78161-49-6

Upstream product

• 42822-13-9 methyl 3,4-di-O-benzyl-α-L-fucopyranoside 
• 115678-13-2 methyl 3,4-di-O-benzyl-6-deoxy-1-thio-α-L-mannopyranoside 
• 5158-64-5 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl bromide 
• 125590-93-4 2,3-di-O-acetyl-1,2-O-(1-ethoxyethylidene)-β-L-rhamnopyranose 
• 245450-63-9 2,3-di-O-benzyl-1,2-O-(1-ethoxyethylidene)-β-L-rhamnopyranose 
• 1431974-50-3 C₁₀H₁₈O₆ 
• 117249-17-9 3,4-di-O-benzyl-L-rhamnal 
• 100-39-0 benzyl bromide 
• 106988-69-6 (2S,3S,4S)-4-(benzyloxy)-2-methyl-3,4-dihydro-2H-pyran-3-ol 

Downstream Products

• 872333-43-2 6-methoxy-6-oxohexyl 3,4-di-O-benzyl-2-O-(2,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl)-6-deoxy-β-L-mannopyranoside 
• 872333-42-1 6-(benzyloxy)-6-oxohexyl 2-O-[3-O-acetyl-2,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl]-3,4-di-O-benzyl-6-deoxy-β-L-mannopyranoside 
• 872333-45-4 6-methoxy-6-oxohexyl O-2,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl-(1->3)-O-2,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl-(1->2)-3,4-di-O-benzyl-6-deoxy-β-L-mannopyranoside 
• 872333-44-3 6-methoxy-6-oxohexyl O-3-O-acetyl-2,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl-(1->3)-O-2,4-di-O-benzyl-6-deoxy-α-L-mannopyranosyl-(1->2)-3,4-di-O-benzyl-6-deoxy-β-L-mannopyranoside 
• 73983-19-4 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-L-mannopyranose 
• 73983-20-7 1,2-di-O-acetyl-3,4-di-O-benzyl-β-L-rhamnopyranose 
• 76251-65-5 cyclohexyl 3,4-di-O-benzyl-2-O-(methylsulfonyl)-α-L-rhamnopyranoside 
• 76251-66-6 cyclohexyl 3,4-di-O-benzyl-2-O-(methylsulfonyl)-β-L-rhamnopyranoside 
• 76251-62-2 Toluene-4-sulfonic acid (2S,3R,4R,5S,6S)-4,5-bis-benzyloxy-3-methanesulfonyloxy-6-methyl-tetrahydro-pyran-2-yl ester 
• 154779-60-9 1,2-anhydro-3,4-di-O-benzyl-6-deoxy-α-L-glucopyranose 
• 76251-60-0 3,4-di-O-benzyl-2-O-(methylsulfonyl)-L-rhamnopyranosyl-α-chloride 
• 76251-61-1 3,4-di-O-benzyl-2-O-(methylsulfonyl)-L-rhamnopyranosyl-β-chloride 
• 872333-41-0 6-(benzyloxy)-6-oxohexyl 3,4-di-O-benzyl-6-deoxy-β-L-mannopyranoside 

Relevant academic research and scientific papers

C-Glycoside D-galacturonates suitable as glycosyl acceptors for the synthesis of allyl C-homo- and rhamno-galacturonan modules

Methyl 2,3-di-O-benzyl-1-deoxy-1-(prop-2-enyl)-α-D- galactopyranuronate and benzyl 2,3-di-Obenzyl- 1-deoxy-1-(prop-2-enyl)-α- D-galactopyranuronate were prepared as glycosyl acceptors. The glycosyl donors benzyl 4-O-acetyl-2,3-di-O-benzyl-1-(trichloroacet

Studies towards a conjugate vaccine for anthrax: Synthesis of the tetrasaccharide side chain of the Bacillus anthracis exosporium

The first synthesis of β-L-glycoside 17 of the tetrasaccharide β-Ant-(1 → 3)-α-L-Rhap-(1 → 3)-α-L-Rhap-(1 → 2)-L-Rhap is described (Schemes 1-3). Its spacer can be functionalized to make it amenable to conjugation to proteins by different conjugation meth

A new method for the stereoselective synthesis of α- and β-glycosylamines using the Burgess reagent

Although glycosylamines constitute an important group of carbohydrates from the standpoint of biology and medicine, methods for their synthesis typically lack substrate generality and/or result in variable stereoselectivity, especially in complex contexts

Synthesis of β-D-Mannopyranosides and β-L-Rhamnopyranosides by Glycosidation at C-1

A stereoselective synthesis of β-D-mannopyranosides and β-L-rhamnopyranosides has been achieved by glycosidation at C-1.Treatment of the 1-O-tosyl derivative 2 with 1 equiv of methanol in acetonitrile gave methyl 3,4,6-tri-O-benzyl-2-O-(methylsulfonyl)-β-