@article { ISI:000323093300010,
	title = {Short synthesis of (2S,3S)-3-hydroxypipecolic acid},
	journal = {Tetrahedron Letters},
	volume = {54},
	number = {36},
	year = {2013},
	month = {SEP},
	pages = {4851-4853},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A convenient synthesis of (2S,3S)-3-hydroxypipecolic acid starting from cheap and abundant L-(+)-tartaric acid has been achieved. The strategy employs selective ester reduction and reductive lactamization as key steps. (C) 2013 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Reductive lactamization, Selective deprotection, Wittig reaction},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2013.06.111},
	author = {Chavan, Subhash P. and Harale, Kishor R. and Pawar, Kailash P.}
}
@article { ISI:000351584500007,
	title = {Synthesis of 3-ethyl-4-metyl-1h,5-dihydro-2h-pyrrol-2-one by novel palladium(ii)-catalyzed cyclization and ring-closing metathesis},
	journal = {Synthesis-Stuttgart},
	volume = {47},
	number = {7},
	year = {2015},
	month = {APR},
	pages = {955-960},
	publisher = {GEORG THIEME VERLAG KG},
	type = {Article},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>Synthesis of 3-ethyl-4-methyl-1,5-dihydro-2H-pyrrol-2-one is described starting from commercially available allylamine and 4-methoxybenzylamine employing palladium-catalyzed cyclization or ring-closing metathesis as the key steps.</p>},
	keywords = {antidiabetic, cyclization, glimepiride, lactams, metabolite, pyrrolinone, Ring-closing metathesis},
	issn = {0039-7881},
	doi = {10.1055/s-0034-1379985},
	author = {Chavan, Subhash P. and Pathak, Ashok B. and Pawar, Kailash P.}
}
