藤田 栄一 | Institute For Chemical Research Kyoto University
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概要
関連著者
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藤田 栄一
Institute For Chemical Research Kyoto University
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藤田 栄一
Institute for Chemical Research, Kyoto University
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藤田 栄一
Osaka University Of Pharmaceutical Sciences
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藤田 栄一
京都大学化学研究所
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冨士 薫
Institute For Chemical Research Kyoto University
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長尾 善光
Institute for Chemical Research, Kyoto University
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長尾 善光
Institute For Chemical Research Kyoto University
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野出 学
Institute For Chemical Research Kyoto University
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藤多 哲朗
徳島大学薬学部
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藤多 哲朗
Institute for Chemical Research, Kyoto University
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野出 学
Kyoto Pharmaceutical University
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落合 正仁
Institute for Chemical Research, Kyoto University
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落合 正仁
Institute For Chemical Research Kyoto University
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落合 正仁
徳島大学大学院ヘルスバイオサイエンス研究部精密薬品製造学分野
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落合 正仁
京都大学化学研究所
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渋谷 雅之
Institute For Chemical Research Kyoto University
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藤田 榮一
Osaka University of Pharmaceutical Sciences
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太田 敬一郎
Institute For Chemical Research Kyoto University
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山田 敏英
Tokushima Research Institute Otsuka Pharmaceutical Co. Ltd.
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山田 敏英
Institute for Chemical Research, Kyoto University
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田岡 学
Institute For Chemical Research Kyoto University
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西出 喜代治
京都薬科大学薬品製造学教室 創薬科学フロンティア研究センター
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川端 猛夫
京都大学化学研究所
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伊藤 望
Research Laboratories Nippon Shoji Kaisha Ltd.
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中村 薫竹
Institute for Chemical Research, Kyoto University
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伊藤 望
Institute for Chemical Research, Kyoto University
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河野 辰彦
Institute for Chemical Research, Kyoto University
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川端 猛夫
京大化研
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河野 辰彦
Institute For Chemical Research Kyoto University
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中村 薫竹
Institute For Chemical Research Kyoto University
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角 昭久
Institute For Chemical Research Kyoto University
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山口 秀夫
Osaka University of Pharmaceutical Sciences
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金子 喜三好
Institute For Chemical Research Kyoto University
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別所 清
Institute For Chemical Research Kyoto University
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堀 均
Institute For Chemical Research Kyoto University
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中井 博
Shionogi Research Laboratories
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城 始勇
Research And Development Division Rigaku Industrial Corporation
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城 始勇
Shionogi Research Laboratory, Shionogi & Co.
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有本 正生
Osaka College of Pharmacy
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角 昭久
Institute for Chemical Research, Kyoto University
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川端 猛夫
Institute for Chemical Research, Kyoto University
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西出 喜代治
Institute for Chemical Research, Kyoto University
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渡辺 宏二
Institute for Chemical Research, Kyoto University
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河野 辰彦
Research Laboratories, Nippon Shinyaku Co., Ltd.
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有本 正生
大阪薬大
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中井 博
Shionogi Research Laboratories Shionogi & Co. Ltd.
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有本 正生
Osaka University Of Pharmaceutical Sciences
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渡辺 宏二
Institute For Chemical Research Kyoto University
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中井 博
Shionogi Research Laboratories, Shionogi & Co., Ltd.,
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武田 節夫
Tokushima Institute, Taiho Pharmaceutical Co., Ltd.,
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黒田 浩之
Kyoto College Of Pharmacy
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野出 学
京都薬科大学薬品製造
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富松 利明
Faculty of Pharmaceutical Sciences of Kyushu University
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堀 均
Pharmaceutical Institute School Of Medicine Keio University
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片山 肇
Institute For Chemical Research Kyoto University
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吉村 陽子
Shionogi Research Laboratories Shionogi & Co. Ltd.
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川端 浩二
Institute For Chemical Research Kyoto University
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稲山 誠一
Pharmaceutical Institute, School of Medicine, Keio University
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栗山 馨
Shionogi Research Laboratory
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瀬野 薫
Institute for Chemical Research, Kyoto University
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宮坂 忠与
Institute for Chemical Research, Kyoto University
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高尾 佐知子
Institute for Chemical Research, Kyoto University
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藤田 栄一
京大・化研
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八木 政広
Research Laboratories Nippon Shinyaku Co. Ltd.
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Katoh Takahiro
Department Of Pharmaceutical Manufacturing Chemistry 21st Century Coe Program Kyoto Pharmaceutical U
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梶本 哲也
京都薬大
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野出 学
京大・化研
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藤田 栄一
京大化研
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岡田 泰守
Institute for Chemical Research, Kyoto University
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鈴木 豊子
Institute for Chemical Research, Kyoto University
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岩田 辰夫
Shionogi Research Laboratories, Shionogi & Co., Ltd.
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村田 弘之
Institute for Chemical Research, Kyoto University
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佐井 みどり
Faculty of Pharmaceutical Sciences, Setsunan University
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釆見 憲男
Research Laboratory, Taiho Pharmaceutical Co., Ltd.
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太田 啓一郎
Institute for Chemical Research, Kyoto University
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川端 武夫
Institute for Chemical Research, Kyoto University
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宮坂 忠与
福山大学薬学部
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吉村 陽子
Institute for Chemical Research, Kyoto University
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梶本 哲也
Institute for Chemical Research, Kyoto University
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黒田 浩之
Central Research Laboratories, Takara Shuzo Co. Ltd.,
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富松 利明
Faculty Of Pharmaceutical Sciences University Of Tokushima
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藤田 栄一
徳島大学薬学部
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堀 均
京大・化研
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佐伯 行一
Institute for Chemical Research, Kyoto University Uji, Kyoto-fu, 611, Japan
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佐伯 行一
京大化研
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鷲見 賢三
Institute for Chemical Research, Kyoto University
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浮田 辰三
Institute for Chemical Research, Kyoto University
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藤田 哲郎
Institute for Chemical Research, Kyoto University
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藤田 栄一
Faculty of Pharmacy, Tokushima University
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松田 真人
Research Laboratories, Nippon Shinyaku Co., Ltd.
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尾崎 正邦
Research Laboratories, Nippon Shinyaku Co., Ltd.
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林 道子
Institute for Chemical Research, Kyoto University
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松田 真人
日本新薬株式会社創薬第二研究所
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尾崎 正邦
日本新薬株式会社創薬第二研究所
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市川 皇陛
Institute for Chemical Research, Kyoto University
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稲山 誠一
Institute Of Oriental Medical Sciences
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稲山 誠一
Pharmaceutical Institute School Of Medicine Keio University
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稲山 誠一
慶應義塾大学医学部薬化学研究所
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浮田 辰三
Institute For Chemical Research Kyoto University
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鈴木 豊子
Institute For Chemical Research Kyoto University
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松岡 正人
Chemistry Laboratories And Biology Laboratories Nippon Shinyaku Company Ltd.
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采見 憲男
Tokushima Institute Taiho Pharmaceutical Co. Ltd.
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釆見 憲男
Research Laboratory Taiho Pharmaceutical Co. Ltd.
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武田 節夫
Tokushima Institute Taiho Pharmaceutical Co. Ltd.
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藤田 哲郎
Institute For Chemical Research Kyoto University
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林 道子
Institute For Chemical Research Kyoto University
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松田 真人
Research Laboratories Nippon Shinyaku Co. Ltd.
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Katoh Takahiro
Department Of Pharmaceutical Manufacturing Chemistry Kyoto Pharmaceutical University
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佐伯 行一
Institute For Chemical Research Kyoto University Uji Kyoto-fu 611 Japan
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藤田 栄一
Faculty Of Pharmacy Tokushima University
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佐井 みどり
Faculty Of Pharmaceutical Sciences Setsunan University
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栗山 馨
Shionogi Research Laboratories Shionogi And Co.
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Kajimoto Tetsuya
Department Of Pharmaceutical Manufacturing Chemistry Kyoto Pharmaceutical University
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岩田 辰夫
Shionogi Research Laboratories Shionogi & Co. Ltd.
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尾崎 正邦
Research And Development Laboratory Nippon Shinyaku Co. Ltd.
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高尾 佐知子
Institute For Chemical Research Kyoto University
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市川 皇陛
Institute For Chemical Research Kyoto University
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瀬野 薫
Institute For Chemical Research Kyoto University
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岡田 泰守
Institute For Chemical Research Kyoto University
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Kato Takahiro
Department Of Pharmaceutical Manufacturing Chemistry Kyoto Pharmaceutical University
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鷲見 賢三
Institute For Chemical Research Kyoto University
著作論文
- Monitored Aminolysis of 3-Acyl-1,3-thiazolidine-2-thiones : Synthesis of Amides and Amide Alkaloids
- Terpenoids. XXIV. Isolation of Isodonal and Epinodosin from Isodon japonicus and Structure Elucidation of Sodoponin and Epinodosinol, Novel Diterpenoids of the Same Plant
- Terpenoids. XXI. The Structure and Stereochemistry of Isodotricin, a Diterpenoid of Isodon trichocarpus and I. japonicus
- Terpenoids. XVII. Chemical Conversion of Trichokaurin into Isodocarpin via a Direct Pathway
- Terpenoids. IX. The Structure and Absolute Configuration of Isodocarpin, a New Diterpenoid from Isodon trichocarpus KUDO and I. japonicus HARA
- Terpenoids. VII. The Structure and Absolute Configuration of Nodosin, a New Diterpenoid from Isodon Species
- On the Constituents of Nauclea orientalis L. I. Noreugenin and Naucleoside, A New Glycoside. : Terpenoids V
- The Absolute Configuration of Enmein Transformation of Enmein into (-)-Kaurane
- Lythraceous Alkaloids. XIV. Kinetic Equalization of Carbon-13 Nuclear Magnetic Resonance Chemical Shifts in N, O-Dimethyllythranidine, a Cyclophane Bearing Asymmetric Carbon Atoms
- Lythraceous Alkaloids. XIII. X-Ray Determination of the Molecular Structures of O-Methyllythranidine N, O, O-Triformate, 22-Bromolythranine N, O, O-Triacetate, and O-Methyldeacetyllythramine
- Lythraceous Alkaloids. XII. Circular Dichroism Studies on Lythranine-Type Alkaloids
- Lythraceous Alkaloids. X. Alkaloids of Lagerstroemia subcostata and L. favriei : A Contribution to the Chemotaxonomy
- Lythraceous Alkaloids. II. The Structure of O-Methyllythranidine
- Lythraceous Alkaloids. I. Characterization of the Novel Alkaloids, Lythranine, Lythranidine, and Lythramine isolated from Lythrum anceps MAKINO
- Hard Acid and Soft Nucleophile System. VII. A Convenient Reduction of Functionalized Polyarenes to Parent Polyarenes
- ANTITUMOR ACTIVITY OF DITERPENOIDS, TRICHORABDALS A, B, AND C, AND THE RELATED COMPOUNDS : SYNERGISM OF TWO ACTIVE SITES
- RADICAL CATION INDUCED REDUCTIVE DEHALOGENATION OF ORTHO- AND PARA-HALOPHENOLS AND THEIR DERIVATIVES
- Hard Acid and Soft Nucleophile System. VI. A Convenient Synthesis of Alkylthiopolycyclic Aromatics with a Metal Halide and Thiol System
- Studies on the Alkaloids of Thalictrum Thunbergii DC. XVIII. Total Synthesis of optically Active Natural O-Methylthalicberine
- SELECTIVE DEMETHYLATION OF ALIPHATIC METHYL ETHER IN THE PRESENCE OF AROMATIC METHYL ETHER WITH THE ALUMINUM CHLORIDE-SODIUM IODIDE-ACETONITRILE SYSTEM
- THREE NEW 8,9-SECO-ENT-KAURANE DITERPENOIDS FROM RABDOSIA SHIKOKIANA (LABIATAE)
- Antitumor Activity of Rabdosia and Teucrium Diterpenoids against P 388 Lymphocytic Leukemia in Mice
- Hard Acid and Soft Nucleophile System. IV. Removal of Benzyl Protecting Group with Boron Trifluoride Etherate and Dimethyl Sulflide
- Terpenoids. XXXVII. Hypoiodite Reactions with 6-Hydroxy-17-norkaurane- and 7-Norgibberellane-derivatives
- 22 C_ジベレリンの合成研究
- Absolute Configuration of Lythrancine-I, -II, -III, -IV, Lythrancepine-I, -II, and -III
- 12 ミソハギの新塩基Lythrancine-I〜IV及びLythrancepine-I〜IIIの構造について
- Silicon-Assisted Ring Opening of Cyclopropyl Ketones with Boron Trifluoride-Acetic Acid Complex
- Stereoselective Syntheses of E- and Z-9,11-Dodecadien-1-yl Acetates : The Major Sex Pheromones of the Red Bollworm Moth
- Umpolung of Reactivity of Allylsilane, Allylgermane, and Allylstannane via Their Reaction with Thallium (III) Salt : A New Allylation Reaction for Aromatic Compounds
- Umpolung of Reactivity of Allylsilane, Allylgermane, and Allylstannane : Allylation of Aromatic Compounds with Allylmetal and Arylthallium Bis (trifluoroacetate)
- Terpenoids. XLIII. Total Synthesis of rac-Kaur-16-ene-11α, 15α-diol
- Terpenoids. XLII. A Convenient Stereoselective Transformation of 16-Exocyclic Methylene Group into Carboxy Group in ent-Kaurene and Its 19-Oic Acid
- Terpenoids. XXXIII. Chemical Conversion of Enmein into Enmelol
- Terpenoids. XXVI. Structures of Lasiokaurinol and Lasiokaurinin, Two Novel Diterpenoids of Isodon lasiocarpus (HAYATA) KUDO
- Terpenoids. XX. The Structure and Absolute Configuration of Lasiokaurin and Lasiodonin, New Diterpenoids from Isodon lasiocarpus (HAYATA) KUDO
- Studies on the Alkaloids of Thalictrum Thunbergii DC. II. A Quaternary Base in the Stem and Leaves.
- Antitumor Activity of Acylated Oridonin
- An Efficient Method for Selective Acetylation of Alcoholic Hydroxyl Groups
- Utilization of Derivatives of Thiazolidine-2-thione : Esterification
- Useful Dethioacetalization with Soft Acid Metal Salts : Thallium Trinitrate and Mercuric Perchlorate
- Dethioacetalization with Thallium (III) Nitrate
- A Versatile Synthesis of (±)-Solenopsin A
- Total Synthesis of Optically Active Natural O-Methylthalicberine