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Archive | 2002

Major Synthetic Routes for Modern Herbicide Classes and Agrochemical Characteristics

Kenji Hirai; Atsushi Uchida; Ryuta Ohno

Practical herbicides are classified into several groups according to their mode of action by the Herbicide Resistance Action Committee (HRAC) in cooperation with the Weed Science Society of America (WSSA). The actual classification is composed of 15 groups with 9 subgroups and currently contains a total of 269 kinds of herbicides. Chapters 1–8 deal with representative herbicides belonging to 8 HRAC groups; B (acetolactate synthase inhibitors), F1—F3 (carotenoid biosynthesis inhibitors), G (EPSP synthase inhibitors), H (glutamine synthetase inhibitors), A (ACCase inhibitors), K3 (very long-chain fatty acid, VLCFAs biosynthesis inhibitors), L (cellulose biosynthesis inhibitors) and E (protoporphyrinogen-IX oxidase, PPO inhibitors). Each group contains 50, 19, 2, 2,16, 21, 4 and 26 kinds of practical herbicides, respectively. This chapter briefly summarizes agrochemical characteristics and major synthetic routes for these modern herbicides and chronologically reviews the structural evolution of related compounds (more than 900) disclosed since 1990 except for the PPO inhibitors since 1995.


Journal of Chemical Ecology | 1995

IDENTIFICATION OF FEMALE SEX PHEROMONE COMPONENTS OF RICE LOOPER, Plusia festucae (L.), (LEPIDOPTERA: NOCTUIDAE)

Tetsu Ando; Ryuta Ohno; Tomoyuki Kokuryu; Atsunori Funayoshi; Masashi Nomura

The rice looper,Plusia festucae, is a defoliator of the rice plant. Chromatographic behavior, chemical reactions, and GC-MS analyses of the female sex pheromone revealed that the main component was (Z)-5-dodecenyl acetate (Z5–12: OAc, component I). The GC-MS analysis also indicated that the pheromone gland extract included another three monounsaturated components, (Z)-5-dodecen-l-ol (Z5–12: OH, component II), (Z)-7-tetradecenyl acetate (Z7–14: OAc, component III), and (Z)-7-tetradecen-l-ol (Z7–14: OH, component IV) in the following ratio: I:II:III:IV=100:6:15:1. In a paddy field, the mixture of synthetic I, II, and III in a ratio of 100:6:15 showed stronger attractancy than the virgin female, while the role of IV was unknown.


Journal of Pesticide Science | 2004

Synthesis and Herbicidal Activity of New Pyrazole-4-carboxamide Derivatives

Ryuta Ohno; Atsuko Watanabe; Tomoko Matsukawa; Takuya Ueda; Hiroshi Sakurai; Masahiro Hori; Kenji Hirai


Archive | 2000

Pyrazole derivatives, intermediates for the preparation thereof, processes for the preparation of both and herbicides containing the derivatives as the active ingredient

Kenji Hirai; Ryuta Ohno; Atsuko Yamada; Tomoko Matsukawa; Takuya Ueda


Archives of Insect Biochemistry and Physiology | 1998

Stereochemistry of Δ11‐desaturation and inhibitors of Δ10,12‐desaturation in the biosynthesis of bombykol, sex pheromone of the female silkworm moth, examined with deuterated precursors

Tetsu Ando; Kazuhisa Ikemoto; Ryuta Ohno; Masanobu Yamamoto


Journal of Pesticide Science | 2004

Synthesis and Herbicidal Activity of New 1-Alkyl-3-aryloxypyrazole-4-carboxamide Derivatives

Ryuta Ohno; Atsuko Watanabe; Maho Nagaoka; Takuya Ueda; Hiroshi Sakurai; Masahiro Hori; Kenji Hirai


Journal of Pesticide Science | 1995

Cyclopropene Fatty Acid and Amide

Tetsu Ando; Ryuta Ohno; Kazuhisa Ikemoto; Yohko Yajima


Journal of Pesticide Science | 2010

Synthesis and insecticidal activity of novel 1-alkyl-3-sulfonyloxypyrazole-4-carboxamide derivatives

Ryuta Ohno; Maho Nagaoka; Kenji Hirai; Atsushi Uchida; Shin-ichiro Kochi; Osamu Yamada; Jun Tokumura


Journal of Agricultural and Food Chemistry | 1996

Structure−Activity Relationships of Cyclopropene Compounds, Inhibitors of Pheromone Biosynthesis in Bombyx mori

Tetsu Ando; Ryuta Ohno; Kazuhisa Ikemoto; Masanobu Yamamoto


Journal of Pesticide Science | 2010

Convenient screening of 4-hydroxyphenylpyruvate dioxygenase inhibitors by UV absorbance detection in the presence of Fe2+ ion.

Yumi Ikeda; Ryuta Ohno; Yukiharu Sato

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Kenji Hirai

Tokyo Institute of Technology

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Natsuko Okano

Mitsubishi Chemical Corporation

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Tetsu Ando

Tokyo University of Agriculture and Technology

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Kazuhisa Ikemoto

Tokyo University of Agriculture and Technology

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Takehito Mouri

Tokyo University of Agriculture and Technology

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