Nobukatsu Katsui
Hokkaido University
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Featured researches published by Nobukatsu Katsui.
Phytochemistry | 1987
Mitsuo Takasugi; Shinji Kawashima; Kenji Monde; Nobukatsu Katsui; Tadashi Masamune; Akira Shirata
Abstract An induced and six preformed antifungal compounds were isolated from Chinese yam ( Dioscorea batatas ) inoculated with the bacterium Pseudomonas cichorii . The induced compound, a phytoalexin, was identified as dihydropinosylvin. The preformed compounds were characterized as oxygenated bibenzyls and phenanthrenes.
Journal of The Chemical Society, Chemical Communications | 1986
Mitsuo Takasugi; Nobukatsu Katsui; Akira Shirata
Inoculation of Chinese cabbage heads with the bacterium Pseudomonas cichorii induced the production of three major phytoalexins named methoxybrassinin (1), brassinin (2), and cyclobrassinin (3), whose structures have been elucidated on the basis of spectroscopic studies and synthesis.
Phytochemistry | 1987
Mitsuo Takasugi; Shinji Kawashima; Nobukatsu Katsui; Akira Shirata
Abstract Treatment of sliced burdock root tissue with copper (II) sulphate stimulated phytoalexin formation. Two were isolated and characterized as ( S )-12,1
Journal of The Chemical Society, Chemical Communications | 1985
Mitsuo Takasugi; Shigetomo Okinaka; Nobukatsu Katsui; Tadashi Masamune; Akira Shirata; Muneki Ohuchi
Inoculation of lettuce (Lactua sativa var. capitata) leaves with the pathogenic bacterium Pseudomonas cichorii induced the production of two antifungal sesquiterpenes, costunolide and anew compound named lettucenin A, whose structure has been elucidated on the basis of spectroscopic studies.
Journal of The Chemical Society, Chemical Communications | 1977
Akio Murai; Nobukatsu Katsui; Fujio Yagihashi; Tadashi Masamune; Yukio Ishiguri; Kohei Tomiyama
The title compounds metabolites of rishitin (1a) in healthy potato tuber tissues, are determined to possess structures (2a) and (3a).
Journal of The Chemical Society, Chemical Communications | 1986
Akio Murai; Yuko Yoshizawa; Mitsuhiko Ikura; Nobukatsu Katsui; Tadashi Masamune
Feeding experiments with (–)-[12,12-2H2]rishitin (1-D) in healthy potato tuber tissues indicated that metabolism of (1) into rishitin M-2 (3) proceeded with a stereospecific 1,2-migration of an olefinic hydrogen at C-12 of (1) in contrast with formation of rishitin M-1 (2) by direct oxygenation on C-13 of (1).
Journal of The Chemical Society, Chemical Communications | 1982
Akio Murai; Shingo Sato; Atsushi Osada; Nobukatsu Katsui; Tadashi Masamune
The biosynthetic production of rishitin from solavetivone via lubimin oxylubimin has been established on the basis of experiment with (±)-[8,8-2H2]solavetivone.
Bulletin of the Chemical Society of Japan | 1988
Mitsuo Takasugi; Kenji Monde; Nobukatsu Katsui; Akira Shirata
Nature | 1982
Tadashi Masamune; Masaki Anetai; Mitsuo Takasugi; Nobukatsu Katsui
Chemistry Letters | 1987
Mitsuo Takasugi; Kenji Monde; Nobukatsu Katsui; Akira Shirata