@article { ISI:000279746300009,
	title = {Enantioselective synthesis of (+)-alpha-conhydrine and (-)-sedamine by L-proline-catalysed alpha-aminooxylation},
	journal = {European Journal of Organic Chemistry},
	number = {18},
	year = {2010},
	month = {JUN},
	pages = {3437-3444},
	publisher = {WILEY-BLACKWELL},
	address = {COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA},
	abstract = {<p>An efficient organocatalytic approach to the enantioslective synthesis of two important piperidine alkaloids, namely (+)-alpha-conhydrine (98\% ee) and (-)-sedamine (95\% ee), by L-proline-catalysed alpha-aminooxylation of aldehydes has been developed. The strategy involves an intramolecular cyclization to construct the piperidine core.</p>},
	keywords = {alkaloids, Amino acids, Aminooxylation, Enantioselectivity, organocatalysis},
	issn = {1434-193X},
	doi = {10.1002/ejoc.201000169},
	author = {Shaikh, Tanveer Mahamadali and Sudalai, Arumugam}
}
