92646-34-9

Upstream product

• 743364-14-9 (+/-)-3-Amino-1.2-diphenyl-propanon-⁽¹⁾ 
• 63471-68-1 α-cyano-α'-hydroxy-bibenzyl 
• 4452-11-3 1,2-diphenylprop-2-en-1-one 
• 108973-75-7 (+/-)-erythro-3-Acetamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 71312-66-8 3-hydroxy-2,3-diphenylpropionitrile 
• 103385-06-4 3-Acetamino-1.2-diphenyl-propanon-⁽¹⁾ 
• 140-29-4 phenylacetonitrile 
• 134-81-6 benzil 
• 92435-53-5 3-chloro-1,2-diphenylpropan-1-one 
• 5623-26-7 α-methylbenzoin 
• 451-40-1 phenyl benzyl ketone 
• 856608-74-7 (+/-)-3-Isopropylidenamino-1.2-diphenyl-propanon-⁽¹⁾ 
• 86387-72-6 phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone 
• 100-46-9 benzylamine 

Downstream Products

• 88783-35-1 opt. inakt. 3-Isopropylidenamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 114381-17-8 (+/-)-erythro-3-Thiobenzamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 114381-17-8 (+/-)-threo-3-Thiobenzamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 18456-33-2 (+/-)-threo-3-Dimethylamino-1,2-diphenyl-propanol-⁽¹⁾ 
• 102313-61-1 (+/-)-erythro-N-<3-Hydroxy-2,3-diphenyl-propyl>-benzamidin 

Relevant academic research and scientific papers

Synthesis of a potent wide-spectrum serotonin-, norepinephrine-, dopamine-reuptake inhibitor (SNDRI) and a species-selective dopamine-reuptake inhibitor based on the gamma-amino alcohol functional group

A series of gamma-amino alcohols were synthesized and screened for reuptake inhibition and noncompetitive NMDA antagonism. Compound (±)-3f simultaneously and potently inhibits reuptake of 5-HT, NE, and DA, representing a potential wide-spectrum reuptake inhibitor antidepressant. In addition, comparative rat and human studies uncovered a species-selective DA reuptake inhibitor (±)-2e, K(D)(hDAT)/K(D)(rDAT) = 97.

Syntheses of amino nitrones. Potential intramolecular traps for radical intermediates in monoamine oxidase-catalyzed reactions

Monoamine oxidase (MAO) is a flavin-dependent enzyme that catalyzes the oxidative deamination of a variety of amine neurotransmitters and toxic amines. Although there have been several studies that support the intermediacy of an amine radical cation and a

Anti-Selective Aldol Reaction of Benzylic Nitriles and Synthesis of γ-Amino Alcohols

The stereochemistry of the aldol reaction of seven benzylic nitriles 1a-g and four aldehydes 2-5 has been studied.In all cases studied the reaction is anti-selective.Good to excellent selectivity (10:1 -> 20:1) can be obtained if aldehydes with bulky secondary or tertiary substituents are used.The resulting aldols 6-9 are easily transformed to the corresponding γ-amino alcohols 12-15, which may possess useful antidepressant activity.