149598-04-9

Upstream product

• 149632-19-9 (1S,2R)-(+)-1-cyclohexyl-2,3-epoxy-1-phenyl-1-propanol 
• 78620-93-6 (+/-)-3-cyclohexyl-3-hydroxy-3-phenylpropanoic acid 
• 462093-58-9 (2E)-3-cyclohexyl-3-phenylprop-2-en-1-ol 
• 26482-37-1 (+/-)-3-cyclohexyl-3-hydroxy-3-phenylpropanoic acid ethyl ester 
• 712-50-5 Cyclohexyl phenyl ketone 
• 149597-99-9 (S)-(+)-3-cyclohexyl-3-hydroxy-3-phenylpropyl 4-nitrobenzenesulfonate 
• 114531-89-4 (S)-(-)-3-cyclohexyl-3-hydroxy-3-phenylpropanoic acid 
• 114499-81-9 (S)-(+)-1-cyclohexyl-1-phenyl-1,3-propanediol 
• 135033-61-3 (S)-(+)-1-cyclohexyl-1-phenyl-2-propen-1-ol 

Downstream Products

• 149598-05-0 (2S,3S)-(+)-3-cyclohexyl-2,3-epoxy-3-phenylpropyl 4-nitrobenzenesulfonate 

Relevant academic research and scientific papers

Enantioselective iminium-catalyzed epoxidation of hindered trisubstituted allylic alcohols

The reactivity of diastereomeric biaryl iminium cations made of a (Ra)-5,5′,6,6′,7,7′,8,8′-octahydrobinaphthyl core and exocyclic appendages derived from (S)- or (R)-3,3-dimethylbutyl-2-amine was investigated with hindered trisubstituted allylic alcohols

Anticholinergic Agents 3. Synthesis and Configurational Assignment of the Four Stereoisomers of 1-Cyclohexyl-1,2-epoxy-1-phenyl-3-piperidinylpropane

The four stereoisomers of 1-cyclohexyl-1,2-epoxy-1-phenyl-3-piperidylpropane which are putative muscarinic antagonists, have been synthesised employing (S)- and (R)-1-cyclohexyl-1-phenyl-1,3-propanediol as chiral synthons.The relative configuration of the