Chiral iridium(I) bis(NHC) complexes as catalysts for asymmetric transfer hydrogenation

The common use of NHC complexes in transition-metal mediated C–C coupling and metathesis reactions in recent decades has established N-heterocyclic carbenes as a new class of ligand for catalysis. The field of asymmetric catalysis with complexes bearing NHC-containing chiral ligands is dominated by mixed carbene/oxazoline or carbene/phosphane chelating ligands. In contrast, applications of complexes with chiral, chelating bis(NHC) ligands are rare. In the present work new chiral iridium(I) bis(NHC) complexes and their application in the asymmetric transfer hydrogenation of ketones are described. A series of chiral bis(azolium) salts have been prepared following a synthetic pathway, starting from L-valinol and the modular buildup allows the structural variation of the ligand precursors. The iridium complexes were formed via a one-pot transmetallation procedure. The prepared complexes were applied as catalysts in the asymmetric transfer hydrogenation of various prochiral ketones, affording the corresponding chiral alcohols in high yields and moderate to good enantioselectivities of up to 68%. The enantioselectivities of the catalysts were strongly affected by the various, terminal N-substituents of the chelating bis(NHC) ligands. The results presented in this work indicate the potential of bis-carbenes as stereodirecting ligands for asymmetric catalysis and are offering a base for further developments. Copyright c © 2010 John Wiley & Sons, Ltd.