48229-10-3

Upstream product

• 65556-30-1 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 108-24-7 acetic anhydride 
• 89157-97-1 1,6-anhydro-2,3,4-tri-O-benzyl-β-L-idopyranose 
• 1117805-53-4 C₃₉H₄₈O₆SSi 

Downstream Products

• 65556-30-1 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 641635-63-4 methyl 2,3,4-tri-O-benzyl-α-L-idopyranoside 
• 205192-05-8 methyl 2,3,4-tri-O-benzyl-β-L-idopyranoside 
• 109914-80-9 methyl 2-acetamido-6-O-benzyl-2-deoxy-4-O-sulfo-3-O-(2,3,4-tri-O-benzyl-β-L-idopyranosyluronic acid)-β-D-galactopyranoside, disodium salt 
• 109914-80-9 methyl 2-acetamido-6-O-benzyl-2-deoxy-4-O-sulfo-3-O-(2,3,4-tri-O-benzyl-α-L-idopyranosyluronic acid)-β-D-galactopyranoside, disodium salt 
• 109914-81-0 methyl 2-acetamido-2-deoxy-3-O-(β-L-idopyranosyluronic acid)-4-O-sulfo-β-D-galactopyranoside, disodium salt 
• 109914-74-1 methyl 2-azido-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-β-L-idopyranosyluronic acid)-β-D-galactopyranoside 
• 109914-70-7 methyl 2-azido-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-idopyranosyluronic acid)-β-D-galactopyranoside 
• 109914-69-4 Acetic acid (2R,3R,4R,5R,6R)-5-azido-2-benzyloxymethyl-6-methoxy-4-((2S,3R,4S,5R,6S)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester 
• 109914-68-3 methyl 4-O-acetyl-2-azido-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-idopyranosyl)-β-D-galactopyranoside 
• 109914-84-3 methyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-β-L-idopyranosyluronic acid)-β-D-galactopyranoside 
• 109914-78-5 methyl 2-acetamido-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-idopyranosyluronic acid)-β-D-galactopyranoside 
• 109914-83-2 methyl 2-acetamido-4-O-acetyl-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-β-L-idopyranosyl)-β-D-galactopyranoside 
• 109914-77-4 methyl 2-acetamido-4-O-acetyl-6-O-benzyl-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-idopyranosyl)-β-D-galactopyranoside 

Relevant academic research and scientific papers

1,5-α-D-mannoseptanosides, ring-size isomers that are impervious to α-mannosidase-catalyzed hydrolysis

1,5-D-Mannoseptanosyl di-and trisaccharide ring-size isomers of the corresponding mannopyranosyl oligosaccharides have been prepared. Remarkably, these compounds show no inhibition of the α-mannosidase-catalyzed hydrolysis of p-nitrophenyl-α-D-mannopyrano

Mechanistic studies on the stereoselective formation of β-mannosides from mannosyl iodides using α-deuterium kinetic isotope effects

(Chemical Equation Presented) Stereoselective synthesis of β-mannosides is one of the most challenging linkages to achieve in carbohydrate chemistry. Both the anomeric effect and the C2 axial substituent favor the formation of the axial glycoside (α-produ

Divergent synthesis of L-sugars and L-iminosugars from D-sugars

An efficient divergent synthesis of L-sugars and L-iminosugars from D-sugars is described. The important intermediate. δ-hydroxyalkoxamate. prepared from D-glucono-/galactono-1,5-lactone, was cyclized under Mitsunobu conditions to give the O-cyclized oxim

Novel 1,6-Stannylenes of Glucose, Galactose and Mannose

Treatment of 2,3,4-tri-O-benzyl-gluco-, manno-, and -galactopyranose with dibutyltin oxide leads to the 1,6-di-O-stannylene products 2, 5 and 7, whereas no such products are formed by treatment of the 3-O-axially configured ido and allo sugars.Spectroscop

SYNTHESIS OF DERMATAN SULFATE FRAGMENTS: A CHEMICAL SYNTHESIS OF METHYL 2-ACETAMIDO-2-DEOXY-3-O-(α-L-IDOPYRANOSYLURONIC ACID)-4-O-SULFO-β-D-GALACTOPYRANOSIDE DISODIUM SALT AND ITS NON-SULFATED ANALOGUE

Methyl 2-azido-2-deoxy-β-D-galactopyranoside was subjected in sequence to isopropylidenation, benzylation, acid hydrolysis, and selective acetylation of HO-4, to give amorphous methyl 4-O-acetyl-2-azido-6-O-benzyl-2-deoxy-β-D-galactopyranoside.Condensatio