http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15540
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)
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- 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
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- 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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