@article { ISI:000354982900007,
	title = {Concise enantioselective synthesis of naturally active (S)-3-hydroxypiperidine},
	journal = {Synthetic Communications},
	volume = {45},
	number = {13},
	year = {2015},
	month = {APR},
	pages = {1559-1565},
	publisher = {TAYLOR \& FRANCIS INC},
	address = {530 WALNUT STREET, STE 850, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>A short and efficient enantioselective synthesis of natural product (S)-3-hydroxypiperidine has been achieved starting from commercially available raw materials employing two catalytic routes: (i) cocatalyzed hydrolytic kinetic resolution (HKR) of racemic methyl-3-(oxiran-2-yl)propanoate; (ii) proline-catalyzed -aminooxylation followed by Horner-Wardsworth-Emmons olefination in high enantiomeric purity (97\% ee) and high overall yield (38\%).</p>},
	keywords = {Asymmetric synthesis, bioactivity, Enantioselectivity, Natural products, organocatalysis},
	issn = {0039-7911},
	doi = {10.1080/00397911.2015.1033428},
	author = {Dey, Soumen and Karabal, Pratibha U. and Sudalai, Arumugam}
}
