「基礎科学特別研究員制度」設立に関連して想う
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概要
- 論文の詳細を見る
- 公益社団法人日本薬学会の論文
- 1990-11-01
著者
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大石 武
理研
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大石 武
Faculty Of Engineering Yokohama National University:(present Address)meiji College Of Pharmacy
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大石 武
理化学研究所
関連論文
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- ENZYMATIC HYDROLYSIS IN ORGANIC SOLVENTS FOR KINETIC RESOLUTION OF WATER-INSOLUBLE α-ACYLOXY ESTERS WITH IMMOBILIZED LIPASES
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- 23 スウィンホライドAおよびその関連化合物の合成研究(口頭発表の部)
- The Synthesis of 3-Spirooxindole Derivatives. IX. The Reactions of 2-Hydroxytryptamine with Hemiacetals
- 77 マイカラミドAおよび関連化合物の合成研究(ポスター発表の部)
- 72 ジテルペン系フェノール誘導体のオゾン酸化 : 光学活性ドリマン型セスキテルペン類及びフラノセスキテルペンの合成
- A Facile Chemoenzymatic Route to Optically Active 4,5-Disubstituted-2E-hexenoate Derivatives. I
- Enantioselective Acetylation of an α-Hydroxy Ester by Using Ether-Linked Lipid-Lipase Aggregates in Organic Solvents
- A Formal Total Synthesis of (-)-Oudemansin B
- A Lipid-Lipase Aggregate with Ether Linkage as a New Type of Immobilized Enzyme for Enantioselective Hydrolysis in Organic Solvents
- A FACILE CHEMOENZYMATIC ROUTE TO ENANTIOMERICALLY PURE 4,5-DISUBSTITUTED-2-HEXENOATE DERIVATIVES
- A LIPID LIPASE AGGREGATE AS A NEW TYPE OF IMMOBILIZED ENZYME
- Asymmetric Reduction of α-Methyl β-Keto Esters by Microbial Cells Immobilized with Prepolymer(Organic,Chemical)
- 38 生体触媒を用いるキラルシントンの合成とその天然物合成への応用
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- Microbiologically Modified Chiral Synthon. III. 4,9-Dimethyl-3,5-dioxo-Δ^-octalin for Formal Total Syntheses of Certain Sesquiterpenoids
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- Microbiologically Modified Chiral Synthon. II. : 4,9-Dimethyl-3,7-dioxo-Δ^-octalin for Formal Total Syntheses of Certain C(8) Oxygenated Sesquiterpenoids
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- 37 中環状テルペン類の合成研究 : カリオフィレン類の全合成
- Chemical Synthesis of Deoxyribonucleotides Containing Deoxyadenosine at the 3'-End on a Polystyrene Polymer Support
- 2'- AND 3'-SUBSTITUTED SANGIVAMYCINS : CONFORMATIONAL RESTRICTION BY THE GAUCHE EFFECT
- Synthesis of (+)- and (-)-cis-α-Irones
- Studies on Taxane Synthesis III.Stereocontrolled Synthesis of a Twelve-Membered Lactam Sulfide as a Precursor of 4,8,11,11-Tetramethyl-3-oxobicyclo[5.3.1]undec-8-ene
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- Studies on Taxane Synthesis. II. : Synthese of 3,8,11,11-Tetramethyl-4-oxo- and 4,8,11,11-Tetramethyl-3-oxo-bicyclo[5.3.1]undec-8-enes Corresponding to the A- and B-Rings of Taxane Diterpenes
- Studies on Taxane Synthesis. I. : Synthesis of 3,8,11,11-Tetramethyl-4-oxobicyclo[5.3.1]undecane as a Model for Taxane Synthesis
- エリスロマイシンA合成研究をめぐって
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- A NEW SYNTHETIC METHOD FOR β, γ-UNSATURATED KETONES AND A TOTAL SYNTHESIS OF EGOMAKETONE
- 大環状ラクタムスルフィドの分子内閉環反応を基盤とする中環状化合物の合成 (中・大環状天然物合成の新展開) -- (炭素環状化合物の形成反応とテルペノイドおよびその関連化合物の合成)
- Forced Nucleophilic Substitution Reaction of Chlorobenzenes bearing Electron-Donating Groups by the Use of"Naked"Methoxide Anion
- Revised Stereostructure for (+)-Roemecarine and Synthesis of (±)-, (+)-, and (-)-Roemercarine and (±)-Epiroemecarine
- Kinetic Resolution of (±)-4-Acyloxy-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisopuinolines by Use of Immobilized Lipases in Organic Solvents
- 11 (+)-Pederinの全合成
- The Reactions of Activated Amides. I. The Reactions of Iminoethers derived from the Secondary Amides with the Nucleophiles
- 12 微生物還元を利用する光学活性有用化合物の合成およびその天然物合成への応用
- The Fischer Indole Synthesis with Formic Acid.I.A Convenient Synthesis of 4a-Ethyl-9-formyl-1,2,3,4,4a, 9a-hexahydro-9H-carbazole
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- DETERMINATION OF THE STEREOSTRUCTURE OF THE δ-LACTONES OF 5,7-DIHYDROXY-2,3-UNSATURATED ACIDS BY ^1H NMR SPECTROSCOPY(Communications to the Editor)
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- A FORMAL SYNTHESIS OF l-α-SANTONIN FROM CHIRAL α, β-EPOXYEUDESMANOLIDE VIA ENZYME-CATALYZED HYDROLYSIS
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- Chemoenzymatic Carbon-Carbon Bond Formation Leading to Non-carbohydrate Derivative. Stereoselective Synthesis of Pentamycin C-11-C-16 Fragment
- Structural Characteristics of Lipid-Lipase Aggregates for Enantioselective Hydrolysis in Organic Solvents
- リパーゼを用いる光学活性ヒドロキシエステルの創製とその生理活性化合物合成への応用 : ベンツリシジンA, Bアグリコンの全合成
- The Reactions of Activated Amides. VI. The Reactions of 1-Methyl-2-pyrrolidone Dimethylacetal and 2-Methylmercapto-1-methyl-2-pyrroline with Dimethyl Acetylenedicarboxylate
- The Fischer Indole Synthesis with Formic Acid. II. The Synthesis of Hexahydrocyclopent (b) indoles
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- The Synthesis of 3-Spirooxindole Derivatives. VII. Total Synthesis of Alkaloids (±)-Rhynchophylline and (±)-Isorhynchophylline
- The Reactions of Activated Amides. V. The Reactions of Cyclic Amide Acetals with Electrophiles
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- Activation of Weak Organic Bases. III. The Reactions of Divalent Sulfides with Acid Chlorides in the Presence of Friedel-Crafts Catalysts
- The Reactions of Activated Amides. IV. The Reactions of Amide Acetals with Esters
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- The Synthesis of 3-Spirooxindole Derivatives. III. Stereospecific Syntheses of rac-N-Methylrhynchophyllane for Stereochemistry of Rhynchophylline and Isorhynchophylline.
- The Synthesis of 3-Spirooxindole Derivatives. II. Syntheses of 1-Methylspiro-[indoline-3,1'-pyrrolizidine and Indolizidine]-2-one.
- The Synthesis of 3-Spirooxindole Derivatives. I. Syntheses of 1-Methyl-2', 3', 10', 10'a-tetrahydrospiro [indoline-3,1' (5'H)-pyrrolo [1,2-b]-isoquinoline]-2-one and its Homologs.
- β-HYDROXY-δ-LACTONES AS CHIRAL BUILDING BLOCKS INVOLVING 1,3-DIHYDROXYL FUNCTIONS. 1. : NEW STRATEGIES FOR STREOSELECTIVE CONSTRUCTION OF 2-METHYL-3,5-DIHYDROXY ESTERS
- Highly syn-Selective Reduction of α-Phenylthio-β-methoxy Ketones with Super-hydride
- 非環状化合物におけるケトンの立体選択的還元と天然物合成への応用
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