Volume 56, Issue 17 p. 4632
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Inside Cover: Reagent- and Metal-Free Anodic C−C Cross-Coupling of Aniline Derivatives (Angew. Chem. Int. Ed. 17/2017)

Lara Schulz

Lara Schulz

Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10–14, 55128 Mainz, Germany

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Mathias Enders

Mathias Enders

Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10–14, 55128 Mainz, Germany

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Dr. Bernd Elsler

Dr. Bernd Elsler

Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10–14, 55128 Mainz, Germany

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Dr. Dieter Schollmeyer

Dr. Dieter Schollmeyer

Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10–14, 55128 Mainz, Germany

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Dr. Katrin M. Dyballa

Dr. Katrin M. Dyballa

Evonik Performance Materials GmbH, Paul-Baumann-Strasse 1, 45772 Marl, Germany

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Prof. Dr. Robert Franke

Prof. Dr. Robert Franke

Evonik Performance Materials GmbH, Paul-Baumann-Strasse 1, 45772 Marl, Germany

Lehrstuhl für Theoretische Chemie, Ruhr-Universität Bochum, 44780 Bochum, Germany

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Prof. Dr. Siegfried R. Waldvogel

Corresponding Author

Prof. Dr. Siegfried R. Waldvogel

Institut für Organische Chemie, Johannes Gutenberg-Universität Mainz, Duesbergweg 10–14, 55128 Mainz, Germany

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First published: 22 March 2017

Graphical Abstract

The formation of polyanilines is avoided in an anodic coupling of anilines with simple and easily removable carbonyl-based protecting groups. In their Communication on page 4877 ff., S. R. Waldvogel and co-workers present a facile method for the electrolytic synthesis of protected 2,2′-diaminobiaryl derivatives in high yield and excellent selectivity by oxidative cross-coupling. The use of 1,1,1,3,3,3-hexafluoro-2-propanol as the solvent allows for clean electrochemical conversion.

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