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
Studies on the Chemical Constituents of Rutaceous Plants. XXXV. Structural Establishment and Synthesis of Bocconoline. Photochemical Reaction of a Benzo [c] phenanthridinium Salt with Methanol
Studien uber die Alkaloide der Papaveraceen. XVII. Die Alkaloide von Corydalis incisa. (10). Uber die Struktur des (+)-14-Epicoryno1ins
Untersuchung uber die Alkaloide der Papaveraceen. XIV. Die Alkaloide von Corydalis incisa. (9). Die Abbaureaktion des Corynolins und Corynoloxins
Untersuchung uber die Alkaloide der Papaveraceen. XIII. Die Alkaloide von Corydalis incisa. (8). Uber die Struktur des Corynoloxins
Untersuchung uber Alkaloide von Papaveraceen. VII. Alkaloide von Corydalis incisa. (6). Uber die Struktur des Corynolins. (2).
Untersuchung uber Alkaloide von Papaveraceen. VI. Alkaloide von Corydalis incisa. (5). Uber die Struktur des Corynolins. (1).

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