Synthesis of Axially Chiral 2,2'-Bisphosphobiarenes via a Nickel-Catalyzed Asymmetric Ullmann Coupling: General Access to Privileged Chiral Ligands without Optical Resolution

J Am Chem Soc. 2021 Jan 27;143(3):1328-1333. doi: 10.1021/jacs.0c12843. Epub 2021 Jan 13.

Abstract

We report an asymmetric homocoupling of ortho-(iodo)arylphosphine oxides and ortho-(iodo)arylphosphonates resulting in highly enantioenriched axially chiral bisphosphine oxides and bisphosphonates. These products are readily converted to enantioenriched biaryl bisphosphines without need for chiral auxiliaries or optical resolution. This provides a practical route for the development of previously uninvestigated atroposelective biaryl bisphosphine ligands. The conditions have also proven effective for asymmetric dimerization of other, non-phosphorus-containing aryl halides.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Benzodioxoles / chemical synthesis*
  • Biphenyl Compounds / chemical synthesis*
  • Catalysis
  • Coordination Complexes / chemistry*
  • Dimerization
  • Ligands
  • Nickel / chemistry
  • Oxazoles / chemistry
  • Oxidation-Reduction
  • Phosphorous Acids / chemical synthesis*
  • Pyridines / chemistry
  • Stereoisomerism

Substances

  • Benzodioxoles
  • Biphenyl Compounds
  • Coordination Complexes
  • Ligands
  • Oxazoles
  • Phosphorous Acids
  • Pyridines
  • Nickel