Synthesis of Substituted 3‐Allyl‐1‐Methylindolin‐2‐Ones by Palladium‐Catalyzed Cyclization of N‐(2‐Iodophenyl)‐N‐Methylbicyclo[1.1.0]Butane‐1‐Carboxamides

As a novel class of reactive electrophiles, bicyclo[1.1.0]butanes (BCB) remain relatively underexplored. Herein, a palladium‐catalyzed reaction of bicyclo[1.1.0]butanes is disclosed that provides a variety of 3‐allylindolin‐2‐ones in moderate‐to‐excellent yields with very good functional group tolerance. This protocol features mild reaction conditions and broad substrate scope.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-05-19
DOI
https://doi.org/10.1002/ejoc.202500321
Citations
1
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.94

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article

Synthesis of Substituted 3‐Allyl‐1‐Methylindolin‐2‐Ones by Palladium‐Catalyzed Cyclization of N‐(2‐Iodophenyl)‐N‐Methylbicyclo[1.1.0]Butane‐1‐Carboxamides

Wei Guo, Yongdong Li, Anzhi Li, Jiali Lin et al.
1 citations
European Journal of Organic Chemistry
Asymmetric Synthesis and Catalysis
0.94
article

Synthesis of Substituted 3‐Allyl‐1‐Methylindolin‐2‐Ones by Palladium‐Catalyzed Cyclization of N‐(2‐Iodophenyl)‐N‐Methylbicyclo[1.1.0]Butane‐1‐Carboxamides

Wei Guo, Yongdong Li, Anzhi Li, Jiali Lin, Shuyu Jia, Jiayi Shen, Sheng Chen, Zhiyong Tan
article en
1 citations

Abstract

As a novel class of reactive electrophiles, bicyclo[1.1.0]butanes (BCB) remain relatively underexplored. Herein, a palladium‐catalyzed reaction of bicyclo[1.1.0]butanes is disclosed that provides a variety of 3‐allylindolin‐2‐ones in moderate‐to‐excellent yields with very good functional group tolerance. This protocol features mild reaction conditions and broad substrate scope.

European Journal of Organic ChemistryVol. 28(29)
Gannan Normal University (CN), Jiangxi College of Applied Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 26%
Asymmetric Synthesis and Catalysis
0.94
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