Citation: Zhiyuan Bao, Chao Chen. Efficient synthesis of cyclic imides by the tandem N-arylation-acylation and rearrangement reaction of cyanoesters with diaryliodonium salts[J]. Chinese Chemical Letters, ;2023, 34(5): 107913. doi: 10.1016/j.cclet.2022.107913 shu

Efficient synthesis of cyclic imides by the tandem N-arylation-acylation and rearrangement reaction of cyanoesters with diaryliodonium salts

Zhiyuan Bao ,
Chao Chen ^*,

MOE Key Laboratory of Bioorganic Phosphorus Chemistry & Chemical Biology, Department of Chemistry, Tsinghua University, Beijing 100084, China

chenchao01@mails.tsinghua.edu.cn

Received Date: 22 August 2022
Revised Date: 9 October 2022
Accepted Date: 17 October 2022
Available Online: 20 October 2022

Figures(7)

Available online An efficient method for the synthesis of multi-substituted cyclic imides was developed with cyanoesters and diaryliodonium salts. This method proceeds through a cascade of N-arylation-acylation and rearrangement to give target heterocycles in good yields (up to 99%). This method has the major advantages of a broad substrate scope, excellent functional group compatibility. The strategy was also extended to the fused cyclic imides, such as malonimides, succinimides and glutarimides.
- Cyclic imides,
- Cyanoesters,
- Diaryliodonium salts,
- N-Arylation-acylation,
- Rearrangement
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