated ester. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2010.02.019},
	author = {George, Shyla and Suryavanshi, Gurunath and Sudalai, Arumugam}
}
