104873-95-2Relevant academic research and scientific papers
NADH MODELS XXI. STEREOSELECTIVE REDUCTION OF CHIRAL IMINES WITH HANTZSCH ESTER
van Niel, Johannes C.G.,Pandit, Upendra K.
, p. 6005 - 6012 (2007/10/02)
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
