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- W1966734504 abstract "The titled compound (5) has been prepared from 3′,4′-dideoxyneamine or ribostamycin via 1,6-cyclic carbamate intermediates (2 and 12). 3′,4′-Dideoxygenation, which is the key step in the synthesis from ribostamycin, was accomplished by the hydrogenation of 3′,4′-unsaturated derivative which was prepared from the corresponding 3′,4′-di-O-mesyl derivative by the action of sodium iodide and zinc dust in DMF. The title compound was found to have an improved antibacterial spectrum broader than 3′,4′-dideoxyneamine." @default.
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- W1966734504 date "1974-12-01" @default.
- W1966734504 modified "2023-10-18" @default.
- W1966734504 title "Synthesis of 1-<i>N</i>-[(<i>S</i>)-4-Amino-2-hydroxybutyryl]-3′,4′-dideoxyneamine" @default.
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- W1966734504 doi "https://doi.org/10.1246/bcsj.47.3139" @default.
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