The asymmetric reduction of enamides with molecular, hydrogen and catalytic
amounts of rhodium, iridium or ruthenium complexes containing chiral N,S-l
igands is reported. Various enantiomerically pure mono- and dithioureas wer
e examined. The C-2-symmetry of the dithiourea ligands seems essential to t
he enantioselectivity achieved. Ee values of up to 70% were observed. (C) 2
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