Total Synthesis of Berkeleyone A and Preaustinoid A through Epoxypolyene Cyclization
Abstract A bioinspired Lewis acid‐catalyzed epoxypolyene cyclization was developed to construct the tetracyclic framework containing a bicyclo[3.3.1]nonane core and seven chiral centers. The usage of this approach for assembling these natural products of 6/6/6/6 tetracyclic skeleton with bicyclo[3.3.1]nonane core is demonstrated by the total synthesis of highly oxidized berkeleyone A and preaustinoid A.
Authors
- Z. Chang (ORCID: https://orcid.org/0009-0008-5272-0364)
- Shengfu Duan
- Zhixiang Xie (ORCID: https://orcid.org/0000-0001-5809-3084)
- Xingyi Li (ORCID: https://orcid.org/0000-0002-6004-4174)
Institutions
- State Key Laboratory of Applied Organic Chemistry
- Lanzhou University (CN)
Publication Details
- Journal
- Angewandte Chemie
- Published
- 2024-10-24
- DOI
- https://doi.org/10.1002/ange.202416211
- Primary Topic
- Marine Sponges and Natural Products
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China