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Structure-Activity Relationship and Molecular Design of Peroxidizing Herbicides with Cyclic Imide Structures and Their Relatives

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Peroxidizing Herbicides

Abstract

Since oxadiazon (1) and chlorophthalim (2: X = 4-Cl) were patented around 1970 (Boesch and Metivier 1963; Matsui et al. 1973), numerous trials have been undertaken to optimize and elaborate their structural features as being N-phenyl-nitrogen-heterocyclic. At present, there is a great variety of their structural analogs including C-phenyl-nitrogen-heterocycles known as peroxidizing herbicides and candidates. As recognized from preceding Chapters (2 and 3) of this volume, there seem to be broadly two facets in the structure transformation trials. One is to disclose optimal substituents as well as to identify the best substitution patterns in the phenyl moiety. The other is to discover novel nitrogen-heterocyclic skeletons with well-matched substituents.

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Author information

Authors and Affiliations

  1. EMIL Project, #305 Heights Kyogosho, 492 Umeyacho, Kyoto, 604-8057, Japan

    Toshio Fujita

  2. Odawara Research Center, Nippon Soda Co. Ltd, 345 Takada, Odawara, 250-0216, Japan

    Akira Nakayama

Authors
  1. Toshio Fujita
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  2. Akira Nakayama
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Editors and Affiliations

  1. Department of Plant Physiology and Biochemistry, University of Konstanz, D-78457, Konstanz, Germany

    Peter Böger

  2. Department of Physiology and Biochemistry, Tamagawa University, Machida-shi, Tokyo, 194-8610, Japan

    Ko Wakabayashi

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Fujita, T., Nakayama, A. (1999). Structure-Activity Relationship and Molecular Design of Peroxidizing Herbicides with Cyclic Imide Structures and Their Relatives. In: Böger, P., Wakabayashi, K. (eds) Peroxidizing Herbicides. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-58633-0_4

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  • DOI: https://doi.org/10.1007/978-3-642-58633-0_4

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-63674-5

  • Online ISBN: 978-3-642-58633-0

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