Total Synthesis of (±)-Crokonoid A
We report herein a total synthesis of crokonoid A, featuring a dually bridged 6/7/6/5-fused tetracyclic carbon framework incorporating an unprecedented tricyclo[4.4.1.1<sup>1,4</sup>]dodecane-2,11-dione core. The synthesis is highlighted by the following key transformations: (a) a regioselective decarboxylative allylation of a 1,3-dienyl carbonate to furnish an α-allyl-β,γ-unsaturated ketone; (b) a domino sequence involving ozonolysis, intramolecular aldol reaction, and acetalization to construct the bicyclo[4.3.1]decanedione core from a fused ring system, in which the acetalization step effectively stabilized the otherwise unstable aldol intermediate; (c) a palladium-catalyzed intramolecular cycloalkenylation of a ketone to assemble the bicyclo[3.2.1]octanedione system, in which the hybridization state of the neighboring carbon proved crucial for the success of this cyclization; and (d) SmI<sub>2</sub>-HMPA-mediated regio- and stereoselective reduction of the C14 ketone.
Authors
- Dan Forster
- Jieping Zhu (ORCID: https://orcid.org/0000-0002-8390-6689)
- Qian Wang
Institutions
- Chemical Synthesis Lab (SG)
- École Polytechnique Fédérale de Lausanne (CH)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2025-09-26
- DOI
- https://doi.org/10.1021/jacs.5c14479
- Citations
- 1
- Primary Topic
- Bioactive Natural Diterpenoids Research
- Type
- article
- Field-Weighted Citation Impact
- 0.81