@article { ISI:000238111400016,
	title = {Enantioselective synthesis of (2R,3R)- and (2S,3S)-beta-hydroxyornithine},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {25},
	year = {2006},
	month = {JUN},
	pages = {4167-4169},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient and short synthesis of (2R,3R)- and (2S,3S)-beta-hydroxyornithine 1a-b is described using Sharpless asymmetric dihydroxylation and regioselective nucleophilic opening of a cyclic sulfite as the key steps. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.04.055},
	author = {Pandey, Satyendra Kumar and Kumar, Pradeep}
}
@article { ISI:000243519300018,
	title = {Efficient total synthesis of (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid},
	journal = {European Journal of Organic Chemistry},
	number = {2},
	year = {2007},
	month = {JAN},
	pages = {369-373},
	publisher = {WILEY-V C H VERLAG GMBH},
	type = {Article},
	address = {PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY},
	abstract = {<p>An efficient enantioselective synthesis of (-)-(3S,6R)-3,6-dihydroxy-10-methylundecanoic acid (1) from epichlorohydrin is described. The key steps include Jacobsen{\textquoteright}s HKR, Sharpless asymmetric dihydroxylation, regioselective opening of epoxide and cyclic sulfate. ((c) Wiley-VCH Verlag GmbH \&amp; Co. KGaA, 69451 Weinheim, Germany, 2007).</p>},
	keywords = {cyclic sulfate, Dihydroxylation, Grignard reaction, hydroboration-oxidation, Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR), regio selectivity},
	issn = {1434-193X},
	doi = {10.1002/ejoc.200600690},
	author = {Pandey, Satyendra Kumar and Kumar, Pradeep}
}
