875799-03-4

Upstream product

• 146953-71-1 (S)-3-phenyl-2-trifluoromethanesulfonyloxy-propionic acid benzyl ester 
• 221344-09-8 (1S,2S,4R,5S)-4,5-Dihydroxy-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 7622-21-1 benzyl-(S)-(-)-2-hydroxy-3-phenylpropionate 

Downstream Products

• 934482-16-3 (1S,2S,4R,5S)-4-((R)-1-benzyloxycarbonyl-2-phenyl-ethoxy)-5-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 934482-20-9 (1S,2S,4R,5S)-4-((R)-1-carboxy-2-phenyl-ethoxy)-5-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 934482-21-0 (1S,2S,4R,5S)-4-((R)-1-carboxy-2-phenyl-ethoxy)-5-(2-acetamido-3,4,6-O-triacetyl-2-deoxy-β-D-glucopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 934482-22-1 (1S,2S,4S,5R)-4-((R)-1-carboxy-2-phenyl-ethoxy)-5-(2-acetamido-4,6-O-dipivaloyl-3-O-acetyl-2-deoxy-β-D-galactopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 934482-18-5 (1S,2S,4S,5R)-4-((R)-1-benzyloxycarbonyl-2-phenyl-ethoxy)-5-(2-acetamido-4,6-O-dipivaloyl-3-O-acetyl-2-deoxy-β-D-galactopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 934482-17-4 (1S,2S,4R,5S)-4-((R)-1-benzyloxycarbonyl-2-phenyl-ethoxy)-5-(2-acetamido-3,4,6-O-triacetyl-2-deoxy-β-D-glucopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 875801-24-4 4-[5-acetoxy-6-acetoxymethyl-3-acetylamino-4-(3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy]-5-(1-benzyloxycarbonyl-2-phenyl-ethoxy)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 
• 934482-15-2 (1S,2S,4R,5S)-4-((R)-1-benzyloxycarbonyl-2-phenyl-ethoxy)-5-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-cyclohexane-1,2-dicarboxylic acid di-tert-butyl ester 

Relevant academic research and scientific papers

Intramolecular carbohydrate-aromatic interaction and intermolecular van der Waals interactions enhance the molecular recognition ability of GM1 glycomimetics for cholera toxin

The design and synthesis of two GM1 glycomimetics, 6 and 7, and analysis of their conformation in the free state and when complexed to cholera toxin is described. These compounds, which include an (R)-cyclohexyllactic acid and an (R)-phenyllactic acid fra

A simple model system for the study of carbohydrate-aromatic interactions

A molecular scaffold was identified which enables the establishment of intramolecular interactions between a monosaccharide and a nearby phenyl ring. A group of molecules containing four different monosaccharides (glucose, galactose, N-acetyl-glucosamine,

Ganglioside GM1 mimics: Lipophilic substituents improve affinity for cholera toxin

Ganglioside GM1 mimics including (R)-2-hydroxy-3-cyclohexylpropionic acid or (R)-2-hydroxy-3-phenylpropionic acid as replacements for NeuAc are stronger cholera toxin binders than the parent ligand 2, which includes (R)-2-hydroxy-propionic acid.