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Readily Available Chiral Phosphine-Aminophosphine Ligands for Highly Efficient Rh-Catalyzed Asymmetric Hydrogenation of -Enol Ester
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A new class of unsymmetrical hybrid phosphine-aminophosphine ligands has been prepared from commerciallyavailable, inexpensive (S)-1-phenylethylamine through aconcise synthetic procedure. These ligands are not verysensitive to air and moisture, and displayed good enantioselectivities in the Rh-catalyzed asymmetric hydrogenation ofvarious dimethyl -benzoyloxyethenephosphonates bearing-aryl, -alkyl, and -alkoxy substituents and N-benzyloxycarbonyl -enamido phosphonates, in which up to 97% eewas obtained. A side-by-side comparison study disclosed thatthese new phosphine-aminophosphine ligands showed betterenantioselectivity than BoPhoz ligands.

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