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.

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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
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article

Total Synthesis of (±)-Crokonoid A

Dan Forster, Jieping Zhu, Qian Wang
1 citations
Journal of the American Chemical Society
Bioactive Natural Diterpenoids Research
0.81
article

Total Synthesis of (±)-Crokonoid A

Dan Forster, Jieping Zhu, Qian Wang
article en
1 citations

Abstract

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.

Journal of the American Chemical SocietyVol. 147(40)
Chemical Synthesis Lab (SG), École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 23%
Bioactive Natural Diterpenoids Research
0.81
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