159249-18-0

Upstream product

• 35132-20-8 (R,R)-1,2-diphenylethylenediamine 
• 67-64-1 acetone 

Downstream Products

• 171822-04-1 (4R,5R)-1,3-Diisopropyl-4,5-diphenyl-imidazolidine-2-carbaldehyde 
• 171822-10-9 Acetic acid (S)-1-((4R,5R)-1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-hexyl ester 
• 915192-97-1 3-benzyloxy-1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-2-methyl-3-phenyl-propan-1-ol 
• 915302-29-3 1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-2-methyl-3-phenyl-propane-1,3-diol 
• 915192-95-9 1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-2-methyl-3-phenyl-propane-1,3-diol 
• 915302-31-7 1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-2-methyl-3-phenyl-propane-1,3-diol 
• 915302-27-1 1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one 
• 915192-94-8 1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one 
• 915302-28-2 1-(1,3-diisopropyl-4,5-diphenyl-imidazolidin-2-yl)-3-hydroxy-2-methyl-3-phenyl-propan-1-one 

Relevant academic research and scientific papers

Asymmetric Catalytic Reduction of Carbonyl Compounds Using C2 Symmetric Diamines as Chiral Ligands

The catalytic asymmetric reduction of prochiral ketones by hydride transfer using various C2 symmetric chiral diamines as ligands and rhodium complexes is studied.Kinetic studies show an increase of the enantiomeric excess with the conversion.