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

IF 4.9 1区 化学 Q1 CHEMISTRY, ORGANIC Organic Letters Pub Date : 2024-09-17 DOI:10.1021/acs.orglett.4c02985
Yingfei Tan, Meiting Pei, Kang Yang, Tingting Zhou, Anhua Hu, Jing-Jing Guo
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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.

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通过电子供体-受体复合物光激发催化生成吡啶基自由基:2-Pyridylindole-Based Heterobiaryls 的合成
我们报告了通过光激发电子供体-受体(EDA)复合物催化生成吡啶基自由基的过程,从而实现了吲哚在环境条件下的 C2 选择性杂芳基化。在该歧管中,催化三芳基胺和氯吡啶在无机碱存在下聚合成一个 EDA 复合物,使容易获得的氯吡啶成为生成各种吡啶基的良好前体。鉴于反应范围广泛,这种催化 EDA 复合物方案为获得广泛存在于重要生物分子中的杂多芳基支架提供了可靠的途径。
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来源期刊
Organic Letters
Organic Letters 化学-有机化学
CiteScore
9.30
自引率
11.50%
发文量
1607
审稿时长
1.5 months
期刊介绍: Organic Letters invites original reports of fundamental research in all branches of the theory and practice of organic, physical organic, organometallic,medicinal, and bioorganic chemistry. Organic Letters provides rapid disclosure of the key elements of significant studies that are of interest to a large portion of the organic community. In selecting manuscripts for publication, the Editors place emphasis on the originality, quality and wide interest of the work. Authors should provide enough background information to place the new disclosure in context and to justify the rapid publication format. Back-to-back Letters will be considered. Full details should be reserved for an Article, which should appear in due course.
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