The new lactosyl donor 8, bearing an Fmoc-protected hydroxy group, has been
prepared from lactose for the solid-phase synthesis of lactose-containing
oligosaccharides. In addition to the preparation of 3b-O-fucosyllactoside 1
(with donor 4), use of this new building block has permitted the syntheses
of 3b-O-mannosyllactoside 2 and of human milk oligosaccharide lacto-N-tetr
aoside 3, with known donors 5 and 6, respectively. These successful. high-y
ielding syntheses demonstrate the usefulness of Fmoc-protected O-glycosyl t
richloroacetimidate 8 for the solid-phase construction of oligosaccharides,
by an ester-type linker strategy.