Abstract
(±)-1-Deoxy-muco-inosamine-4, (±)-1-scyllo-inosamine-2 and (±)-2-deoxy-allo-inosadiamine-3, 5 pentaacetates have been synthesized from 1-deoxy-myo-inositol (I). The hydroxyl groups of I are mesylated, and the mesyloxy groups are replaced by azido groups. The reduction of the azido compounds, followed by acetylation, gives the pentaacetyl-deoxyinosamines and deoxyinosadiamine. Their structures have been established by means of a study of the proton magnetic resonance spectra.

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