@article { ISI:000295564100011,
	title = {Formal synthesis of valiolamine from myo-inositol},
	journal = {Tetrahedron},
	volume = {67},
	number = {41},
	year = {2011},
	month = {OCT},
	pages = {7963-7970},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient formal synthesis of racemic valiolamine starting from readily available myo-inositol is reported. In all the synthetic steps only one regioisomer is formed, which circumvents laborious purification of products. Regioselective benzylation of myo-inositol orthoformate, super-hydride mediated deoxygenation of a cyclitol derivative and stereoselective addition of dichloromethyllithium to an inosose are the key reactions in the synthesis. (C) 2011 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Amino sugar, Carbohydrate, Cyclitol, Inositol, Natural product, Valiolamine},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2011.08.027},
	author = {Jagdhane, Rajendra C. and Shashidhar, Mysore S.}
}
