16741-15-4

Upstream product

• 1040165-16-9 benzyl 2-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranoside 
• 10343-13-2 benzyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 141410-43-7 benzyl 6-O-(tert-butyldiphenylsilyl)-β-D-galactopyranoside 
• 141410-44-8 benzyl 6-O-(tert-butyldiphenylsilyl)-3,4-O-isopropylidene-β-D-galactopyranoside 
• 4304-12-5 benzyl β-D-galactopyranoside 
• 100-51-6 benzyl alcohol 
• 693219-38-4 benzyl 2-O-benzoyl-6-O-(tert-butyldiphenylsilyl)-3,4-O-isopropylidene-β-D-galactopyranoside 
• 4163-60-4 β-D-galactose peracetate 

Downstream Products

• 155194-92-6 benzyl 3-O-benzoyl-β-D-galactopyranoside 

Relevant academic research and scientific papers

Acyl group migration and cleavage in selectively protected β-D-galactopyranosides as studied by NMR spectroscopy and kinetic calculations

The migration of acetyl, pivaloyl, and benzoyl protective groups and their relative stabilities at variable pH for a series of β-D-galactopyranoses were studied by NMR spectroscopy. The clockwise and counterclockwise migration rates for the different este

Selectively protected galactose derivatives for the synthesis of branched oligosaccharides

Synthesis and characterization of several new anomerically pure galactose derivatives, based on simple and effective protective group manipulations of benzyl β-D-galactopyranoside, are reported. The monosaccharides described contain selectively protected/deprotected hydroxyl functionalities at their 1,2,3,4- and 6-positions rendering them useful as building blocks for construction of branched oligosaccharides.