Catalytic Generation of Pyridyl Radicals via Electron Donor–Acceptor Complex Photoexcitation: Synthesis of 2-Pyridylindole-Based Heterobiaryls

We report the catalytic generation of pyridyl radicals through photoexcitation of the electron donor-acceptor (EDA) complex, which enables the C2-selective heteroarylation of indole under ambient conditions. In this manifold, catalytic triarylamine and chloropyridine aggregate into an EDA complex in the presence of an inorganic base, making readily available chloropyridines good precursors for the generation of diverse pyridyl radicals. Given the broad reaction scope, this catalytic EDA complex protocol provides robust access to heterobiaryl scaffolds that are widely present in biologically important molecules.

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Publication Details

Journal
Organic Letters
Published
2024-09-17
DOI
https://doi.org/10.1021/acs.orglett.4c02985
Citations
8
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
2.00

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article

Catalytic Generation of Pyridyl Radicals via Electron Donor–Acceptor Complex Photoexcitation: Synthesis of 2-Pyridylindole-Based Heterobiaryls

Yingfei Tan, Jingjing Guo, Tingting Zhou, Anhua Hu et al.
8 citations
Organic Letters
Radical Photochemical Reactions
2.00
article

Catalytic Generation of Pyridyl Radicals via Electron Donor–Acceptor Complex Photoexcitation: Synthesis of 2-Pyridylindole-Based Heterobiaryls

Yingfei Tan, Jingjing Guo, Tingting Zhou, Anhua Hu, Meiting Pei, Kang Yang
article en
8 citations

Abstract

We report the catalytic generation of pyridyl radicals through photoexcitation of the electron donor-acceptor (EDA) complex, which enables the C2-selective heteroarylation of indole under ambient conditions. In this manifold, catalytic triarylamine and chloropyridine aggregate into an EDA complex in the presence of an inorganic base, making readily available chloropyridines good precursors for the generation of diverse pyridyl radicals. Given the broad reaction scope, this catalytic EDA complex protocol provides robust access to heterobiaryl scaffolds that are widely present in biologically important molecules.

Organic LettersVol. 26(38)
Lanzhou University (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 14%
Radical Photochemical Reactions
2.00
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