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. 2015 Sep 1;54(36):10545-9.
doi: 10.1002/anie.201504524. Epub 2015 Jul 15.

Iron-Catalyzed Cross-Coupling of Alkenyl Acetates

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Iron-Catalyzed Cross-Coupling of Alkenyl Acetates

Dominik Gärtner et al. Angew Chem Int Ed Engl. .

Abstract

Stable C-O linkages are generally unreactive in cross-coupling reactions which mostly employ more electrophilic halides or activated esters (triflates, tosylates). Acetates are cheap and easily accessible electrophiles but have not been used in cross-couplings because the strong C-O bond and high propensity to engage in unwanted acetylation and deprotonation. Reported herein is a selective iron-catalyzed cross-coupling of diverse alkenyl acetates, and it operates under mild reaction conditions (0 °C, 2 h) with a ligand-free catalyst (1-2 mol%).

Keywords: Grignard reaction; alkenes; cross-coupling; enols; iron catalysis.

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