Phytochemistry2022,Vol.2007.DOI:10.1016/j.phytochem.2022.113205

Reassignment of the structures of pestalopyrones A–D

Wang W.-X. Li J. Tan Y.-F. Liu S. Tan G.-S. Wu X.-Q. Wang J. Xu K.-P. Zou Z.-X.
Phytochemistry2022,Vol.2007.DOI:10.1016/j.phytochem.2022.113205

Reassignment of the structures of pestalopyrones A–D

Wang W.-X. 1Li J. 2Tan Y.-F. 2Liu S. 2Tan G.-S. 2Wu X.-Q. 1Wang J. 1Xu K.-P. 1Zou Z.-X.1
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作者信息

  • 1. Xiangya School of Pharmaceutical Sciences
  • 2. Department of Pharmacy Xiangya Hospital
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Abstract

? 2022Pestalopyrones A–D are four unusual tricyclic pyrone derivatives with flexible chiral structures, isolated from the endophytic fungus Pestalotiopsis neglecta S3. The full elucidation of their structures was a challenging task, and remained unsolved in the original article. Herein, the relative configurations of pestalopyrones A and pestalopyrones B were unambiguously assigned by detailed analyses on spectroscopic data and GIAO 13C NMR calculation method with sorted training sets (STS). The planar structures of pestalopyrones C and pestalopyrones D were revised by reinterpretation of their reported spectroscopic data, and then their relative configurations were deduced by STS GIAO 13C NMR calculation and NOE analysis. The absolute configurations of all the mentioned compounds were determined by the comparison of their experimental and calculated ECD curves.

Key words

Amphisphaeriaceae/ECD/GIAO 13C NMR calculation/Pestalotiopsis neglecta/Relative configuration assignment/Structure revision

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出版年

2022
Phytochemistry

Phytochemistry

CCR
ISSN:0031-9422
参考文献量49
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