Abstract
Abstract The title compound was synthesized from methyl 4-O-benzyl-2,6-dideoxy-β-l-threo-hexopyranosid-3-ulose (19) through cyanomesylation, reductive spiro aziridine formation, and reductive ring-opening. When (2-methoxyethoxymethyl) group was used as the protecting group at O-4 of the above intermediate, it could not be removed at the final stage.
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