Summary
Ferocin and ferocinin — esters of the new sesquiterpene alcohol fecerol with p-hydroxybenzoic and vanillic acids, respectively — have been isolated from the roots ofFerula ceratophylla.
On the basis of spectral characteristics and chemical transformations, the structure of 1,1,8-trimethylcycloundeca-2,4(14),7-trien-10-ol is proposed for fecerol.
Similar content being viewed by others
Literature cited
L. A. Golovina and G. K. Nikonov, Khim. Prirodn. Soedin., 707 (1977).
L. A. Smedman, E. Zavarin, and R. Teranishi, Phytochemistry,8, 1457 (1969).
J. Jano and T. Nishijama, Photochemistry,13, 1207 (1974).
G. J. Poos, G. E. Arth, R. E. Beyler, and L. H. Sarett, J. Am. Chem. Soc.,75, 422 (1953).
Additional information
Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 796–800, November–December, 1977.
Rights and permissions
About this article
Cite this article
Golovina, L.A., Saidkhodzhaev, A.I. The structures of ferocin and ferocinin. Chem Nat Compd 13, 671–674 (1977). https://doi.org/10.1007/BF00565515
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF00565515