Development of Practical Rhodium Phosphine Catalysts for the Hydrogenation of beta-Dehydroamino Acid Derivatives (Articolo in rivista)

Type
Label
  • Development of Practical Rhodium Phosphine Catalysts for the Hydrogenation of beta-Dehydroamino Acid Derivatives (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1021/op0602270 (literal)
Alternative label
  • Enthaler S.; Erre G.; Junge K.; Holz J.; Börner A.; Alberico E.; Nieddu I.; Gladiali S.; Beller M. (2007)
    Development of Practical Rhodium Phosphine Catalysts for the Hydrogenation of beta-Dehydroamino Acid Derivatives
    in Organic process research & development; American Chemical Society, Washington (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Enthaler S.; Erre G.; Junge K.; Holz J.; Börner A.; Alberico E.; Nieddu I.; Gladiali S.; Beller M. (literal)
Pagina inizio
  • 568 (literal)
Pagina fine
  • 577 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://pubs.acs.org/doi/abs/10.1021/op0602270 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 11 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 3 (literal)
Note
  • Scopu (literal)
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Chimica Biomolecolare - CNR, Sassari; Leibniz Institut fuer Katalyse an der UniVersitaet Rostock e.V., Albert-Einstein Strasse 29a, 18059 Rostock, Germany; Università degli Studi di Sassari (literal)
Titolo
  • Development of Practical Rhodium Phosphine Catalysts for the Hydrogenation of beta-Dehydroamino Acid Derivatives (literal)
Abstract
  • The rhodium-catalyzed asymmetric hydrogenation of various beta-dehydroamino acid derivatives to give optically active beta-amino acids has been examined. Chiral monodentate 4,5-dihydro-3Hdinaphthophosphepines, which are easily tuned and accessible in a multi-10-g scale, have been used as ligands. The enantioselectivity is largely dependent on the nature of the substituent at the phosphorous atom and on the structure of the substrate. Applying optimized conditions up to 94% ee was achieved. (literal)
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