62867-75-8

Upstream product

• 613-90-1 benzoyl cyanide 
• 62867-72-5 benzyl 2,3-di-O-acetyl-4,6-O-benzylidene-β-D-galactopyranosyl-(1→4)-2,3-di-O-acetyl-β-D-glucopyranoside 
• 100-39-0 benzyl bromide 
• 67398-59-8 benzyl 2,3,6-tri-O-acetyl-4-O-(2,3-di-O-acetyl-4,6-O-benzylidene-β-D-galactopyranosyl)-β-D-glucopyranoside 

Downstream Products

• 62867-88-3 benzyl 2,3,6-tri-O-benzyl-4-O-(2,3-di-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 62867-79-2 benzyl 2,3,6-tri-O-benzyl-4-O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranoside 
• 112014-36-5 benzyl 2,3,6,2',3',6' hexa-O-benzyl-4'-O--β-lactoside 
• 62867-79-2 benzyl O-(2,3,6-tri-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of Globotriaosylceramide (Gb3) and Isoglobotriaosylceramide (isoGb3)

The synthesis of globotriaosylceramide (1) was based on O-galactosyl trichloroacetimidate 5α as donor and 4b-O-unprotected lactose 7 as acceptor; 7 was readily accessible from lactose.Glycosylation by an "inverted procedure" afforded preferentially the α-

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