@article { ISI:000274985000008,
	title = {Convenient synthesis of enantiomerically pure (R)-mexiletine using hydrolytic kinetic resolution method},
	journal = {Tetrahedron-Asymmetry},
	volume = {20},
	number = {24},
	year = {2009},
	month = {DEC},
	pages = {2814-2817},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Enantiopure (R)-mexiletine was prepared in a simple and practical way using hydrolytic kinetic resolution method of terminal epoxide by Jacobsen catalyst. High enantiomeric purity (98\% ee) was achieved and the method is well amenable to industrial scale-up. (C) 2009 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2009.11.014},
	author = {Sasikumar, Murugesan and Nikalje, Milind D. and Muthukrishnan, Murugan}
}
@article { ISI:000286862600011,
	title = {Facile enantioselective synthesis of enantiomerically pure (R)-phenoxybenzamine hydrochloride using the hydrolytic kinetic resolution method},
	journal = {Tetrahedron-Asymmetry},
	volume = {21},
	number = {23},
	year = {2010},
	month = {DEC},
	pages = {2825-2829},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A practical and highly efficient enantioselective synthesis of (R)-phenoxybenzamine hydrochloride has been described for the first time using Jacobsen{\textquoteright}s hydrolytic kinetic resolution of a terminal epoxide as a key step and source of chirality. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2010.11.011},
	author = {Nikalje, Milind D. and Sasikumar, Murugesan and Muthukrishnan, Murugan}
}
