@article { ISI:000468868900013,
	title = {Biologically active branched-chain aminocyclopentane tetraols from d-galactose},
	journal = {MONATSHEFTE FUR CHEMIE},
	volume = {150},
	number = {5, SI},
	year = {2019},
	month = {MAY},
	pages = {861-870},
	abstract = {From 1,2;3,4-di-O-isopropylidene-d-galactopyranose, a series of highly functionalized branched-chain cyclopentanes was easily available. The initial partially protected cyclopentane tetraol is a versatile central intermediate and was exploited as subject to various highly regio- and stereoselective structural alterations with a view to prepare selective -d-galactosidase inhibitors. In line with our findings on recently reported constitutional isomers featuring amino substituents, basic derivatives are medium activity inhibitors of -d-galactosidases with side activities for beta-glucosidases. {[}GRAPHICS] .},
	issn = {0026-9247},
	doi = {10.1007/s00706-019-02428-0},
	author = {Schalli, Michael and Weber, Patrick and Nasseri, Seyed A. and Gomez, Ana Torvisco and Mueller, Philipp and Stuetz, Arnold E. and Withers, Stephen G. and Wolfsgruber, Andreas and Wrodnigg, Tanja M.}
}
