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New O-acyl derivatives of lariciresinol

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Summary

In an investigation of the composition of the extractive substance of the wood ofAbies sibirica Ledeb. andA. nephrolepis Maxim., new O-acylated lignans, previously unknown in nature, have been isolated. The structures of the two new compounds have been established by physicochemical methods and by independent synthesis: they are lariciresinol coumarate and ferulate.

The PMR spectra of laricyl coumarate and laricyl ferulate were taken by G. A. Kalabin.

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Literature cited

  1. W. J. Taylor and A. R. Battersby, Oxidation Coupling of Phenols, N. J. (1976), p. 276.

  2. S. A. Medvedeva, L. D. Modonova, V. G. Leont'eva, V. N. Glazkova, and N. A. Tyukavkina, Khim. Prirodn. Soedin., 113 (1971).

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  5. L. D. Modonova, V. K. Voronov, V. G. Leont'eva and N. A. Tyukavkina, Khim. Prirodn. Soedin., 165 (1972).

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Authors
  1. V. G. Leont'eva
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  2. L. D. Modonova
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  3. V. K. Voronov
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  4. N. A. Tyukavkina
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Additional information

Irkutsk Institute of Organic Chemistry, Siberian Branch of the Academy of Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 162–166, March–April, 1976.

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Leont'eva, V.G., Modonova, L.D., Voronov, V.K. et al. New O-acyl derivatives of lariciresinol. Chem Nat Compd 12, 147–150 (1976). https://doi.org/10.1007/BF00566332

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  • DOI: https://doi.org/10.1007/BF00566332

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