Zusammenfassung
Axillarin (5, 7, 3′, 4′-Tetrahydroxy-3,6-dimethoxyflavon). 5,3′,4′-Trihydroxy-3,6,7-trimethoxyflavon und 5,7,3′,4′-Tetrahydroxy-3,8-dimethoxyflavon wurden synthetisiert.
Literatur
A. O. Taylor andE. Wong, Tetrahedron Lett.41, 3675 (1965).
W. Herz, L. Farkas, V. Sudarsanam, H. Wagner, L. Hörhammer andR. Rüger, Chem. Ber.99, 3539 (1966).
E. L. Ghisalberti, P. R. Jefferies andC. I. Stacey, Aust. J. Chem.20, 1049 (1967).
C. A. Henrick andP. R. Jefferies, Tetrahedron21, 3219 (1965).
L. Farkas andM. Nogradi, Tetrahedron Lett.31, 3759 (1966).
K. Fukui, T. Matsumoto, S. Nakamura, M. Nakayama andT. Horie, Experientia24, 108 (1968); Bull. chem. Soc. Japan41, No. 6 (1968).
K. Fukui, M. Nakayama andT. Horie, Experientia24, 417 (1968).
Natural axillarin and its tetraethyl ether, kindly supplied by Prof.W. Herz, the Florida State University, were measured in this laboratory.
D. K. Bhadwaj, S. Neelakantan andT. R. Seshadri, Indian J. Chem.4, 417 (1966).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Fukui, K., Nakayama, M. & Horie, T. The syntheses of axillarin and its related compounds. Experientia 24, 769–770 (1968). https://doi.org/10.1007/BF02144856
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF02144856