古賀 憲司 | Faculty of Pharmaceutical Sciences, University of Tokyo
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概要
関連著者
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古賀 憲司
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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山田 俊一
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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富岡 清
Faculty of Pharmaceutical Sciences, University of Tokyo
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古賀 憲司
東京大学
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富岡 清
京都大学大学院薬学研究科
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小田嶋 和徳
Faculty of Pharmaceutical Sciences, University of Tokyo
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小田嶋 和徳
Graduate School Of Pharmaceutical Sciences The University Of Tokyo
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松尾 寿之
Faculty Of Pharmaceutical Sciences University Of Tokyo
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古賀 憲司
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
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伊古田 暢夫
National Institute Of Radiological Sciences
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石黒 恒男
Faculty of Pharmaceutical Sciences, University of Tokyo
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石黒 恒男
Central Research Laboratories Ajinomoto Co. Inc.
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橋本 俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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山田 俊一
東京大学
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吉野 収
(present Address)national Institute Of Radiological Sciences
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寺島 孜郎
(財)相模中央化学研究所
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伊古田 暢夫
Faculty of Pharmaceutical Sciences, University of Tokyo
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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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SASAKI Shigeki
Graduate School of Pharmaceutical Sciences, Kyushu University
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佐々木 茂貴
Faculty Of Pharmaceutical Sciences Kyushu University
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水口 英道
Faculty of Pharmaceutical Sciences, University of Tokyo
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水口 英道
Faculty Of Pharmaceutical Sciences University Of Tokyo
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佐々木 茂貴
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)faculty Of Pharmaceutical Sc
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橋本 俊一
Faculty Of Pharmaceutical Sciences Hokkaido University
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中島 誠
Faculty Of Pharmaceutical Sciences University Of Tokyo
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関 英男
Faculty of Pharmaceutical Sciences, University of Tokyo
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青木 一真
Faculty Of Pharmaceutical Sciences University Of Tokyo
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川上 肇
Faculty Of Pharmaceutical Sciences University Of Tokyo
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佐々木 茂貴
Faculty of Pharmaceutical Sciences, Kyusyu University
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国枝 武久
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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曽 仲奇
Faculty Of Pharmaceutical Sciences University Of Tokyo
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吉野 収
Faculty of Pharmaceutical Sciences, University of Tokyo
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三宅 宗晴
College Of Pharmacy Nihon University
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安酸 達郎
Faculty of Pharmaceutical Sciences, University of Tokyo
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桐沢 誠
College of Pharmacy, Nihon University
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関 英男
Research Laboratories Fujisawa Pharmaceutical Co. Ltd.
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国枝 武久
Faculty Of Pharmaceutical Sciences Kumamoto University
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柴田 久就
Faculty Of Pharmaceutical Sciences University Of Tokyo
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谷口 誠朗
東大薬
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谷口 誠朗
Faculty of Pharmaceutical Sciences, University of Tokyo
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呉 欽敬
Faculty Of Pharmaceutical Sciences University Of Tokyo
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安酸 達郎
Faculty Of Pharmaceutical Sciences University Of Tokyo
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塩入 孝之
Faculty of Pharmaceutical Sciences, Nagoya City University
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村上 泰興
Faculty of Pharmaceutical Sciences, University of Tokyo
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大木 貞雄
Tokyo College of Pharmacy
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松尾 市郎
Medical School, Self Defence Force
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飯高 洋一
Faculty of Pharmaceutical Sciences, The University of Tokyo
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富岡 清
京大院薬
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三輪 篤史
Faculty Of Pharmaceutical Sciences University Of Tokyo
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村上 泰興
東邦大学薬学部
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新藤 充
東大・薬
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辻原 健二
Research Laboratories, Tanabe Seiyaku Co., Ltd.
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竹内 義雄
Faculty Of Pharmaceutical Sciences University Of Tokyo
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伊古田 暢夫
放射線医学総合研究所重粒子医科学センター
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小林 通洋
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)research Laboratory Kissei P
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白井 隆一
Faculty of Pharmaceutical Sciences, Science University of Tokyo
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塩入 孝之
Faculty Of Pharmaceutical Sciences Nagoya City University
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高橋 俊也
Faculty Of Pharmaceutical Sciences University Of Tokyo
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松尾 市郎
Junsei Pure Chemicals Co. Ltd.
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川崎 元士
相模中研
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田中 正英
Faculty of Pharmaccutical Sciences, Hokkaido University
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荘 祚敏
Institute of Applied Chemistry, National Chiao-Tung University
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米島 伸泰
Faculty of Pharmaceutical Sciences, University of Tokyo
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清水 公博
Faculty of Pharmaceutical Sciences, University of Tokyo
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SASAKI Isabelle
Faculty of Pharmaceutical Sciences, University of Tokyo
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高橋 一朗
Faculty Of Pharmaceutical Sciences University Of Tokyo
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田中 正英
Faculty Of Pharmaceutical Sciences University Of Tokyo
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田中 正英
Faculty Of Pharmaccutical Sciences Hokkaido University
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佐藤 大作
Faculty of Pharmaceutical Sciences, University of Tokyo
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金 熙斗
Faculty of Pharmaceutical Sciences, University of Tokyo
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村形 政利
Faculty of Pharmaceutical Sciences, University of Tokyo
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富岡 清
(Present address)Institute of Scientific and Industrial Research, Osaka University
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杉森 正道
Exploratory Research Laboratories I, Daiichi Pharmaceutical Co., Ltd.
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真鍋 敬
Faculty of Pharmaceutical Sciences, University of Tokyo
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親見 裕一
Faculty of Pharmaceutical Sciences, University of Tokyo
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椎名 邦彦
Faculty of Pharmaceutical Sciences, University of Tokyo
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伊古田 暢夫
(Present address)National Institute of Radiological Sciences
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河崎 久
Faculty of Pharmaceutical Sciences, University of Tokyo
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新藤 充
Faculty of Pharmaceutical Sciences, University of Tokyo
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村岡 正実
Faculty of Pharmaceutical Sciences, University of Tokyo
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CAPO Magdalena
Faculty of Pharmaceutical Sciences, University of Tokyo
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桐澤 誠
College of Pharmacy, Nihon University
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LAI Chung-Fang
Faculty of Pharmaceutical Sciences, University of Tokyo
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米島 伸泰
Pharmaceutical Research Laboratory Kirin Brewery Co. Ltd.
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松井 武明
Faculty Of Pharmaceutical Sciences University Of Tokyo
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佐藤 大作
Faculty Of Pharmaceutical Sciences University Of Tokyo
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酒井 広志
Faculty Of Pharmaceutical Sciences University Of Tokyo
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杉森 正道
Exploratory Research Laboratories I Daiichi Pharmaceutical Co. Ltd.
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杉森 正道
Faculty of Pharmaceutical Sciences, University of Tokyo
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朱 尚渉
東大薬
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辻原 健二
Lead Optimization Research Laboratory Tanabe Seiyaku Co. Ltd.
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Capo Magdalena
Faculty Of Pharmaceutical Sciences University Of Tokyo
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Lai Chung-fang
Faculty Of Pharmaceutical Sciences University Of Tokyo
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白井 隆一
Faculty Of Pharmaceutical Sciences Science University Of Tokyo
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辻原 健二
Faculty of Pharmaceutical Sciences, University of Tokyo
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Tomioka K
Graduate School Of Pharmaceutical Sciences Kyoto University
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桐沢 誠
College Of Pharmacy Nihon University
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石墨 紀久夫
Sumitomo Pharmaceuticals Research Center
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金 熙斗
Faculty Of Pharmaceutical Sciences University Of Tokyo
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川崎 元士
Faculty of Pharmaceutical Sciences, University of Tokyo
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飯高 洋一
Faculty Of Pharmaceutical Sciences The University Of Tokyo
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関 秀雄
Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)fujisawa Pharmaceutical Co.
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清水 公博
Faculty Of Pharmaceutical Sciences University Of Tokyo
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朱 尚渉
Faculty of Pharmaceutical Sciences, University of Tokyo
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山本 芳光
Faculty Of Pharmaceutical Sciences University Of Tokyo
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村形 政利
Faculty Of Pharmaceutical Sciences University Of Tokyo
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村岡 正実
Faculty Of Pharmaceutical Sciences University Of Tokyo
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荘 祚敏
Institute Of Applied Chemistry National Chiao-tung University
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桐澤 誠
College Of Pharmacy Nihon University
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椎名 邦彦
Faculty Of Pharmaceutical Sciences University Of Tokyo
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親見 裕一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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荘 祚敏
Faculty of Pharmaceutical Sciences, University of Tokyo
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石墨 紀久夫
Faculty of Pharmaceutical Sciences, University of Tokyo
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Sasaki Isabelle
Faculty Of Pharmaceutical Sciences University Of Tokyo
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楊 正勝
Faculty of Pharmaceutical Sciences, University of Tokyo
著作論文
- Stereochemical Studies. XIII. Determination of the Absolute Configuration of Mercaptosuccinic Acid by Chemical Correlation with Glyceraldehyde
- Studies on Opically Active Amino Acids. VII. Stereoselective Synthesis of l-Norephedrine Hydrochloride from D-Phenylalanine
- Studies on Optically Active Amino Acids. V. Synthesis of Optically Active α-Aminoalcohols by the Reduction of α-Amino Acid Esters with Sodium Borohydride
- Studies on Optically Active Amino Acids. IV. A New Synthetic Approach to Chloramphenicol Base from L-Phenylalanine.
- Stereoselective Reactions. XVI. : Total Synthesis of (-)-β-Bourbonene by Employing Asymmetric (2+2) Photocycloaddition Reaction of Chiral Butenolide
- Stereoselective Reactions. II. Asymmetric Synthesis of β-Substituted Aldehydes by Michael Reaction using Chiral α, β-Unsaturated Aldimines
- Stereoselective Reactions. I. A highly Efficient Asymmetric Synthesis of β-Substituted Aldehydes via 1,4-Addition of Grignard Reagents to optically Active α, β-Unsaturated Aldimines
- Stereochemical Studies. LIV. A Biogenetic-type Asymmetric Synthesis of optically Active Galanthamine from L-Tyrosine
- MOLECULAR RECOGNITION AND DISCRIMINATION OF HYDROPHOBIC GUESTS IN WATER BY QUATERNARY AMMONIUM CYCLOPHANES HAVING DIARHLMETHANE UNITS
- DESIGN, SYNTHESIS, AND PROPERTIES OF NOVEL WATER-SOLUBLE CYCLOPHANES HAVING NAPHTHYLPHENYLMETHANE UNITS AS HOSTS FOR ALIPHATIC AND AROMATIC GUESTS
- ASYMMETRIC REDUCTION OF ARYLGLYOXYLIC ACIDS VIA・HOST-GUEST COMPLEX FORMATION WITH OPTICALLY ACTIVE PARACYCLOPHANES
- Stereoselective Reactions. III. A highly Efficient Method for the Asymmetric Synthesis of 2-Alkylcycloalkanones via Chiral Chelated Lithioenamines
- Stereoselective Reactions. XXII. Design and Synthesis of Chiral Chelated Lithium Amides for Enantioselective Reactions
- REINVESTIGATION ON THE OPTICAL PURITIES OF OPTICALLY ACTIVE TRIMETHYLSILYL ENOL ETHERS OF 4-SUBSTITUTED CYCLOHEXANONES
- Biomimetic Studies Using Artificial Systems. VI. Design and Synthesis of Novel Cyclophanes Having Eight Carboxyl Groups on the Aromatic Rings
- A NOVEL WATER-SOLUBLE CYCLOPHANE AS A HOST FOR CATIONIC, ANIONIC, AND NEUTRAL AROMATIC GUESTS
- Chromatographic Separation of Armatic Guest Compounds by a Gel-Immobilized Water-Soluble Cyclophane
- Stereoselective Reactions. XIX. Asymmetric Dihydroxylation of Olefins by Employing Osmium Tetroxide-Chiral Amine Complexes
- ENANTIOSELECTIVE DARZENS REACTION : ASYMMETRIC SYNTHESIS OF trans-GLYCIDIC ESTERS MEDIATED BY CHIRAL LITHIUM AMIDES
- Amino Acids and Peptides. II. A One-Step Synthesis of Atropine and Other Related Alkaloids from dl-Phenylalanine 3α-Tropanyl Ester
- Stereochemical Studies. XVII. Nitrous Acid Deaminations of (R)-α-Methylphenylalanine and Its Methyl Ester in Acetic Acid
- Stereoselective Reactions. XX. Synthetic Studies on Optically Active β-Lactams. III. Stereocontrolled Synthesis of Chiral Intermediate to (+)-Thienamycin from D-Glucose
- Stereoselective Reactions. XVIII. : Synthesis and Cytotoxicity of the Demethyl Derivatives of Steganes
- ASYMMETRIC α-ALKYLATION OF CYCLOHEXANONE BY MEDIATION OF A CHIRAL LIGAND AND THE LEAVING-GROUP EFFECT OF ELECTROPHILES ON ENANTIOSELECTIVITY
- Biomimetic Studies Using Astificial Systems. V. : Design and Synthesis of Novel Water-Soluble Bis-cyclophanes
- Stereoselective Reactions. XI. : Asymmetric Alkylation of Cyclohexanone via Chiral Chelated Lithioenamines Derived from D-Camphor Derivatives
- SYNTHETIC STUDIES TOWARD TRICHOTHECENE SESQUITERPENES. SYNTHESIS OF AN OPTICALLY PURE KEY INTERMEDIATE FOR CALONECTRIN USING HIGHLY STEREOSELECTIVE CYCLIZATION(Communications to the Editor)
- NOVEL BICYCLIC CHIRAL CROWN ETHERS HAVING A p-XYLENEDIOXY UNIT WITH INPROVED COMPLEX STABILITY AND RATE-ENHANCEMENT IN THE INTRA-COMPLEX THIOLYSIS OF α-AMINO ACID ESTER SALTS
- Stereoselective Reactions. V. Design of the Asymmetric Synthesis of Lignan Lactones. Synthesis of optically Active Podorhizon and Deoxypodorhizon by 1,3-Asymmetric Induction
- Biomimetic Studies Using Artificial Systems. II. Enantioselective Thiolysis of D- or L-α-Amino Acid Ester Salts by Thiol-Bearing Chiral Crown Ethers as an Enzyme Model
- Studies on Optically Active Amino Acids.XIII.Racemization of N-Benzoylanilides of Optically Active Proline and Pipecolic Acid
- Studies on Optically Active Amino Acids. XII.Synthesis, Resolution and Racemization of Bicyclic α-Amino-ketones
- Stereoselective Reactions. IX. Synthetic Studies on Optically Active β-Lactams. I. Chiral Synthesis of Carbapenam and Carbapenem Ring Systems Starting from (S)-Aspartic Acid
- SYNTHETIC STUDIES ON OPTICALLY ACTIVE β-LACTAMS. STEREOCONTROLLED SYNTHESIS OF CHIRAL THIENAMYCIN INTERMEDIATE FROM D-GLUCOSE
- Stereoselective Reactions. XII. : Synthesis of Antitumor-Active Steganacin Analogs, Picrosteganol and Epipicrosteganol, by Selective Isomerization
- 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
- Functionalized Macrocycles. I. Synthesis of Thiol-bearing Crown Ethers as an Approach to Regioselective Catalysts
- Chemistry of Amino Acids. III. Reduction of Phenylalanine Ethyl Ester and Its Derivatives with Sodium Borohydride.
- Stereochemical Studies. XII. Effects of Neighboring Functional Groups on 1,2-Asymmetric Induction in the Reduction of Propiophenone Derivatives by Catalytic Hydrogenation
- Stereochemical Studies. XXXI. Total Synthesis of Several D-Pentose Derivatives. Stereochemical Courses of the Synthesis of Four Methyl 2,3-Anhydro-5-O-benzyl-D-pentofuranosides from L-Glutamic Acid and Their Reactions with Nucleophiles
- Stereochemical Studies. XVI. Deaminative Acetolyses of L-Valine and L-Valine Benzyl Ester
- Biomimetic Studies Using Artificial Systems. IV. : Biomimetic Peptide Synthesis by Using Multi-Functionalized Crown Ethers as a Novel Enzyme Model. A New Concept in Mimicking of Enzyme-Catalyzed Bond-Forming Reactions
- Amino Acids and Peptides. III. A New Synthetic Approach to N-Acylated α-Amino Aldehydes from N-Acylated α-Amino Acids by Catalytic Reduction of Their Mixed Carbonic-Carboxylic Acid Anhydrides with Palladium-Charcoal
- Stereochemical Studies. XV. Neighboring Aryl Group Participation in Nitrous Acid Deaminations of L-Phenylalanine and Its p-Nitro and p-Methoxy Derivatives. Conversion of L-Phenylalanine to naturally Occurring S-Tropic Acid
- Stereochemical Studies. XIV. Studies on the Neighboring Aryl Group Participation in Nitrous Acid Deaminations of L-Phenylalanine Ethyl Ester and Its p-Nitro and p-Methoxy Derivatives
- Stereochemical Studies. LII. Studies on the Stereochemical Courese in Deaminative Bromination of 3,5-Dichloro-L-tyrosine and in Amination of the Corresponding α-Bromo Acid. Existence of Strong Neighboring "Phenoxide"Group Participation
- Chemistry of Sodium Borohydride and Diborane. IV. Reduction of Carboxylic Acids to Alcohols with Sodium Borohydride through Mixed Carbonic-Carboxylic Acid Anhydrides
- Stereoselective Reactions. VIII. Stereochemical Requirement for the Benzylic Oxidation of Lignan Lactone. A Highly Selective Synthesis of the Antitumor Lignan Lactone Steganacin by the Oxidation of Stegane
- Stereoselective Reactions. VII. Synthesis of Racemic and Optically Pure Stegane, Isostegane, Picrostegane, and Isopicrostegane via Highly Selective Isomerization
- Stereoselective Reactions. X. Total Synthesis of Optically Pure Antitumor Lignan, Burseran
- Stereochemical Studies. L. Reductive Decyanization of α-Amino Nitriles with Sodium in Liquid Ammonia. An Alternate Method for the Application to the Asymmetric Synthesis of optically Active Natural Products
- Stereochemical Studies. XLIX. A Biogenetic-type Total Synthesis of Natural (+)-Maritidine from L-Tyrosine using highly Specific Asymmetric Cyclization
- Stereochemical Studies. XVIII. Nitrous Acid Deaminations of threo- and erythro-Phenylserine and Their Methyl Esters in Acetic Acid
- Stereochemical Studies. XI. Changes in the Stereochemical Course of 1,2-Asymmetric Induction in the Reduction of N-Substituted 2-Aminopropiophenone Derivatives with Sodium Borohydride
- Stereochemical Studies. X. Effects of Neighboring Functional Groups on 1,2-Asymmetric Induction in the Reduction of Propiophenone Derivatives with Sodium Borohydride