The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Reductive Cross‐Coupling Reactions between Two Electrophiles
Abstract
Reductive cross‐electrophile coupling reactions have recently been developed to a versatile and sustainable synthetic tool for selective CC bond formation. The employment of cheap and abundant electrophiles avoids the pre‐formation and handling of organometallic reagents. In situ reductive coupling is effected in the presence of a transition‐metal catalyst (Ni, Co, Pd, Fe) and a suitable metallic reductant (Mn, Zn, Mg). This Concept article assesses the current state of the art and summarizes recent protocols with various combinations of alkyl, alkenyl, allyl, and aryl reagents and highlights key mechanistic studies.
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Citations
Cites
Palladium‐Catalyzed Cross‐Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize
Johansson Seechurn, C. C. C., Kitching, M. O., Colacot, T. J., & Snieckus, V. (2012) · Angewandte Chemie International Edition · doi:10.1002/anie.201107017 · Cited by 3,007
Montalti, M., Credi, A., Prodi, L., & Gandolfi, M. T. (2006) · CRC Press eBooks · doi:10.1201/9781420015195 · Cited by 2,167
Cross‐Coupling Reactions Of Organoboranes: An Easy Way To Construct CC Bonds (Nobel Lecture)
Suzuki, A. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101379 · Cited by 2,055
Franke, R., Selent, D., & Börner, A. (2012) · Chemical Reviews · doi:10.1021/cr3001803 · Cited by 1,668
Magical Power of Transition Metals: Past, Present, and Future (Nobel Lecture)
Negishi, E. (2011) · Angewandte Chemie International Edition · doi:10.1002/anie.201101380 · Cited by 759
Coming of Age: Sustainable Iron‐Catalyzed Cross‐Coupling Reactions
Czaplik, W. M., Mayer, M., Cvengroš, J., & von Wangelin, A. J. (2009) · ChemSusChem · doi:10.1002/cssc.200900055 · Cited by 570
Palladiumkatalysierte Kreuzkupplungen: eine historische Perspektive im Kontext der Nobel‐Preise 2010
Johansson Seechurn, C. C. C., Kitching, M. O., Colacot, T. J., & Snieckus, V. (2012) · Angewandte Chemie · doi:10.1002/ange.201107017 · Cited by 499
35 years of palladium-catalyzed cross-coupling with Grignard reagents: how far have we come?
Knappke, C. E. I., & Jacobi von Wangelin, A. (2011) · Chemical Society Reviews · doi:10.1039/c1cs15137a · Cited by 251
Self-citationEstimation of Standard Reduction Potentials of Halogen Atoms and Alkyl Halides
Isse, A. A., Lin, C. Y., Coote, M. L., & Gennaro, A. (2011) · The Journal of Physical Chemistry B · doi:10.1021/jp109613t · Cited by 243
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Cited by
A Pharmaceutical Industry Perspective on Sustainable Metal Catalysis
Hayler, J. D., Leahy, D. K., & Simmons, E. M. (2019) · Organometallics · doi:10.1021/acs.organomet.8b00566 · Cited by 323
Stereospecific and stereoconvergent cross-couplings between alkyl electrophiles
Lucas, E. L., & Jarvo, E. R. (2017) · Nature Reviews Chemistry · doi:10.1038/s41570-017-0065 · Cited by 300
Iron‐Catalyzed Cross‐Couplings in the Synthesis of Pharmaceuticals: In Pursuit of Sustainability
Piontek, A., Bisz, E., & Szostak, M. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201800364 · Cited by 285
Sharif, F., Tayebi, B., Buzsáki, G., Royer, S., & Fernandez-Ruiz, A. (2021) · Neuron · doi:10.1016/j.neuron.2020.10.034 · Cited by 111
Metadata
- Authors
- Knappke, C. E. I., Grupe, S., Gärtner, D., Corpet, M., Gosmini, C., & Jacobi von Wangelin, A.
- Venue
- Chemistry – A European Journal
- Publisher
- Wiley
- Published
- 2014-05-13
- Volume
- 20
- Issue
- 23
- Pages
- 6828-6842
- ISSN
- 0947-6539 (ISSN-L)
- 1521-3765
- OpenAlex
- W2117123115
- Cited by
- 757
- References
- 11
- FWCI
- 16.48
- Type
- journal article
- Language
- en
- Open access
- closed
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- Knappke, C. E. I., Grupe, S., Gärtner, D., Corpet, M., Gosmini, C., & Jacobi von Wangelin, A. (2014). Reductive Cross‐Coupling Reactions between Two Electrophiles. Chemistry – A European Journal. https://doi.org/10.1002/chem.201402302
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