79705-28-5

Upstream product

• 70056-64-3 3-O-Acetyl-1,6-anhydro-2-O-benzyl-β-D-galactopyranose 
• 76909-65-4 1,6-Anhydro-2-O-benzyl-3,4-O-(1-methoxyethyliden)-β-D-galactopyranose 
• 55287-63-3 1,6-anhydro-2-O-benzyl-β-D-galactopyranose 
• 86861-42-9 1,6-anhydro-2,4-di-O-benzyl-β-D-mannopyranose 
• 100-39-0 benzyl bromide 
• 86900-44-9 1,6-anhydro-4-O-benzyl-β-D-mannopyranose 
• 108-24-7 acetic anhydride 
• 61074-17-7 1,6-Anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 79705-26-3 1,6-Anhydro-2-O-benzyl-3,4-O-(1-ethoxyethyliden)-β-D-galactopyranose 
• 79705-27-4 3-O-Acetyl-1,6-anhydro-2,4-di-O-benzyl-β-D-galactopyranose 
• 86861-43-0 3-O-Acetyl-1,6-anhydro-2,4-di-O-benzyl-β-D-mannopyranose 

Downstream Products

• 79705-38-7 Benzyl-4-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranosyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 
• 79705-37-6 Benzyl-4-O-(3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranosyl)-2,3-O-isopropyliden-α-L-rhamnopyranosid 
• 143826-32-8 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-3-O-levulinoyl-β-D-galactopyranoside 
• 143826-29-3 N-benzyloxycarbonyl-3-aminopropyl 3,6-di-O-acetyl-2,4-di-O-benzyl-β-D-galactopyranoside 
• 143826-33-9 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-3-O-levulinoyl-β-D-galactopyranoside 
• 143826-31-7 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-6-O-tert-butyldimethylsilyl-β-D-galactopyranoside 
• 143826-30-6 N-benzyloxycarbonyl-3-aminopropyl 2,4-di-O-benzyl-β-D-galactopyranoside 
• 114283-82-8 Acetic acid (2R,3S,4S,5R)-2-acetoxymethyl-3,5-bis-benzyloxy-6-hydroxy-tetrahydro-pyran-4-yl ester 
• 79705-30-9 3,6-di-O-acetyl-2,4-di-O-benzyl-α-D-galactopyranosyl bromide 

Relevant academic research and scientific papers

Synthesis of a pentasaccharide and a heptasaccharide corresponding to an ovarian glycoprotein; studies towards glycosylations

The syntheses of pentasaccharide I and heptasaccharide II, which correspond to an ovarian O-glycoprotein, are presented. The protected pentasaccharide 1 was prepared by condensing a trisaccharide donor (18c) with a disaccharide acceptor (8b), while conden

Building Units of Oligosaccharides, XLVII. - Synthesis of Tri- and Tetrasaccharide Sequences of N-Glycoproteins Including a β-D-Mannosidic Linkage

The trisaccharides α-D-Man-p-(1 -> 6)-β-D-Man-p-(1 -> 4)-D-GlcNAc (37) and α-D-Man-p-(1 -> 3)-β-D-Man-p-(1 -> 4)-D-GlcNAc (43) as well as the key tetrasaccharide α-D-Man-p-(1 -> 3)- 6)>-β-D-Man-p-(1 -> 4)-D-GlcNAc (51), which are parts of th

Bausteine von Oligosacchariden, XXIX. Synthese des Trisaccharids aus N-Acetylglucosamin, Galactose und Rhamnose einer O-determinanten Kette von Escherichia coli. Abhaengigkeit der Stereoselektivitaet der α-Glycosidsynthese von der Reaktivitaet des Pyranos

The mercury salt catalysed reaction of substituted α-D-galactosyl halides with the reactive 4-OH groups of the rhamnosides 18 and 19 were studied.The order of reactivity of the halides increases with the following substituents: O-acetyl O-glucosyl O-b