Electrochemical Cascade Reactions of 1,2,3-Benzotriazinones with Alkynes to Assemble 3,4-Dihydroisoquinolin-1(2<i>H</i>)-ones

An unexpected electrochemical cascade reaction of 1,2,3-benzotriazinones with alkynes to assemble 3,4-dihydroisoquinolin-1(2<i>H</i>)-ones has been developed, which avoids the use of pressurized H<sub>2</sub>, any metal catalysts, and stoichiometric redox agents. This route tolerates a wide range of functional groups in both reactants and can be performed under an air atmosphere. The process of continuous cathodic reduction was demonstrated by control experiments and cyclic voltammograms. Moreover, the gram-scale reaction confirmed the potential of this environmentally benign method for practical applications.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-04-21
DOI
https://doi.org/10.1021/acs.joc.5c00022
Citations
1
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
0.94
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article

Electrochemical Cascade Reactions of 1,2,3-Benzotriazinones with Alkynes to Assemble 3,4-Dihydroisoquinolin-1(2H)-ones

Jinkang Chen, Q. H. Song, Da-Ming Wei, A. A. Chen et al.
1 citations
The Journal of Organic Chemistry
Synthesis and Biological Evaluation
0.94
article

Electrochemical Cascade Reactions of 1,2,3-Benzotriazinones with Alkynes to Assemble 3,4-Dihydroisoquinolin-1(2H)-ones

Jinkang Chen, Q. H. Song, Da-Ming Wei, A. A. Chen, Zhijun Lei, Xudong Wu, Quan Huang, Min Liu, S. L. Lu, Sanfei Nian
article en
1 citations

Abstract

An unexpected electrochemical cascade reaction of 1,2,3-benzotriazinones with alkynes to assemble 3,4-dihydroisoquinolin-1(2<i>H</i>)-ones has been developed, which avoids the use of pressurized H<sub>2</sub>, any metal catalysts, and stoichiometric redox agents. This route tolerates a wide range of functional groups in both reactants and can be performed under an air atmosphere. The process of continuous cathodic reduction was demonstrated by control experiments and cyclic voltammograms. Moreover, the gram-scale reaction confirmed the potential of this environmentally benign method for practical applications.

The Journal of Organic ChemistryVol. 90(17)
Zhejiang Hisun Pharmaceutical (China) (CN), Yibin University (CN), Zhejiang Pharmaceutical College (CN)
Openalex Percentile: Top 27%
Synthesis and Biological Evaluation
0.94
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