80856-56-0

Upstream product

• 80874-22-2 3-O-(6-O-acetyl-2-azido-4-O-benzyl-2-desoxy-β-D-galactopyranosyl)-1,6-anhydro-2,4-di-O-benzyl-β-D-galactopyranose 

Downstream Products

• 80856-54-8 3-O-<2-Acetamido-3-O-(2-acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-galactopyranosyl)-6-O-acetyl-4-O-benzyl-2-desoxy-β-D-galactopyranosyl>-1,6-anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 80856-62-8 3-O-<2-Acetamido-3-O-(2-acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-galactopyranosyl)-6-O-acetyl-4-O-benzyl-2-desoxy-β-D-galactopyranosyl>-6-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranosylbromid 
• 80856-61-7 3-O-<2-Acetamido-3-O-(2-acetamido-6-O-acetyl-3,4-di-O-benzyl-2-desoxy-α-D-galactopyranosyl)-6-O-acetyl-4-O-benzyl-2-desoxy-β-D-galactopyranosyl>-1,6-di-O-acetyl-2,4-di-O-benzyl-α,β-D-galactopyranose 

Relevant academic research and scientific papers

Building Units of Oligosaccharides, XXXVI. - Investigation of Reactivity in Tri-and Pentasaccharide Syntheses. Improved Synthesis of the Pentasaccharide Chain of the Forssman Antigen

The dependence of selectivity and yield upon the initial saccharide's reactivity is shown for the syntheses of the trisaccharides 7, 8, 9, and 12.From 8 comes the trisaccharide halide 15 which, together with 22 in a block synthesis, yields the pentasaccha