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Updated: Feb 14, 2026

Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Construction of bridged cyclic N,O-ketal spirooxindoles through a Michael addition/N,O-ketalization sequence
Yanshuo Zhu1, Jia Guo, Shaojing Jin
1Institute of Functional Organic Molecular Engineering, College of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, China. wangqilin@henu.edu.cn buzhanwei@henu.edu.cn.
Abstract:
The first highly diastereoselective TfOH-catalyzed Michael addition/N,O-ketalization sequence of 3-aminooxindoles and ortho-hydroxychalcones was achieved, delivering a wide range of bridged cyclic N,O-ketal spirooxindoles with complex and strained structures in 41-97% yields. Moreover, a gram-scale experiment and some chemical conversions were conducted to further demonstrate the synthetic value.
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