The asymmetric hydrogenation of prochiral electron-rich enamines with rhodi
um(I) diphosphine and diphosphinite catalysts is described. The reaction is
strongly sensitive to the ligand applied. Good results are observed with c
atalysts based on (R,R)-DIOP, K-beta(+)-OH, (R,R)-bdpch and other ligands f
orming seven-membered chelates with the metal. It is shown, that by convers
ion of a cyclic imine, which could not be hydrogenated, into the correspond
ing enamine a substrate is formed which is smoothly reduced at 1 bar initia
l hydrogen pressure by up to 72% ee. (C) 2000 Elsevier Science Ltd. All rig
hts reserved.