99409-28-6

Upstream product

• 107802-83-5 O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-(1-> 3)-[O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-(1-> 4)]-6-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl trichloroacetimidate 
• 118590-83-3 C₁₂₉H₁₃₃NO₂₆ 
• 120316-18-9 C₁₂₇H₁₃₅NO₂₇ 
• 99422-52-3 ethyl 6-O-benzyl-2-deoxy-2-phthalimido-4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-1-thio-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-β-D-glucopyranoside 
• 169048-88-8 ethyl 6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 
• 61134-30-3 benzyl 3,4,6-tri-O-benzyl-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis of a nonasaccharide with two Lewis x trisaccharides anchored onto a branched trimannoside

Double condensation of phenyl 3,4,6-tri-O-benzyl-2-O-[6-O-benzyl-2-deoxy-2-phthalimido-4-O-(2,3,4,6- tetra-O-benzoyl-β-D-galactopyranosyl)-3-O-(2,3,4-tri-O-benzyl-α-L-fu copyranosyl)-β-D-glucopyranosyl]-1-thio-α-D-mannopyranoside 31 with methyl 2,4-di-O-b

A TOTAL SYNTHESIS OF DIMERIC Lex ANTIGEN, III3V3Fuc2nLc6Cer: PIVALOYL AUXILIARY FOR STEREOCONTROLLED GLYCOSYLATION

A first total synthesis of dimeric Lex glycooctaosyl ceramide was achieved in a stereocontrolled manner.Synthetic experiments were designed so as to evidence the advantage for the use of O-2a pivaloyl over O-2a acetyl group as a stereocontrolli

Synthesis of a tetra- and a nona-saccharide which contain alpha-L-fucopyranosyl groups and are part of the complex type of carbohydrate moiety of glycoproteins.

Methyl trifluoromethanesulfonate-promoted condensation of ethyl 6-O-benzyl-2-deoxy-2-phthalimido-4-O-(2,3,4,6-tetra-O-acetyl-beta-D- galactopyranosyl)-1-thio-3-O-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)- beta-D- glucopyranoside with benzyl 3,4,6-tri-O-b