Iron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents
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- 1 March 2004
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 126 (12), 3686-3687
- https://doi.org/10.1021/ja049744t
Abstract
An iron-catalyzed cross-coupling reaction of a primary or secondary alkyl halide with an aryl Grignard reagent proceeds under mild conditions to give the corresponding coupling product in quantitative yield.Keywords
This publication has 8 references indexed in Scilit:
- Ni- or Cu-Catalyzed Cross-Coupling Reaction of Alkyl Fluorides with Grignard ReagentsJournal of the American Chemical Society, 2003
- Palladium-Catalyzed Coupling of Alkyl Chlorides and Grignard ReagentsAngewandte Chemie International Edition, 2002
- Cobalt-Catalyzed Coupling Reaction of Alkyl Halides with Allylic Grignard ReagentsAngewandte Chemie International Edition, 2002
- Nickel-Catalyzed Cross-Coupling Reaction of Grignard Reagents with Alkyl Halides and Tosylates: Remarkable Effect of 1,3-ButadienesJournal of the American Chemical Society, 2002
- Possibility of Living Radical Polymerization of Vinyl Acetate Catalyzed by Iron(I) ComplexMacromolecules, 2001
- Novel tridentate diamino organomanganese(II) complexes as homogeneous catalysts in manganese(II)/copper(I) catalyzed carbon–carbon bond forming reactionsJournal of Organometallic Chemistry, 1998
- New Cobalt‐ and Iron‐Catalyzed Reactions of Organozinc compoundsAngewandte Chemie International Edition in English, 1996
- Vinylation of Grignard reagents. Catalysis by ironJournal of the American Chemical Society, 1971