@article { ISI:000335921200039,
	title = {Concise synthesis of C-1-cyano-iminosugars via a new Staudinger/aza Wittig/Strecker multicomponent reaction strategy},
	journal = {BIOORGANIC \& MEDICINAL CHEMISTRY LETTERS},
	volume = {24},
	number = {12},
	year = {2014},
	month = {JUN 15},
	pages = {2777-2780},
	abstract = {A new Staudinger/aza Wittig/Strecker multicomponent reaction sequence to C-1-cyano iminoalditols has been developed. When applied to 5-azidodeoxy-D-xylose and -D-glucose as substrates the method leads smoothly in good yield and with excellent stereoselectivity to respectively, 1,5-dideoxy-1,5-imino-D-idurono nitrile and 2,6-didesoxy-2,6-imino-D-glycero-D-ido-heptononitrile. (C) 2014 Published by Elsevier Ltd.},
	issn = {0960-894X},
	doi = {10.1016/j.bmcl.2014.03.069},
	author = {Zoidl, Manuel and Mueller, Bernhard and Torvisco, Ana and Tysoe, Christina and Benazza, Mohamed and Siriwardena, Aloysius and Withers, Stephen G. and Wrodnigg, Tanja M.}
}
