@article { ISI:000236923500003,
	title = {Efficient and selective cleavage of the tert-butoxycarbonyl (Boc) group under basic condition},
	journal = {Arkivoc},
	number = {14},
	year = {2005},
	month = {MAY},
	pages = {20-28},
	publisher = {ARKAT USA INC},
	type = {Article},
	address = {C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA},
	abstract = {<p>A simple, efficient and mild method for the selective cleavage of tert-butoxycarbonyl (Boc) from dicarbamates and a carbonyl or aromatic ring in conjugation with the nitrogen atom bearing the Boc-group is described under basic condition.</p>},
	keywords = {alpha-amino acids, celogenitins, di-t-butylimidodicarbonate, racemization, Selective deprotection},
	issn = {1424-6376},
	author = {Mohapatra, Debendra K. and Durugkar, Kulbhushan A.}
}
@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.}
}
