NMR study of fumarprotocetraric acid, a complex lichen depsidone derivative from Cladonia furcata

Abstract A lichen depsidone derivative, fumarprotocetraric acid, was obtained as the major constituent of Cladonia furcata (Huds.) Schrad. collected in Iceland. In the 1 H NMR spectrum (in DMSO‐ d 6 ) of this compound, the trans double bond proton signals of the fumaryl unit appeared as overlapping...

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Bibliographic Details
Published in:Magnetic Resonance in Chemistry
Main Authors: Su, Bao‐Ning, Cuendet, Muriel, Nikolic, Dejan, Kristinsson, Hördur, Ingólfsdóttir, Kristín, van Breemen, Richard B., Fong, Harry H. S., Pezzuto, John M., Kinghorn, A. Douglas
Other Authors: National Cancer Institute
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2003
Subjects:
Doublets
Iceland
Online Access:http://dx.doi.org/10.1002/mrc.1181
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmrc.1181
https://onlinelibrary.wiley.com/doi/full/10.1002/mrc.1181
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Summary:Abstract A lichen depsidone derivative, fumarprotocetraric acid, was obtained as the major constituent of Cladonia furcata (Huds.) Schrad. collected in Iceland. In the 1 H NMR spectrum (in DMSO‐ d 6 ) of this compound, the trans double bond proton signals of the fumaryl unit appeared as overlapping singlets. To confirm the presence of a trans double bond in the molecule, fumarprotocetraric acid was treated with triethylamine. The 1 H NMR spectrum of the resultant triethylamine salt displayed a pair of clear doublets with coupling constants of 15.7 Hz, which are characteristic of a trans double bond. Unambiguous 1 H and 13 C NMR spectral data for both fumarprotocetraric acid and its triethylamine salt were assigned for the first time based on the interpretation of their 2D NMR (HMQC, HMBC and NOESY) spectra. Copyright © 2003 John Wiley & Sons, Ltd.

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