An Infrared Study of the C=N Stretching Frequency in N-Benzylideneaniline Derivatives
スポンサーリンク
概要
- 論文の詳細を見る
A series of 131 N-benzylideneaniline derivatives was prepared, and their infrared spectra were measured in the same conditions. Statistical tests showed that differences of substitution in benzene ring of benzylidene group affected acceptably on the region of C=N stretching absorption peak, but those in benzene ring of aniline group had smaller effect on it.
- 社団法人日本薬学会の論文
- 1967-05-25
著者
-
中村 優
Faculty Of Pharmaceutical Sciences Fukuoka University
-
小松 京子
Faculty Of Pharmaceutical Sciences Fukuoka University
-
権藤 宜子
Faculty of Pharmaceutical Sciences, Fukuoka University
-
太田 紀代子
Faculty of Pharmaceutical Sciences, Fukuoka University
-
上田 陽
Faculty of Pharmaceutical Sciences, Kyushu University
-
権藤 宜子
Faculty Of Pharmaceutical Sciences Fukuoka University
-
上田 陽
Faculty Of Pharmaceutical Sciences Kyushu University
-
太田 紀代子
Faculty Of Pharmaceutical Sciences Fukuoka University
関連論文
- An Infrared Study of the C=N Stretching Frequency in N-Benzylideneaniline Derivatives
- Chemiluminescent Products of Reaction between α-Keto Acids and 4,5-Diaminophthalhydrazide
- Determination of 21-Hydroxycorticosteroids in Human Urine by High-Performance Liquid Chromatography with Fluorescence Detection
- High-Performance Liquid Chromatography of Arachidonic Acid Metabolites and Its Application to the Determination of Leukotriene B_4 in Stimulated Leukocytes
- 3-Bromomethyl-6,7-methylenedioxy-1-methyl-2(1H)-quinoxalinone as a Highly Sensitive Fluorescence Derivatization Reagent for Carboxylic Acids in High-Performance Liquid Chromatography
- 1,2-Diamino-4,5-methylenedioxybenzene as a Highly Sensitive Fluorogenic Reagent for α-Keto Acids(Analytical,Chemical)
- An Ultramicro Fluorimetric Determination of Total Ascorbic Acid in Human Serum Using 1,2-Diamino-4,5-dimethoxybenzene
- Fluorescent Products of Reaction between α-Keto Acids and 1,2-Diamino-4,5-dimethoxybenzene
- Fluorescent Product in the Determination of Aromatic Aldehydes with 4,5-Dimethoxy-1,2-diaminobenzene
- Extension of the CNDO/S Method to the Calculation of Aromatic and Heterocyclic Compounds Containing Si, P, S and Cl
- Spectroscopic Investigation on the Mechanisms of Oxygenation Reactions of Skatole Catalyzed by Co (II) (p-OCH_3) TPP and ClCo (III) (p-OCH_3) TPP
- π-π^* Transition Energies of Steroid Polyenes and Steroid Polyenyl Cations
- Studies on the Catalytic Oxidation Reactions of Skatole using Cobalt Complexes
- Quantum Chemical Study on the Cytochrome P-450-Catalyzed Hydroxylation of 1,2,3,4-Tetrahydronaphthalene and Indane
- Quantum Chemical Study on the Cytochrome P-450 catalyzed Hydroxylation of Aromatic Hydrocarbons
- Color Reaction Product of Urea with Diacetyl Monoxime and Glucuronolactone. III. Structures of Two Major Reaction Products of the Color Reaction of Butylurea with 1-Phenyl-1,2-propanedione
- Study on the Correspondence of Color Change with Polyenyl Cation Formation of Cholesterol in Strong Acids
- Tautomerism of 4-Amino- and 4-Arylamino-1,2-naphthoquinones
- Mechanism of the Color Reaction between Aldehyde and Diazotized Aromatic Amine. I. Color Reaction Products of Formaldehyde with Diazotized Sulfanilamide and with Diazotized p-Aminobenzoic Acid
- Mechanism of the Color Reaction of 4,5-Dinitroveratrole with Reducing Sugars. : Organic Analysis. LXIV
- Organic Analysis. XXXVI. Identification of Amines as the Salts of 3,6-Dinitrophthalic Acid.
- Organic Analysis. XXXIII. Mechanism of the Color Reaction between Fructose and N-Methyldiphenylamine.
- Organic Analysis. XXV. Mechanism of the Reaction between Fructose and Diphenylamine
- Mechanism of the Reaction between Fructose and Diphenylamine
- The Models for the Active Site of Pyridoxal Enzymes. Calculations of π-π^* Transition Energies of Electronic Absorption
- Substituent Effects on the Mass Spectra of ortho-Hydroxyaromatic Aldehyde para-Substituted Benzylidenehydrazones
- Molecular Orbital Interpretation of Infrared Absorption Frequencies. II. α, β-Unsaturated Carbonyl, para-and meta-Substituted Aromatic Carbonyl Compounds, an Introduction of the Mutual Additive Substituent Parameter
- Molecular Orbital Interpretation of Infrared Absorption Frequencies. I. Selection of HMO Hetero-atomic Parameters
- Tricyanovinylation of Imidazole Derivatives with Tetracyanoethylene
- Mechanism of the Molisch Reaction
- Study on the Color Reaction Mechanism of the Seliwanoff Reaction with 4-Ethylresorcinol as the Color-Developing Reagent
- Interaction of Imidazole Derivatives with Electron Acceptors. II. Reaction Products of Imidazole with p-Benzoquinone
- Color Reaction Mechanism of Cholesterol in Zak-Henly's Method. (Organic Analysis. LVII.)
- Color Reaction Mechanism of Cholesterol with Perchloric Acid, Phosphoric Acid and Ferric Chloride Reagent. I. (Organic Analysis. LVIII.)
- Color Reaction Product of Urea with Diacetyl Monoxime and Glucuronolactone. I. On the Reaction of Urea Derivatives with Diacetyl Monoxime and Glucuronolactone
- Molecular Orbital Interpretation of Infrared Absorption Frequencies. III. Nitrobenzene Derivatives, Cyano Compounds and an Application of Mutual Additive Substituent Parameters to Benzophenone Derivatives
- Studies on the Physical Properties of Aromatic Sulfinamides. II. Infrared Absorption Spectrum
- Interaction of Imidazole Derivatives with Electron-Acceptor. I. Isolation of Imidazolium 1,1,2,3,3-Pentacyanopropenide Derivatives
- Color Reaction Product of Urea with Diacetyl Monoxime and Glucuronolactone. II. On the Reaction of Butylurea with Diacetyl, 1-Phenyl-1,2-propanedione, 1-Phenyl-1-hydroxyimino-2-propanone, and 1-Phenyl-2-hydroxyimino-1-propanone
- Organic Analysis. LVI. Determination of Free Cholesterol in Blood Serum. An Application of Perchloric Acid-Phosphoric Acid-Ferric Chloride Reagent to Cholesteryl Digitonide.