142452-45-7

Upstream product

• 64-04-0 phenethylamine 
• 1439-07-2 trans-Stilbene oxide 
• 1564-19-8 N-(2-Phenethyl)-α-cyanobenzylamine 
• 100-52-7 benzaldehyde 
• 122-78-1 phenylacetaldehyde 
• 530-36-9 2-amino-1,2-diphenylethanol 
• 142452-50-4 2-Benzyl-4,5-diphenyl-oxazolidine 

Relevant academic research and scientific papers

One-pot synthesis of trisubstituted 1,2-amino alcohols from deprotonated α-amino nitriles

A short synthesis of N,1,2-trisubstituted vicinal amino alcohols by 1,2-addition of deprotonated N-monosubstituted α-amino nitriles to aldehydes and subsequent one-pot reduction of the intermediates with borane-THF is described. This procedure leads to the predominant formation of the anti-configured products. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Facile Preparation of Some Highly Hindered Chiral 1,2-Diphenyl-2-(N-monoalkyl)amino Alcohols and N-Benzylbornamine

The preparation of some novel chiral 1,2-diphenyl-2-(N-monoalkyl)amino alcohols by a facile one-pot procedure and the synthesis of N-benzylbornamine by a reduction process are described herein.