158716-10-0

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 2936-70-1 (2R,3S,4S,5S,6R)-2-Hydroxymethyl-6-phenylsulfanyl-tetrahydro-pyran-3,4,5-triol 
• 100-39-0 benzyl bromide 
• 158716-04-2 phenyl exo(phenyl)-2,3:4,6-di-O-benzylidene-1-thio-α-D-mannopyranoside 
• 177943-74-7 methyl 2-O-benzyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-1-thio-α-D-mannopyranoside 
• 168138-26-9 phenyl 4,6-O-benzylidene-3-O-(4-methoxybenzyl)-1-thio-α-D-mannopyranoside 
• 159407-19-9 phenyl 4,6-O-benzylidene-1-thio-α-D-mannopyranoside 
• 108-24-7 acetic anhydride 
• 158716-08-6 phenyl 4,6-O-benzylidene-2-O-benzyl-1-deoxy-1-thio-α-D-mannopyranoside 

Downstream Products

• 216758-83-7 methyl (3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranosyl)-(1-2)-3-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 1200440-94-3 C₄₁H₄₉O₁₅P 
• 1200440-95-4 C₄₂H₄₉O₁₈P 
• 1200440-96-5 C₃₉H₄₇O₁₄P 
• 1200440-97-6 C₅₇H₆₁O₁₅P 
• 1200440-98-7 C₄₉H₅₉O₁₇P 
• 1200440-99-8 C₅₀H₅₃O₁₅P 
• 1200441-00-4 C₅₇H₆₁O₁₅P 
• 1257634-78-8 3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-1-deoxy-1-allyl-β-D-mannopyranose 
• 1257634-65-3 3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-1-deoxy-1-allyl-α-D-mannopyranose 
• 1257634-76-6 4,6-O-benzylidene-2-O-benzyl-3-O-tert-butyldimethylsilyl-1-deoxy-1-(2-oxo-2-phenylethyl)-β-D-mannopyranose 
• 1257634-67-5 3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-1-deoxy-1-(2-oxo-2-phenylethyl)-α-D-mannopyranose 
• 1257634-66-4 3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-1-deoxy-(3,3-dimethyl-2-oxo-butyl)-α-D-mannopyranose 
• 1096119-93-5 6'-azidohexyl 3-O-acetyl-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 

Relevant academic research and scientific papers

Studies of Catalyst-Controlled Regioselective Acetalization and Its Application to Single-Pot Synthesis of Differentially Protected Saccharides

This article describes studies on the regioselective acetal protection of monosaccharide-based diols using chiral phosphoric acids (CPAs) and their immobilized polymeric variants, (R)-Ad-TRIP-PS and (S)-SPINOL-PS, as the catalysts. These catalyst-controll

Highly stereoselective synthesis of α-D-mannopyranosyl phosphosugars

(Chemical Equation Presented) α-Mannopyranosyl phosphosugars are obtained in 61-90% yields from 4,6-O-benzylidene-protected mannosyl thioglycosides bearing ester functionality in the 3-O-position by coupling reactions with ammonium salts of phosphosugars

A synthetic approach to the glycan chain of high mannose type N-glycoprotein

The syntheses of α-D-glucopyranose-(1→3)-D-mannopyranose, methyl α-D-glucopyranose-(1→3)-α-D-mannopyranoside and methyl α-D-glucopyranose-(1→3)-α-D-mannopyranose-(1→2)-α-D- mannopyranoside are reported. High stereoselectivity was observed during the coupl