Articles producció científica> Química Física i Inorgànica

Asymmetric Pd-catalyzed allylic substitution using a large sugar-based monophosphite ligand library. Scope and limitations

  • Identification data

    Identifier: PC:1256
    Authors:
    Montserrat DiéguezSabina AlegreYvette MataOscar Pàmies
    Abstract:
    We have applied a modular sugar-based phosphite ligand library for the Pd-catalyzed allylic substitution reactions of several substrates. These ligands are derived from D-(+)-glucose, D-(+)-galactose and D-(+)- fructose, which lead to a wide range of sugar backbones, and contain several substituents at the C-3 carbon of the furanoside backbone and several substituents/ configurations in the biaryl moiety, with different steric and electronic properties. Systematic variation of the ligand parameters indicates that the catalytic performance (activities and enantioselectivities) is highly affected by sugar backbone, the substituents at the C-3 carbon of the furanoside backbone, the configurations at the C-3 and C-4 carbons of the ligand backbone and the type of substituents/configurations in the biaryl phosphite moiety as well as the substrate type. For disubstituted substrates moderate enantioselectivities (up to 72%) were achieved using ligand L8d, while for monosubstituted substrates the highest enantioselectivities (up to 40%) were obtained using ligand L9a
  • Others:

    Author, as appears in the article.: Montserrat Diéguez Sabina Alegre Yvette Mata Oscar Pàmies
    Department: Química Física i Inorgànica
    URV's Author/s: DIÉGUEZ FERNÁNDEZ, MONTSERRAT Sabina Alegre Yvette Mata PAMIES OLLÉ, OSCAR
    Keywords: asymmetric catalysis palladium allylic substitution
    Abstract: We have applied a modular sugar-based phosphite ligand library for the Pd-catalyzed allylic substitution reactions of several substrates. These ligands are derived from D-(+)-glucose, D-(+)-galactose and D-(+)- fructose, which lead to a wide range of sugar backbones, and contain several substituents at the C-3 carbon of the furanoside backbone and several substituents/ configurations in the biaryl moiety, with different steric and electronic properties. Systematic variation of the ligand parameters indicates that the catalytic performance (activities and enantioselectivities) is highly affected by sugar backbone, the substituents at the C-3 carbon of the furanoside backbone, the configurations at the C-3 and C-4 carbons of the ligand backbone and the type of substituents/configurations in the biaryl phosphite moiety as well as the substrate type. For disubstituted substrates moderate enantioselectivities (up to 72%) were achieved using ligand L8d, while for monosubstituted substrates the highest enantioselectivities (up to 40%) were obtained using ligand L9a
    Research group: Organometàl.lics i Catàlisi Homogènia
    Thematic Areas: Química Química Chemistry
    licence for use: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 2300-4630
    Author identifier: 0000-0002-8450-0656 n/a n/a 0000-0002-2352-8508
    Record's date: 2015-11-18
    Last page: 39
    Papper version: info:eu-repo/semantics/publishedVersion
    Licence document URL: https://repositori.urv.cat/ca/proteccio-de-dades/
    Entity: Universitat Rovira i Virgili
    Journal publication year: 2014
    First page: 32
    Publication Type: Article
  • Keywords:

    Catàlisi asimètrica
    Pal·ladi (Element químic)
    asymmetric catalysis
    palladium
    allylic substitution
    Química
    Química
    Chemistry
    2300-4630
  • Documents:

  • Cerca a google

    Search to google scholar