Enantioselective Total Synthesis of (+)-Fusicoccadiene via Photocatalytic Polyene Isomerization

The fusicoccane diterpenes have amassed interest for their intricate 5-8-5 tricyclic framework and ability to interface with diverse signaling proteins. Herein, we report an enantioselective synthetic platform for the rapid assembly of fusicoccanes where the 5-8-5 motif is prepared via valence bond isomerization of a polyene precursor. A series of regio- and stereoselective modifications to the periphery of this substructure provides entry to diverse fusicoccane congeners. The utility of this strategy is demonstrated with a concise total synthesis of (+)-fusicoccadiene.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-12-31
DOI
https://doi.org/10.1021/jacs.5c19654
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39
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article

Enantioselective Total Synthesis of (+)-Fusicoccadiene via Photocatalytic Polyene Isomerization

James H. Frederich, Jacqueline Pinkerton, Vitalii S. Basistyi, James A. Law et al.
1 citations
Journal of the American Chemical Society
Microbial Natural Products and Biosynthesis
1.39
article

Enantioselective Total Synthesis of (+)-Fusicoccadiene via Photocatalytic Polyene Isomerization

James H. Frederich, Jacqueline Pinkerton, Vitalii S. Basistyi, James A. Law, Tyler Weinhold
article en
1 citations

Abstract

The fusicoccane diterpenes have amassed interest for their intricate 5-8-5 tricyclic framework and ability to interface with diverse signaling proteins. Herein, we report an enantioselective synthetic platform for the rapid assembly of fusicoccanes where the 5-8-5 motif is prepared via valence bond isomerization of a polyene precursor. A series of regio- and stereoselective modifications to the periphery of this substructure provides entry to diverse fusicoccane congeners. The utility of this strategy is demonstrated with a concise total synthesis of (+)-fusicoccadiene.

Journal of the American Chemical SocietyVol. 148(1)
Florida State University (US), Laboratory of Molecular Genetics (PL)
Openalex Percentile: Top 13%
Microbial Natural Products and Biosynthesis
1.39
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