The DOI matches its Crossref record; 68 of the 68 references it cites were found in a registry or an index.
Alkyl Carbon–Carbon Bond Formation by Nickel/Photoredox Cross‐Coupling
Open accessAbstract
The union of photoredox and nickel catalysis has resulted in a renaissance in radical chemistry as well as in the use of nickel‐catalyzed transformations, specifically for carbon–carbon bond formation. Collectively, these advances address the longstanding challenge of late‐stage cross‐coupling of functionalized alkyl fragments. Empowered by the notion that photocatalytically generated alkyl radicals readily undergo capture by Ni complexes, wholly new feedstocks for cross‐coupling have been realized. Herein, we highlight recent developments in several types of alkyl cross‐couplings that are accessible exclusively through this approach.
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Cites
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Photoredox Catalysis in Organic Chemistry
Shaw, M. H., Twilton, J., & MacMillan, D. W. C. (2016) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.6b01449 · Cited by 3,186
Palladium‐Catalyzed Cross‐Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize
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The Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates
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Dual Catalysis Strategies in Photochemical Synthesis
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Recent advances in homogeneous nickel catalysis
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The merger of transition metal and photocatalysis
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Catalysis for fluorination and trifluoromethylation
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Late-stage C–H functionalization offers new opportunities in drug discovery
Guillemard, L., Kaplaneris, N., Ackermann, L., & Johansson, M. J. (2021) · Nature Reviews Chemistry · doi:10.1038/s41570-021-00300-6 · Cited by 837
Tay, N. E. S., Lehnherr, D., & Rovis, T. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00384 · Cited by 518
Strategic Use of Visible-Light Photoredox Catalysis in Natural Product Synthesis
Pitre, S. P., & Overman, L. E. (2022) · Chemical Reviews · doi:10.1021/acs.chemrev.1c00247 · Cited by 486
New Redox Strategies in Organic Synthesis by Means of Electrochemistry and Photochemistry
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Metadata
- Authors
- Milligan, J. A., Phelan, J. P., Badir, S. O., & Molander, G. A.
- Venue
- Angewandte Chemie International Edition
- Publisher
- Wiley
- Published
- 2019-02-27
- Volume
- 58
- Issue
- 19
- Pages
- 6152-6163
- ISSN
- 1433-7851 (ISSN-L)
- 1521-3773
- OpenAlex
- W2895656588
- Cited by
- 623
- References
- 68
- FWCI
- 26.38
- Type
- journal article
- Language
- en
- Open access
- green
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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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