The hydrogenation of acetoacetanilide in the presence of optically act
ive ruthenium catalysts leads to 3-hydroxy-N-phenylbutanamide in good
yield anti high enantioselectivity (ee>95%). Its direct phosphinylatio
n with chlorodiphenylphosphine affords a new bifunctional amido-phosph
inite ligand that can easily be coordinated to [(arene)RuCl2] and to t
he CpRuCl(PPh3) moiety with very good stereoselectivity from CpRuCl(PP
h3)(2). (C) 1998 Elsevier Science Ltd. All rights reserved.