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.

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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

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article

Ru-Catalyzed Asymmetric Hydrogenation of Chiral δ-Hydroxy-β-Keto Acid Derivatives

Zhaoguo Zhang, Yuxuan Zhang, Limin Xu, Yan Lu
The Journal of Organic Chemistry
Asymmetric Hydrogenation and Catalysis
article

Ru-Catalyzed Asymmetric Hydrogenation of Chiral δ-Hydroxy-β-Keto Acid Derivatives

Zhaoguo Zhang, Yuxuan Zhang, Limin Xu, Yan Lu
article en

Abstract

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.

The Journal of Organic ChemistryVol. 90(21)
Shanghai Jiao Tong University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 91%
Asymmetric Hydrogenation and Catalysis
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