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- W1963739163 abstract "The synthesis of the disaccharide present in the hydrophobia region of many endotoxins, a 2-amino-2-deoxy-β-D-glucopyranosyl-(1 → 6)-2-amino-2-deoxy-D-glucose in which the amino groups are acylated by (3R)-3-hydroxytetradecanoic acid residues and the 4″-hydroxy group is esterified by phosphate, is described. Two synthons carrying the specific substituents were prepared and condensed; stepwise removal of the protecting groups from the disaccharide thus formed afforded the title compound." @default.
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- W1963739163 date "1984-01-01" @default.
- W1963739163 modified "2023-10-18" @default.
- W1963739163 title "Chemistry of bacterial endotoxins. Part 1. Block synthesis of 6-O-{4-O-ammonio(hydrogen)phosphono-2-deoxy-2-[(3R)-3-hydroxy-tetradecanamido]-β-<scp>D</scp>-glucopyranosyl}-2-deoxy-2-[(3R)-3-hydroxy-tetradecanamido]-<scp>D</scp>-glucose" @default.
- W1963739163 doi "https://doi.org/10.1039/p19840000275" @default.
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