Rhodium/MonoPhos-Catalysed Asymmetric Hydrogenation of Enamides

Michel van den Berg, Robert M. Haak, Adriaan J. Minnaard, André H.M. de Vries, Johannes G. de Vries, Bernard Feringa

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Abstract

The monodentate phosphoramidite MonoPhos has been used in the rhodium-catalysed asymmetric hydrogenation of N-acetyl-α-arylenamides. This ligand is readily available via a one-step procedure and is air stable. Its Rh(I) complex, which is an effective catalyst precursor for the hydrogenation of dehydroamino acids, also gives high enantioselectivities for this class of substrates. Because of the facile synthesis and stability of MonoPhos, its complex provides a general solution in preparing chiral amine derivatives through asymmetric hydrogenation.
Original languageEnglish
Pages (from-to)1003-1007
Number of pages5
JournalAdvanced Synthesis & Catalysis
Volume344
Issue number9
DOIs
Publication statusPublished - 2002

Keywords

  • asymmetric catalysis
  • chiral amines
  • enamides
  • enantioselective hydrogenation
  • homogeneous
  • phosphoramidites
  • rhodium
  • HIGHLY ENANTIOSELECTIVE HYDROGENATION
  • LIGANDS
  • PHOSPHOLANE
  • OLEFINS

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