Visible light induced hydroxyfluoroalkylation of quinoxalin-2(1<i>H</i>)-ones with <i>N</i>-trifluoroethoxyphthalimide under catalyst-free conditions

For the first time, we achieved visible light-induced direct C3-hydroxyfluoroalkylation of quinoxalin-2(1<i>H</i>)-ones using <i>N</i>-trifluoroethoxyphthalimide as the trifluoroethanol radical precursor, without the need for a photocatalyst. The metal-free and catalyst-free nature of this method makes it an efficient and environmentally friendly approach for synthesizing C3-hydroxyfluoroalkylated quinoxalin-2(1<i>H</i>)-ones.

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Publication Details

Journal
Organic & Biomolecular Chemistry
Published
2024-11-22
DOI
https://doi.org/10.1039/d4ob01616e
Citations
3
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.75
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article

Visible light induced hydroxyfluoroalkylation of quinoxalin-2(1H)-ones with N-trifluoroethoxyphthalimide under catalyst-free conditions

Kui Lu, Xia Zhao, Siqi Li, Jing Liu et al.
3 citations
Organic & Biomolecular Chemistry
Synthesis and Biological Evaluation
0.75
article

Visible light induced hydroxyfluoroalkylation of quinoxalin-2(1H)-ones with N-trifluoroethoxyphthalimide under catalyst-free conditions

Kui Lu, Xia Zhao, Siqi Li, Jing Liu, Liting Liu, Mengfei Yang
article en
3 citations

Abstract

For the first time, we achieved visible light-induced direct C3-hydroxyfluoroalkylation of quinoxalin-2(1<i>H</i>)-ones using <i>N</i>-trifluoroethoxyphthalimide as the trifluoroethanol radical precursor, without the need for a photocatalyst. The metal-free and catalyst-free nature of this method makes it an efficient and environmentally friendly approach for synthesizing C3-hydroxyfluoroalkylated quinoxalin-2(1<i>H</i>)-ones.

Organic & Biomolecular ChemistryVol. 23(3)
Tianjin University of Science and Technology (CN), Tianjin Normal University (CN), China International Science and Technology Cooperation (CN)
Openalex Percentile: Top 31%
Synthesis and Biological Evaluation
0.75
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