76251-67-7

Upstream product

• 34212-64-1 methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 74372-90-0 1,2-anhydro-3,4,6-tri-O-benzyl-β-D-mannopyranose 
• 16697-49-7 3,4,6-tri-O-benzyl-1,2-O-(methoxyethylidene)-β-D-mannopyranose 
• 130525-72-3 ethyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside 
• 129163-10-6 methyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-α-D-mannopyranoside 
• 186540-03-4 tert-Butyl-diphenyl-((2R,3R,4S,5S,6S)-3,4,5-tris-benzyloxy-6-methoxy-tetrahydro-pyran-2-ylmethoxy)-silane 
• 131089-34-4 3-O-benzoyl-6-O-(t-butyldiphenyl)silyl-α-D-mannopyranoside 
• 73045-72-4 Benzoic acid (2R,3S,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-2-(toluene-4-sulfonyloxy)-tetrahydro-pyran-3-yl ester 
• 68536-49-2 1,2-di-O-benzoyl-3,4,6-tri-O-benzyl-D-mannopyranose 
• 68536-53-8 2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 
• 65827-59-0 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl chloride 
• 20231-36-1 methyl 6-O-trityl-α-D-mannopyranoside 
• 13242-53-0 acetobromomannose 
• 225924-46-9 1,2-O-<1-(R)-methoxyethylidene>-β-D-mannopyranose 

Downstream Products

• 76251-58-6 methyl 2,3,4-tri-O-benzyl-6-O-(3,4,6-tri-O-benzyl-2-O-(methylsulfonyl)-α-D-mannopyranosyl)-α-D-mannopyranoside 
• 183885-23-6 methyl 2,3,4-tri-O-benzyl-6-O-(2,6-di-O-acetyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside 
• 195875-44-6 methyl 2-O-acetyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-(1→6)-2,3,4-tri-O-benzyl-α-D-mannopyranoside 
• 183885-26-9 methyl 2,3,4-tri-O-benzyl-6-O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-α-D-mannopyranoside 

Relevant academic research and scientific papers

Synthesis and structural investigation of a series of mannose-containing oligosaccharides using mass spectrometry

A series of compounds associated with naturally occurring and biologically relevant glycans consisting of α-mannosides were prepared and analyzed using collision-induced dissociation (CID), energy-resolved mass spectrometry (ERMS), and 1H nucle

Mannose-binding geometry of pradimicin A

Pradimicins (PRMs) and benanomicins are the only family of non-peptidic natural products with lectin-like properties, that is, they recognize D-mannopyranoside (Man) in the presence of Ca2+ ions. Coupled with their unique Man binding ability, t

Synthesis of a tetrasaccharide fragment of cobra venom factor oligosaccharide

Synthesis of a tetrasaccharide fragment, α-L-Fuc-(1→3)-β-D-GlcNAc-(1→2)-α-D-Man-(1→6)-α-D-Man-OMe of the cobra venom factor (CVF) oligosaccharide is described. Copyright (C) 1999 Elsevier Science Ltd.

Synthesis of laminin hexasaccharide analogue

The synthesis of laminin hexasaccharide analogue di-O-[Gal-β-(1→4)-Glc-β]-(1→2)-(1→6)-man-α- (1→6)-man-α-Me derivative (1) was achieved with 1,2-anhydromannopyranose benzyl ether (3) as the key intermediate. Coupling of 3 with methyl 2,3,4-tri-O-benzyl-α-D-mannopyranoside (4) promoted by ZnCl2 gave methyl 2,3,4-tri-O-benzyl-6-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-α-D- mannopyranoside (2a). Selective 6-O-debenzylation of 2b with ZnCl2-Ac2O-HOAc followed by coupling with acetobromolactopyranose afforded 1.

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-