95504-11-3

Upstream product

• 137491-98-6 2,2,2-trichloroethyl 4,6-O-benzylidene-α-D-mannopyranoside 
• 105165-52-4 2,2,2-trichloroethyl 2,3-di-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside 
• 145350-27-2 2,3-di-O-benzyl-α-D-mannopyranoside 
• 114079-09-3 2,2,2-trichloroethyl 2,3-di-O-benzyl-α-D-mannopyranoside 
• 100-39-0 benzyl bromide 
• 68536-42-5 acetyl 4,6-di-O-acetate-2,3-di-O-benzyl-α-D-mannopyranoside 

Downstream Products

• 145350-28-3 2,3-di-O-acetyl-1,6-anhydro-4-O-(4,6-di-O-acetyl-2,3-di-O-benzyl-β-D-mannopyranosyl)-β-D-glucopyranose 
• 160204-39-7 cyclohexyl 4,6-di-O-acetyl-2,3-di-O-benzyl-β-D-mannopyranoside 
• 145350-29-4 O-(4,6-di-O-acetyl-2,3-di-O-benzyl-β-D-mannopyranosyl)-(1<*>4)-1,2,3,6-tetra-O-acetyl-α-D-glucopyranose 
• 145350-29-4 O-(4,6-di-O-acetyl-2,3-di-O-benzyl-β-D-mannopyranosyl)-(1<*>4)-1,2,3,6-tetra-O-acetyl-β-D-glucopyranose 
• 160204-43-3 cyclohexyl 2,3-di-O-benzyl-4,6-bis-O-(tert-butyldimethylsilyl)-β-D-mannopyranoside 
• 160204-46-6 cyclohexyl 2,3-di-O-benzyl-4,6-bis-O-trimethylsilyl-β-D-mannopyranoside 
• 160204-41-1 cyclohexyl 2,3-di-O-benzyl-β-D-mannopyranoside 

Relevant academic research and scientific papers

Convenient synthesis of pyruvate acetals of carbohydrates by coupling of trialkylsilylated diols and pyruvates

Hexopyranoside diols, mainly 4,6-diols with α-gluco, β-gluco, α-galacto, β-galacto, and α-manno configurations could be converted effectively (40-74% yields), to the corresponding pyruvate acetals by the coupling of the O-trialkylsilylated, namely, O-TBDM

Synthetic studies on oligosaccharide of a glycolipid from the spermatozoa of bivalves. VII. The synthesis of di-, tri-, tetrasaccharides related to glycosphingolipid

The three kinds of oligosaccharides that constitute the partial structure of lipid IV (1) were synthesized as follows. The disaccharide O-β-D-mannopyranosyl-(1 → 4)-D-glucopyranose (13), the trisaccharide O-α-D-mannopyranosyl-(1 → 3)-O-β-D-mannopyranosyl-