Issue 19, 2007
From the journal:

Chemical Communications

Iron-catalyzed aryl–aryl cross-coupling reaction tolerating amides and unprotected quinolinones†

Christiane C. Kofink,a   Benoît Blank,a   Sandro Pagano,a   Nadine Götza  and  Paul Knochel*a  

* Corresponding authors

a Ludwig-Maximilians-Universität, Department Chemie und Biochemie, Ludwig-Maximilians-Universität München, Butenandtstr. 5-13, Haus F, München, Germany
E-mail: paul.knochel@cup.uni-muenchen.de
Fax: +49 (0) 89 2180 77680
Tel: + 49 (0) 89 2180 77679

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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Article information

DOI
https://doi.org/10.1039/B618617C
Article type
Communication
Submitted
20 Dec 2006
Accepted
26 Jan 2007
First published
16 Feb 2007

Chem. Commun., 2007, 1954-1956

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Iron-catalyzed aryl–aryl 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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