Improved Access to Succinimide-Fused Cyclobutenes

Succinimide-fused cyclobutenes are valuable building blocks for the synthesis of highly functionalized polycyclic structures. However, methods for constructing these structures-especially the N-aryl ones-remain limited. Herein, we provided an improved and rapid access to N-substituted succinimide-fused cyclobutenes by leveraging the copper-catalyzed Chan-Lam coupling. Desired products are afforded in 45-99% yields. Furthermore, this method features a broad substrate scope and good functional group compatibility.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-11-06
DOI
https://doi.org/10.1021/acs.joc.6c02123
Primary Topic
Catalytic Alkyne Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Improved Access to Succinimide-Fused Cyclobutenes

Zhanhui Yang, Jiaxi Xu, Xinru Zhang, Xiaojing Hou
The Journal of Organic Chemistry
Catalytic Alkyne Reactions
article

Improved Access to Succinimide-Fused Cyclobutenes

Zhanhui Yang, Jiaxi Xu, Xinru Zhang, Xiaojing Hou
article en

Abstract

Succinimide-fused cyclobutenes are valuable building blocks for the synthesis of highly functionalized polycyclic structures. However, methods for constructing these structures-especially the N-aryl ones-remain limited. Herein, we provided an improved and rapid access to N-substituted succinimide-fused cyclobutenes by leveraging the copper-catalyzed Chan-Lam coupling. Desired products are afforded in 45-99% yields. Furthermore, this method features a broad substrate scope and good functional group compatibility.

The Journal of Organic Chemistry
Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, Beijing Municipal Natural Science Foundation
Openalex Percentile: Top 27%
Catalytic Alkyne Reactions
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