Terada Akira | Department of Chemistry, Faculty of Science, Osaka City University
スポンサーリンク
概要
関連著者
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Terada Akira
Department of Chemistry, Faculty of Science, Osaka City University
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Tanoue Yasuhiro
Department of Chemistry, Kyushu Institute of Technology
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Terada Akira
Department Of Computer Science Tokyo Institute Of Technology
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Terada Akira
Department of Chemistry, Kyushu Institute of Technology
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Tokunaga Takenobu
Department of Computer Science Tokyo Institute of Technology
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Terada A
Department Of Computer Science Tokyo Institute Of Technology
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Tsuboi Toshiyuki
Department Of Molecular Science And Technology Kyushu University:(present Address)nippon Kankoh-shik
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Sakamoto Hiroshi
Deparment Of Biology Faculty Of Science Kobe University
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Tsuge Otohiko
Research Institute of Industrial Science, and Department of Molecular Science and Technology, Interdisciplinary Graduate School of Engineering Sciences Kyushu University
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Tsuge Otohiko
Research Institute of Industrial Science, Kyushu University
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Tanoue Yasuhiro
Department of Food Science and Technology, Shimonoseki University of Fisheries
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Umezu Yasuo
Department of Chemistry, Kyushu Institute of Technology
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Hatada Akira
Department of Chemistry, Kyushu Institute of Technology
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Torisu Kazuhiko
Department of Chemistry, Kyushu Institute of Technology
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Taniguchi Hiroshige
Department of Chemistry, Kyushu Institute of Technology
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Umezu Yasuo
Department of Applied Chemistry, Kyushu Institute of Technology
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Hayashida Takayuki
Department of Chemistry, Kyushu Institute of Technology
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Sakamoto Hiroshi
Department of Chemistry, Kyushu Institute of Technology
著作論文
- Corpus Based Method of Transforming Nominalized Phrases into Clauses for Text Mining Application(Special Issue on Text Processing for Information Access)
- Synthesis of Naphthoquinone Derivatives. Paper XI. A Fusarubin Isomer.
- Synthesis of 5,8-dihydroxy-2-methoxy-1,4-naphthoquinone derivatives. A major naphthoquinone moiety of some of naphthoquinone antibiotics.
- Synthesis of shikalkin (.+-.shikonin) and related compounds.
- Monosubstituted Tetramethoxynaphthalenes
- Fries rearrangement of 1-methoxy-4-(4-methyl-2- and -3-pentenoyloxy)benzenes.