Butyrolactone 1 was isolated from the EtOAc fraction of the EtOH extract of the aerial part of Geranium charlesii (Aitch. & Hemsl.) Vved. The configurations of all chiral centers of 1 were established by an X-ray crystal structure analysis. The structure of 1 was (3S,4R,5S,6R,7S)-3-p-hydroxyphenyl-5,6,7-trihydroxyoxolan-1,4-olide or the trivial name sawaranin. The dynamics of sawaranin conformers were studied as a function of time in DMSO-d6 solution using NMR spectroscopy and quantum-chemical calculations.
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Translated from Khimiya Prirodnykh Soedinenii, No. 6, November–December, 2021, pp. 862–865.
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Siddikov, D.R., Bobakulov, K.M., Turgunov, K.K. et al. Conformational Dynamics and Absolute Configuration of Sawaranin. Chem Nat Compd 57, 1005–1009 (2021). https://doi.org/10.1007/s10600-021-03538-0
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DOI: https://doi.org/10.1007/s10600-021-03538-0