Two known C-glycosylflavones, swertisin and embinoidin, were isolated from the leaves of Anthurium aripoense, and characterized by room temperature 1D and 2DNMR experiments. At this temperature, the 1H-and 13C-NMR spectra of these C-glycosylflavones revealed doubling of signals, which suggested the presence of two rotamers in solution. Variable-temperature (VT) 1H-NMR studies supported this hypothesis. The T-ROESY data, in addition to the theoretical (MM2) calculations utilizing the Chem3D Pro software, confirmed the hypothesis that the two rotamers interchange via rotation about the C-glycosidic bond. © 2012 by the authors.
CITATION STYLE
Frank, J. H., Powder-George, Y. L., Ramsewak, R. S., & Reynolds, W. F. (2012). Variable-temperature 1H-NMR studies on two C-glycosylflavones. Molecules, 17(7), 7914–7926. https://doi.org/10.3390/molecules17077914
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