@article { ISI:000249894100012,
	title = {Convenient formal synthesis of (+/-)-paroxetine},
	journal = {Synthetic Communications},
	volume = {37},
	number = {18},
	year = {2007},
	month = {SEP},
	pages = {3143-3149},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>A formal total synthesis of antidepressant (+/-)-paroxetine employing a solvent-free Heck reaction is disclosed.</p>},
	keywords = {antidepressants, carbamate, electrophile, Heck reaction, piperidines},
	issn = {0039-7911},
	doi = {10.1080/00397910701545130},
	author = {Chavan, Subhash P. and Khobragade, Dushant A. and Pathak, Ashok B. and Kalkote, Uttam R.}
}
@article { ISI:000328606500015,
	title = {Concise enantioselective syntheses of (+)-L-733,060 and (2S,3S)-3-hydroxypipecolicw acid by cobalt(III)(salen)-catalyzed two-stereocenter hydrolytic kinetic resolution of racemic azido epoxides},
	journal = {Synlett},
	volume = {25},
	number = {1},
	year = {2014},
	month = {JAN},
	pages = {102-104},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>An efficient synthesis of the 2,3-disubstituted piperidines (+)-L-733,060 and (2S,3S)-3-hydroxypipecolic acid (99\% ee) in high optical purity from commercially available starting materials is described. The strategy involves a cobalt-catalyzed hydrolytic kinetic resolution of a racemic azido epoxide with two stereocenters and an intramolecular reductive cyclization as key reactions.</p>},
	keywords = {azides, cyclizations, epoxides, piperidines, stereoselective synthesis, Wittig reactions},
	issn = {0936-5214},
	doi = {10.1055/s-0033-1340074},
	author = {Devalankar, Dattatray A. and Chouthaiwale, Pandurang V. and Sudalai, Arumugam}
}
