36667-55-7

Upstream product

• 1445-91-6 (S)-1-phenylethanol 
• 16433-43-5 (R)-4-phenylpentanoic acid 
• 36617-82-0 (-)-(R)-N,N-dimethyl-4-phenylpentanamide 
• 36617-85-3 (-)-R-N,N-Dimethyl-4-phenylpentylamin 
• 36617-72-8 (-)-(R)-1-Chlor-2-phenyl-butan 
• 2031-46-1 (R)-3-phenylbutanol 
• 772-14-5 (R)-3-phenylbutyric acid 
• 35010-24-3 (-)-(R)-2-phenyl-pentanoic acid methyl ester 
• 172424-30-5 (R)-2-phenylpentan-1-ol 
• 130-95-0 Quinine 
• 1459-15-0 (R)-1-chloro-1-phenylethane 
• 5676-32-4 α-n-propylstyrene 
• 107773-77-3 toluene-4-sulfonic acid-((R)-2-phenyl-pentyl ester) 
• 30273-14-4 4-((R)-1-methyl-butyl)-aniline 

Downstream Products

• 1196-58-3 (1-ethylpropyl)benzene 
• 71-43-2 benzene 

Relevant academic research and scientific papers

Synthesis of (R)-2-diphenylphosphino-2′-diphenylphosphinomethyl-1,1′-binaphthyl and its use for asymmetric hydrogenation of α-alkylstyrenes

A new chiral bisphosphine ligand ((R)-2-diphenylphosphino-2′-diphenylphosphinomethyl-1,1′-binaphthyl) was synthesized from enantiomerically pure (R)-1,1′-binaphthalene-2,2′-diol. Rhodium(I) complexes of this bisphosphine ligand have been used as catalysts for asymmetric hydrogenation of α-alkylstyrenes to give the corresponding aromatic hydrocarbons in up to 77% ee.