Catalytic Asymmetric Intramolecular Domino Allylic O-Alkylation/Allylic Dearomatization of Allyl Aryl Ethers

An intramolecular asymmetric allylic O-alkylation/allylic dearomative spirocyclization cascade has been successfully developed with allyl aryl ethers. In the presence of palladium and a phosphoramidite ligand, a series of spirocyclohexadienones with an exocyclic double bond were obtained in up to 98% yield with 98% ee. The asymmetric allylic alkylation mechanism was elucidated through control experiments. In addition, scale-up of the reaction and further transformations of the spirocyclic products were also performed, demonstrating the potential application of this method.

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Publication Details

Journal
Organic Letters
Published
2025-06-02
DOI
https://doi.org/10.1021/acs.orglett.5c01540
Citations
3
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
2.81

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article

Catalytic Asymmetric Intramolecular Domino Allylic O-Alkylation/Allylic Dearomatization of Allyl Aryl Ethers

Dong‐Chao Wang, Kun Wang, Hai‐Ming Guo, Yinglong Li et al.
3 citations
Organic Letters
Asymmetric Synthesis and Catalysis
2.81
article

Catalytic Asymmetric Intramolecular Domino Allylic O-Alkylation/Allylic Dearomatization of Allyl Aryl Ethers

Dong‐Chao Wang, Kun Wang, Hai‐Ming Guo, Yinglong Li, Yun-Qiao Zhang
article en
3 citations

Abstract

An intramolecular asymmetric allylic O-alkylation/allylic dearomative spirocyclization cascade has been successfully developed with allyl aryl ethers. In the presence of palladium and a phosphoramidite ligand, a series of spirocyclohexadienones with an exocyclic double bond were obtained in up to 98% yield with 98% ee. The asymmetric allylic alkylation mechanism was elucidated through control experiments. In addition, scale-up of the reaction and further transformations of the spirocyclic products were also performed, demonstrating the potential application of this method.

Organic LettersVol. 27(23)
Henan Normal University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Henan Province, Henan Key Laboratory of Organic Functional Molecules and Drug Innovation
Openalex Percentile: Top 10%
Asymmetric Synthesis and Catalysis
2.81
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Catalytic Asymmetric Intramolecular Domino Allylic O-Alkylation/Allylic Dearomatization of Allyl Aryl Ethers — Dong‐Chao Wang, Kun Wang, et al. · Organic Letters (2025) | TGRS Research Map | TGRS