高尾楢雄 | Kobe Women's College of Pharmacy

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著作論文

Quantitative Structure-Activity Relationships of Anticonvulsant Aralkyl and Alkyl Carbamates
A Quantitative Structure-Activity Study of Anticonvulsant Phenylacetanilides
A Quantitative Structure-Activity Study of Anticonvulsant Benzyl N, N-Dimethylcarbamates
Conformational Features of 5'-O-[N-(L-Alanyl)sulfamoyl]adenosine, a Substrate Analogue of Alanyl-tRNA Synthetase, Studied by ^1H-NMR and Energy Calculation Methods
Stereochemistry of Quinolizidines. V. Protonation of Benzo [α] quinolizidines and Determination of Their Nitrogen Inversion Rates
Pyrolysis and Photolysis of the N-Oxides of Protopines and Hexahydrobenzo [c] phenanthridines. Syntheses of the Secoberbines and Benzo [c] phenanthridines
Behavior of Hydrochlorides and Methiodides of N-Substituted 4-Piperidones in Methanol
^C NMR Spectral Behavior of N-Substituted-4-piperidones in Methanol. Possibility of Distinguishing between Acetal and Hemiacetal
^C NMR Studies of the Reaction between N-Ethyl-piperidones and Methanol
Studies on the Alkaloids of Papaveraceous Plants. XXX. Conformational Analysis of Some Hydrobenzo [c]-phenanthridine-type Alkaloids
Studies on the Alkaloids of Papaveraceous Plants. XXIX. Conformational Analysis of Tetrahydroprotoberberines by Carbon-13 Magnetic Resonance Spectroscopy
Studies on the Alkaloids of Papaveraceous Plants. XXV. Biosynthesis of the Alkaloids of Corydalis incisa PERS. and Chelidonium majus L. Incorporations of Tetrahydroprotoberberines, N-Methosalts of Tetrahydroprotoberberines, and Protopine
Degradation of Some Phthalideisoquinolines with Ethyl Chloroformate-Stereochemical Aspects
Stereochemistry of Quinolizidines. II. Carbon-13 Magnetic Resonance Spectra of N-Methylquinolizidinium Ions
Studies on the Alkaloids of Papaveraceous Plants. XXVI. Stereo-structure of Tetrahydroprotoberberine-type Alkaloids
Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. IX. Relationship between Capacity Factor and Water-Octanol Partition Coefficient of Monosubstituted Pyrimidines
Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. VII. Hydrogen-Bond Effects in Prediction of the log P Values for Benzyl N, N-Dimethylcarbamates
Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. V. Relationship between the Capacity Factor and the Octanol-Water Partition Coefficient for Simple Heteroaromatic Compounds and Their Ester Derivatives
Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. III. Influence of Stationary and Mobile Phases on the Relationship between the Capacity Factor and the Octanol-Water Partition Coefficient for Pyrazine Derivatives
Hydrophobicity Parameters Determined by Reversed-Phase Liquid Chromatography. II. Dependence of Retention Behavior of Pyrazines on Mobile Phase Composition
Hydrophobic Properties of Anticonvulsant Phenylacetanilides. Relationship between Octanol-Water Partition Coefficient and Capacity Factor Determined by Reversed-Phase Liquid Chromatography
Electronic Properties of Anticonvulsant Amides. A C-13 Nuclear Magnetic Resonance Study of Phenylacetanilides

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