666753-83-9

Upstream product

• 1245566-78-2 phenyl 2-azido-2-deoxy-3-O-benzyl-4,6-O-p-methoxybenzylidene-1-thio-β-D-glucopyranoside 
• 277756-86-2 phenyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-1-thio-β-D-glucopyranoside 
• 166516-67-2 phenyl 2-azido-2-deoxy-1-thio-β-D-glucopyranoside 
• 1394857-30-7 phenyl 4,6-O-benzylidene-1-thio-β-D-glucosaminopyranoside 
• 371123-22-7 phenyl 2-amino-2-deoxy-1-thio-β-D-glucopyranoside 
• 108-98-5 thiophenol 
• 1075217-39-8 phenyl 2-azido-3-O-benzyl-2-deoxy-4,6-O-(1-naphthylmethylidene)-1-thio-β-D-glucopyranoside 

Downstream Products

• 1053555-47-7 2,2,2-Trichloro-acetimidic acid (2R,3S,4R,5R,6S)-5-azido-4-benzyloxy-3-hydroxy-6-phenylsulfanyl-tetrahydro-pyran-2-ylmethyl ester 
• 1245566-82-8 C₂₀H₂₃N₃O₆S₂ 
• 1394857-33-0 phenyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-1-thio-β-D-glucopyranoside 
• 1394857-35-2 phenyl 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-1-thio-4-trichloroacetyl-β-D-glucopyranoside 
• 1394857-42-1 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trichloroacetyl-1-O-trichloroacetimidate-β-D-glucopyranoside 
• 1394857-60-3 2-azido-6-O-benzoyl-3-O-benzyl-2-deoxy-4-O-trichloroacetyl-1-O-trichloroacetimidate-α-D-glucopyranoside 
• 1245566-83-9 phenyl 2-azido-2-deoxy-3-O-benzyl-6-deoxy-6-phthalimido-1-thio-β-D-glucopyranoside 
• 1245566-85-1 C₁₉H₂₀N₆O₃S 
• 1245566-97-5 C₂₇H₃₄N₁₀O₇ 
• 1245566-93-1 methyl (2-azido-2-deoxy-3-O-benzyl-6-deoxy-6-phthalimido-α-D-glucopyranosyl)-(1->4)-2,6-diazido-2,6-dideoxy-3-O-benzyl-α-D-glucopyranoside 
• 1245566-92-0 methyl (4-O-acetyl-2-azido-2-deoxy-3-O-benzyl-6-deoxy-6-phthalimido-α-D-glucopyranosyl)-(1->4)-2,6-diazido-2,6-dideoxy-3-O-benzyl-α-D-glucopyranoside 
• 1379976-86-9 C₃₇H₃₈N₁₀O₁₀ 
• 1379976-91-6 C₂₉H₃₄N₁₂O₈ 
• 1379976-89-2 C₂₉H₃₄N₁₂O₈ 

Relevant academic research and scientific papers

Synthesis and scalable conversion of L-iduronamides to heparin-related Di- and tetrasaccharides

A diastereomerically pure cyanohydrin, preparable on kilogram scale, is efficiently converted in one step into a novel L-iduronamide. A new regioselective acylation of this iduronamide and a new mild amide hydrolysis method mediated by amyl nitrite enable

Oligo-Aminosaccharide compound

An oligo-aminosaccharide compound formed by binding 3 to 6 saccharides, such as 2,6-diamino-2,6-dideoxy-α-(1→4)-D-glucopyranose oligomers, or a salt thereof, which has high affinity to a double-stranded nucleic acid.

Synthesis of the putative minimal FGF binding motif heparan sulfate trisaccharides by an orthogonal protecting group strategy

The synthesis of two trisaccharides, the putative minimal heparan sulfate sequences responsible for binding to acidic and basic fibroblast growth factors, respectively, is described from a common protected intermediate using an orthogonal protecting group strategy.