@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:000255827100025,
	title = {Concise synthesis of protected (2S,4R)-4-hydroxyornithine},
	journal = {Tetrahedron Letters},
	volume = {49},
	number = {20},
	year = {2008},
	month = {MAY},
	pages = {3297-3299},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A short synthesis of the nonproteinogenic amino acid, (2S,4R)-4-hydroxyornithine is described. Starting from racemic benzyl glycidol, the scaffold of the target compound was constructed in high enantio- and diastereoselectivity using Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR) and regioselective opening of an epoxide as key steps. (c) 2008 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Epoxide, Grignard reaction, hydroxyornithine, Jacobsen{\textquoteright}s HKR, Natural product},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2008.03.076},
	author = {Pandey, Satyendra Kumar and Pandey, Menaka and Kumar, Pradeep}
}
