Enantioselective Synthesis of Hydrindanes via Palladium-Catalyzed Asymmetric Desymmetrization of Cyclohexadiene Derivatives
We herein disclose a strategy for the asymmetric desymmetrization of cyclohexadiene derivatives via a palladium-catalyzed Heck and tandem Heck/Tsuji-Trost allylic alkoxylation reaction. By employing DCE as the solvent, we obtained a variety of chiral hydrindanes containing an all-carbon quaternary carbon center and a tertiary carbon chiral center in good yields with excellent enantioselectivities. With alcohols as the solvent, the valuable chiral hydrindanes with one quaternary stereocenter and two tertiary centers were constructed with a high level of enantioinduction.
Authors
- Aijun Lin (ORCID: https://orcid.org/0000-0001-5786-4537)
- Jiajun Lu
- Miaomiao Li (ORCID: https://orcid.org/0000-0003-2132-6168)
- Chi Yang (ORCID: https://orcid.org/0000-0002-3436-8554)
- Yue Huang (ORCID: https://orcid.org/0000-0001-5845-4839)
- Shu Sen Wu
Institutions
- China Pharmaceutical University (CN)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-02-05
- DOI
- https://doi.org/10.1021/acs.orglett.4c04733
- 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 Jiangsu Province
- State Key Laboratory of Natural Medicines