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Faculty of Pharmaceutical Sciences, Osaka University | 論文
- On the Estimation of the Quantitative Structure-Activity Relationships Descriptor σ_ for Aliphatic Compound
- Revised Substituent Entropy Constants σ_ for Di- and Tri-Substituted Benzene Derivatives, and Their Applications for Substrates Having Two Substituted Phenyl Rings
- Procedures on the Estimation of the Novel Quantitative Structure-Activity Relationship (QSAR) Descriptor σ_ for Poly-Substituted Benzene Series, and Their Polarizabilities
- Estimation of the Quantitative Structure-Activity Relationship Descriptor σ_ for Di- and Tri-Substituted Benzene Derivatives
- Solute-Stationary Phase Interaction in Gas-Liquid Chromatography. : Evaluation of the Relative Retention Value for Substituted Halogenobenzene Derivatives
- On the Solute-Stationary Phase Interaction in Gas-Liquid Chromatorgaphy. Evaluation on the Relative Retention Values for Mono- and Polyalkyo-Substituted Benzene Derivatives
- Determination of the Novel Quantitative Structure-Activity Relationships Descriptor σ_ for Di- and Trisubstituted Benzene Derivatives
- Feasibility of Estimating the Novel Quantitative Structure-Activity Relationship (QSAR) Descriptor σ_ by Means of Gas-Liquid Chromatography. I. : Halogenobenzene Derivatives
- Comparison of Novel Descriptors σ_ and μ^2/α with Topological Indices in Quantitative Structure-Activity Relationships Analyses
- Substitutent Entropy constant σ_ and Descriptor μ^2/α of sym-Disubstituted Benzene Derivatives. : Estimation and Validity of Novel Quantitative Structure-Activity Relationships Descriptors
- Availability of Substituent Entropy Constants σ_ and Descriptor μ^2/α as Predictors of Relative Retention Values on Gas-Liquid Chromatography of Substituted Propane and Butane Derivatives
- On the Novel Quantitative Structure-Activity Relationships (QSAR)Descriptors σ_ and μ^2/α Deduced from the Modified Lennard-Jones 12,6 Potentials
- Photochemical Dealkylation of 2-Acyl-3-alkylamino-5,5-dimethyl-2-cyclohexen-1-ones
- Synthesis and Photocyclization of 2-Aroyl-3-methylcyclohex-2-enones
- Mild and Facile Cleavage of 2-Cyanoethyl Ester Using Sodium Sulfide or Tetrabutylammonium Fluoride. Synthesis of 1,4-Dihydropyridine Monocarboxylic Acids and Unsymmetrical 1,4-Dihydropyridine Dicarboxylates
- Protecting Group for Carboxyl Function : Mild and Facile Cleavage of 2-Cyanoethyl Ester under Non-hydrolytic Conditions
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-r-ones as Synthetic Intermediates. V. : An Improved Synthesis of (±)-Pentalenene
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-3-ones as Synthetic Intermediates. IV. : A Further Examination of Cyclopropane Ring Opening in the Tricyclo[3.3.0.0^]octan-3-one System
- Synthetic Studies on Spiroketal Natural Producys. III. : Enantioselective Synthesis of 1,6-Dioxaspiro[4.5]decane Compounds
- Study on Some Factors Affecting the Precision of Luminescence Analyses