Iron-Catalyzed Cross-Coupling of Alkenyl Acetates
- PMID: 26184455
- DOI: 10.1002/anie.201504524
Iron-Catalyzed Cross-Coupling of Alkenyl Acetates
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.
© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
LinkOut - more resources
Full Text Sources
