@article { ISI:000286862200012,
	title = {Asymmetric total synthesis of (2S,3S)-3-hydroxypipecolic acid},
	journal = {Tetrahedron Letters},
	volume = {52},
	number = {3},
	year = {2011},
	month = {JAN},
	pages = {404-406},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A synthetic route to (2S,3S)-3-hydroxypipecolic acid was achieved from readily available nonchiral pool starting material cis-2-butene-1,4-diol and involved Claisen orthoester rearrangement, Sharpless asymmetric dihydroxylation and intramolecular lactamisation of azido lactone as the key steps. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2010.11.062},
	author = {Chavan, Subhash P. and Dumare, Nilesh B. and Harale, Kishor R. and Kalkote, Uttam R.}
}
