55439-11-7

Basic information

• Product Name: (2SR,3SR)-2,3-diphenyl-1,2,3,4-tetrahydroquinoline
• Synonyms: (2SR,3SR)-2,3-diphenyl-1,2,3,4-tetrahydroquinoline
• CAS NO: 55439-11-7
• Molecular Weight: 285.389
• Mol File: 55439-11-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2SR,3SR)-2,3-diphenyl-1,2,3,4-tetrahydroquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: (2SR,3SR)-2,3-diphenyl-1,2,3,4-tetrahydroquinoline(55439-11-7)
• EPA Substance Registry System: (2SR,3SR)-2,3-diphenyl-1,2,3,4-tetrahydroquinoline(55439-11-7)

Safety Data

• Hazardous Substances Data: 55439-11-7(Hazardous Substances Data)

Upstream product

• 3193-62-2 N-benzyl-1-phenylethylamine 
• 704200-89-5 2-(2-methoxyphenyl)-1-phenylethan-1-amine 
• 612-16-8 (2-methoxyphenyl)methanol 
• 52289-93-7 o-Methoxybenzyl bromide 
• 100-52-7 benzaldehyde 
• 22514-82-5 2,3-diphenyl quinoline 
• 5344-90-1 2-Aminobenzyl alcohol 
• 451-40-1 phenyl benzyl ketone 
• 64-17-5 ethanol 
• 64-19-7 acetic acid 

Relevant articles and documents

Highly Diastereo- And Enantioselective Ir-Catalyzed Hydrogenation of 2,3-Disubstituted Quinolines with Structurally Fine-Tuned Phosphine-Phosphoramidite Ligands

A highly diastereo- and enantioselective Ir-catalyzed hydrogenation of unfunctionalized 2,3-disubstituted quinolines, especially 3-alkyl-2-arylquinolines, has been realized. The success of this hydrogenation is ascribed to the use of a structurally fine-tuned chiral phosphine-phosphoramidite ligand with a (Sa)-3,3′-dimethyl H8-naphthyl moiety and (Rc)-1-phenylethylamine backbone. The hydrogenation displayed broad functional group tolerance, thus furnishing a wide range of optically active 2,3-disubstituted tetrahydroquinolines in up to 96% ee and with perfect cis-diastereoselectivity.