95580-54-4

Upstream product

• 10378-06-0 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 
• 121237-39-6 (2R,3R,4S,5R,6S)-5-(benzyloxy)-2-((benzyloxy)methyl)-4-hydroxy-6-(((2R,3R,4S,5R,6R)-4,5,6-tris(benzyloxy)-2-((benzyloxy)methyl)tetrahydro-2H-pyran-3-yl)oxy)tetrahydro-2H-pyran-3-yl acetate 
• 95580-52-2 Benzyl-O-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)-(1->3)-O-(4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranosid 

Relevant academic research and scientific papers

A convenient synthesis of partially benzylated derivative of β-DGlcpNAc-(1→3)-β-D-Galp-(1→4)-β-D-Glcp-1-OBn as a versatile building block for sialyl lewis X antigens

Synthesis of the trisaccharide, benzyl 2-acetamido-3,6-di-O-benzyl-2-deoxy-β-Dglucopyranosyl-(1→3)-2,4,6-tri-O-benzyl-β-D-galactopyranosyl-(1→4)-2,3,6-tri-O-benzyl-β-Dglucopyranoside (9), was achieved from building block derivatives of the component mono-

Building Units of Oligosaccharides, LVIII. - Regioselective Glycosylation at 3'-OH or 4'-OH of Lactose Using Different Catalyst Systems

The lactose derivative 4 with unsubstituted 3'-OH and 4'-OH groups makes regioselective glycosylation reactions possible depending on the chosen type of catalyst system.In the presence of silver triflate, 4 reacts in homogenic phase with the phthalimido b