Visible Light-Induced Arylation/Alkylation/Phosphorylation of Isocyanides via EDA Complex Activation

Shichao Yang , Xiangwen Tan , Dan Liu , Huanfeng Jiang , Wanqing Wu

Chinese Journal of Chemistry ›› 2025, Vol. 43 ›› Issue (12) : 1379 -1384.

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Chinese Journal of Chemistry ›› 2025, Vol. 43 ›› Issue (12) : 1379 -1384. DOI: 10.1002/cjoc.70000
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Visible Light-Induced Arylation/Alkylation/Phosphorylation of Isocyanides via EDA Complex Activation

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Abstract

Herein, it is reported that the aryl radicals derived from aryl thianthrenium salts are used as coupling partner in the arylation reactions of isocyanides, simultaneously as initiators for the formation of alkyl and phosphoryl radicals from ethers and diarylphosphine oxides. This cascade cyclization reaction leads to diverse arylated, alkylated and phosphorylated heteroaromatic compounds. Notably, this transformation can be achieved without the aid of metals or photocatalysts, exhibiting a wide substrate applicability and operational simplicity. Mechanistic studies suggest the involvement of radical processes and electron donor-acceptor (EDA) complexes in this transformation.

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Aryl thianthrenium salts / Isocyanides / Cascade cyclization / Heteroaromatic compounds / Electron donor-acceptor (EDA) / Photoredox catalysis / Cyclization / Hydrogen atom transfer

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Shichao Yang, Xiangwen Tan, Dan Liu, Huanfeng Jiang, Wanqing Wu. Visible Light-Induced Arylation/Alkylation/Phosphorylation of Isocyanides via EDA Complex Activation. Chinese Journal of Chemistry, 2025, 43(12): 1379-1384 DOI:10.1002/cjoc.70000

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