339316-75-5

Upstream product

• 76-83-5 trityl chloride 
• 80035-32-1 benzyl 2-deoxy-2-phthalimido-β-D-glucopyranoside 
• 7772-87-4 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl chloride 
• 80035-31-0 benzyl 2-phthalimido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 100-51-6 benzyl alcohol 

Downstream Products

• 339316-76-6 benzyl 2-deoxy-3,4-di-O-benzyl-2-phthalimido-6-O-triphenylmethyl-β-D-glucopyranoside 
• 339316-77-7 benzyl 2-deoxy-3,4-di-O-benzyl-2-phthalimido-β-D-glucopyranoside 
• 339316-78-8 benzyl 2-amino-2-deoxy-3,4-di-O-benzyl-β-D-glucopyranoside 
• 339316-80-2 benzyl 2-deoxy-3,4-di-O-benzyl-2-[(R)-3-tetradecanoyloxytetradecanamido]-β-D-glucopyranoside 
• 85065-35-6 benzyl 2-deoxy-6-O-(2-deoxy-2-phthalimido-β-D-glucopyranosyl)-2-phthalimido-β-D-glucopyranoside 
• 85065-37-8 benzyl 2-<(3R)-3-acetoxytetradecanamido>-6-O-<2-<(3R)-3-acetoxytetradecanamido>-2-deoxy-β-D-glucopyranosyl>-2-deoxy-β-D-glucopyranoside 
• 85071-06-3 benzyl 3,4-di-O-acetyl-2-deoxy-2-phthalimido-6-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-β-D-glucopyranoside 
• 85065-38-9 benzyl 2-<(3R)-3-acetoxytetradecanamido>-6-O-<2-<(3R)-3-acetoxytetradecanamido>-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl>-2-deoxy-β-D-glucopyranoside 
• 85065-40-3 benzyl 2-<(3R)-3-acetoxytetradecanamido>-6-O-<2-<(3R)-3-acetoxytetradecanamido>-3-O-acetyl-2-deoxy-β-D-glucopyranosyl>-3,4-di-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 85065-39-0 benzyl 2-<(3R)-3-acetoxytetradecanamido>-6-O-<2-<(3R)-3-acetoxytetradecanamido>-3-O-acetyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranosyl>-3,4-di-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 85065-41-4 benzyl 2-<(3R)-3-acetoxytetradecanamido>-6-O-<2-<(3R)-3-acetoxytetradecanamido>-3-O-acetyl-6-O-benzyloxymethyl-2-deoxy-β-D-glucopyranosyl>-3,4-di-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 85065-36-7 benzyl 2-amino-6-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-β-D-glucopyranoside 
• 85065-34-5 benzyl 3,4-di-O-acetyl-2-deoxy-2-phthalimido-6-O-triphenylmethyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Monophosphoryl lipid A analogues with varying 3-O-substitution: synthesis and potent adjuvant activity

Structurally defined immunostimulatory adjuvants play important roles in the development of new generation vaccines. Here described are the syntheses of three monophosphoryl lipid A analogues (1-3) with different substitution at 3-O-position of the reduci

Chemistry of Bacterial Endotoxins. Part 2. A Practical Synthesis of 6-O--β-D-glucopyranosyl>-2-deoxy-2--D-glucose

An improved method for the preparation of the phosphorylated disaccharide named in the title, via benzyl 2-amino-6-O-(2-amino-2-deoxy-β-D-glucopyranosyl)-2-deoxy-β-D-glucopyranoside, is described.