@article { ISI:000355987900093,
	title = {Enantioselective syntheses of (R)-pipecolic acid, (2R,3R)-3-hydroxypipecolic acid, beta-(+)-conhydrine and (-)-swainsonine using an aziridine derived common chiral synthon},
	journal = {RSC Advances},
	volume = {5},
	number = {62},
	year = {2015},
	month = {MAY},
	pages = {50580-50590},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Concise total syntheses of (R)-pipecolic acid, (R)-ethyl-6-oxopipecolate, (2R, 3R)-3-hydroxypipecolic acid and formal syntheses of beta-(+)-conhydrine, (-)-lentiginosine, (-)-swainsonine and 1,2-di-epi-swainsonine have been accomplished starting from a common chiral synthon. The present strategy employs regioselective aziridine ring opening, Wittig olefination and RCM as the key chemical transformations.</p>},
	issn = {2046-2069},
	doi = {10.1039/c5ra06429e},
	author = {Chavan, Subhash P. and Khairnar, Lalit B. and Pawar, Kailash P. and Chavan, Prakash N. and Kawale, Sanket A.}
}
