Photocatalytic Diheteroarylation of [1.1.1]Propellane for the Construction of 1,3-Diheteroaryl Bicyclo[1.1.1]pentanes

Herein, we report a visible light-induced diheteroarylation reaction of [1.1.1]propellane to synthesize 1,3-diheteroaryl bicyclo[1.1.1]pentanes (BCPs). In this approach, heteroaryl radicals are generated from heteroaryl halides via photocatalysis and subsequently added to [1.1.1]propellane. The <i>in situ</i> generated BCP radicals are then trapped by various heterocycles to furnish 1,3-diheteroaryl BCPs. Notably, this strategy features metal-free, mild conditions and utilizes inexpensive catalyst. For the first time, the diheteroarylation of [1.1.1]propellane could be achieved via a radical strategy, allowing for the efficient synthesis of 1,3-diheteroaryl BCPs with various applications in organic and medicinal chemistry.

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Publication Details

Journal
Organic Letters
Published
2024-10-23
DOI
https://doi.org/10.1021/acs.orglett.4c03198
Citations
9
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
2.25

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article

Photocatalytic Diheteroarylation of [1.1.1]Propellane for the Construction of 1,3-Diheteroaryl Bicyclo[1.1.1]pentanes

Xinpeng Jiang, Zhihao Yu, Guoxiang Bao, Yue Wang et al.
9 citations
Organic Letters
Radical Photochemical Reactions
2.25
article

Photocatalytic Diheteroarylation of [1.1.1]Propellane for the Construction of 1,3-Diheteroaryl Bicyclo[1.1.1]pentanes

Xinpeng Jiang, Zhihao Yu, Guoxiang Bao, Yue Wang, Jiacheng Li, Wenhao Xu, Wei Zhou, Longyi Li
article en
9 citations

Abstract

Herein, we report a visible light-induced diheteroarylation reaction of [1.1.1]propellane to synthesize 1,3-diheteroaryl bicyclo[1.1.1]pentanes (BCPs). In this approach, heteroaryl radicals are generated from heteroaryl halides via photocatalysis and subsequently added to [1.1.1]propellane. The <i>in situ</i> generated BCP radicals are then trapped by various heterocycles to furnish 1,3-diheteroaryl BCPs. Notably, this strategy features metal-free, mild conditions and utilizes inexpensive catalyst. For the first time, the diheteroarylation of [1.1.1]propellane could be achieved via a radical strategy, allowing for the efficient synthesis of 1,3-diheteroaryl BCPs with various applications in organic and medicinal chemistry.

Organic LettersVol. 26(43)
Pharmaceutical Biotechnology (Czechia) (CZ), Zhejiang University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 12%
Radical Photochemical Reactions
2.25
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Photocatalytic Diheteroarylation of [1.1.1]Propellane for the Construction of 1,3-Diheteroaryl Bicyclo[1.1.1]pentanes — Xinpeng Jiang, Zhihao Yu, et al. · Organic Letters (2024) | TGRS Research Map | TGRS