Journal of Organometallic Chemistry p. 23 - 30 (1985)
Update date:2022-08-22
Topics:
Bakos, Jozsef
Toth, Imre
Heil, Balint
Marko, Laszlo
Asymmetric heterogeneous hydrogenation of acetylacetone was applied for the preparation of both enantiomers (2R,4R and 2S,4S) of 2,4-bis(diphenylphosphino)pentane (BDPP).Among the chiral phosphine prepared up to now BDPP appears to be unique in the sense that its rhodium(I) complexes serve as effective homogeneous asymmetric hyrogenation catalysts not only for the reduction Z-α-amidoacrylic acids but also for the reduction of α-ethylstyrene, acetophenone, and acetophenonebenzylimine.The analogous phosphinite ligand BDPOP yields a less active catalyst
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