548486-16-4

Upstream product

• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 100-52-7 benzaldehyde 
• 548486-24-4 2-(4-bromophenyl)-2-oxoethyl (R)-3-benzyloxyhexadecanoate 

Downstream Products

• 775341-79-2 4-oxo-pentanoic acid 1-({6-[3-benzyloxy-5-(3-benzyloxy-hexadecanoylamino)-4-hydroxy-6-phenylsulfanyl-tetrahydro-pyran-2-ylmethoxy]-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-ylcarbamoyl}-methyl)-tetradecyl ester 
• 1080017-77-1 dimethylthexylsilyl 6-O-{4,6-O-benzylidene-2-deoxy-2-[(R)-3-hexadecanoyloxy-15-methylhexadecanoylamino]-3-O-levulinoyl-β-D-glucopyranosyl}-4-O-benzyl-3-O-[(R)-3-(benzyloxy)hexadecanoyl]-2-[(R)-3-benzyloxy-15-methylhexadecanoylamino]-2-deoxy-β-D-glucopyranoside 
• 548486-17-5 phenyl 4-O-benzyl-6-O-{4,6-O-benzylidene-3-O-[(R)-3-benzyloxy-hexadecanoyl]-2-deoxy-2-[(R)-3-octacosanoyloxy-hexadecan]amido-β-D-glucopyranosyl}-2-[(R)-3-benzyloxy-hexadecan]amido-3-O-[(R)-3-benzyloxy-hexadecanoyl]-2-deoxy-1-thio-α-D-glucopyranoside 

Relevant academic research and scientific papers

Preparation of a lipid A derivative that contains a 27-hydroxyoctacosanoic acid moiety

(Chemical Equation Presented) A general synthetic strategy for long-chain ω-1 hydroxy fatty acids has been developed, which employs as a key reaction step a cross metathesis between ω-unsaturated ester and 3-butene-2-ol. The resulting lipids were used for

Synthesis and biological evaluation of Rhizobium sin-1 lipid A derivatives

A highly convergent strategy for the synthesis of several derivatives of the lipid A of Rhizobium sin-1 has been developed. The approach employed the advanced intermediate 3-O-acetyl-6-O-(3-O-acetyl-4,6-O-benzylidene-2-deoxy-2-phthalimido- β-D-glucopyrano