106022-67-7

Upstream product

• 28715-21-1 (R)-3-hydroxytetradecanoic acid 
• 111247-06-4 benzyl 2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-β-D-glucopyranoside 
• 112475-20-4 (3R)-3-tetradecanoyloxytetradecanoic acid phenacyl ester 
• 102794-17-2 benzyl 2-amino-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside 
• 87357-65-1 (3R)-3-hydroxytetradecanoic acid phenacyl ester 
• 87357-76-4 (R)-3-(dodecanoyloxy)tetradecanoic acid 
• 111247-07-5 benzyl 2-deoxy-4,6-O-isopropylidene-2-<(3R)-3-tetradecanoyloxytetradecanamido>-3-O-<(3R)-3-tetradecanoyloxytetradecanoyl>-β-D-glucopyranoside 

Downstream Products

• 111247-08-6 (R)-3-Tetradecanoyloxy-tetradecanoic acid (2R,3R,4R,5S,6R)-2-benzyloxy-5-hydroxy-3-((R)-3-tetradecanoyloxy-tetradecanoylamino)-6-trityloxymethyl-tetrahydro-pyran-4-yl ester 
• 117779-94-9 benzyl 6-O-tert-butyldimethylsilyl-2-deoxy-2-<(R)-3-tetradecanoyloxytetradecanamido>-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-β-D-glucopyranoside 
• 113783-72-5 benzyl 2-deoxy-2-<(R)-3-tetradecanoyloxytetradecanamido>-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-(benzyl-5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-β-D-galacto-2-nonulopyranosyl)-β-D-glucopyranoside 
• 113783-72-5 benzyl 2-deoxy-2-<(R)-3-tetradecanoyloxytetradecanamido>-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-(benzyl-5-acetamido-4,7,8,9-tetra-O-acetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosyl)-β-D-glucopyranoside 
• 118190-52-6 benzyl 2-deoxy-2-<(R)-3-tetradecanoyloxytetradecanamido>-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-6-O-(benzyl-5-acetamido-4,7,8,9-tetra-O-monochloroacetyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosyl)-β-D-glucopyranoside 
• 106022-69-9 C₉₂H₁₄₉NO₂₂ 
• 106022-69-9 benzyl 6-O-(benzyl 4,5,7,8-tetra-O-acetyl-3-deoxy-α-D-manno-2-octulopyranosylonate)-2-deoxy-2-<(R)-3-tetradecnanoyloxytetradecanamido>-3-O-<(R)-3-tetradecanoyloxytetradecanoyl>-β-D-glucopyranoside 

Relevant academic research and scientific papers

SYNTHESIS OF THE OPTICALLY ACTIVE 4-O-PHOSPHONO-D-GLUCOSAMINE DERIVATIVES RELATED TO THE NONREDUCING-SUGAR SUBUNIT OF BACTERIAL LIPID A

The optically active lipid A-subunit homologs named GLA-46, GLA-47, GLA-59, and GLA-60 have been synthesized stepwise by successive acylation at N-2 and O-3 of benzyl 2-amino-2-deoxy-4,6-O-isopropylidene-β-D-glucopyranoside with the 3-O-(benzyloxy)methyl