-
- 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)
- Tweet
キーワード
詳細情報 詳細情報について
-
- CRID
- 1360565169059848832
-
- NII論文ID
- 130003515566
-
- ISSN
- 13480715
- 03667022
-
- データソース種別
-
- Crossref
- CiNii Articles
- OpenAIRE