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SHR Neuro Krebs Kardio Lipid Stoffw Microb

Schalli, M; Weber, P; Nasseri, SA; Gomez, AT; Muller, P; Stutz, AE; Withers, SG; Wolfsgruber, A; Wrodnigg, TM.
Biologically active branched-chain aminocyclopentane tetraols from d-galactose
MONATSH CHEM. 2019; 150(5): 861-870. Doi: 10.1007/s00706-019-02428-0
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Führende Autor*innen der Med Uni Graz
Schalli Michael
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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] .

Find related publications in this database (Keywords)
Aminoalcohols
Carbocycles
Carbohydrates
Cyclizations
Ene reactions
Structure-activity relationships
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