Hydrolysis and Phytotoxic Activity of Cyclic Imides(Pesticide Chemistry)
スポンサーリンク
概要
- 論文の詳細を見る
In order to explain the close phytotoxic activities of N-aryl-3,4,5,6-tetrahydrophthalimides and their hydrolyzed products, N-aryl-3,4,5,6-tetrahydrophthalamic acids, five sets of both types of compounds possessing the same aryl residues were prepared. Their phytotoxic activity against sawa millett (E. utilis) and green microalga (S. acutus), and the relationship of interconversion between the imides and amide acids during the bioassay were investigated. In almost all cases, the imides showed stronger activity than the corresponding amide acids. The hydrolysis of the imides and the cyclization of amide acids were observed in respect of the aryl residues. The phytotoxicity caused by the imides and amide acids tested was influenced by this interconversion.
- 社団法人日本農芸化学会の論文
- 1991-11-23
著者
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Sato Yukiharu
Faculty Of Agriculture Tamagawa University
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Wakabayashi Ko
Faculty Of Agriculture Tamagawa University
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Watanabe Hiroyuki
Research & Development Division, Daido Steel Co.
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KOJIMA Takashi
Faculty of Agriculture, Tamagawa University
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GOTO Toshiyuki
Faculty of Agriculture, Tamagawa University
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OOMIKAWA Reiko
Faculty of Agriculture, Tamagawa University
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Oomikawa Reiko
Faculty Of Agriculture Tamagawa University
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Kojima Takashi
Faculty Of Agriculture Tamagawa University
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Watanabe H
Yamagata Univ. Yamagata Jpn
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Goto Toshiyuki
Faculty Of Agriculture Tamagawa University
関連論文
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- Hydrolysis and Phytotoxic Activity of Cyclic Imides(Pesticide Chemistry)
- 1,3-Dipolar cycloadditions to 2-phenyl-1-azaspiro[2.2]pent-1-ene.