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The C 12 -aminoalditol H 2 NCH 2 -(CHOBn) 10 -CH 2 OH was prepared from two simple monosaccharide building blocks. The synthesis was realized by a regioselective introduction of the azide group and subsequent protection-deprotection transformations. The chemical reactivity of the aminoalditol was tested in the reductive amination reaction with a selectively protected sucrose monoaldehyde.

An efficient synthesis of a C12-higher sugar aminoalditol

An efficient synthesis of a C₁₂-higher sugar aminoalditol