Total Synthesis and Stereochemical Assignment of Alternapyrone

Alternapyrone, a bioactive polyketide produced by the fungal host <i>Aspergillus oryzae</i>, is biosynthesized by a polyketide synthase encoded by the <i>alt1-5</i> gene cluster. Despite its known bioactivity, the stereochemical configuration of the three stereogenic centers in its polyketide backbone has remained unresolved. In this study, we determined the complete stereostructure of alternapyrone using an integrative approach that combines predictive, rule-based stereochemical analysis with experimental validation through total synthesis. The efficient total synthesis enabled the precise assignment of the hypothesized stereochemistry by matching the synthetic product to the natural compound. This comprehensive study conclusively established the absolute configuration of alternapyrone.

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Publication Details

Journal
Molecules
Published
2025-04-03
DOI
https://doi.org/10.3390/molecules30071597
Citations
1
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
1.39

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Total Synthesis and Stereochemical Assignment of Alternapyrone

Chao Xu, Bencan Tang, Hui Zhang, Di Wang et al.
1 citations
Molecules
Microbial Natural Products and Biosynthesis
1.39
article

Total Synthesis and Stereochemical Assignment of Alternapyrone

Chao Xu, Bencan Tang, Hui Zhang, Di Wang, Tao Ye, Jiaxuan Feng
article en
1 citations

Abstract

Alternapyrone, a bioactive polyketide produced by the fungal host <i>Aspergillus oryzae</i>, is biosynthesized by a polyketide synthase encoded by the <i>alt1-5</i> gene cluster. Despite its known bioactivity, the stereochemical configuration of the three stereogenic centers in its polyketide backbone has remained unresolved. In this study, we determined the complete stereostructure of alternapyrone using an integrative approach that combines predictive, rule-based stereochemical analysis with experimental validation through total synthesis. The efficient total synthesis enabled the precise assignment of the hypothesized stereochemistry by matching the synthetic product to the natural compound. This comprehensive study conclusively established the absolute configuration of alternapyrone.

MoleculesVol. 30(7)
University of Nottingham Ningbo China (CN), Peking University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Guangdong Province
Openalex Percentile: Top 22%
Microbial Natural Products and Biosynthesis
1.39
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