New explortion of 2-(Diphenylphosphino)benzaldehyde

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 50777-76-9, you can also check out more blogs about50777-76-9

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.50777-76-9, Name is 2-(Diphenylphosphino)benzaldehyde, molecular formula is C19H15OP. In a Article,once mentioned of 50777-76-9, Product Details of 50777-76-9

Several chiral and unsymmetrical tridentate [NNP]-type ligands with sp 2-N and sp3-N were synthesized from monosulfonamide of (1R, 2R)-1,2-diaminocyclohexane and 2-(diphenylphosphino)benzaldehyde. Their ruthenium(II) complexes have been used in the enantioselective asymmetric hydrogen transfer reduction of acetophenone in 2-propanol with selectivities in the range 14-99% e.e. The good enantioselectivity with the ligands with sp 2-N and sp3-N is believed to be due to formation of hexacoordinated complexes with a 2:1 ligand to metal ratio.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Product Details of 50777-76-9, you can also check out more blogs about50777-76-9

Reference:
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate