http://www.cnr.it/ontology/cnr/individuo/prodotto/ID15421
Expanding the Scope of Atropisomeric Monodentate P-donor Ligands in Asymmetric Catalysis. Hydrogen Transfer Reduction of alfa,beta-unsaturated Acid Derivatives by Rhodium/Ph-BINEPINE Catalysts. (Articolo in rivista)
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- Expanding the Scope of Atropisomeric Monodentate P-donor Ligands in Asymmetric Catalysis. Hydrogen Transfer Reduction of alfa,beta-unsaturated Acid Derivatives by Rhodium/Ph-BINEPINE Catalysts. (Articolo in rivista) (literal)
- Anno
- 2006-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/hlca.200690169 (literal)
- Alternative label
Alberico E.; Nieddu I.; Taras R.; Gladiali S. (2006)
Expanding the Scope of Atropisomeric Monodentate P-donor Ligands in Asymmetric Catalysis. Hydrogen Transfer Reduction of alfa,beta-unsaturated Acid Derivatives by Rhodium/Ph-BINEPINE Catalysts.
in Helvetica chimica acta; Wiley-VCH Verlag Gmbh, Weinheim (Germania)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Alberico E.; Nieddu I.; Taras R.; Gladiali S. (literal)
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- http://onlinelibrary.wiley.com/doi/10.1002/hlca.200690169/abstract;jsessionid=D18C25CEB6135C5969C0BC306DE628D2.d02t01 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Chimica Biomolecolare, CNR, Sassari; Università degli Studi di Sassari (literal)
- Titolo
- Expanding the Scope of Atropisomeric Monodentate P-donor Ligands in Asymmetric Catalysis. Hydrogen Transfer Reduction of alfa,beta-unsaturated Acid Derivatives by Rhodium/Ph-BINEPINE Catalysts. (literal)
- Abstract
- A range of alfa,beta-unsaturated acids and esters have been selectively reduced to the corresponding saturated
acid derivatives by hydrogen transfer. As the reducing agent, formic acid was used in the presence
of RhI complexes formed with the powerful chiral ligand Ph-binepine (1), an axially chiral binaphthalenetype
monodentate P-donor ligand. Very high stereoselectivities (up to 97% ee) were obtained in the case
of itaconic acid (2a). (literal)
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