Experientia

, Volume 24, Issue 8, pp 769–770

The syntheses of axillarin and its related compounds

  • K. Fukui
  • M. Nakayama
  • T. Horie
Specialia Chimica. Biochimica. Biophysica

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

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    A. O. Taylor andE. Wong, Tetrahedron Lett.41, 3675 (1965).PubMedGoogle Scholar
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    W. Herz, L. Farkas, V. Sudarsanam, H. Wagner, L. Hörhammer andR. Rüger, Chem. Ber.99, 3539 (1966).Google Scholar
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    E. L. Ghisalberti, P. R. Jefferies andC. I. Stacey, Aust. J. Chem.20, 1049 (1967).Google Scholar
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    C. A. Henrick andP. R. Jefferies, Tetrahedron21, 3219 (1965).Google Scholar
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    L. Farkas andM. Nogradi, Tetrahedron Lett.31, 3759 (1966).Google Scholar
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    K. Fukui, T. Matsumoto, S. Nakamura, M. Nakayama andT. Horie, Experientia24, 108 (1968); Bull. chem. Soc. Japan41, No. 6 (1968).Google Scholar
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    K. Fukui, M. Nakayama andT. Horie, Experientia24, 417 (1968).Google Scholar
  8. 8.
    Natural axillarin and its tetraethyl ether, kindly supplied by Prof.W. Herz, the Florida State University, were measured in this laboratory.Google Scholar
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    D. K. Bhadwaj, S. Neelakantan andT. R. Seshadri, Indian J. Chem.4, 417 (1966).Google Scholar

Copyright information

© Birkhäuser Verlag 1968

Authors and Affiliations

  • K. Fukui
    • 1
    • 2
  • M. Nakayama
    • 1
    • 2
  • T. Horie
    • 1
    • 2
  1. 1.Department of Chemistry, Faculty of ScienceHiroshima UniversityHiroshima
  2. 2.Department of Applied Chemistry, Faculty of EngineeringUniversity of TokushimaJapan

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