Rhodium-Catalyzed Asymmetric Allylic Dearomatization of β-Naphthols via Tandem Etherification/Claisen Rearrangement

Transition metal-catalyzed asymmetric allylic dearomatization of β-naphthols provides efficient access to enantioenriched naphthalenones. However, these reactions generally suffer from limited substrate scope, incompatibility with alkyl-substituted allylic electrophiles, and poor understandings of the reaction mechanism. Herein, we report a rhodium-catalyzed asymmetric allylic dearomatization of β-naphthols utilizing a bisdihydrobenzooxaphosphole (BIBOP) chiral ligand. This catalytic system displays high yields and enantioselectivity and broad substrate scope, efficiently accommodating both alkyl- and aryl-substituted allylic carbonates. Detailed mechanistic studies reveal that the reaction proceeds through a tandem asymmetric allylic etherification/Claisen rearrangement sequence. This provides critical insights into the fundamental pathways for the asymmetric allylic dearomatization of naphthols.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-08-20
DOI
https://doi.org/10.1021/jacs.5c11943
Citations
6
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
5.62

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article

Rhodium-Catalyzed Asymmetric Allylic Dearomatization of β-Naphthols via Tandem Etherification/Claisen Rearrangement

Hu-Chong Wang, Ting-Jia Sun, Ziqi Yang, Qing Gu et al.
6 citations
Journal of the American Chemical Society
Asymmetric Synthesis and Catalysis
5.62
article

Rhodium-Catalyzed Asymmetric Allylic Dearomatization of β-Naphthols via Tandem Etherification/Claisen Rearrangement

Hu-Chong Wang, Ting-Jia Sun, Ziqi Yang, Qing Gu, Shu‐Li You
article en
6 citations

Abstract

Transition metal-catalyzed asymmetric allylic dearomatization of β-naphthols provides efficient access to enantioenriched naphthalenones. However, these reactions generally suffer from limited substrate scope, incompatibility with alkyl-substituted allylic electrophiles, and poor understandings of the reaction mechanism. Herein, we report a rhodium-catalyzed asymmetric allylic dearomatization of β-naphthols utilizing a bisdihydrobenzooxaphosphole (BIBOP) chiral ligand. This catalytic system displays high yields and enantioselectivity and broad substrate scope, efficiently accommodating both alkyl- and aryl-substituted allylic carbonates. Detailed mechanistic studies reveal that the reaction proceeds through a tandem asymmetric allylic etherification/Claisen rearrangement sequence. This provides critical insights into the fundamental pathways for the asymmetric allylic dearomatization of naphthols.

Journal of the American Chemical SocietyVol. 147(35)
Shanghai Institute of Organic Chemistry (CN), University of Chinese Academy of Sciences (CN)
National Natural Science Foundation of China, Ministry of Science and Technology of the People's Republic of China, Shanghai Municipal Education Commission, Science and Technology Commission of Shanghai Municipality
Openalex Percentile: Top 4%
Asymmetric Synthesis and Catalysis
5.62
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