Reactivity in Nickel Catalyzed Multicomponent Sequential Reductive Cross-Coupling Reactions
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Angew Chem Int Ed - 2022 - Chen - Reactivity in Nickel Catalyzed Multicomponent Sequential Reductive Cross‐Coupling.pdf
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2023-06-21
Type
ArticleKAUST Department
King Abdullah University of Science and Technology KAUST Catalysis Center Chemical Science Program SAUDI ARABIAKAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division
Chemical Science Program
Date
2022-06-21Embargo End Date
2023-06-21Permanent link to this record
http://hdl.handle.net/10754/679245
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A nickel-catalyzed three-component reductive carbonylation of alkyl halides, aryl halides, and ethyl chloroformate is described. Ethyl chloroformate is utilized as a safe and readily available source of CO in this multi-component protocol, providing an efficient and practical alternative for the synthesis of aryl-alkyl ketones. The reaction exhibits a wide substrate scope and good functional group compatibility. Experimental and DFT mechanistic studies highlight the complexity the cross-electrophile coupling and provide insight into the sequence of the three consecutive oxidative additions of aryl halide, chloroformate and akyl halide.Citation
Chen, H., Yue, H., Zhu, C., & Rueping, M. (2022). Reactivity in Nickel Catalyzed Multicomponent Sequential Reductive Cross-Coupling Reactions. Angewandte Chemie International Edition. Portico. https://doi.org/10.1002/anie.202204144Sponsors
The authors thank the King Abdullah University of Science and Technology (KAUST) for financial support and the KAUST Supercomputing Laboratory for providing the computational resources of the Shaheen II supercomputer.Publisher
WileyAdditional Links
https://onlinelibrary.wiley.com/doi/10.1002/anie.202204144ae974a485f413a2113503eed53cd6c53
10.1002/anie.202204144