Oxidative C-H homodimerization of phenylacetamides

Didier G. Pintori, Michael F. Greaney

    Research output: Contribution to journalArticlepeer-review


    A range of secondary and tertiary phenylacetamides undergo oxidative homodimerization to afford biaryls. The reaction proceeds under palladium catalysis in the presence of a copper cocatalyst and oxygen and is most effective for electron-rich substrates. © 2011 American Chemical Society.
    Original languageEnglish
    Pages (from-to)5713-5715
    Number of pages2
    JournalOrganic Letters
    Issue number21
    Publication statusPublished - 4 Nov 2011


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