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.
Authors
- Xinpeng Jiang (ORCID: https://orcid.org/0000-0002-8205-1455)
- Zhihao Yu (ORCID: https://orcid.org/0000-0002-2437-0167)
- Guoxiang Bao
- Yue Wang (ORCID: https://orcid.org/0000-0002-4664-4587)
- Jiacheng Li (ORCID: https://orcid.org/0000-0002-4404-4895)
- Wenhao Xu (ORCID: https://orcid.org/0000-0001-7694-4268)
- Wei Zhou
- Longyi Li
Institutions
- Pharmaceutical Biotechnology (Czechia) (CZ)
- Zhejiang University of Technology (CN)
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
Funders
- National Natural Science Foundation of China