Abstract
The title compound, C28H41NO6, was obtained by reduction of benzyl 2-deoxy-2-(3,5-di-tert-butylsalicylideneamino)-α-d-glucopyranoside. The benzyl substituent is in an axial position, whereas the 3,5-di-tert-butylsalicylamino substituent and the hydroxyl groups are in equatorial positions. The enantiomerically pure title compound is a potential O,N,O-chelate ligand suitable as a precursor for chiral transition metal complexes. The absolute configuration was determined by NMR experiments.
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