134750-75-7

Upstream product

• 134780-72-6 (1R,2S)-2-Methoxymethoxy-1-phenyl-cyclohexanol 
• 17540-15-7 (1R,2S)-1-phenyl-1,2-cyclohexanediol 
• 134750-74-6 C₃₂H₄₆O₇ 
• 134750-73-5 (-)-cis-2-(Methoxymethoxy)-1-phenylcyclohexanol 
• 23313-43-1 cis-acetic acid 2-hydroxy-2-phenyl-cyclohexyl ester 
• 4912-59-8 1-phenyl-1,2-cyclohexanediol 
• 4912-59-8 (1R,2R)-1-phenyl-1,2-cyclohexanediol 
• 134750-74-6 (+)-2,2'-Oxydiethylenedioxybis(2-phenylcyclophenylethyl methyl ether) 

Downstream Products

• 167356-43-6 (4R,9R,17R,22R)-9,17-diphenyl-27,29-dimethoxy-3,10,13,16,23-pentaoxatetracyclo<23.3.1.0^4,9.0^17,22>nonacosa-1(28),25(29),26(27)-triene 

Relevant academic research and scientific papers

Preparation and Enantiomer Recognition Behaviour of Crown Ethers containing cis-1-Phenylcyclohexane-1,2-diol and trans-1,2-Diphenylcyclohexane-1,2-diol as a Chiral Subunit

Pig liver esterase-mediated hydrolysis of (+/-)-cis-2-acetoxy-1-phenylcyclohexanol 5 gave (+)-cis-1-phenylcyclohexane-1,2-diol 4 of high optical purity, from which (-)-trans-1,2-diphenylcyclohexane-1,2-diol 8 has been prepared.Using these diols (+)-4 and

Synthesis and Enantiomer Recognition of Crown Ethers containing Cyclohexane-1,2-diol Derivatives as the Chiral Centre and Enzymatic Resolution of the Chiral Subunits

The cyclohexane-1,2-diol derivatives 1 and 4 of high optical purity have been prepared by enantioselective hydrolysis of their acetates (+/-)-2 and (+/-)-5 using pig liver esterase.The enantiomer recognition behaviour of the chiral crown ethers 11, 14, 15