Carbonylative homocoupling of arylzinc compounds 1 using 1 atm of CO and 1, 2- dibromoethane as an oxidant was achieved in the presence of Rh− dppf catalyst, affording symmetrical diaryl ketones in good yields. Under similar conditions, Pd or Ni catalysts induced oxidative homocoupling of 1 to yield biaryls instead. The beneficial catalysis by Rh in the carbonylation was presumed to stem from the facility by which the migration of the ...
[O'Brien, Christopher J.; Kantchev, Eric Assen B.; Valente, Cory; Hadei, Niloufar; Chass, Gregory A.; Lough, Alan; Hopkinson, Alan C.; Organ, Michael G. Chemistry - A European Journal, 2006 , vol. 12, # 18 p. 4743 - 4748]