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.
Authors
- Dong‐Chao Wang (ORCID: https://orcid.org/0000-0002-5037-4727)
- Kun Wang (ORCID: https://orcid.org/0000-0002-4563-0212)
- Hai‐Ming Guo (ORCID: https://orcid.org/0000-0003-0629-4524)
- Yinglong Li (ORCID: https://orcid.org/0000-0001-9098-5314)
- Yun-Qiao Zhang
Institutions
- Henan Normal University (CN)
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
Funders
- National Natural Science Foundation of China
- Natural Science Foundation of Henan Province
- Henan Key Laboratory of Organic Functional Molecules and Drug Innovation