Molecular editing of 3-hydroxyphenyl oxindole derivatives <i>via</i> formal O-insertion and N-insertion: synthesis of dioxolane spirooxindoles and quinoxalin-2(1 <i>H</i> )-ones

Molecular editing of 3-hydroxyphenyl oxindole derivatives via formal O-insertion and N-insertion has been developed for synthesis of dioxolane spirooxindoles and quinoxalin-2(1 H )-ones.

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Publication Details

Journal
Organic Chemistry Frontiers
Published
2025-10-22
DOI
https://doi.org/10.1039/d5qo01334h
Citations
4
Primary Topic
Synthesis and Biological Evaluation
Type
article
Field-Weighted Citation Impact
3.74
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article

Molecular editing of 3-hydroxyphenyl oxindole derivatives via formal O-insertion and N-insertion: synthesis of dioxolane spirooxindoles and quinoxalin-2(1 H )-ones

Tiesheng Shi, Fangzhi Hu, Houchen Wang, Yao‐Bin Shen et al.
4 citations
Organic Chemistry Frontiers
Synthesis and Biological Evaluation
3.74
article

Molecular editing of 3-hydroxyphenyl oxindole derivatives via formal O-insertion and N-insertion: synthesis of dioxolane spirooxindoles and quinoxalin-2(1 H )-ones

Tiesheng Shi, Fangzhi Hu, Houchen Wang, Yao‐Bin Shen, Peng Wang, Shuai‐Shuai Li, Jiawei Li
article en
4 citations

Abstract

Molecular editing of 3-hydroxyphenyl oxindole derivatives via formal O-insertion and N-insertion has been developed for synthesis of dioxolane spirooxindoles and quinoxalin-2(1 H )-ones.

Organic Chemistry FrontiersVol. 13(1)
Qingdao Agricultural University (CN), Zaozhuang University (CN)
Openalex Percentile: Top 7%
Synthesis and Biological Evaluation
3.74
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