Benzaldehyde- And Nickel-Catalyzed Photoredox C(sp3)-H Alkylation/Arylation with Amides and Thioethers

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Abstract

Herein a synergistic combination of a nickel catalyst and benzaldehyde for the utilization of amides and thioethers in C(sp3)-H alkylation and arylation reactions employing simple aryl or alkyl halides is reported. This method provides a simple and cheap strategy for the direct functionalization of amides and thioethers. Readily available starting materials, mild reaction conditions, a good functional-group tolerance, and a broad substrate scope make this methodology attractive and practical for pharmaceutical and synthetic chemistry.

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Si, X., Zhang, L., & Hashmi, A. S. K. (2019). Benzaldehyde- And Nickel-Catalyzed Photoredox C(sp3)-H Alkylation/Arylation with Amides and Thioethers. Organic Letters, 21(16), 6329–6332. https://doi.org/10.1021/acs.orglett.9b02226

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