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Showing papers by "Seiichiro Ogawa published in 1968"



Journal ArticleDOI
TL;DR: In this paper, a mechanism of the bromination reaction is presented, based on the configuration of a bromo-compound, and the new compounds obtained were established by nuclear magnetic resonance and chemical evidences.
Abstract: Bromination of myo-inosadiamine-l,3 dihydrochloride or its di-N-acetyl derivative with acetyl bromide and acetic anhydride yielded pentaacetyl-2-bromo-2-deoxy-scyllo-inosadiamine-1,3 (III), which upon reductive debromination afforded pentaacetyl-2-deoxystreptamine (IV). The configurations of the new compounds obtained were established by nuclear magnetic resonance and chemical evidences. A mechanism of the bromination reaction is presented, based on the configuration of the bromo-compound.

13 citations