The DOI matches its Crossref record; 12 of the 12 references it cites were found in a registry or an index.
Cross‐Coupling of Alkyl Halides with Aryl Grignard Reagents Catalyzed by a Low‐Valent Iron Complex
Abstract
A striking reversal of the usual reactivity pattern of aryl Grignard reagents is observed for reactions in the presence of catalytic amounts of the “bare” ferrate complex [Li(tmeda)]2[Fe(C2H4)4] (1). Highly reduced iron–magnesium clusters may play a decisive role in the exceptionally facile and chemoselective cross-coupling reaction with alkyl halides (see scheme).
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Citations
Cites
Iron-Catalyzed Cross-Coupling Reactions
Fürstner, A., Leitner, A., Méndez, M., & Krause, H. (2002) · Journal of the American Chemical Society · doi:10.1021/ja027190t · Cited by 823
Self-citationIron-Catalyzed Cross-Coupling of Primary and Secondary Alkyl Halides with Aryl Grignard Reagents
Nakamura, M., Matsuo, K., Ito, S., et al. (2004) · Journal of the American Chemical Society · doi:10.1021/ja049744t · Cited by 524
Fürstner, A., & Leitner, A. (2002) · Angewandte Chemie International Edition · doi:10.1002/1521-3773(20020215)41:4<609::aid-anie609>3.0.co;2-m · Cited by 432
Self-citationRoom-Temperature Alkyl−Alkyl Suzuki Cross-Coupling of Alkyl Bromides that Possess β Hydrogens
Netherton, M. R., Dai, C., Neuschütz, K., & Fu, G. C. (2001) · Journal of the American Chemical Society · doi:10.1021/ja011306o · Cited by 419
Highly Stereo- and Chemoselective Iron-Catalyzed Alkenylation of Organomagnesium Compounds
Cahiez, G., & Avedissian, H. (1998) · Synthesis · doi:10.1055/s-1998-2135 · Cited by 380
Scheiper, B., Bonnekessel, M., Krause, H., & Fürstner, A. (2004) · The Journal of Organic Chemistry · doi:10.1021/jo0498866 · Cited by 339
Self-citationIron-Catalyzed Grignard Cross-Coupling with Alkyl Halides Possessing β-Hydrogens
Nagano, T., & Hayashi, T. (2004) · Organic Letters · doi:10.1021/ol049779y · Cited by 295
Catalysis‐Based Total Synthesis of Latrunculin B
Fürstner, A., De Souza, D., Parra‐Rapado, L., & Jensen, J. T. (2003) · Angewandte Chemie International Edition · doi:10.1002/anie.200352413 · Cited by 172
Self-citationIron-Catalyzed Cross-Coupling Reactions. A Scalable Synthesis of the Immunosuppressive Agent FTY720
Seidel, G., Laurich, D., & Fürstner, A. (2004) · The Journal of Organic Chemistry · doi:10.1021/jo049885d · Cited by 153
Self-citationTetrakis(ethylene)irondilithium and Bis(η4‐1,5‐cy‐clooctadiene)irondilithium
Jonas, K., Schieferstein, L., Krüger, C. R., et al. (1979) · Angewandte Chemie International Edition in English · doi:10.1002/anie.197905501 · Cited by 77
Cited by
The Promise and Challenge of Iron-Catalyzed Cross Coupling
Sherry, B. D., & Fürstner, A. (2008) · Accounts of Chemical Research · doi:10.1021/ar800039x · Cited by 1,235
Self-citationFürstner, A. (2016) · ACS Central Science · doi:10.1021/acscentsci.6b00272 · Cited by 746
Self-citationAdvances in Iron Catalyzed Cross Coupling Reactions
Fürstner, A., & Martin, R. (2005) · Chemistry Letters · doi:10.1246/cl.2005.624 · Cited by 472
Self-citationRiener, K., Haslinger, S., Raba, A., Högerl, M. P., Cokoja, M., Herrmann, W. A., & Kühn, F. E. (2014) · Chemical Reviews · doi:10.1021/cr4006439 · Cited by 411
Katalyse von Radikalreaktionen: Konzepte aus Sicht der Radikalchemie
Studer, A., & Curran, D. P. (2016) · Angewandte Chemie · doi:10.1002/ange.201505090 · Cited by 313
Metadata
- Authors
- Martin, R., & Fürstner, A.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2004-07-20
- Volume
- 43
- Issue
- 30
- Pages
- 3955-3957
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2049151058
- Cited by
- 400
- References
- 12
- FWCI
- 13.35
- Type
- journal article
- Language
- en
- Open access
- closed
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- Martin, R., & Fürstner, A. (2004). Cross‐Coupling of Alkyl Halides with Aryl Grignard Reagents Catalyzed by a Low‐Valent Iron Complex. Angewandte Chemie International Edition. https://doi.org/10.1002/anie.200460504
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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