Chiral binuclear metal complexes for stereoselective hydrolysis of saccharides and glycosides
AssigneeBoard of Trustees of the University of Arkansas
InventorSusanne Striegler
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AssigneeBoard of Trustees of the University of Arkansas
InventorSusanne Striegler
Estimating the term…
Disclosed herein is a class of chiral binuclear metal complexes for stereoselective hydrolysis of saccharides and glycosides, and more particular chiral binuclear transition metal complex catalysts that discriminate epimeric glycosides and α- and β-glycosidic bonds of saccharides in aqueous solutions at near physiological pHs. The chiral binuclear metal complexes include a Schiff-base-type ligand derived from a chiral diamino building block, and a binuclear transition metal core, each which can be varied for selectivity. The metal core is a Lewis-acidic metal ion, such as copper, zinc, lanthanum, iron and nickel. The Schiff-base may be a reduced or non-reduced Schiff-base derived from aliphatic linear, aliphatic cyclic diamino alcohols or aromatic aldehydes. The ligand can be a penta- or heptadentate ligand derived from pyridinecarbaldehydes, benzaldehydes, linear or cyclic diamines or diamino alcohols.
An enantiopure asymmetric chiral binuclear transition metal (II) complex for discriminating α-glycosidic bonds of saccharides in aqueous solutions, wherein the formula of said enantiopure asymmetric chiral binuclear transition metal (II) complex is:
An enantiopure asymmetric chiral binuclear transition metal (II) complex for discriminating β-glycosidic bonds of saccharides in aqueous solutions, wherein the formula of said enantiopure asymmetric chiral binuclear transition metal (II) complex is:
A method of hydrolysis of saccharides and glycosides, said method comprising the steps of:
Dependencies are inferred from the claim text.