1446944-41-7

Upstream product

• 1117-61-9 (3R)-citronellol 
• 67214-54-4 (R)-citronellyl tosylate 
• 55816-07-4 (R)-3,7-dimethyl-6-octenyl iodide 
• 173913-23-0 (R)-5,9-dimethyl-1-(trimethylsilyl)-dec-8-en-1-yne 
• 5949-05-3 (S)-Citronellal 
• 79015-77-3 (R)-(+)-5,9-dimethyldec-8-en-1-yne 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 100-44-7 benzyl chloride 
• 629-11-8 1,6-hexanediol 
• 71126-73-3 6-benzyloxyhexan-1-ol 
• 41144-01-8 (S)-3,7-dimethyl-6-octenyl tosylate 
• 126519-80-0 6-benzyloxyhexyl 4-methylbenzenesulfonate 
• 97510-97-9 (((6-iodohexyl)oxy)methyl)benzene 
• 145678-85-9 (S)-8-iodo-2,6-dimethyloct-2-ene 

Downstream Products

• 1446944-44-0 (S)-11-methylpentadecyl tosylate 
• 1446944-42-8 (S)-1-benzyloxy-11-methyl-14-pentadecen-7-yne 

Relevant academic research and scientific papers

Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal

The enantiomers of citronellal were converted to all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2- octadecanone, the female-produced sex pheromone components of the Lyclene dharma dharma moth. Three wellestablished procedures, the Wittig reaction, alkylation of alkynes, and acetoacetic ester synthesis, were employed for the carbon-carbon bond formation to connect the building blocks.