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Issue 19, 2007
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Iron-catalyzed arylaryl cross-coupling reaction tolerating amides and unprotected quinolinones

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Abstract

The iron(III)-catalyzed cross-coupling reaction between functionalized arylcopper reagents and aromatic iodides bearing an amide function or an unprotected quinolinone leads smoothly to polyfunctionalized biphenyls in excellent yields due to an intramolecular chelating effect of the amide group.

Graphical abstract: Iron-catalyzed aryl–aryl cross-coupling reaction tolerating amides and unprotected quinolinones

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Publication details

The article was received on 20 Dec 2006, accepted on 26 Jan 2007, published on 16 Feb 2007 and first published online on 16 Feb 2007


Article type: Communication
DOI: 10.1039/B618617C
Citation: Chem. Commun., 2007, 1954-1956
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    Iron-catalyzed arylaryl cross-coupling reaction tolerating amides and unprotected quinolinones

    C. C. Kofink, B. Blank, S. Pagano, N. Götz and P. Knochel, Chem. Commun., 2007, 1954
    DOI: 10.1039/B618617C

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