Michael addition of nitromethane to non-racemic chiral Cr(CO)3 complexes of ethyl cinnamate derivatives: stereoselective synthesis of (R)-(-)-baclofen (Articolo in rivista)

Type
Label
  • Michael addition of nitromethane to non-racemic chiral Cr(CO)3 complexes of ethyl cinnamate derivatives: stereoselective synthesis of (R)-(-)-baclofen (Articolo in rivista) (literal)
Anno
  • 2000-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/S0957-4166(00)00123-3 (literal)
Alternative label
  • Baldoli, Clara; Maiorana, Stefano; Licandro, Emanuela; Perdicchia, Dario; Vandoni, Barbara (2000)
    Michael addition of nitromethane to non-racemic chiral Cr(CO)3 complexes of ethyl cinnamate derivatives: stereoselective synthesis of (R)-(-)-baclofen
    in Tetrahedron: asymmetry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Baldoli, Clara; Maiorana, Stefano; Licandro, Emanuela; Perdicchia, Dario; Vandoni, Barbara (literal)
Pagina inizio
  • 2007 (literal)
Pagina fine
  • 2014 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 11 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 9 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Università degli Studi di Milano; CNR-Istituto di Scienze e Tecnologie Molecolari (literal)
Titolo
  • Michael addition of nitromethane to non-racemic chiral Cr(CO)3 complexes of ethyl cinnamate derivatives: stereoselective synthesis of (R)-(-)-baclofen (literal)
Abstract
  • We carried out a highly stereoselective Michael addition (96% de) of nitromethane to enantiomerically pure tricarbonyl(ethyl-4-chloro-2-trimethylsilylcinnamate)chromium(0). This reaction is the key step in the synthesis of (R)-(^)-baclofen, a potent antispastic drug. (literal)
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