910541-11-6

Upstream product

• 23190-16-1 (1R,2S)-2-Amino-1,2-diphenylethanol 
• 1148-11-4 N-Benzyloxycarbonyl-L-proline 

Downstream Products

• 529486-25-7 (2S,1'S,2'R)-pyrrolidine-2-carboxylic acid (2-hydroxy-1,2-diphenylethyl)amide 

Relevant academic research and scientific papers

Novel small organic molecules for a highly enantioselective direct aldol reaction

Novel organic molecules containing an l-proline amide moiety and a terminal hydroxyl for catalyzing direct asymmetric aldol reactions of aldehydes in neat acetone are designed and prepared. Catalyst 3d, prepared from l-proline and (1S,2S)-diphenyl-2-amino

Enantioselective conjugate addition of ketones to β-nitrostyrenes catalyzed by 1,2-amino alcohol-derived prolinamides

Various l-prolinamides 14, prepared from l-proline and chiral β-amino alcohols, are active bifunctional catalysts for the direct nitro-Michael addition of ketones to β-nitrostyrenes. In particular, catalyst 14e prepared from l-proline and (1S,2R)-cis-1-am