@article { ISI:000260843700019,
	title = {Total synthesis of (+)-isolaurepan},
	journal = {Tetrahedron Letters},
	volume = {49},
	number = {49},
	year = {2008},
	month = {DEC},
	pages = {7012-7014},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A versatile and efficient method for the enantioselective synthesis of 2,7-cis-disubstituted oxepane 1c, (+)-isolaurepan, using oxidative resolution of a secondary alcohol and highly diastereoselective Et(3)SiH/TMSOTf-promoted reductive cyclization of a hydroxy ketone is described. (C) 2008 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Cis-selective cyclization, Cyclic ethers, Isolaurepan, Oxepanes, Oxidative resolution of secondary alcohols},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2008.09.134},
	author = {Tripathi, Divya and Kumar, Pradeep}
}
