128705-82-8

Upstream product

• 139684-71-2 methyl 5-acetamido-4,7,8,9-tetra-O-benzyl-3,5-dideoxy-3-phenylthio-D-erythro-β-L-gluco-2-nonulopyranosonate 
• 108-98-5 thiophenol 
• 931-59-9 benzenesulfenyl chloride 
• 125288-69-9 5-acetamido-4,7,8,9-tetra-O-benzyl-2,3-dehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonic acid 
• 116096-67-4 methyl 5-acetamido-4,7,8,9-tetra-O-benzyl-2,3,5-trideoxy-2-fluoro-3-phenylseleno-D-erythro-α-L-gluco-nonulopyranosate 
• 125288-70-2 methyl 5-acetamido-4,7,8,9-tetra-O-benzyl-3,5-dideoxy-3-phenylseleno-D-erythro-β-L-gluco-2-nonulopyranosonate 
• 128596-95-2 (3R,4R,5S,6R)-5-Acetylamino-4-benzyloxy-2-hydroxy-3-phenylsulfanyl-6-((1S,2R)-1,2,3-tris-benzyloxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 129234-78-2 methyl 5-acetamido-4,7,8,9-tetra-O-benzyl-3-bromo-3,5-dideoxy-D-erythro-L-gluco-2-nonulopyranosonate 
• 129234-78-2 methyl 5-acetamido-4,7,8,9-tetra-O-benzyl-3-bromo-3,5-dideoxy-D-erythro-L-manno-2-nonulopyranosonate 
• 116096-63-0 methyl 5-acetamido-4,7,8,9-tetra-O-benzyl-2,3-dehydro-3,5-dideoxy-D-glycero-D-galacto-2-nonulopyranosonate 
• 73960-72-2 methyl-2,3-didehydro-4,7,8,9-tetra-O-acetyl-N-acetylneuraminate 
• 100-39-0 benzyl bromide 

Downstream Products

• 136514-63-1 C₁₀₈H₁₁₈N₂O₂₃S 
• 125288-74-6 methyl O--(2->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 120315-58-4 methyl O--(2->6)-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 120308-60-3 C₁₀₀H₁₀₅NO₁₉S 
• 120308-59-0 benzyl O--(2->3)-O-(2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 120308-59-0 benzyl O--(2->3)-O-(2,6-di-O-benzyl-β-D-galactopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Stereocontrolled Synthesis of Sialyl Lex, the Oligosaccharide Binding Ligand to ELAM-1 (Sialyl = N-acetylneuramin)

Sialyl Lex 1 the oligosaccharide binding ligand to ELAM-1 is synthesized from building blocks 2-5 via a short route featuring the principle of a neighbouring PhS group as an auxiliary to facilitate and stereochemically control the formation of

HIGHLY STEREOSELECTIVE GLYCOSYLATION OF SIALIC ACID AIDED BY STEREOCONTROLLING AUXILIARIES

α-Selective glycosylation of sialic acid was achieved by using a sialic acid donor which carries a stereocontrolling auxiliary such as selenide or sulfide group at C-3 position.