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Synthesis and NMR Spectra of New C-Modified Glycyrrhetic Acid Derivatives

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Chemistry of Natural Compounds Aims and scope

New oxidative and skeletal transformations of olean-9(11),12(13)-dien-30-oic acid that were based on ozonolysis and UV irradiation produced the 9α,11α-epoxide and opened ring C.

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Acknowledgment

The work was supported financially by the RFBR (Grant 11-03-00462a) and NSh 7014.2012.3.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Ufa Scientific Center, Russian Academy of Sciences, 450054, Ufa, Prosp. Oktyabrya, 71, Russia

    A. S. Budaev, L. R. Mikhailova, L. V. Spirikhin & L. A. Baltina

Authors
  1. A. S. Budaev
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  2. L. R. Mikhailova
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  3. L. V. Spirikhin
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  4. L. A. Baltina
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Corresponding author

Correspondence to L. A. Baltina.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 2, March–April, 2014, pp. 265–267.

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Budaev, A.S., Mikhailova, L.R., Spirikhin, L.V. et al. Synthesis and NMR Spectra of New C-Modified Glycyrrhetic Acid Derivatives. Chem Nat Compd 50, 302–304 (2014). https://doi.org/10.1007/s10600-014-0937-5

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  • DOI: https://doi.org/10.1007/s10600-014-0937-5

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