114760-75-7

Upstream product

• 114817-16-2 (1S,3R)-3-Methyl-1-phenyl-cyclohexylamine; compound with (E)-but-2-enedioic acid 
• 114693-38-8 N-(1(S)-phenyl-3(R)-methylcyclohexyl)-5-chlorovaleramide 
• 114693-39-9 N-(1(S)-phenyl-3(R)-methylcyclohexyl)-δ-valerolactam 

Relevant academic research and scientific papers

Synthesis, pharmacological action, and receptor binding affinity of the enantiomeric 1-(1-phenyl-3-methylcyclohexyl)piperidines

The cis and trans enantiomers of the 1-(1-phenyl-3-methylcyclohexyl)piperidines were prepared from either 3(R)- or 3(S)-methylcyclohexanone through the Bruylents reaction or a modified azide route, respectively. Separation of the intermediate amines (5 an