Ishido Yoshiharu | Department Of Chemistry Tokyo Institute Of Technology
スポンサーリンク
概要
関連著者
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Ishido Yoshiharu
Department Of Chemistry Tokyo Institute Of Technology
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Yoshino Teruo
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Araki Younosuke
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Matsuura Kazuo
Department Of Breast Oncology Saitama International Medical Center Saitama Medical University
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Maeda Sadao
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Inaba Shigeru
Department Of Ergonomics Faculty Of Engineering Chiba University
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Ichikawa Tetsuya
Department Of Orthopaedic Surgery Enshu Hospital
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Sato Tetsuo
Departmelet Of Organic Chemistry Tokyo Institute Of Technology Ookayama
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Hosono Akira
Department of Applied Biological Chemistry, The University of Tokyo
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Araki Younosuke
Department of Chemistry, Tokyo Institute of Technology
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Okamoto Toshiro
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Tanaka Hisayuki
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Sekiya Masao
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Komura Hajime
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Yamada Koh
Department Of Anesthesiology Kansai Medical University
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Hosono Akira
Department Of Chemistry Tokyo Institute Of Technology
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Hosono Akira
Department Of Biochemistry Osaka Medical College
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Sekine Mitsuo
Department Of Life Chemistry Tokyo Institute Of Technology
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Sato Tetsuo
Department of Chemistry, Tokyo Institute of Technology
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ISHIDO YOSHIHARU
Department of Chemistry, Tokyo Institute of Technology
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Matsuba Teruo
Department of Chemistry, Tokyo Institute of Technology
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Sato Tetsuo
Department Of Chemistry Tokyo Institute Of Technology
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Matsuba Teruo
Department Of Chemistry Tokyo Institute Of Technology
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Sakakibara Tohru
Department Of Chemistry Yokohama City University
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Yamaguchi Kazuo
Department Of Biological Sciences Graduate School Of Natural Science And Technology Kanazawa Univers
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SUGIYAMA Hiroshi
Chemical Research Institute of Non-aqueous Solution, Tohoku University
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Hata Tsujiaki
Department of Chemistry Tokyo Institute of Technology
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Sekine Mitsuo
Department of Life Chemistry, Tokyo Institute of Technology
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Seto Shuichi
Chemical Research Institue of Non-Aqueous Solutions, Tohoku University
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Yamaoka Naotaka
Faculty of Pharmaceutical Science, Kitazato University
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Shimizu Bunji
Central Research Laboratory, Sankyo Ltd.
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Shimizu Bunji
Central Research Laboratories, Sankyo Co., Ltd.
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Yamaoka Naotaka
Faculty of Agriculture Tohoku Univerisity
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Maeda Sadao
Department of Chemistry, Tokyo Institute of Technology
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Ohdan Shohji
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Sato Tetsuo
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Fujii Kiyohisa
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Tada Toshizo
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Ohgo Yohko
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Sakairi Nobuo
Department of Chemistry, Tokyo Institute of Technology
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Hosono Akira
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Yamaguchi Kazuo
Department of Life Chemistry, Tokyo Institute of Technology
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Manandhar Mangala
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Ohkita Noriaki
Department of Chemistry, Yokohama City University
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Nakazaki Nobuo
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Gokita Noboru
Department of Life Chemistry, Tokyo Institute of Technology
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Nishiyama Kazunari
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Ichikawa Tetsuya
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Sugiyama Hiroshi
Chemical Research Institue of Non-Aqueous Solutions, Tohoku University
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Inoue Kimio
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
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Tsutsumi Hideo
Department of Chemistry, Faculty of Science, Tokyo Institute of Technology
著作論文
- D-8-1 Syntheses of Purine Nucleosides by the Fusion Method(Nucleosides)
- Synthetic Studies of Carbohydrate Derivatives with Photochemical Reactions. IX. The Photochemical Addition of 1,3-Dioxolane to Several Enoses
- On the Mechanism of the Acid Catalysis and New Activating Agents in the Fusion Reaction of an Acylated Sugar with a Purine Derivative
- Studies on chemical synthesis of mRNAs. I. Synthesis and properties of N2-tritylguanosine derivatives and application to synthesis of pGpUpU.
- Carbon-13 Nuclear Magnetic Resonance Spectra of α-Ribonucleosides
- Synthetic Studies of Carbohydrate Derivatives with Photochemical Reaction. II. Photochemistry of Benzylidene Sugar Derivatives
- Synthetic Studies of Amino Acids by the Use of Copper Complex. II. The Condensation Reaction of N-Pyruvylideneglycinatocopper(II) Complexes with various Aldehydes
- Synthetic Studies of Carbohydrate Derivatives with Photochemical Reaction. VIII. Photochemical Desulfurization of Some Sugar Diethyl Dithioacetal Acetates into the Corresponding 1-S-Ethyl-1-thioalditol Acetates
- Synthetic Studies of Amino Acids by the Use of Copper(II) Complex. III. Syntheses of Several 2-Amino-2-deoxyaldonic Acids by the Use of Bisglycinato- and N-Pyruvylideneglycinatoaquocopper(II)
- Kinetic and NMR Spectroscopic Studies of the Fusion Reactions of Chloropurines with 1,2,3,5-Tetra-O-acetyl-D-ribofuranoses
- Preparation of 2-nitromethyl-2-cycloalkenol and 2-nitromethyl-2-cycloalkenone.
- Condensation Reactions of Adenine Derivatives with 1-O-Acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose in Nitrophenols
- Synthetic Studies by the Use of Carbonates, II. An Easy Method of Preparing Cyclic Carbonates of Polyhydroxy Compounds by Transesterification with Ethylene Carbonate
- Synthetic Studies by the Use of Carbonates. I. The Nucleophilic Substitution Reaction of Ethylene Carbonate with Amine Hydrohalides
- Synthetic Studies by the Use of Carbonates. III. The Condensation Reactions of Ethylene Carbonate with a Variety of Phenols Catalyzed by Lithium Hydride or Tetraethylammonium Halides
- The regioselective C-hydroxyalkylation of 1,3-diphenyl-1,3-propanedione with halo alcohols, involving intramolecular alcoholysis: the synthesis of oxoalkyl esters.