Synthesis and Herbicidal Activity of Opened Hydantoin-ring Derivatives of Hydantocidin

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概要

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• We synthesized three hydantocidin derivatives and evaluated their herbicidal activity in order to elucidate the role of the spirohydantoin system at the anomeric center of hydantocidin. With application to foliage at 1000 ppm, only α-ureidoamide 14 demonstrated activity, the remaining compounds being found to be inactive.

• 社団法人日本農芸化学会の論文
• 1996-07-23

著者

• Kitagawa Junko

  Agroscience Research Laboratories Sankyo Co. Ltd.

• Sano Hiromi

  Agroscience Research Laboratories Sankyo Co. Ltd.

• MIO Shigeru

  Agroscience Research Laboratories, Sankyo Co. Ltd.

• KUMAGAWA Yuko

  Agroscience Research Laboratories, Sankyo Co. Ltd.

• SHINDOU Masahiro

  Agroscience Research Laboratories, Sankyo Co. Ltd.

• HONMA Toyokuni

  Agroscience Research Laboratories, Sankyo Co. Ltd.

• SUGAI Soji

  Agroscience Research Laboratories, Sankyo Co. Ltd.

• Honma T

  Godo Shusei Co. Ltd. Chiba Jpn

• Honma Toyokuni

  Agroscience Research Laboratories Sankyo Co. Ltd.

• Sugai Soji

  Agroscience Research Laboratories Sankyo Co. Ltd.

• Sugai S

  Agroscience Research Laboratories Sankyo Co. Ltd.

• Mio S

  Agroscience Research Laboratories Sankyo Co. Ltd.

• Kumagawa Yuko

  Agroscience Research Laboratories Sankyo Co. Ltd.

• MIO Shigeru

  Agroscience Research Laboratories, Sankyo Agro Co., Ltd.

関連論文

• Synthesis and Herbicidal Activity of Opened Hydantoin-ring Derivatives of Hydantocidin
• Synthesis and Herbicidal Activity of Hydantocidin Analogues : Modification of the Carbonyl Groups in Spirohydantoin
• Synthesis and Insecticidal Activity of Novel N-Oxydihydropyrrole Derivatives with a Substituted Spirocyclohexyl Group(Organic Chemistry)
• Synthesis and Insecticidal Activity of N-Oxydihydropyrroles : 4-Hydroxy-3-mesityl-5, 5-dimethyl Derivatives with Various Substituents at the 1-Position(Organic Chemistry)
• Synthesis and Herbicidal Activity of Deoxy Derivatives of (+)-Hydantocidin(Organic Chemistry)
• 4-Sulfenyl-2-carbamoyl-4-isoxazolin-3-ones : Biological Isostere to 4-Chloro-2-carbamoyl-4-isoxazolin-3-ones

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