- Selective monoarylation of acetate esters and aryl methyl ketones using aryl chlorides.
Selective monoarylation of acetate esters and aryl methyl ketones using aryl chlorides.
Organic letters (2009-03-20)
Mark R Biscoe, Stephen L Buchwald
PMID19296693
ZUSAMMENFASSUNG
Simple, efficient procedures for the monoarylation of acetate esters and aryl methyl ketones using aryl chlorides are presented. Previously, no general method was available to ensure the highly selective monoarylation of these classes of substrates using aryl chlorides. Using palladium precatalysts recently reported by our group, these reactions are easily accomplished under mild conditions that tolerate a wide array of heterocyclic substrates.
MATERIALIEN
Produktnummer
Marke
Produktbeschreibung
Sigma-Aldrich
Chloro-[2-(di-tert.-butylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl][2-(2-aminoethyl)-phenyl)]-palladium(II)