86657-56-9

Upstream product

• 13266-02-9 n-tridecyltriphenylphosphonium bromide 
• 765-09-3 1-bromotridecane 
• 603-35-0 triphenylphosphine 

Downstream Products

• 1204527-69-4 C₅₀H₇₁N₃O₉ 
• 1384423-78-2 1-O-(α-D-galactopyranosyl)-2-(11-(4-phenoxyphenyl)undecanoyl)amino-D-ribo-1,3,4-octadecanetriol 
• 600168-66-9 3,4-O-isopropylidene-1-O-triphenylmethyl-D-arabino-octadecane-1,2,3,4-tetraol 
• 600168-67-0 2-azido-3,4-O-isopropylidene-1-O-triphenylmethyl-D-arabino-octadecane-1,3,4-triol 
• 158021-47-7 (2S,3S,4R)-1-(α-D-glucopyranosyloxy)-2-hexacosanoylamino-3,4-octadecanediol 
• 160280-62-6 3,4-O-isopropylidene-1-O-triphenylmethyl-D-arabino-octadec-5-en-1,2,3,4-tetraol 
• 155332-03-9 (Z)-(S)-1-Benzyloxy-octadec-5-en-2-ol 

Relevant academic research and scientific papers

HUMAN iNKT CELL ACTIVATION USING GLYCOLIPIDS

Glycosphingolipids (GSLs) compositions and methods for iNKT-independent induction of chemokines are disclosed.

Synthesis of [13]-membered macrocyclic stevastelins via a transesterification reaction as the key step: Total synthesis of stevastelin C3

A new synthesis of stevastelin C3 (3), a [13]-membered ring component of the stevastelin family, whose structure was recently revised, is reported. Initially, a macrolactonization approach was attempted to generate the [13]-membered macrolactone but this

Ozonolysis of alkenes and study of the reactions of polyfunctional compounds. XXXIV. Regiospecific synthesis of diastereomeric (+/-)-7,11-dimethyloctadecane and (+/-)-17,21-dimethylheptatriacontane

(Z,Z)-1,5-Dimethyl-1,5-cyclooctadiene upon partial ozonolysis with subsequent two-step olefination of the isoprenoid ketoaldehyde formed gives 8,12-dimethyl-4,8,12-octadecatriene and 17,21-dimethyl-13,17,21-heptatriacontatriene, whose hexahydro derivative