Abstract
The 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 of the cross-electrophile coupling and provide insight into the sequence of the three consecutive oxidative additions of aryl halide, chloroformate, and alkyl halide.
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Chen, H., Yue, H., Zhu, C., & Rueping, M. (2022). Reactivity in Nickel-Catalyzed Multi-component Sequential Reductive Cross-Coupling Reactions. Angewandte Chemie - International Edition, 61(33). https://doi.org/10.1002/anie.202204144
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