- ASYMMETRIC HYDROGENATION CATALYZED BY AMINOPHOSPHINE-PHOSPHINITERHODIUM COMPLEXES DERIVED FROM NATURAL AMINOALCOHOLS AND X-RAY CRYSTAL STRUCTURE OF (1,5-CYCLOOCTADIENE)-(S)-N-(DIPHENYLPHOSPHINO)-2-DIPHENYLPHOSPHINOXYMETHYLPYRROLIDINERHODIUM(I) PERCHLORATE
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From the cheap and readily available amino alcohols (S)-pyrrolidinemethanol ((S)-prolinol), and (S)-α-N-ethyl-aminobutanol, we have obtained two new aminophosphine-phosphinite ligands: (S)-N-(diphenylphosphino)-2-diphenylphosphinooxymethylpyrrolidine ((S)-Prolophos) and (S)-1-diphenylphosphinoxy-2-N-ethyl-N-diphenylphosphinoaminobutane ((S)-Butaphos).The rhodium(I) complexes of these phosphines act as efficient homogeneous hydrogenation catalysts at ambient temperature and pressures for dehydro N-acetyl amono acids, dehydro N-benzoyl amino acids and itaconic acid.An X-ray diffraction study of the complex *THF has been shown that the crystals belong to the monoclinic space group P21 with a 10.680(2), b 10.448(2), c 18.207(3) Angstroem and β 104.97(1)o.Refinements based on 2105 significant counter reflections led to a final R value of 0.060.The cation is in a distorted square planar geometry, the rhodium atom being bound to the two phosphorus atoms and to the two double bonds of the diene molecule.
- Cesarotti, E.,Chiesa, A.,Ciani, G.,Sironi, A.
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- ASYMMETRIC HYDROGENATION BY CHIRAL AMINOPHOSPHINE-PHOSPHINITE RHODIUM COMPLEXES
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The ligands (S)-N-(diphenylphosphino)-2-diphenylphosphinomethylpyrrolidine, (S)-prolophos, and (S)-1-diphenylphosphinoxy-2-N-ethyl-N-diphenylphosphinoaminobutane,(S)-butaphos, have been prepared.The Rh(I) complexes of these phosphines act as an efficient homogenous hydrogenation catalysts at ambient temperature and pressure for α-N-acetaminoacrylic acid and itaconic acid.
- Cesarotti, E.,Chiesa, A.,D'Alfonso, G.
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p. 2995 - 2996
(2007/10/02)
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