SYNTHESIS OF NEOBAVAISOFLAVONE

DOI DOI PDF 参考文献1件 オープンアクセス
  • Mitsuru Nakayama
    Department of Chemistry, Faculty of Science, Hiroshima University
  • Shûichi Hayashi
    Department of Chemistry, Faculty of Science, Hiroshima University
  • Mitsuo Masumura
    Department of Applied Chemistry, Faculty of Engineering, Tokushima University
  • Tokunaru Horie
    Department of Applied Chemistry, Faculty of Engineering, Tokushima University
  • Masao Tsukayama
    Department of Applied Chemistry, Faculty of Engineering, Tokushima University
  • Toshihide Yamada
    Department of Applied Chemistry, Faculty of Engineering, Tokushima University

説明

<jats:title>Abstract</jats:title> <jats:p>Condensation of 7-benzoyldaidzein (III) with 2-methyl-3-buten-2-ol gave 7-benzoyl-3′-(3-methyl-2-butenyl)daidzein (IV). Hydrolysis of IV with dilute alkali gave 3′-(3-methyl-2-butenyl)daidzein (neobavaisoflavone) (I), which was converted into isoneobavaisoflavone (VI) when heated with formic acid. 7-Benzyldaidzein (VII) was condensed with 2-methyl-3-buten-2-ol to give a chroman derivative (VIII), which was converted into VI by hydrogenolysis.</jats:p>

収録刊行物

  • Chemistry Letters

    Chemistry Letters 4 (4), 281-282, 1975-04

    Oxford University Press (OUP)

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