寺島孜郎 | Faculty Of Pharmaceutical Sciences University Of Tokyo:(present Address)sagami Chemical Research Cen

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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
Studies on Optically Active Amino Acids. XIV. Studies on α-Alkyl-α-amino acids. VII. Determination of Absolute Configuration of Optically Active α-Methylphenylglycine Configuration of Optically Active α-Methylphenylglycine and 1-Methyl-1-phenylpropylamine
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
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
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
Studies on Optically Active Amino Acids. XV. Studies on α-Alkyl-α-amino Acids. VIII. Absolute Configuration of Optically Active α-Methylserine and 2-Amino-2-methyl-3-butenoic Acid.
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
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
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

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