top of page
Search

PyBOX Ligands for Asymmetric Catalysis

  • ascensusspec
  • Feb 3
  • 2 min read

Bis(oxazoline) Pyridine Derivatives Have Been Found to be Effective Ligands for Enantioselective Transformations.


PyBOX represents a very important subgroup of bis(oxazoline) (BOX) ligands for asymmetric synthesis. Often in PyBOX two enantiomeric oxazoline rings containing a bulky substituent at the 4- and/or the 5-carbon positions are bridged with the pyridine, forming a C2 symmetrical molecule.


PyBOX is a tridentate “pincer-type” ligand and able to coordinate with a wide range of metals including alkaline earth, d- and f-transition metal atoms. Upon coordination of oxazoline rings through the N atoms, two stereogenic centers are produced near the metal center.  This can influence and control the enantioselective process.


Pyridine-linked bis(oxazoline) ligands were introduced by Hisao Nishiyama in 1989. He used RuCl3/(S)-(i-Pr)-PyBOX (07-0307) catalyst for asymmetric hydrosilylation of ketones [2]. (R)- isomer of (i-Pr)-PyBOX (07-0306) is also highly effective in enantioselective transformations, e.g. Mannich reaction [3].















Today PyBOX ligands exist with a wide range of structural diversities. Metal complexes incorporating Phenyl [(R,R)-Ph-PyBOX (07-0303) (S,S)-Ph-PyBOX (07-0304)], benzyl [(R) 07-0390 and (S) 07-0391 and Indenyl-PYBOX (07-0280) ligands are effective enantioselective catalysts for a variety of asymmetric synthesis.



For more detailed descriptions of each catalytic process please review the corresponding technical note for each item on our website.

 

References:

1.      Chem. Rev., 2006, 106, 3561.; Chem. Rev. 2011, 111, PR284

2.      Organometallics, 1989, 8, 846.

3.      Organometallics, 1991, 10, 500.

4.      Chem. Eur. J., 2013, 19, 10142.

 


Products mentioned in this blog and related products:







 

 

Visit the below links to view related oxazoline literature on our website:

SpinPhox-Ir Catalyst Kit

 
 
bottom of page