@article { ISI:000261163300008,
	title = {1-Deoxygalactonojirimycin-lysine hybrids as potent D-galactosidase inhibitors},
	journal = {BIOORGANIC \& MEDICINAL CHEMISTRY},
	volume = {16},
	number = {24},
	year = {2008},
	month = {DEC 15},
	pages = {10216-10220},
	abstract = {Cyclization by double reductive amination of L-arabino-hexos-5-ulose with suitably protected D- as well as L-lysine derivatives provided 1-deoxygalactonojirimycin lysine hybrids without any observable epimer formation at C-5. Modi. cations on the lysine moiety by acylation gave access to lipophilic derivatives which exhibited excellent D-galactosidase inhibitory activities. (C) 2008 Elsevier Ltd. All rights reserved.},
	issn = {0968-0896},
	doi = {10.1016/j.bmc.2008.10.054},
	author = {Steiner, Andreas J. and Schitter, Georg and Stuetz, Arnold E. and Wrodnigg, Tanja M. and Tarling, Chris A. and Withers, Stephen G. and Fantur, Katrin and Mahuran, Don and Paschke, Eduard and Tropak, Michael}
}
