The synthesis of new chiral multidentate amino- and amidophosphine ligands
bearing up to six potential coordination sites were synthesized starting fr
om L-valine. Based on these compounds chiral Ru(II) complexes were prepared
, characterized and tested in the asymmetric transfer hydrogenation of aryl
-alkyl ketones. In all cases investigated the catalyst bearing additional h
ydroxy groups gave lower conversions than the complex without hydroxy group
s. Highest enantioselectivity was achieved with isobutyrophenone as substra
te (69%ee). (C) 2000 Elsevier Science Ltd. All rights reserved.