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.
Authors
- pengfei yu
- Xingang Xie (ORCID: https://orcid.org/0000-0002-0707-1229)
- Tao Liu (ORCID: https://orcid.org/0000-0001-6763-6271)
- Yunxia Yang (ORCID: https://orcid.org/0000-0003-3545-9244)
- Gaoyuan Zhao (ORCID: https://orcid.org/0000-0003-4838-865X)
- Huilin Li (ORCID: https://orcid.org/0000-0001-8088-6718)
- Jia Li (ORCID: https://orcid.org/0000-0002-3148-6897)
- Xuegong She (ORCID: https://orcid.org/0000-0002-3002-2433)
- Yan Zhang
- Kai Liu
Institutions
- Lanzhou University (CN)
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
- Field-Weighted Citation Impact
- 0.00