Structure Elucidation of Biflavones With Ether Bonds by NMR‐Spectroscopy—Structure Revisions of Loniflavone and Methylloniflavone

For the structure elucidation of biflavones in which the subunits are linked by an ether bridge, two NMR spectroscopic approaches are shown to determine the position of the ether bridge, without derivatization of the compound. We show that the structures of the biflavones loniflavone and methylloniflavone, isolated from the leaves of Lonicera japonica Thunb. (Caprifoliaceae), have to be revised to ochnaflavone and methylochnaflavone, respectively.

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Publication Details

Journal
Magnetic Resonance in Chemistry
Published
2025-11-10
DOI
https://doi.org/10.1002/mrc.70058
Primary Topic
Biological Activity of Diterpenoids and Biflavonoids
Type
article
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article

Structure Elucidation of Biflavones With Ether Bonds by NMR‐Spectroscopy—Structure Revisions of Loniflavone and Methylloniflavone

Franz Bučar, L. D. Haas, Eva‐Maria Pferschy‐Wenzig, Fabian Alperth et al.
Magnetic Resonance in Chemistry
Biological Activity of Diterpenoids and Biflavonoids
article

Structure Elucidation of Biflavones With Ether Bonds by NMR‐Spectroscopy—Structure Revisions of Loniflavone and Methylloniflavone

Franz Bučar, L. D. Haas, Eva‐Maria Pferschy‐Wenzig, Fabian Alperth, Klaus Zangger, Olaf Kunert
article en

Abstract

For the structure elucidation of biflavones in which the subunits are linked by an ether bridge, two NMR spectroscopic approaches are shown to determine the position of the ether bridge, without derivatization of the compound. We show that the structures of the biflavones loniflavone and methylloniflavone, isolated from the leaves of Lonicera japonica Thunb. (Caprifoliaceae), have to be revised to ochnaflavone and methylochnaflavone, respectively.

Magnetic Resonance in ChemistryVol. 64(2)
University of Graz (AT), Research Center Pharmaceutical Engineering (Austria) (AT)
Openalex Percentile: Top 70%
Biological Activity of Diterpenoids and Biflavonoids
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