Iron-Catalyzed Arylation of Aromatic Ketones and Aldehydes Mediated by Organosilanes

Risto Savela, Marcin Majewski, Reko Leino

    Tutkimustuotos: LehtiartikkeliArtikkeliTieteellinenvertaisarvioitu

    18 Sitaatiot (Scopus)

    Abstrakti

    A simple and efficient iron-catalyzed method for arylation of aromatic carbonyl compounds is reported. The use of 4% FeCl3 or Fe(acac)(3) as the catalyst, in combination with a slight excess of chlorotrimethylsilane and triethylsilane, chlorination of benzylic ketones and aldehydes with subsequent Friedel-Crafts alkylation of arenes is achieved. Although the method is limited by the general constraints associated with Friedel-Crafts alkylation reactions, robust applications for the synthesis of pharmaceutical intermediates and so on can be envisioned.
    AlkuperäiskieliEi tiedossa
    Sivut4137–4147
    Sivumäärä11
    JulkaisuEuropean Journal of Organic Chemistry
    Numero19
    DOI - pysyväislinkit
    TilaJulkaistu - 2014
    OKM-julkaisutyyppiA1 Julkaistu artikkeli, soviteltu

    Keywords

    • Homogeneous catalysis
    • Iron
    • Silanes
    • Synthetic methods

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