70056-63-2

Upstream product

• 20888-02-2 1,6-anhydro-2,3,4-tri-O-benzyl-β-D-mannopyranose 
• 65556-30-1 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranoside 

Downstream Products

• 87424-13-3 Acetic acid (2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-((2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-2-ylmethyl ester 
• 87424-14-4 Acetic acid (2R,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-((2S,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-methoxy-tetrahydro-pyran-3-yloxy)-tetrahydro-pyran-2-ylmethyl ester 
• 83259-23-8 Benzyl-2-acetamido-4-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-3,6-di-O-benzyl-2-desoxy-α-D-glucopyranosid 
• 105592-47-0 trideuteriomethyl 6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranoside 
• 136944-97-3 8-Ethoxycarbonyloctyl-6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranosid 
• 136944-97-3 8-Ethoxycarbonyloctyl-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranosid 
• 70056-69-8 benzyl 6-O-acetyl-2,3,4-tri-O-benzyl-β-D-mannopyranoside 
• 87735-64-6 p-trifluroacetamidophenyl 2,3-O-isopropylidene-4-O-(2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-α-L-rhamnopyranoside 
• 105072-66-0 4-0-(6-0-acetyl-2,3,4-tri-0-benzyl-β-D-mannopyranosyl)-3-0-allyl-1,6-anhydro-2-azido-2-deoxy-β-D-glucopyranose 
• 186765-90-2 2-acetamido-2-deoxy-4-O-(β-D-mannopyranosyl)-β-D-glucosamine 
• 86861-54-3 1,6-Anhydro-2-azido-3-O-benzyl-4-O-(2,3,4-tri-O-benzyl-β-D-mannopyranosyl)-2-desoxy-β-D-glucopyranose 
• 140182-87-2 8-methoxycarbonyloctyl 6-O-(6-O-acetyl-2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-2,3,4-tri-O-benzyl-β-D-mannopyranoside 
• 140182-88-3 8-methoxycarbonyloctyl 2,3,4-tri-O-benzyl-6-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-β-D-mannopyranoside 
• 136944-98-4 8-methoxycarbonyloctyl 2,3,4-tri-O-benzyl-β-D-mannopyranoside 

Relevant academic research and scientific papers

First total synthesis of a GPI-anchored peptide

A GPI-anchored dipeptide of sperm CD52 antigen was prepared through a convergent synthesis. First, the dipeptide with its C-terminus free and the GPI with its nonreducing end phosphoeth-anolamine bearing a free amino group were synthesized separately. Then, the two building blocks were coupled with use of EDC/HOBt as the condensation reagent. Finally, the GPI-anchored peptide was deprotected to give the target molecule 1.

Synthesis of a tetrasaccharide acceptor for use in the assay of UDP-GlcpNAc:β-D-Galp-(1 → 4)-β-D-GlcpNAc (GlcNAc to Gal) β(1 → 3)-N-acetylglucosaminyltransferase activity and the pentasaccharide product that would be formed by its enzymic glycosylation

The tetrasaccharide β-D-Galp-(1 → 4)-β-D-GlcpNAc-(1 → 6)-α-D-Manp-(1 → 6)-β-D-Manp-OR (2) and the pentasaccharide β-D-GlcpNAc-(1 → 3)-β-D-Galp-(1 → 4)-β-D-GlcpNAc-(1 → 6)-α-D-Manp-(1 → 6)-β-D-Manp-OR (3), where R = (CH2)8COOMe, have

Bausteine von Oligosacchariden, XXX. Neue effektive β-Glycosidsynthese fuer Mannose-Glycoside. Synthesen von Mannose-haltigen Oligosacchariden

A new method was developed for the stereo selective synthesis of oligosaccharides containing a β-linked mannose-unit which were hitherto not available by direct synthesis.The glycoside synthesis is promoted by a silversilicate-catalyst which was precipita