133699-44-2

Upstream product

• 133699-41-9 (2R,6S)-2,6,9-trimethyldecanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 133699-32-8 (2S,3RS,6R)-2.6.9-trimethyl-3-(phenylsulfonyl)decyl tetrahydropyranyl ether 
• 133699-37-3 (R)-3,6-dimethylheptyl tosylate 
• 133774-43-3 (2R,6S)-2,6,9-trimethyldecyl tetrahydropyranyl ether 
• 133699-35-1 (R)-3,6-dimethylheptyl iodide 
• 133699-30-6 (R)-3,6-dimethyl-6-heptenyl acetate 
• 133699-34-0 (R)-3,6-dimethyl-1-heptanol 

Relevant academic research and scientific papers

Pheromone Synthesis, CXXXI Synthesis of the Four Stereoisomers of 6,10,13-Trimethyl-1-tetradecanol, Aggregation Pheromone of Predatory Stink Bug, Stiretrus anchorago

The synthesis of the four stereoisomers of 6,10,13-trimethyl-1-tetradecanol (1a), the male-produced aggregation pheromone of the predatory stink bug Stiretrus anchorago, was achieved by starting from (R)-citronellol (2a), methyl (R)- or (S)-3-hydroxy-2-methylpropanoate (10) and 4-chloro-1-butanol (12a). - Key Words: Grignard coupling / Phenyl sulfone, alkylation of / Pheromone, enantiomerically pure / Stiretrus anchorago / 1-Tetradecanol, 6,10,13-trimethyl- / Sulfones