Ru-Catalyzed Asymmetric Hydrogenation of Chiral δ-Hydroxy-β-Keto Acid Derivatives
Ru-catalyzed stereoselective asymmetric hydrogenation of multifunctionalized ketones has been a formidable challenge, and few related successful works have been reported. Herein, we report our research on Ru-catalyzed asymmetric hydrogenation of chiral δ-hydroxy-β-keto acid derivatives, which achieves excellent diastereoselectivity (up to >99% <i>de</i>). This procedure provides a new route for the synthesis of pure <i>syn</i>- and <i>anti</i>-3,5-dihydroxy acid derivatives, which serve as key intermediates in natural products and drug molecules, such as statins.
Authors
- Zhaoguo Zhang (ORCID: https://orcid.org/0000-0003-3270-6617)
- Yuxuan Zhang (ORCID: https://orcid.org/0000-0001-6905-3993)
- Limin Xu (ORCID: https://orcid.org/0000-0001-7990-4456)
- Yan Lu (ORCID: https://orcid.org/0000-0001-5148-7910)
Institutions
- Shanghai Jiao Tong University (CN)
Publication Details
- Journal
- The Journal of Organic Chemistry
- Published
- 2025-05-17
- DOI
- https://doi.org/10.1021/acs.joc.4c02766
- Primary Topic
- Asymmetric Hydrogenation and Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China