@article { ISI:000251507000029,
	title = {Concise synthesis of (-)-deoxoprosopinine},
	journal = {Synlett},
	number = {18},
	year = {2007},
	month = {NOV},
	pages = {2894-2896},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A simple and highly efficient approach to (-)-deoxoprosopinine from racemic epoxide as a starting material is described employing a Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR) and Sharpless asymmetric dihydroxylation (AD) as key steps.</p>},
	keywords = {hydroboration-oxidation, Jacobsen{\textquoteright}s HKR, Piperidine alkaloids, sharpless AD, Total synthesis},
	issn = {0936-5214},
	doi = {10.1055/s-2007-991056},
	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}
}
