Synthesis of a biotinylated penta-α-(1→6)-d-glucoside based on the rational design of an α-stereoselective glucosyl donor
Keyword(s):
Rational design of a protecting group pattern in a glucosyl donor allows for the α-selective synthesis of biotinylated pentasaccharides corresponding to the fragment of the α-(1→6)-glucans of Helicobacter pylori.