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

Risto Savela, Marcin Majewski, Reko Leino

    Forskningsoutput: TidskriftsbidragArtikelVetenskapligPeer review

    18 Citeringar (Scopus)

    Sammanfattning

    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.
    OriginalspråkOdefinierat/okänt
    Sidor (från-till)4137–4147
    Antal sidor11
    TidskriftEuropean Journal of Organic Chemistry
    Nummer19
    DOI
    StatusPublicerad - 2014
    MoE-publikationstypA1 Tidskriftsartikel-refererad

    Nyckelord

    • Homogeneous catalysis
    • Iron
    • Silanes
    • Synthetic methods

    Citera det här