959862-94-3

Upstream product

• 220645-16-9 4-methylphenyl 4,6-O-benzylidene-2-deoxyl-1-thio-2-phthalimido-β-D-glucopyranoside 

Downstream Products

• 1221498-78-7 3-oxobutyl 6-O-benzyl-2-deoxy-2-N-phthalimido-β-D-glucopyranoside 
• 1459246-74-2 p-tolyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl-(1→4)-6-O-benzyl-2-deoxy-2-phthalimido-1-thiol-β-D-glucopyranoside 
• 1071226-03-3 p-tolyl (methyl 4,7,8,9-tetra-O-acetyl-3,5-dideoxy-5-trichloroacetamido-D-glycero-α-D-galacto-2-nonulopyranosylonate-(2->3))-2-O-benzoyl-4,6-O-benzylidene-β-D-galactopyranosyl-(1->4)-6-O-benzyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 

Relevant academic research and scientific papers

Syntheses of LewisX and dimeric LewisX: Construction of branched oligosaccharides by a combination of preactivation and reactivity based chemoselective one-pot glycosylations

(Chemical Equation Presented) Two asymmetrically branched oligosaccharides, LewisX and dimeric LewisX, were assembled in one pot with high yields and exclusive regio- and stereoselectivities. p-Tolyl thioglycosides were utilized as t

Synthesis of the tolerance-inducing oligosaccharide lacto-N-fucopentaose III bearing an activated linker

A concise synthetic route to an immunomodulatory pentasaccharide, lacto-N-fucopentaose III (1) and its corresponding human serum albumin conjugate, is described. Key transformations of the strategy include two highly regio- and stereoselective glycosylations for the construction of disaccharide 10 and pentasaccharide 12, a Birch reduction for deprotection of benzyl ethers, and a UV-promoted radical addition of a thiol to an alkene for modification of the aglycone.