Highly diastereoselective synthesis of annulated 2‐acyl‐2,3‐dihydrofurans

Abstract A simple and convenient method to synthesize annulated 2‐acyl‐2,3‐dihydrofuran derivatives by Michael addition‐alkylation reaction of α‐bromochalcones and 5,5‐dimethylcyclohexane‐1,3‐dione is described. This transformation was well compatible with various α‐bromochalcones, and the corresponding 2‐acyl‐2,3‐dihydrofurans were obtained in yields of up to 98%.

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Publication Details

Journal
Journal of the Chinese Chemical Society
Published
2025-03-24
DOI
https://doi.org/10.1002/jccs.70002
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Highly diastereoselective synthesis of annulated 2‐acyl‐2,3‐dihydrofurans

Jun Yang, Lin Li, Jinxiang Feng, Guizhou Yue et al.
Journal of the Chinese Chemical Society
Asymmetric Synthesis and Catalysis
article

Highly diastereoselective synthesis of annulated 2‐acyl‐2,3‐dihydrofurans

Jun Yang, Lin Li, Jinxiang Feng, Guizhou Yue, Wenjie Zou, Qilin Huang, Juhua Feng, Juanhong Li, Ailin Huang, Kuan Liu
article en

Abstract

Abstract A simple and convenient method to synthesize annulated 2‐acyl‐2,3‐dihydrofuran derivatives by Michael addition‐alkylation reaction of α‐bromochalcones and 5,5‐dimethylcyclohexane‐1,3‐dione is described. This transformation was well compatible with various α‐bromochalcones, and the corresponding 2‐acyl‐2,3‐dihydrofurans were obtained in yields of up to 98%.

Journal of the Chinese Chemical SocietyVol. 72(4)
Sichuan Agricultural University (CN)
Natural Science Foundation of Sichuan Province
Openalex Percentile: Top 96%
Asymmetric Synthesis and Catalysis
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