Total Synthesis of (+)-Niduenes A and B
Niduenes A and B, two tetraquinane sesterterpenoids, possess a complex and intriguing 5/5/5/5/6 pentacyclic skeleton with eight contiguous stereocenters. We have achieved the first total synthesis of niduenes A and B in 16 and 14 steps, respectively. The synthesis features a Pauson-Khand reaction to generate the 5/5 bicycle, a Pd-catalyzed oxidative cyclization to construct the congested triquinane framework, and a radical cyclization to assemble the tetraquinane skeleton.
Authors
- Yanxing Jia (ORCID: https://orcid.org/0000-0002-9508-6622)
- Chuanzhen Tan
- H Lin
- Yuan Wang
Institutions
- Peking University (CN)
- State Key Laboratory of Natural and Biomimetic Drugs (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-06-25
- DOI
- https://doi.org/10.1021/jacs.6c08709
- Primary Topic
- Synthetic Organic Chemistry Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- National Outstanding Youth Science Fund Project of National Natural Science Foundation of China