119471-50-0

Upstream product

• 19525-80-5 (3R)-3-hydroxydecanoic acid 
• 70-11-1 α-bromoacetophenone 

Downstream Products

• 119471-51-1 phenacyl (3R)-3-levulinoyloxydecanoate 
• 202824-33-7 (R)-3-[(2R,3R,4aS,5S,7R,8R,8aR)-2,3-Dimethoxy-2,3,5-trimethyl-8-((2S,3R,4R,5S,6S)-3,4,5-tris-benzyloxy-6-methyl-tetrahydro-pyran-2-yloxy)-hexahydro-pyrano[3,4-b][1,4]dioxin-7-yloxy]-decanoic acid 2-oxo-2-phenyl-ethyl ester 
• 202824-35-9 C₆₇H₉₂O₁₆ 
• 206272-07-3 phrnacyl (R)-3-(benzyloxy)decanoate 
• 19525-83-8 (R)-3-(benzyloxy)decanoic acid 
• 206272-23-3 C₆₀H₇₃Cl₆N₂O₁₈P 
• 206272-22-2 C₆₄H₇₇Cl₆N₂O₂₀P 
• 119471-55-5 methyl (3R)-3-<(3R)-3-(3,4-di-O-benzyl-2-O-chloroacetyl-α-L-rhamnopyranosyloxy)decanoyloxy>decanoate 

Relevant academic research and scientific papers

Divergent synthesis and biological activities of lipid A analogues of shorter acyl chains

Novel lipid A analogues which possess four (R)-3-hydroxyacyl moieties of shorter chain length were synthesized via new divergent synthetic route in order to clarify the effect of the chain length of acyl groups to the biological activity: a disaccharide 4

SYNTHESIS OF METHYL 3-DECANOATE, A RHAMNOLIPID FROM Pseudomonas aeruginosa

Condensation of (3R)-3-levulinoyloxydecanoic acid (16) with methyl (3R)-3-hydroxydecanoate (13) afforded, after selective delevulinoylation, methyl (3R)-3-decanoate (18).Boron trifluoride etherate-promoted coupling of 3,4-di-O-b