@article { ISI:000307433600011,
	title = {Formal synthesis of tetrahydrolipstatin and tetrahydroesterastin},
	journal = {Tetrahedron-Asymmetry},
	volume = {23},
	number = {11-12},
	year = {2012},
	month = {JUN},
	pages = {884-890},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A versatile and efficient approach to (3.5,5R)-methyl 3-(benzyloxy)-5-(methoxymethoxy)hexadecanoate, a key chiral building block and a common polyol fragment of the anti-tumor and anti-obesity agents tetrahydrolipstatin 3 and tetrahydroesterastin 4 using both hydrolytic kinetic resolution (HKR) and proline catalyzed sequential alpha-aminoxylation, followed by HWE-olefination reaction is described. (c) 2012 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2012.05.025},
	author = {Tripathi, Divya and Kumar, Pradeep}
}
