390400-48-3Relevant articles and documents
Efficient synthesis of lactosaminylated core-2 O-glycans
Misra, Anup Kumar,Fukuda, Minoru,Hindsgaul, Ole
, p. 2667 - 2669 (2001)
A series of lactosaminylated oligosaccharides found in mucin type O-glycans was synthesized using a generalized block strategy. The synthesis involved the addition of a protected lactosamine donor to a partially protected T-disaccharide derivative. The nonreducing galactose residues of the deblocked oligosaccharide products could be removed by β-galactosidase from jack bean to produce the corresponding GlcNAc terminated compounds. A series of tri- to hexasaccharides was thus efficiently produced.