岡本 敏彦 | Faculty Of Pharmaceutical Sciences University Of Tokyo

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• 岡本 敏彦

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 岡本 敏彦

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 首藤 紘一

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 首藤 紘一

  Facutly Of Pharmaceutical Sciences University Of Tokyo

• 岡本 敏彦

  Sato Pharmaceutical Co. Ltd.

• 岡本 敏彦

  東大・薬

• 磯谷 遙

  工研

• 岡本 敏彦

  千葉大学薬学部

• 岡本 敏彦

  東京大学薬学部

• 岡本 敏彦

  東大薬

• 橋本 祐一

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 夏目 充隆

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 坂井 進一郎

  Faculty of Pharmaceutical Sciences, Chiba University

• 山口 健太郎

  千葉大学分析センター

• 飯高 洋一

  Faculty of Pharmaceutical Sciences, The University of Tokyo

• 高橋 惣四郎

  東大薬

• 小泉 徹

  Faculty Of Pharmaceutical Sciences Toyama Medical And Pharmaceutical University

• 広部 雅昭

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 小菅 卓夫

  静岡薬科大学

• 川添 豊

  Faculty Of Pharmaceutical Sciences Nagoya City University

• 小菅 卓夫

  Cawthron Institute

• 清水 正夫

  Central Research Laboratory, Daiichi Seiyaku Co., Ltd.

• 山本 一郎

  Faculty of Pharmaceutical Sciences, Chiba University

• 小菅 卓夫

  Shizuoka College Of Pharmacy

• 山口 健太郎

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 磯谷 遙

  Biological Institute College of General Education, University of Tokyo

• 鎌田 進

  塩野義研

• 山本 一郎

  Faculty Of Pharmaceutical Sciences Chiba University

• 内丸 文彦

  Research Institute, Daiichi Seiyaku Co., Ltd.

• 高山 広光

  Faculty of Pharmaceutical Sciences, Chiba University

• 山口 啓一

  Faculty of Pharmaceutical Sciences, Chiba University

• 北原 嘉泰

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 川添 豊

  Faculty of Pharmaceutical Sciences, Nagoya City University

• 北原 嘉泰

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 首藤 紘一

  東大薬学

• 首藤 紘一

  東大・薬

• 武田 敬

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 長尾 美奈子

  国立がんセ・研・生化 横浜国大・工

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  Faculty of Pharmaceutical Sciences, University of Tokyo

• 染井 正徳

  東京大学薬学部

• 鳥井 良彦

  東大薬

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  Biological Institute, College of General Education, University of Tokyo

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  東大教養

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  Faculty of Pharmaceutical Sciences, The University of Tokyo

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  Faculty Of Pharmaceutical Sciences Teikyo University

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  Department Of Pharmacy Shinsyu University Hospital

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  Faculty of Pharmaceutical Sciences, University of Tokyo

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  National Cancer Center Research Institute

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  National Cancer Center Research Institute

• 三條 秀直

  Faculty of Pharmaceutical Sciences, Tokyo University

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  Faculty of Pharmaceutical Sciences, Tokyo University

• 奥田 晴宏

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 吉野 明江

  Faculty Of Pharmaceutical Sciences Tokyo University

• 磯谷 遙

  東大教養

• 秋山 稔

  東大薬

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  東大薬学部

• 前田 孝

  Faculty of Pharmaceutical Sciences, University of Tokyo

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  信州大学医学部

• 高橋 浩

  Hoshi Institute of Pharmaceutical Sciences

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  東大・教養

• 八並 高志

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 前田 孝

  Faculty Of Pharmaceutical Sciences University Of Tokyo

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  Faculty of Pharmaceutical Sciences, University of Tokyo

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  Faculty Of Pharmaceutical Science Hoshi University

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  National Cancer Center Research Institute

• 菰田 泰夫

  Institute for Medical and Dental Engineering, Tokyo Medical and Dental University

• 萩庭 丈寿

  千葉大学薬学部

• 土屋 悦輝

  東京都立衛生研究所

• 杉村 隆

  国立がんセンター研究所

• 河内 恵美子

  東京医歯大・生材研:東京医歯大・疾患生命

• 河内 恵美子

  東大・薬

• 橋本 祐一

  東大薬

• 辻 邦郎

  静岡薬科大学

• 辻 邦郎

  静岡県大 薬

• 小倉 治夫

  School Of Pharmaceutical Sciences Kitasato University

• 板井 昭子

  東大・薬

• 古賀 弘

  Exploratory Research Laboratories Chugai Pharmaceutical Co. Ltd.

• 辻 邦郎

  静岡県大・薬

• 古賀 弘

  Faculty of Pharmaceutical Sciences, Kumamoto University

• 三宅 真二

  東大薬

• 磯谷 遙

  College of General Education, University of Tokyo

• 板井 昭子

  Faculty of Pharmaceutical Science, University of Tokyo

• 清野 祐子

  National Cancer Center Institute

• 太田 敏晴

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 津田 恭介

  共立薬科大学:日本学士院

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  Shizuoka College of Pharmacy

• 若林 敬二

  National Cancer Center Research Institute

• 津田 恭介

  Institut fur angewandte Mikrobiologie, Universitat Tokio

• 佐藤 良博

  Institute of Applied Microbiology, University of Tokyo

• 落合 英二

  Pharmazeutische Fakultat, Universitat Tokio

• 大沢 昭緒

  東京大学薬学部

• 土屋 悦輝

  東京都立衛生研究所水質研究科

• 染井 正徳

  東大薬

• 佐藤 八重子

  Biological Institute, College of General Education, University of Tokyo

• 秋山 稔

  東大薬学部

• 岡本 敏彦

  東大薬学部

• 磯谷 遙

  東大教養学部

• 岡本 敏彦

  Laboratory of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo

• Shudo K

  Res. Foundation Itsuu Lab. Tokyo Jpn

• 三条 秀直

  東京大学 薬

• 李 金星

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 黒崎 文也

  東京大学薬学部

• 山田 久美子

  Department of Biology, College of General Education, University of Tokyo

• 森 幸雄

  Faculty Of Pharmaceutical Sciences University Of Tokyo

• 荻庭 丈寿

  千葉大 薬

• 萩庭 文寿

  千葉大・藥

• 相見 則郎

  千葉大院葉

• 宮田 直樹

  National Institute Of Hygienic Sciences University Of Tokyo

• 宮田 直樹

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 山本 武司

  藤永製薬株式会社

• 飯高 洋一

  東大薬

• 若林 敬二

  国立がんセンター研究所

• 首藤 紘一

  東京大学薬学部

• 河内 恵美子

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 石崎 孝義

  東京大学薬学部

• 小倉 治夫

  School of Pharmaceutical Sciences, Kitasato University

• 高柳 弘明

  School of Pharmaceutical Sciences, Kitasato University

• 杉村 隆

  国立ガンセンター

• 河内 卓

  国立ガンセンター

• 長尾 美奈子

  国立ガンセンター

• 矢作 多喜江

  国立ガンセンター

• 清野 祐子

  国立ガンセンター

• 武田 敬

  東大薬

• 山口 健太郎

  東大薬

• 板井 昭子

  東大薬

• 小菅 卓夫

  静岡薬大

• 辻 邦郎

  静岡薬大

• 若林 敬二

  静岡薬大

• 山本 武司

  静岡薬大

• 権田 金治

  東京電機大学理工学部

• 網谷 孝

  Hokkaido Institute Of Pharmaceutical Sciences

• 横田 正実

  静岡県大薬

• 高柳 弘明

  北里大学薬学部薬化学教室

• 高柳 弘明

  School Of Pharmaceutical Sciences Kitasato University

• 河内 恵美子

  東大薬

• 斎藤 肇

  熊本大学 薬

• 糠谷 東雄

  静岡大学・薬

• 辻 邦郎

  Shizuoka College Pharmacy

• 糠谷 東雄

  Shizuoka College of Pharmacy

• 寺田 章男

  Central Health Center of Shizuoka City

• 小杉 敦子

  National Cancer Center Research Institute

• 斎藤 肇

  National Cancer Center Research Institute

• 長谷川 弘子

  Institute of Applied Microbiology, University of Tokyo

• 萩庭 丈寿

  Faculty of Pharmaceutical Sciences, Chiba University

• 長谷川 弘子

  Institute Of Applied Microbiology University Of Tokyo

• 金子 力

  Faculty of Pharmaceutical Sciences, Tokyo University

• 横田 正実

  Shizuoka College of Pharmacy

• 成田 九州男

  Shizuoka College of Pharmacy

• 前田 満和

  National Cancer Center Research Institute

• 成田 九州男

  Department of Radiobiochemistry, School of Pharmaceutical Sciences, University of Shizuoka

• 早津 彦哉

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 染井 正徳

  Faculty of Parmaceutical Sciences, Kanazawa University

• 末松 和美

  東大薬

• 川田 健司

  東大薬

• 永田 亘

  シオノギ研

• 若林 利生

  シオノギ研

• 成定 昌幸

  シオノギ研

• 速瀬 善男

  シオノギ研

• 鎌田 進

  シオノギ研

• 磯谷 遥

  College of General Education

• 西野 武則

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 山口 久夫

  東大薬

• 吉田 明

  東大薬

• 広部 雅昭

  東大薬学部

• 磯谷 遙

  東大教授

• 鳥井 良彦

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 磯谷 謡

  東大教養

• 鳥越 泰義

  Laboratory of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo

• 佐藤 盛幸

  Laboratory of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo

• 菰田 泰夫

  Laboratory of Pharmaceutical Chemistry, Faculty of Pharmaceutical Science, University of Tokyo

• 成田 九州男

  Department Of Radiobiochemistry School Of Pharmaceutical Sciences University Of Shizuoka

• 山田 裕

  東京大学薬学部

• 保戸田 勝己

  千葉大学薬学部

• 長谷川 杉生

  千葉大学薬学部

• 長谷川 杉生

  Faculty of Pharmaceutical Sciences, Chiba University

• 池田 勝

  Product Development Laboratories Sankyo Co. Ltd.

• 尾沢 鉄男

  Faculty Of Parmaceutical Sciences University Of Tokyo

• 黒崎 文也

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 黒崎 文也

  東大・薬

• 岡崎 利夫

  Faculty Of Pharmaceutical Sciences Chiba University

• 岡本 敏彦

  Experimental Station for Medicinal Plant Studies, Faculty of Pharmaceutical Sciences, University of

• 首藤 紘一

  Experimental Station for Medicinal Plant Studies, Faculty of Pharmaceutical Sciences, University of

• 高橋 惣四郎

  Laboratory of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo

• 八並 高志

  Laboratory of Pharmaceutical Chemistry, Faculty of Pharmaceutical Sciences, University of Tokyo

• 磯谷 遙

  Department of Biology, College of General Education, University of Tokyo

• 磯谷 遥

  Department of Biology College of General Education, University of Tokyo

• 金子 雅英

  Pharmazeutische Fakultat Universitat Tokyo

• 望月 正隆

  Kyoritsu College of Pharmacy

• 揚田 富子

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 山本 和子

  Kobe Women's College Of Pharmacy

• 山本 和子

  Faculty of Pharmacy, Meijo University

• 永田 亘

  塩野義製薬株式会社研究所

• 成定 昌幸

  塩野義製薬株式会社研究所

• 望月 正隆

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 網谷 孝

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 佐藤 盛幸

  Faculty of Pharmaceutical Sciences, Hokkaido University

• 室伏 良信

  Chemical Research Laboratories:sankyo Company Ltd.

• 首藤 絋一

  Faculty of Pharmaceutical Sciences, University of Tokyo

• 荻庭 丈寿

  Faculty of Pharmaceutical Sciences, Chiba University

• 坂口 正一

  School Of Pharmaceutical Sciences Kitasato University

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著作論文

• Reactions of K-Region Oxides of Carcinogenic and Noncarcinogenic Aromatic Hydrocarbons. Comparative Studies on Reactions with Nucleophiles and Acid-catalyzed Reactions
• 2 アミノ酸熱分解物中に含まれる変異原物質 : 分離・構造・合成および生物活性
• 18 サイトカイニン作用をもつ二,三のウレア化合物のイネ苗条テストで示す伸長促進作用
• 4-Pyridylureas are surprisingly Potent Cytokinins. The Structure-Activity Relationship
• Synthesis of a Mutagenic Principle isolated from Tryptophan Pyrolysate
• ISOLATION AND STRUCTURAL DETERMINATION OF MUTAGENIC SUBSTANCES IN COAL TAR
• THE STRUCTURE AND ABSOLUTE CONFIGURATION OF SADOSINE
• THE STRUCTURE OF IGNAVINE
• A Potent Mutagen isolated from a Pyrolysate of L-Ornithine
• Ultramicro Analysis of Benzo [α] pyrene in Food
• Synthesis and Mutagenicity of 10-Azabenzo [α] pyrene-4,5-oxide and Other Pentacyclic Aza-arene Oxides
• A Novel Method for Angular Functionalized Methylation via Ring Opening of Bromocyclopropane
• 35 MorphinanおよびB/C trans-morphinanの合成
• 不活性C-H結合に対する新攻撃法とそのエンメインよりジベレリンA_合成への応用 : ダイテルペノイドの化学的研究(第1報)
• 6. dl-ジベレリンA_の生理活性
• 9. 4-カルボアニリドイミダゾール及び関連化合物のサイトカイニン活性
• A Novel Method for Attacking Non-activated C-H Bond and Its Application to the Synthesis of Gibberellin-A_ from Enmein
• 38 新不活性C-H結合攻撃法と,そのEnmeinよりGibberellin A_合成への応用
• Plant Growth Regulators in the Pea Plant (Pisum sativum L.)
• Quantitative Estimation of Auxins and Antiauxin in Etiolated Seedlings of Phaseolus Bean by Gas Chromatography and Colorimetry. I
• Studies on Plant-Growth Regulators. IV. Structure of Growth Retardants and Syntheses of Related Compounds
• 3. 化学構造とcytokinin活性
• 26 三員環の選択的開裂を経由する核間位への官能基を有する炭素化法
• Reaction of 4α, 10α-Bromomethano-1,1-dimethyl-9-oxo-1,2,3,4-tetrahydrophenanthrene with Nucleophiles
• 12. 化学構造とCytokinin活性
• 5. 新植物生長調整物質Lycoricidi-nol,Lycoricidineの単離と生理作用
• Lycoricidinol and Lycoricidine, New Plant-growth Regulators in the Bulbs of Lycoris radiata HERB.
• 12 Lycoricidinol,Lycoricidine : ヒガンバナ鱗茎中の新植物生長調整物貭
• Synthesis of s-Triazolo [1,5-a] pyrazine Derivatives and Cytokinin Activity
• Synthesis of 4α-Formyl-1,2,3,4,4α, 10-hexahydrophenanthrene. A New Method for Angular Formylation
• Isolation of a Plant Growth Inhibitory Substance from Garden Peas (Pisum sativum L.) and Its Identification with (+)-Abscisin-II
• Structure Elucidation of a New Aconite Alkaloid, 15-α-Hydroxyneoline
• Structural and Biological Links between Urea- and Purine-cytokinins
• 19 尿素系サイトカイニンとアデニン系サイトカイニンの作用点について
• Shoot Formation of Tobacco Callus by Various Cytokinin-Active Ureas and Pyrimidines
• 12. アミノピリミジン誘導体のサイトカイニン作用
• Cytokinin Activity of Pyrimidine Derivatives
• Studies on the Constituents of Isodon trichocarpus KUDO. II. The Structures of Enmenin, Enmelol, and Ememodin
• Studies on the Constituents of Isodon trichocarpus KUDO. I. Isolation of the Constituents and the Structures of Isodonol, Enmedol, and Enmenol
• Reaction Mechanism in Aromatic Heterocyclic Compounds. X. Kinetics of the Reaction of Carcinogenic 4-Nitroquinoline 1-Oxide and Its Derivatives with Sodium Ethoxide
• The Structure of Lucidusculine and the Absolute Configuration of Songorine
• Novel Rearrangement of Pyrazole N-Imines with Acetic Anhydride
• Syntheses of Novel Antimicrobial Compounds : Pyrazolo [5,1-b] thiazole, Imidazo [1,2-b] pyrazole, and Thiazolo [3,2-b] dihydro-1,2-diazepine
• THREE NEW ALKALOIDS, RYOSENAMINE, RYOSENAMINOL, AND IBUKINAMINE FROM ACONITUM IBUKIENSE NAKAI
• The Structure of Nobilonine. The Second Alkaloid from Dendrobium nobile
• The Structure of Dendrobine
• Rearrangement of 4-Acetoxy-2H-1,4-benzoxazin-3 (4H)-one
• A Fungal Metabolite, Novel Isocyano Epoxide
• The Crystal Structure of the Bromoacetylated Dimer-A synthesized by the Reaction of Acridine with Hydroxylamine-O-sulfonic Acid
• Uber die Shimoburobase-II und die Takaobase-I
• THE CONVERSION OF PSEUDOKOBUSINE TO KOBUSINE
• THE STRUCTURE OF THE NEW DITERPENE ALKALOID NOMININE AND THE ABSOLUTE CONFIGURATION OF KOBUSINE
• THE STRUCTURE OF A NEW DITERPENE ALKALOID : SANYONAMINE
• THE STRUCTURE OF HYPOGNAVINE
• THE PARTIAL SYNTHESIS OF ISODELPHININE
• Studies on the Chlorinated α-Santonins. I
• Reaction of Phenanthrene-9,10-oxide with Tetracyanoethylene
• The Structure of Isohypognavine
• Structural Correlation of Kobusine to Pseudokobusine
• Reaction Mechanism in Aromatic Heterocyclic Compounds. III. Kinetics of the Reaction of 4-Haloquinoline 1-Oxides and Related Compounds with Piperidine.
• Chemical Structure of QA_, One of the Covalently Bound Adducts of Carcinogenic 4-Nitroquinoline 1-Oxide with Nucleic Acid Bases of Cellular Nucleic Acids
• Studies on Chemical Alterations of Nucleic Acids and Their Components. VIII. Alkaline Rearrangement of 1-Aminoadenosine to 5-Amino-1-β-D-ribofuranosyl-4-(1,2,4-triazol-3-yl) imidazole
• Application of NMR to Stereochemistry. (I). The Spatial Interaction Effect of the Hydroxyl Group to Methyl Resonance.(53)
• Synthesis of Non-K-region Dihydrodiols and Epoxides of Carcinogenic Dibenz [c, h] acridine
• Identification of an Ultimate Mutagen of 10-Azabenzo [α] pyrene : Microsomal Oxidation of 10-Azabenzo [α] pyrene to 10-Azabenzo [α] pyrene-4,5-oxide
• Aconite Aldaloids. XXIV. The Structure of Ignavine. (4).
• The Aconite Alkaloids. XXIII. The Structure of Ignavine. (3).
• Syntheses of Alkylphenanthrenes. I.
• ヒノリン-N-オキシドのニトロ化反応-チーアミノナフタリンスルホン酸誘導体の日本脳炎ヴイルスに対する作用日本薬学会例会講演要旨-
• Reaction of N-Aminopyridinium Derivatives. V. Syntheses of 1-(N-Methylacetamido) alkylpyridinium Salts and Their Reaction with Cyanide Ion.
• Reaction of N-Aminopyridinium Derivatives. II. The Reactions of 1-(N-Acylalkylamino) pyridinium Salt Derivatives with Cyanide Ion. : A New Synthesis of Primary Amines.
• Synthesis of Mutagens isolated from Tryptophan Pyrolysate and of Some Analogs, 3-Amino-5H-pyrido [4,3-b] indoles
• Synthesis of Mutagenic Principles Isolated from L-Glutamic Acid Pyrolysate
• Further Studies on the Alkaloidal Constituents of Dendrobium nobile (Orchidaceae)-Structure Determination of 4-Hydroxy-dendroxine and Nobilomethylene
• 東京都内水域における水質, かび臭物質および原因微生物について
• 藍藻Oscillatoria sp.および河川水中の臭気物質.2-Methylisoborneol, Geosmin, p-Cresol, Indoleおよび3-Methylindoleの確認
• Studies on Plant Growth Regulators. III. Isolation of Indole-3-acetonitrile and Methyl Indole-3-acetate from the Neutral Fraction of the Moyashi Extract
• Studies on Plant Growth Regulators. II. Isolation of Indole-3-acetic Acid, Phenylacetic Acid, and Several Plant Growth Inhibitors from Etiolated Seedlings of Phaseolus
• Studies on Plant Growth Regulators. I., Isolation of Indole-3-acetamide, 2-Phenylacetamide, and Indole-3-carboxaldehyde from Etiolated Seedlings of Phaseolus
• Alkylation of Phenols by Phenanthrene 9,10-Oxide
• 7 4-ピリダジニルフェニル尿素誘導体のサイトカイニン活性
• STRUCTURE OF NUCLEIC ACID BASES IN CALF THYMUS DNA MODIFIED BY THE POTENT MUTAGEN, 10-AZABENZO[a]PYRENE-4,5-OXIDE
• Reactions of 3-Nitroquinoline Derivatives with Sodium Hypobromite
• Studies on Reaction of Alkali-fusion of Haloquinolones via Aryne Intermediates
• Deoxyribonucleic Acid Modification by Mutagenic 3-Amino-1-methyl-5H-pyrido [4,3-b] indole : The Chemical Events
• FORMATION OF PUMMERER'S KETONE FROM 4-METHYLPHENOXENIUM ION. AN ACID-CATALYZED SOLVOLYSIS OF N-p-TOLUENESULFONYL-O-(4-TOLYL)-HYDROXYLAMINE IN p-CRESOL
• Reaction of Aromatic Heterocyclic Nitro Compounds with Potassium Cyanide. II
• Modification of Deoxyribonucleic Acid with Reductively Activated Mitomycin C. Structures of Modified Nucleotides
• MOLECULAR REQUIREMENTS FOR EPIGENETIC MODULATORS. SYNTHESIS OF ACTIVE FRAGMENTS OF TELEOCIDINS LYNGBYATOXIN
• NEW DIMERIC ANALOGS OF 2-AMINODIPYRIDO [1,2-a : 3', 2'-d] IMIDAZOLE : SYNTHESIS AND INTERACTION WITH DNA
• ALKYLATION OF DNA WITH A MITOMYCIN DERIVATIVE, 7-N-(p-HYDROXYPHENYL)-MITOMYCIN C. REDUCTIVE ALKYLATION AND PREFERENTIAL BINDING TO ADENINE
• Synthesis of Mutagenic Heteroaromatics : 2-Aminoimidazo [4,5-f] quinolines
• 植物のケミカルコントロ-ル (食糧問題と化学--明日の生産技術を探る)
• Reaction of Benzene with Diphenyl Sulfoxides
• Reaction of 1-Naphthylhydroxylamine with Calf Thymus Deoxyribonucleic Acid. Isolation and Synthesis of N-(Guanin-C^8-yl)-1-naphthylamine
• 27 マイトマイシンCと仔牛胸腺DNAとの反応修飾ヌクレオチドの分離と構造
• 複素環芳香族アミンによる変異原性の発現
• Identification of a Reactive Metabolite of the Mutagen, 2-Amino-3-methylimidazolo [4,5-f] quinoline
• 変異原性および発癌性芳香族アミンの化学
• 20 N-フェニール-N'-(2-OH-4-ピリディル)尿素のイネ苗条試験に対する効果
• 87 制癌性および発癌性物質による修飾核酸塩基の構造
• Alkylation of 5'-Guanylic Acid by Reductively Activated Mitomycin C
• Structure of a Base in DNA modified by Glu-P-1
• 11 4-ピリジルフェニル尿素誘導体のサイトカイニン活性
• Structural Identification of a Modified Base in DNA covalently Bound with Mutagenic 3-Amino-1-methyl-5H-pyrido [4,3-b] indole
• Synthesis of Phenanthrene-9,10-imine Tosylate. A Stable Arene Imine
• Photoisomerisation of N-Carboethoxy-2,3-homoazepine
• Wave Length Dependent Photolysis of Phenanthrene Oxide
• Synthesis of Gibbane Derivatives from Enmein
• Conversion of Enmein to (-)-Kaurane. The Absolute Stereochemistry of Enmein
• Chemical Conversion of Kobusine. Cleavage and Regeneration of the Bridged C_-C_ Bond
• Reaction of N-Aminopyridinium Derivatives. IV. Syntheses of N-Aminoquinolinium Salts and Their Reaction with Cyanide Ion
• The Structure of Dendramine (6-Oxydendrobine) and 6-Oxydendroxine The Fourth and Fifth Alkaloid from Dendrobium nobile
• The Structure of Dendroxine The Third Alkaloid from Dendrobium nobile
• Chemical Conversion of Kobusine : Cleavage of the Bridged C-C Bond by a Novel Fragmentation Reaction
• Acid-Catalyzed Double-Cyclization Reactions of N, N-Dibenzylamino-acetaldehyde Dialkyl Acetals and Related Compounds : General Sunthesis of 7,12-Dihydro-5H-6,12-methanodibenz-[c, f]azocines and Related Compounds
• A One-step Synthesis of Purine Ring from Formamide
• Reaction of Aromatic Heterocyclic Nitro Compounds with Potassium Cyanide. III. Some Nitroquinoline 1-Oxides
• Reaction of Aromatic Heterocyclic Nitro Compound with Potassium Cyanide. I. 3-Nitroquinoline
• Reductive Radical Formation of Hetero Aromatic N-Oxides
• Reaction Gas Chromatography. : Determination of Skeletal Structure by Means of Reaction Gas Chromatography
• Reaction Mechanism in Aromatic Heterocyclic Compounds. V. Kinetics of the Reaction of 4-Nitroquinoline 1-Oxide and Related Compounds with Thioglycolic Acid.
• The Reaction of N-Alkoxypyridinium Derivatives. (6). The Reaction of N-Methoxyquinolinium Salt with Ketones.
• Teflon Coated Support for Gas Chromatography at a Lower Temperature
• Reaction Mechanism in Aromatic Heterocyclic Compound. I. The Reactions of N-Alkoxypyridinium Derivarives
• Application of Nuclear Magnetic Resonance to Stereochemistry. II. Determination of the Conformation of Hydroxyl Groups by Nuclear Magnetic Resonance ; Androst-4-en-3-one and Pregn-4-en-3-one Series.
• C-Glycosyl Nucleoside. XI. Interaction of Schiff Bases with Metal Halides in Dimethyl Sulfoxide
• Reaction of N-Aminopyridinium Derivatives. VI. Properties of s-Triazolo [1,5-α] pyridine Ring.
• Reaction of N-Aminopyridinium Derivatives. III. Synthesis of s-Triazolo [1,5-α]-pyridine Ring.
• Synthesis of 2- and 4-Cyanopyridines
• Reaction of N-Aminopyridinium Derivatives. XIII. Syntheses of Pyrazolodiazines by Cyclization of N-Aminodiazinium Salts
• Reaction of N-Aminopyridinium Salt with Cyanide Ion

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