Chemical Synthesis of Polygalacic Acid from Oleanolic Acid Enabled by Three Site-Selective C–H Oxidations

Abstract The first chemical synthesis of polygalacic acid was accomplished from readily available oleanolic acid through three complementary site-selective C–H oxidation reactions. Key transformations include palladium-catalyzed directed C–23 oxidation, base-promoted C–2 α-oxidation, and copper-mediated directed C–16 hydroxylation, enabling selective installation of three oxygen functionalities onto the pentacyclic triterpenoid scaffold. This work demonstrates an oxidation-based strategy for converting an abundant triterpenoid into a more highly oxygenated natural product.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2026-11-11
DOI
https://doi.org/10.1021/acs.joc.6c02498
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

Chemical Synthesis of Polygalacic Acid from Oleanolic Acid Enabled by Three Site-Selective C–H Oxidations

pengfei yu, Xingang Xie, Tao Liu, Yunxia Yang et al.
The Journal of Organic Chemistry
Natural product bioactivities and synthesis
article

Chemical Synthesis of Polygalacic Acid from Oleanolic Acid Enabled by Three Site-Selective C–H Oxidations

pengfei yu, Xingang Xie, Tao Liu, Yunxia Yang, Gaoyuan Zhao, Huilin Li, Jia Li, Xuegong She, Yan Zhang, Kai Liu
article en

Abstract

Abstract The first chemical synthesis of polygalacic acid was accomplished from readily available oleanolic acid through three complementary site-selective C–H oxidation reactions. Key transformations include palladium-catalyzed directed C–23 oxidation, base-promoted C–2 α-oxidation, and copper-mediated directed C–16 hydroxylation, enabling selective installation of three oxygen functionalities onto the pentacyclic triterpenoid scaffold. This work demonstrates an oxidation-based strategy for converting an abundant triterpenoid into a more highly oxygenated natural product.

The Journal of Organic Chemistry
Lanzhou University (CN)
Natural product bioactivities and synthesis
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