@article { ISI:000266735500021,
	title = {2-Acetamino-1,2-dideoxynojirimycin-lysine hybrids as hexosaminidase inhibitors},
	journal = {TETRAHEDRON-ASYMMETRY},
	volume = {20},
	number = {6-8},
	year = {2009},
	month = {MAY 7},
	pages = {832-835},
	abstract = {Cyclisation by double reductive amination of 2-acetamino-2-deoxy-D-xylo-hexos-5-ulose with N-2 protected L-lysine derivatives provided 2-acetamino-1,2-dideoxynojirimycin derivatives without any observable epimer formation at C-5. Modifications on the lysine moiety gave access to lipophilic derivatives that exhibited improved hexosaminidase inhibitory activities. (C) 2009 Elsevier Ltd. All rights reserved.},
	issn = {0957-4166},
	doi = {10.1016/j.tetasy.2009.02.015},
	author = {Steiner, Andreas J. and Schitter, Georg and Stuetz, Arnold E. and Wrodnigg, Tanja M. and Tarling, Chris A. and Withers, Stephen G. and Mahuran, Don J. and Tropak, Michael B.}
}
