@article { ISI:000266794200009,
	title = {Synthesis and Biological Evaluation of 1,5-Dideoxy-1,5-iminoxylitol-Amino Acid Hybrids as Xylosidase Inhibitors},
	journal = {AUSTRALIAN JOURNAL OF CHEMISTRY},
	volume = {62},
	number = {6},
	year = {2009},
	note = {Symposium on Glycoscience, Chemistry and Chemical Biology, Oslo, NORWAY, 2007},
	pages = {553-557},
	abstract = {1,5-Dideoxy-1,5-iminoxylitol-amino acid hybrids have been synthesized by cyclisation via a double reductive amination of xylo-pentodialdose and the respective amino groups of lysine as well as serine components. Further modification with aromatic substituents gave access to lipophilic derivatives. Kinetic studies revealed that all compounds exhibited better inhibitory properties against beta-xylosidase from Thermoanaerobacterium sacharolyticum than the parent iminosugar.},
	issn = {0004-9425},
	doi = {10.1071/CH09040},
	author = {Steiner, Andreas J. and Stuetz, Arnold E. and Tarling, Chris A. and Withers, Stephen G. and Wrodnigg, Tanja M.}
}
