161905-08-4

Upstream product

• 84237-05-8 (S)-((3,7-dimethyloct-6-enyloxy)methyl)benzene 
• 100-39-0 benzyl bromide 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 

Downstream Products

• 82538-56-5 (S)-(+)-3-methylpentane-1,5-diol 1-benzyl ether 
• 82538-58-7 (3R)-5-(benzyloxy)-3-methylpentanal 
• 161794-89-4 (R)-5-(benzyloxy)-3-methyl-1-(phenylsulfonyl)pentane 
• 161795-01-3 (3S,7S)-3,7-dimethyldecyl tosylate 
• 161795-03-5 (3S,7R)-3,7-dimethyldecyl tosylate 
• 161794-94-1 (3S,7S)-1-(benzyloxy)-3,7-dimethyldecane 
• 162938-42-3 (3S,7R)-1-(benzyloxy)-3,7-dimethyldecane 
• 161794-87-2 (R)-1-(benzyloxy)-5-iodo-3-methylpentane 
• 161794-86-1 (R)-5-(benzyloxy)-3-methylpentyl tosylate 

Relevant academic research and scientific papers

A concise stereoselective formal total synthesis of the cytotoxic macrolide (+)-Neopeltolide via Prins cyclization

A convergent and highly stereoselective formal total synthesis of the naturally occurring, cytotoxic 14-membered macrolide neopeltolide has been achieved via two Prins cyclizations.

Pheromone Synthesis, CLXVII. - Synthesis of All of the Eight Stereoisomers of Methyl 2,6,10-Trimethyltridecanoate, the Male-produced Pheromone of the Stink Bugs, Euschistus heros and E. obscurus

All of the eight possible stereoisomers of methyl 2,6,10-trimethyltridecanoate (1), the male-produced attractant pheromone of the South American soybean pest, Euschistus heros, and that of E. obscurus, are synthesized by starting from the enantiomers of citronellol (2) and methyl 3-hydroxy-2-methylpropanoate (9). - Key Words: Euschistus heros / Euschistus obscurus / Pheromones / Stink bugs / Sulfones, alkylation of / Tridecanoate, methyl 2,6,10-trimethyl-