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.
Authors
- Hu-Chong Wang
- Ting-Jia Sun
- Ziqi Yang (ORCID: https://orcid.org/0000-0003-0784-935X)
- Qing Gu (ORCID: https://orcid.org/0000-0003-4963-2271)
- Shu‐Li You (ORCID: https://orcid.org/0000-0003-4586-8359)
Institutions
- Shanghai Institute of Organic Chemistry (CN)
- University of Chinese Academy of Sciences (CN)
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
Funders
- 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