Base‐Promoted [4 + 2] Annulation for the Synthesis of Tri‐Aryl Substituted <i>α</i>‐Pyrones

A transition‐metal‐free procedure for synthesizing tri‐aryl substituted α ‐pyrones has been developed. It involves conjugate addition, CO bond formation, and CO bond cleavage. This procedure provides an efficient protocol for the synthesis of multisubstituted α ‐pyrones from readily available starting materials. Notable features of this program are high atom economy and transition‐metal‐free.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2025-03-19
DOI
https://doi.org/10.1002/ejoc.202401430
Citations
1
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.94
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article

Base‐Promoted [4 + 2] Annulation for the Synthesis of Tri‐Aryl Substituted α‐Pyrones

Mengdan Wang, Jianyue Li, Fengmin Wu, Bingli Pan et al.
1 citations
European Journal of Organic Chemistry
Asymmetric Synthesis and Catalysis
0.94
article

Base‐Promoted [4 + 2] Annulation for the Synthesis of Tri‐Aryl Substituted α‐Pyrones

Mengdan Wang, Jianyue Li, Fengmin Wu, Bingli Pan, Kun Liu, Junying Ma, Xiaowei Wang, Junling Wang
article en
1 citations

Abstract

A transition‐metal‐free procedure for synthesizing tri‐aryl substituted α ‐pyrones has been developed. It involves conjugate addition, CO bond formation, and CO bond cleavage. This procedure provides an efficient protocol for the synthesis of multisubstituted α ‐pyrones from readily available starting materials. Notable features of this program are high atom economy and transition‐metal‐free.

European Journal of Organic ChemistryVol. 28(21)
Henan University of Science and Technology (CN)
Openalex Percentile: Top 28%
Asymmetric Synthesis and Catalysis
0.94
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