82111-33-9

Upstream product

• 69350-13-6 N-benzylidene-(S)-α-methylbenzylamine 
• 100-52-7 benzaldehyde 
• 82032-22-2 N-(Phenylethyl)-1-phenyl-1-benzoylmethylamine hydrochloride 

Downstream Products

• 82087-17-0 (2R, 4S, 5S, 3'R)-(+)-N,N-bis(1-phenylethyl)-1,2-diphenyl-2-aminoethanol 
• 40648-92-8 (R,R)-(+)-bis[alpha-methylbenzyl]amine hydrochloride 
• 82087-14-7 (2R, 4S, 5S, 3'R)-(-)-N-(1-phenylethyl)-2,4,5-triphenyloxazolidine 

Relevant academic research and scientific papers

Zirconium-Mediated Diastereoselective Coupling Reactions of Chiral Aldimine: Remarkable Temperature-Dependence of Chiral Induction

Zr-mediated coupling reactions of aldehyde with chiral aldimine which is derived from benzaldehyde and (R)-phenylglycinol methyl ether showed a remarkable temperature effect on the sense of chiral induction to yield amino alcohol derivatives with high dia

THE STEREOSELECTIVE REDUCTION OF α-AMINODEOXYBENZOIN DERIVATIVES WITH SODIUM BOROHYDRIDE

Total stereoselectivity is observed in the sodium borohydride reduction of α-aminodeoxybenzoins and their hydrochlorides in various hydroxylic solvents.RS-SR isomer (erythro) was the only aminoalcohol obtained.