4.8 Article

Radical Alkene-Trifluoromethylation-Triggered Nitrile Insertion/Remote Functionalization Relay Processes: Diverse Synthesis of Trifluoromethylated Azaheterocycles Enabled by Copper Catalysis

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ORGANIC LETTERS
卷 24, 期 4, 页码 1110-1115

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AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.2c00083

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  1. National Natural Science Foundation of China [21772063]

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A copper-catalyzed alkene-trifluoromethylation-triggered nitrile insertion/remote functionalization relay process has been developed, which involves the generation of iminyl radical intermediates through interrupted remote 1,n-difunctionalizations of alkenes with nitrite insertion, followed by subsequent 1,n-HAT to achieve remote functionalization. This relay protocol provides a straightforward approach for the assembly of structurally diverse trifluoromethylated azaheterocycles.
A copper-catalyzed alkene-trifluoromethylation-triggered nitrile insertion/remote functionalization relay process has been achieved, in which interrupted remote 1,n-difunctionalizations of alkenes with nitrite insertion can deliver iminyl radical intermediates instead of C-based radicals, followed by subsequent 1,n-HAT to furnish corresponding remote functionalization. This relay protocol enables a straightforward approach to streamline the assembly of structurally diverse trifluoromethylated azaheterocycles.

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