Abstract
The epigeal part ofArtemisia absinthium L. has yielded a new sesquiterpene lactone artemolin, C15H20O5, with mp 205°C, [α] 20D +18° (c 1.0, chloroform). The structure of artemolin has been established on the basis of chemical transformations and spectral characteristics.
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Literature cited
F. Bohlmann, P. K. Mahanta, and L. N. Dutta, Phytochemistry,18, 289 (1979).
K. S. Rybalko, Zh. Obshch. Khim.,33, 2734 (1963).
H. Yoshioka, T. Mabry, and B. Timmerman, Sesquiterpene Lactones, University of Tokyo Press (1973), p. 349.
K. Vokač, Z. Samek, V. Herout, and F. Sorm, Collect. Czech. Chem. Commun.,37, 1346 (1972).
Additional information
Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 658–661, September–October, 1979.
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Kasymov, S.Z., Abdullaev, N.D., Zakirov, S.K. et al. Artemolin — A new guaianolide fromArtemisia absinthium . Chem Nat Compd 15, 577–579 (1979). https://doi.org/10.1007/BF00565928
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DOI: https://doi.org/10.1007/BF00565928