299926-66-2

Upstream product

• 299430-21-0 (2R,4RS,6R)-1-tert-butyldimethylsilyloxy-2,6-dimethyl-4-phenylsulfonyl-7-tetrahydropyranyloxyheptane 
• 299430-20-9 (R)-2-methyl-4-phenylsulfonyl-1-tetrahydropyranyloxybutane 
• 250359-29-6 (R)-3-methyl-4-tetrahydropyranyloxybutyl tosylate 
• 170717-85-8 (R)-3-Methyl-4-<(tetrahydropyranyl)oxy>butan-1-ol 
• 299430-07-2 (R)-3-Methyl-4-<(tetrahydropyranyl)oxy>-1-iodobutane 
• 299430-22-1 (2R,6R)-1-tert-butyldimethylsilyloxy-2,6-dimethyl-7-tetrahydropyranyloxyheptane 
• 98-59-9 p-toluenesulfonyl chloride 
• 299430-23-2 (2R,6R)-2,6-dimethyl-7-tetrahydropyranyloxy-1-heptanol 

Downstream Products

• 375844-71-6 (2R,6S)-2,6-dimethyl-1-tetrahydropyranyloxy-17-octadecene 
• 299430-16-3 (2S,6R)-2,6-dimethylpentadecyl tosylate 
• 299430-26-5 (2R,6S)-2,6-dimethylpentadecyl tosylate 
• 299430-29-8 (2R,6S)-2,6-dimethyltetradecyl tosylate 
• 299430-13-0 (2R,6S)-2,6-dimethyl-1-decyl tosylate 
• 108195-53-5 (5S,9S)-5,9-Dimethylheptadecane 
• 375844-75-0 (2R,6S)-2,6-dimethyl-17-octadecenyl p-toluenesulfonate 

Relevant academic research and scientific papers

Synthesis of all the stereoisomers of 13,17-dimethyl-1-tritriacontene and 13,17-dimethyl-1-pentatriacontene, the contact sex pheromone components of the female tsetse fly, Glossina austeni

All of the stereoisomers of 13,17-dimethyl-1-tritriacontene (1) and 13,17-dimethyl-1-pentatriacontene (2), the contact sex pheromone components of the female tsetse fly (Glossina austeni), were synthesized starting from the enantiomers of the protected syn- and anti-2,6-dimethylheptane-1,7-diol (3), which were prepared from the enantiomers of methyl 3-hydroxy-2-methylpropanoate (4) and methyl phenyl sulfone (5).

Pheromone synthesis, CCIS synthesis of the enantiomers of anti-2,6-dimethylheptane-1,7-diol monotetrahydropyranyl ether and their conversion into the enantiomers of the sex pheromone components of the apple leafminer, Lyonetia prunifoliella

Both (2R,6R)- and (2S,6S)-isomers of 2,6-dimethylheptane-1,7-diol monotetrahydropyranyl ether (4) were synthesized, and converted into the enantiomers of anti-10,14-dimethyl-1-octadecene (1), anti-5,9-dimethyloctadecane (2) and anti-5,9-dimethylheptadecane (3), the sex pheromone components of the apple leafminer (Lyonetia prunifoliella).