Cobalt-Catalyzed Enantioselective Dicarbofunctionalization of Acrylates
Catalytic enantioselective alkene difunctionalization represents a powerful tool for the rapid assembly of complex chiral molecules and has found wide range of applications in synthetic chemistry. Enantioselective control of the newly formed pro-chiral carbon centers using chiral cobalt catalyst, however, remains challenging. Herein, we report the first cobalt-catalyzed enantioselective difunctionalization of industry-relevant acrylates with lithium aryl boronates and α,α-dialkyl bromoacetate for the preparation of enantioenriched glutaric acid derivatives. Facile transformations of the resulting α-aryl esters to other functionalities have been achieved. To further showcase the synthetic utility of the current protocol, application to the enantioselective synthesis of an analog of (−)-preclamol was demonstrated.
Authors
- Yi Xu (ORCID: https://orcid.org/0000-0002-2549-1446)
- Jiejun Li
- Xiaolong Wan (ORCID: https://orcid.org/0000-0002-1138-6274)
- Qilong Shen (ORCID: https://orcid.org/0000-0001-5622-153X)
Institutions
- Shanghai Institute of Organic Chemistry (CN)
- University of Chinese Academy of Sciences (CN)
Publication Details
- Journal
- ACS Catalysis
- Published
- 2024-10-02
- DOI
- https://doi.org/10.1021/acscatal.4c03670
- Citations
- 5
- Primary Topic
- Catalytic C–H Functionalization Methods
- Type
- article
- Field-Weighted Citation Impact
- 1.25
Funders
- National Natural Science Foundation of China
- Chinese Academy of Sciences
- National Key Research and Development Program of China