| Literature DB >> 32277730 |
Qihao Wu1,2, Song-Wei Li1,3, Heng Xu1, Hong Wang2, Pei Hu1, Hao Zhang1, Cheng Luo1,4, Kai-Xian Chen1,4, Bastien Nay5, Yue-Wei Guo1,4, Xu-Wen Li1,4.
Abstract
Placobranchus ocellatus is well known to produce diverse and complex γ-pyrone polypropionates. In this study, the chemical investigation of P. ocellatus from the South China Sea led to the discovery and identification of ocellatusones A-D, a series of racemic non-γ-pyrone polyketides with novel skeletons, characterized by a bicyclo[3.2.1]octane (1, 2), a bicyclo[3.3.1]nonane (3) or a mesitylene-substituted dimethylfuran-3(2H)-one core (4). Extensive spectroscopic analysis, quantum chemical computation, chemical synthesis, and/or X-ray diffraction analysis were used to determine the structure and absolute configuration of the new compounds, including each enantiomer of racemic compounds 1-4 after chiral HPLC resolution. An array of new and diversity-generating rearrangements is proposed to explain the biosynthesis of these unusual compounds based on careful structural analysis and comparison with six known co-occurring γ-pyrones (5-10). Furthermore, the successful biomimetic semisynthesis of ocellatusone A (1) confirmed the proposed rearrangement through an unprecedented acid induced cascade reaction.Entities:
Keywords: Sacoglossan mollusk; biomimetic synthesis; biosynthetic rearrangements; marine natural products; polyketides
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Year: 2020 PMID: 32277730 DOI: 10.1002/anie.202003643
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336