Stereoselective oxazaborolidine-borane reduction of biphenyl alkyl ketons (Articolo in rivista)

Type
Label
  • Stereoselective oxazaborolidine-borane reduction of biphenyl alkyl ketons (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Alternative label
  • Delogu G., Fabbri D., De Candia C., Patti A., Pedotti S. (2002)
    Stereoselective oxazaborolidine-borane reduction of biphenyl alkyl ketons
    in Tetrahedron: asymmetry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Delogu G., Fabbri D., De Candia C., Patti A., Pedotti S. (literal)
Pagina inizio
  • 891 (literal)
Pagina fine
  • 898 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 13 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di chimica biomolecolare (literal)
Titolo
  • Stereoselective oxazaborolidine-borane reduction of biphenyl alkyl ketons (literal)
Abstract
  • Asymmetric reduction of three different biphenyl alkyl ketones with a (R)- oxazaborolidine as catalyst was successfully carried out and the corresponding biphenyl alcohols were obtained in high yield and ee. High diastereoselectivity was achieved with C2-conformationally stable 3,3’-bis- (2-hydroxyethyl)-2,2’,6,6’-tetramethoxybiphenyl and more detailed investigations evidenced a cooperative effect between stereoaxis and stereocentre. (literal)
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