Abstract
An x-ray structural investigation has been made of the sesquiterpene ester ferticin: diffractometer, CuKα radiation, 1037 reflections, direct method, R factor 0.105. The spatial structure of the molecule has been determined.
Similar content being viewed by others
Literature cited
K. Rajendron, S. K. Paknikar, and S. C. Bhattoryya, Indian J. Chem.,1613, No. 1, 4 (1978).
M. G. Valle, G. Appendino, G. M. Nano, and V. Picci, Phytochemistry,26, No. 1, 253 (1987).
C. G. Casinovi, S. Cerrino, O. Motl, G. Fardella, W. Fedeli, E. Gavusso, and D. Lamba, Coll. Czech. Chem. Commun.,48, 2411 (1983).
R. B. Bates, R. E. Klenck, C. K. Mesta, and S. K. Paknikar, Acta Cryst.,39, 1667 (1983).
W. H. Watson, R. P. Kashyap, and I. Tavanaiepour, Acta Cryst.,41, 1650 (1985).
C. Romming and P. E. Hansen, Acta Chem. Scand.,A33, 265 (1979).
J. B. Hendrickson, J. Am. Chem. Soc.,83, 4537 (1961).
B. Tashkhodzhaev, M. K. Makhmudov, L. A. Golovina, A. I. Saikhodzhaev, M. R. Yagudaev, and V. M. Malikov, Khim. Prir. Soedin., 309 (1984).
V. I. Andrianov, Z. Sh. Safina, and B. L. Tarnopol'skii, Zh. Strukt. Khim.,15, 911 (1974).
Additional information
Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 68–73, January–February, 1989.
Rights and permissions
About this article
Cite this article
Makhmudov, M.K., Golovina, L.A., Tashkhodzhaev, B. et al. X-ray structural investigation of sesquiterpene esters from plants of the genus Ferula. V. Structure and stereochemistry of ferticin. Chem Nat Compd 25, 59–63 (1989). https://doi.org/10.1007/BF00596702
Received:
Revised:
Issue Date:
DOI: https://doi.org/10.1007/BF00596702