209474-75-9

Upstream product

• 98847-00-8 9-<(2H-tetrahydropyran-2-yl)oxy>nonan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 3937-56-2 1,9-Nonanediol 
• 110-87-2 3,4-dihydro-2H-pyran 

Downstream Products

• 1283115-95-6 C₂₉H₄₁O₇P 
• 1283115-96-7 C₃₇H₅₇O₇P 
• 1283115-86-5 C₂₅H₄₂O₆S 
• 1333498-78-4 C₃₄H₅₁O₈P 
• 1333498-87-5 C₄₂H₆₇O₈P 
• 1333502-84-3 C₂₉H₄₃O₇P 
• 1333502-86-5 C₃₇H₅₉O₇P 
• 230966-24-2 (10RS,13S)-13-methyl-10-phenylsulfonyl-1-(tetrahydropyran-2-yl)oxyheptacosane 
• 230966-23-1 (10RS,13R)-13-methyl-10-phenylsulfonyl-1-(tetrahydropyran-2-yl)oxyheptacosane 

Relevant academic research and scientific papers

Z-selective intramolecular Horner-Wadsworth-Emmons reaction for the synthesis of macrocyclic alkenes

The Z-selective intramolecular Horner-Wadsworth-Emmons reaction of the substrates 7-12 (RO)2P(O)CHR′CO2Et (R′ = (CH2)nCHO) (R = Ph or o-tBuC6H4) gives the 13-18-membered cyclic alkenes selectively (up to Z:E = 97:3) in good yields using NaH in THF under high dilution conditions.

Pheromone synthesis, CXCIV. - Synthesis of the enantiomers of (Z)-21- methyl-8-pentatriacontene, the major component of the female-produced contact sex pheromone of the yellow-spotted longicorn beetle, Psacothea hilaris

Both the enantiomers of (Z)-21-methyl-8-pentatriacontene (1), the major component of the female-produced contact sex pheromone of the yellow-spotted longicorn beetle (Psacothea hilaris), were synthesized by starting from the enantiomers of citronellol (2).