98713-57-6

Upstream product

• 68690-78-8 (2E)-1-benzyloxy-6-hydroxy-3,7-dimethyl-2,7-octadiene 
• 118512-37-1 (2E)-1-benzyloxy-7,8-epoxy-6-hydroxy-3,7-dimethyl-2-octene 
• 55776-46-0 (3'E)-3-(5'-benzyloxy-3'-methylpent-3'-enyl)-2,2-dimethyloxirane 
• 70238-26-5 8-benzyloxy-2,6-dimethyl-3-phenylthio-1,6(E)-octadiene 
• 81491-12-5 C₂₃H₂₈O₂S 
• 98713-70-3 ((E)-6-Methanesulfonyl-3,7-dimethyl-octa-2,7-dienyloxymethyl)-benzene 
• 98713-68-9 ((E)-6-Methanesulfinyl-3,7-dimethyl-octa-2,7-dienyloxymethyl)-benzene 
• 118512-38-2 (2E,6,7-anti)-1-benzyloxy-6,7-dihydroxy-3,7-dimethyl-2-octene 
• 52188-73-5 geranyl benzyl ether 

Relevant academic research and scientific papers

CONVENIENT SYNTHETIC ROUTE TO (+)-FARANAL AND (+)-13-NORFARANAL; THE TRAIL PHEROMONE OF PHARAOH'S ANT AND ITS CONGENER

(+)-Faranal 1a, the trail pheromone of Pharaoh's ant, and its congener, (+)-13-norfaranal 1b were synthetized from chiral building block 4 employing diastereoselective carbon-carbon bond formation.The application of crude pig liver esterase enzyme for the

Regio- and Stero-selective Desulphurizative γ-Substitution of α-Substituted β-Methylallyl Sulphoxides and Sulphones with Lithium Dialkylcuprates providing Trisubstituted Olefins

α-Substituted β-methylallyl sulphoxides (2) and sulphones (3) undergo regio- and stereo-selective desulphurizative γ-substitution by the action of lithium dialkylcuprates in ether.The reaction provides a new method for the synthesis of trisubstituted E-ol