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Regioselective oxidation of the methyl ester of maleopimaric acid by dimethyldioxirane

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Chemistry of Natural Compounds Aims and scope

Reaction of the methyl ester of maleopimaric acid and dimethyldioxirane resulted in regioselective oxidation of the bridging double bond to form the 13(15)-en-14S-hydroxy derivative.

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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

    T. I. Nazyrov, E. V. Tret’yakova, O. B. Kazakova & L. V. Spirikhin

  2. Bashkir State University, Ufa, Ul. Zaki Validi, 32, Russia

    O. S. Kukovinets

Authors
  1. T. I. Nazyrov
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  2. E. V. Tret’yakova
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  3. O. B. Kazakova
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  4. L. V. Spirikhin
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  5. O. S. Kukovinets
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Correspondence to O. B. Kazakova.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 6, November–December, 2012, pp. 888–889.

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Nazyrov, T.I., Tret’yakova, E.V., Kazakova, O.B. et al. Regioselective oxidation of the methyl ester of maleopimaric acid by dimethyldioxirane. Chem Nat Compd 48, 1002–1003 (2013). https://doi.org/10.1007/s10600-013-0449-8

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  • DOI: https://doi.org/10.1007/s10600-013-0449-8

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