@article { ISI:000342873800010,
	title = {Short enantioselective total synthesis of (R)- and (S)-pipecolic acid},
	journal = {Tetrahedron-Asymmetry},
	volume = {25},
	number = {16-17},
	year = {2014},
	month = {SEP},
	pages = {1246-1251},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A convenient and practical total synthesis of (R)- and (S)-pipecolic acid has been achieved by utilizing chiral cis-aziridine-2-carboxylate as the common synthetic precursor. The synthesis involves regioselective reductive cleavage of the aziridine ring and Wittig olefination as key reactions. (C) 2014 Elsevier Ltd. All rights reserved.</p>},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2014.08.001},
	author = {Chavan, Subhash P. and Khairnar, Lalit B. and Chavan, Prakash N. and Kalbhor, Dinesh B.}
}
@article { ISI:000345660300032,
	title = {Stereospecific synthetic approach towards tamiflu using the ramberg-backlund reaction from cysteine hydrochloride},
	journal = {RSC Advances},
	volume = {4},
	number = {107},
	year = {2014},
	month = {NOV},
	pages = {62281-62284},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>The stereospecific formal synthesis of Tamiflu from L-cysteine hydrochloride as the chiral source is described. The notable feature of the present strategy is the Ramberg-Backlund reaction and Sharpless-Reich protocol as the key chemical transformations to access the cyclohexene skeleton of Tamiflu.</p>},
	issn = {2046-2069},
	doi = {10.1039/c4ra10391b},
	author = {Chavan, Subhash P. and Chavan, Prakash N. and Gonnade, Rajesh G.}
}
