寺島 孜郎 | (財)相模中央化学研究所
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概要
関連著者
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寺島 孜郎
(財)相模中央化学研究所
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寺島 孜郎
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)sagami Chemical Research Cen
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山田 俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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寺島 孜郎
Faculty of Pharmaceutical Sciences, University of Tokyo
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山田 俊一
Faculty of Pharmaceutical Sciences, University of Tokyo
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柴崎 正勝
東大院薬
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柴崎 正勝
Faculty Of Pharmaceutical Sciences Teikyo University:(present Address)faculty Of Pharmacertical Scie
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柴崎 正勝
Faculty Of Pharmaceutical Sciences Hokkaido University
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山田 俊一
東京大学
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曽 仲奇
Faculty Of Pharmaceutical Sciences University Of Tokyo
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Koga Kenjiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
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丹野 紀彦
Faculty Of Pharmaceutical Sciences University Of Tokyo
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古賀 憲司
Faculty of Pharmaceutical Sciences, University of Tokyo
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山田 俊一
東京大学薬学部
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北本 六良
Faculty of Pharmaceutical Sciences, University of Tokyo
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曽根 孝範
Faculty of Pharmaceutical Sciences, University of Tokyo
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我妻 光吉
Faculty of Pharmaceutical Sciences, University of Tokyo
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曽根 孝範
Life-science Institute, Asahi Chemical Industry Co., Ltd.
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曽根 孝範
Life-science Institute Asahi Chemical Industry Co. Ltd.
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我妻 光吉
Faculty Of Pharmaceutical Sciences University Of Tokyo
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北本 六良
Faculty Of Pharmaceutical Sciences University Of Tokyo
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高村 則夫
Organic Chemistry Research Laboratory, Tanabe Seiyaku Co., Ltd.,
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水野 初彦
Faculty of Pharmaceutical Sciences, Osaka University
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佐藤 忠夫
Faculty Of Pharmaceutical Sciences Chiba University
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阿知波 一雄
Faculty of Pharmaceutical Sciences, University of Tokyo
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寺島 孜郎
相模中研
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水野 初彦
Faculty Of Pharmaceutical Sciences University Of Tokyo
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高村 則夫
Faculty of Pharmaceutical Sciences, University of Tokyo
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高村 則夫
Organic Chemistry Research Laboratory Tanabe Seiyaku Co. Ltd.
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益子 敏夫
東京大学薬学部
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寺島 孜郎
東京大学薬学部
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奈良 宗彦
興和(株)東研
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寺島 孜郎
東大・薬
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田本 克己
Faculty Of Pharmaceutical Sciences University Of Tokyo
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田本 克巳
Development Research Laboratories I Sumitomo Pharmaceuticals Research Center
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朱 尚渉
東大薬
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李 功固
Faculty of Pharmaceutical Sciences, University of Tokyo
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李 功固
Faculty Of Pharmaceutical Sciences University Of Tokyo
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広井 邦雄
Faculty Of Pharmaceutical Sciences University Of Tokyo
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柴崎 正勝
東大・薬
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竹内 義雄
Faculty Of Pharmaceutical Sciences University Of Tokyo
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冨士 薫
京都大学化学研究所
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樹林 千尋
東京薬科大学薬学部
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北川 富造
Faculty of Pharmaceutical Sciences, University of Tokyo
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石川 清康
Faculty of Pharmaceutical Sciences, University of Tokyo
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大橋 尚仁
東大薬
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寺島 孜郎
Sagami Chemical Research Center
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古賀 憲司
東大薬
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山田 俊一
城西大・薬
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木村 芳一
相模中研
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高橋 一朗
Faculty Of Pharmaceutical Sciences University Of Tokyo
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大橋 尚仁
Faculty of Pharmaceutical Sciences, University of Tokyo
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亀尾 一弥
Faculty of Pharmaceutical Sciences, University of Tokyo
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明田 耕一
Faculty of Pharmaceutical Sciences, University of Tokyo
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山田 俊一
東大・薬
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高島 克己
Faculty of Pharmaceutical Sciences, University of Tokyo
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平井 功一
三共(株)第二生産技術研究所
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鈴木 三千代
Sagami Chemical Research Center
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木村 芳一
Sagami Chemical Research Center
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北川 富造
東大薬
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明田 耕一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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亀尾 一弥
Research Center Taisho Pharmaceutical Co. Ltd.
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平井 功一
三共(株)研究本部
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石川 清康
Faculty Of Pharmaceutical Sciences University Of Tokyo
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寺島 孜郎
東大薬
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丹野 紀彦
東大薬
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朱 尚渉
Faculty of Pharmaceutical Sciences, University of Tokyo
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高島 克己
Faculty Of Pharmaceutical Sciences University Of Tokyo
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樹林 千尋
東京薬科大学
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奈良 宗彦
Faculty of Pharmaceutical Sciences, University of Tokyo
著作論文
- Stereochemical Studies. XXIX. Asymmetric Synthesis of 2-Alkylcyclohexanones via optically Active Lithioenamines
- Stereochemical Studies. VII. Thermal Rearrangement of α-Hydroxyimines to α-Aminoketones using optically Active Open Chain Compounds
- Studies on optically Active Amino Acids. XVIII. Studies on α-Methyl-α-amino Acids. XIV. Several Optical Properties of α-Methyl-α-amino Acids
- 光学活性化合物に魅せられた50年 : 山田俊一先生にきく
- 立体化学の研究(第56報)(Acetylacetonato)[(1R, 2S)-N-alkylephedrinato]-dioxomolybdenumを不斉触媒とするアリルアルコールの不斉エポキシ化反応
- 立体化学の研究(第55報)不斉エポキシ化触媒としてのモリブデン錯体の合成
- 36 メソ型化合物を用いる光学活性プロスタグランディン,ステロイド中間体の新合成法
- Studies on the Synthesis of 4-[1,8-Dioxygenated-9,10-dioxoanthracen (or anthracen)-2-yl] butanoic Acid Derivatives
- Stereochemical Studies. XXIII. Stereochemistry of the Thermal Isocyanide-Cyanide Rearrangement
- 効率的合成法の開発に感動と興奮を求めて
- 生物活性物質の効率的合成法の開発とその創薬化学への展開
- Stereochemical Studies. XLVII. Asymmetric Reduction of 2-Alkyl-1,3,4-cyclopentanetriones with Lithium Aluminum Hydride decomposed by optically Active β-Aminoalcohols. Syntheses of optically Active Allethrolone and Prostaglandin E_1
- Stereochemical Studies. XLV. A Novel Regiospecific Ring Opening of optically Active 2-Substituted-1-tosylaziridines
- Stereochemical Studies. XLVI. Studies on the Synthesis of 4-Acetoxy-cyclopentane-1,3-dione Derivatives
- Stereochemical Studies. XLIV. Exploitation of the New Synthetic Scheme for Chiral Additives Usable in Asymmetric Syntheses. Novel Syntheses of optically Active γ-Amino Acids and Pyrrolidines from L-α-Amino Acids
- Stereochemical Studies. XLIII. Novel Reactivity of Organometallic Reagents to 5,5-Ethylenedioxy-2-methyl-2-phenylcyclohexanone
- Stereochemical Studies. XLII. Asymmetric Synthesis of naturally Occurring Podocarpic Acid
- Stereochemical Studies. XLI. Asymmetric Synthesis of optically Active 4a-Methyl-4,4a, 9,10-tetrahydro-2 (3H)-phenanthrone Derivatives, Key Intermediates for Total Syntheses of optically Active Diterpenes and Steroids
- Stereochemical Studies. XL. A Biomimetic Conversion of L-Lysine into optically Active 2-Substituted Piperidines. Syntheses of D- and L-Pipecolic Acid, and (S) (+)-Coniine from L-Lysine
- Stereochemical Studies. XXXIX. A Novel Method for the Preparation of Optically Active Aldehydes. Syntheses of Optically Active (R) (+)-α-Cyclocitral, (S) (+)-Dehydrovomifoliol, and (S) (+)-Abscisic Acid
- Stereochemical Studies. XXXV. A Biogenetic-type Asymmetric Cyclization. Syntheses of optically Active α-Cyclocitral and trans-α-Damascone
- Stereochemical Studies. XXXIV. A Novel Biogenetic-type Cyclization of Citral to α-Cyclocitral via an Enamine
- プロスタグランディンの化学合成 (プロスタグランディン)
- 2 光学活性テルペン類の不斉合成 : α-cyclocitralの不斉合成を中心として
- Stereochemical Studies. XXII. Thermal Rearrangement of S(-)-1-Phenylethyl Isocyanide
- Amino Acids and Peptides. I. Novel Peptide Bond Formation Catalyzed by Metal Ions. I. Formation of Glycine Peptide Esters
- 光学活性な生物活性化合物の合成を目指して
- Chemistry of Amino Acids. VI. Studies on α-Alkyl-α-amino Acids. X. Unusual Alkyl Migration in the Hofmann Degradation of 5-(2-Dialkylaminoethyl)-5-methylhydantoin Quarternary Ammonium Hydroxide Anhydronium Base
- Stereochemical Studies. XXI. Studies on α-Alkyl-α-amino Acids. XV. Application of Thermal Isocyanide-Cyanide Rearrangement to R-S Conversion of α-Methylphenylalanine
- Amino Acids and Peptides. VI. Novel Peptide Bond Formation catalyzed by Metal Ions. IV. Formation of optically Active Amino Acid Amides and Peptide Amides
- Stereochemical Studies. VI. Steric Course of Intramolecular Alkylations using optically Active Amine Derivatives
- 薬学における有機合成の現状と将来
- Novel Ethynylcerium(III) Reagents as Efficient Tools for Constructing the α-Hydroxy Methyl Ketone Moiety of Anthracyclinones
- Elucidation of the Racemization Mechanism of the α-Hydroxy Ketone Moiety (C_9-Position) of Optically Active Anthracyclinone Derivatives
- Novel Synthesis of Optically Pure Anthracyclinone Intermediates by the Use of Microbial Asymmetric Reduction with Fermenting Baker's Yeast
- Asymmetric Reduction of Various Types of Ketones with Lithium Aluminum Hydride partially decomposed with (-)-N-Methylephedrine and N-Ethylaniline
- Asymmetric Synthesis of optically Active Anthracyclinone Intermediate and 4-Demethoxyanthracyclinones by the Use of a Novel Chiral Reducing Agent
- Development of a Novel Synthetic Route to optically Active Anthracyclinones : Preliminary Synthesis of the Racemic Key Intermediate
- 30 光学活性アンスラサイクリノンの不斉合成
- Asymmetric Halolactonization Reactions. 3. Asymmetric Synthesis of optically Active Anthracyclinones
- Synthesis of Enantiomeric Pairs of Vicinal-Diols from L-α-Amino Acids by the Use of Organolithium Reagents : Its Application to optically Active Epoxyterpene Synthesis
- Synthesis of optically Active α-Alkyl or α-Aryl Acids from L-α-Amino Acids by the Use of Organocopper Reagents
- 日本薬学会奨励賞受賞 大塚雅巳氏の業績
- Stereochemical Studies. V. Intramolecular C-H Bond Insertion Reaction of Acyl Nitrene generated from optically Active Acyl Azide
- Stereochemical Studies. IV. Studies on α-Alkyl-α-amino Acids. XII. Hofmann and Curtius Rearrangements of S (+)-2-Cyano-2-methyl-3-phenylpropionic Acid
- Stereochemical Studies. III. Chemical Correlation of Absolute Configuration of 2-Cyano-2-methyl-3-phenylpropionic Acid to α-Methyl-α-isopropylsuccinic Acid
- Studies on Optically Active Amino Acids. XVI. Studies on α-Alkyl-α-amino Acids. XI. Synthesis of R-α-Methylphenylalanine from S (+)-2-Methyl-3-phenylpropionic Acid by the Direct Conversion of the optically Active C-H Bond into the C-N Bond
- Stereochemical Studies. II. Thermal and Photochemical Decompositions of Optically Active Alkyl Azidoformates