65017-66-5

Upstream product

• 115148-64-6 [2-(3-Methoxy-phenyl)-1-phenyl-ethyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine 
• 65017-65-4 (+/-)-2-(3-methoxyphenyl)-1-phenylethylamine 

Downstream Products

• 65017-62-1 (-)-2-(3-hydroxyphenyl)-1-phenylethylamine 
• 83508-79-6 3-{(R)-2-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-2-phenyl-ethyl}-phenol 
• 61311-43-1 (-)-1-cyclohexyl-4-<2-(3-hydroxyphenyl)-1-phenylethyl>piperazine 
• 61311-49-7 (-)-1-cyclohexyl-4-<2-(3-methoxyphenyl)-1-phenylethyl>piperazine 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESES IV: ENANTIOSELECTIVE SYNTHESIS OF (R)-BENZYLIC AMINES VIA ALKYLATION OF D-CAMPHOR KETIMINE

An efficient asymmetric synthesis of (R)-benzylic amines in optical purity 36-90percent had been achieved by alkylation of a chiral ketimine prepared from D-camphor and benzylamine.Diastereoselectivity in the alkylation is dependent on the alkyl halides.

Synthesis and structure-activity relationships of 1-substituted 4-(1,2-diphenylethyl)piperazine derivatives having narcotic agonist and antagonist activity

Racemates and enantiomers of 1-substituted 4-[2-(3-hydroxyphenyl)-1-phenylethyl]piperazine derivatives (3-18) were synthesized, and their analgesic and other pharmacological activities and structure-activity relationships were investigated. The S-(+) enan