Visible-Light-Induced Cascade Radical Trifluoromethylation/Cyclization/Dearomatization of Isocyanide-Containing Indoles: Synthesis of Trifluoromethylated 3-Spiroindolines
A visible-light-induced cascade radical trifluoromethylation/cyclization/dearomatization reaction between isocyanide-containing indoles and CF<sub>3</sub>Br has been developed to afford trifluoromethylated spiro[indole-3,3-quinoline] and spiro [indole-3,3-pyrrole] derivatives in good yields. The utility of the process is demonstrated by a scale-up experiment. The mechanism was proposed based on the control experiments. The protocol constitutes a novel and efficient route for the synthesis of trifluoromethylated 3-spiroindolenines with advantages of good generality and practical applicability, broad substrate scope, and green energy source.
Authors
- Yulai Hu (ORCID: https://orcid.org/0000-0002-9630-4150)
- Zhoubin Deng
- Zhiguang Zhu (ORCID: https://orcid.org/0009-0008-7859-9734)
- Danfeng Huang (ORCID: https://orcid.org/0000-0002-5848-1164)
- Yuyu Lv (ORCID: https://orcid.org/0000-0002-9044-3934)
- Junjiao Wang (ORCID: https://orcid.org/0000-0002-5091-5263)
- Ke‐Hu Wang
Institutions
- Northwest Normal University (CN)
- Lanzhou University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2024-12-04
- DOI
- https://doi.org/10.1021/acs.joc.4c02349
- Citations
- 7
- Primary Topic
- Fluorine in Organic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 1.46
Funders
- National Natural Science Foundation of China