109430-87-7

Upstream product

• 65017-65-4 (+/-)-2-(3-methoxyphenyl)-1-phenylethylamine 
• 126003-96-1 C₁₇H₂₃NO 
• 115148-64-6 [2-(3-Methoxy-phenyl)-1-phenyl-ethyl]-[(1R,4R)-1,7,7-trimethyl-bicyclo[2.2.1]hept-(2E)-ylidene]-amine 
• 126004-02-2 (1R,2R,5R)-3-[(E)-(S)-2-(3-Methoxy-phenyl)-1-phenyl-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol 

Downstream Products

• 61311-58-8 (+)-2-(3-hydroxyphenyl)-1-phenylethylamine 
• 83540-73-2 3-{(S)-2-[4-(2-Methoxy-phenyl)-piperazin-1-yl]-2-phenyl-ethyl}-phenol 
• 61331-58-6 (+)-1-cyclohexyl-4-<2-(3-hydroxyphenyl)-1-phenylethyl>piperazine 
• 259086-56-1 (S)-(+)-4-cyclohexyl-1-[2-(3-methoxyphenyl)-1-phenylethyl]piperidine 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS VIII: ENANTIONSELECTIVE SYNTHESIS OF (R) OR (S)-α-SUBSTITUTED BENZYLAMINES VIA CHIRAL PINANONE KETIMINE TEMPLATE

An excellent asymmetric synthesis of both (R) and (S)-α-substituted benzylamines in optical purity 90.4 - 99.9percent has been achieved by alkylation of a chiral ketimine, prepared from pinanone and benzylamine.Diastereoselectivity in the alkylation is not 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

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.