104828-82-2

Upstream product

• 104828-81-1 [1-(4-Bromo-phenyl)-eth-(E)-ylidene]-((R)-1-phenyl-ethyl)-amine 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 99-90-1 para-bromoacetophenone 

Relevant academic research and scientific papers

Asymmetric reduction of enantiopure imines with zinc borohydride: Stereoselective synthesis of chiral amines

The first application of zinc borohydride in the reduction of enantiopure imines for the stereoselective preparation of both the enantiomers of secondary amines is described. A possible explanation of the stereoselectivity and of the reaction mechanism is

NADH MODELS XXI. STEREOSELECTIVE REDUCTION OF CHIRAL IMINES WITH HANTZSCH ESTER

Imines derived from p-substituted acetophenones and (+) R-1-phenylethylamine are reduced by 3,5-diethoxycarbonyl-2,6-dimethyl-1,4-dihydro-pyridine (Hantzsch ester), in acetonitrile, in the presence of magnesium perchlorate, to diastereomeric mixtures of t