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Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Autore Hofmann Klaus <1911-1995.>
Pubbl/distr/stampa New York, : Interscience, 1953
Descrizione fisica 1 online resource (470 p.)
Disciplina 547.59
547/.59/05
Collana Chemistry of heterocyclic compounds
Soggetto topico Imidazoles
Imidazoles - Derivatives
ISBN 1-282-30139-X
9786612301391
0-470-18654-2
0-470-18804-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto IMIDAZOLE and Its Derivatives; Preface; Contents; Section 1 CHEMISTRY OF CLASSES AND DERIVATIVES; I. General Properties and Structure of the Imidazoles; A. Nomenclature; B. Physical Properties; 1. Introduction; 2. Boiling and Melting Points; 3. Solubility; 4. Molecular Weight and Degree of Association; 5. Viscosity; 6. Dipole Moments; 7. Spectroscopic Properties; (a) Ultraviolet Absorption Spectra; (b) Raman Spectra; (c) Chemiluminescence; 8. Miscellaneous Physical Properties; C. Chemical Properties; 1. Basic Strength; 2. Pseudoacidic Character; 3. Chemical Stability and Aromatic Character
D. Structural Considerations1. The Classical Imidazole Formula; 2. Current Views; E. Tautomeric Character; II. The Alkyl- and Arylimidazoles; A. Synthetic Procedures; 1. Introduction; 2. The Radziszewski Synthesis; 3. The Weidenhagen Synthesis; 4. Formation from Carbohydrates; 5. Formation from 2(3H)-Imidazolethiones and Dithiohydantoins; 6. Formation from Imidazolecarboxylic Acids; 7. Formation from 2-Imidazolines; 8. Miscellaneous Procedures; B. Properties and Chemical Behavior; 1. General Properties; 2. Acylation; 3. Alkylation
III. The Oxo- and Hydroxyimidazoles and Their Sulfur AnaloguesA. The Oxoimidazoles; 1. Imidazolecarboxaldehydes; 2. Imidazole Ketones; 3. Imidazolones and Thiones; (a) Nomenclature; (b) Structural Considerations Regarding the 2(3H)-Imidazolones and Thiones; (c) 2(3H)-Imidazolones; (d) 2(3H)-Imidazolethiones; (e) 2(5H)-Imidazolones; (f) 4(5H) (or 5(4H))-Imidazolones; B. The Hydroxyalkylimidazoles; 1. Monohydroxyalkylimidazoles; (a) Hydroxymethylimidazoles; (b) 4(or 5)-(2-Hydroxyethyl)Imidazole; 2. Polyhydroxyalkylimidazoles; (a) 4(or 5)-Polyhydroxyalkylimidazoles
(b)) l-PolyhydroxyalkylimidazolesIV. The Halogenoimidazoles; A. Bromoimidazoles; 1. Preparative Methods; 2. Properties; B. Chloroimidazoles; C. Chloroalkylimidazoles; D. Iodoimidazoles; 1. Preparative Methods; 2. Properties; V. The Nitro-, Arylazo-, and Aminoimidazoles; A. Nitroimidazoles; 1. Synthetic Methods and Orientation of the Nitro Group; 2. Properties; B. Arylazoimidazoles; 1. Formation and Orientation of the Arylazo Group; 2. Application of the Diazo Test to the Identification and Estimation of Imidazoles; 3. Properties; C. Aminoimidazoles; 1. 2-Aminoimidazoles
2. 4(or 5)-AminoimidazolesD. Histamine; 1. Discovery, Distribution in Nature, and Pharmacological Effects; 2. Isolation from Natural Materials; 3. Quantitative Estimation of Histamine; (a) Biological Methods; (b) Colorimetric Methods; 4. Formation by Microorganisms; 5. Preparative Methods; 6. Physical and Chemical Properties; 7. Structural Analogues of Histamine; (a) Position Isomers; (b) Ring-Substitution Products; (c) N-Monoalkyl- and N-Dialkylhistamine Derivatives; (d) Histamine Analogues Possessing Longer or Shorter Aliphatic Side Chains; 8. Pharmacological Specificity
VI. The Imidazolecarboxylic and Sulfonic Acids
Record Nr. UNINA-9910144289503321
Hofmann Klaus <1911-1995.>  
New York, : Interscience, 1953
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Autore Hofmann Klaus <1911-1995.>
Pubbl/distr/stampa New York, : Interscience, 1953
Descrizione fisica 1 online resource (470 p.)
Disciplina 547.59
547/.59/05
Collana Chemistry of heterocyclic compounds
Soggetto topico Imidazoles
Imidazoles - Derivatives
ISBN 1-282-30139-X
9786612301391
0-470-18654-2
0-470-18804-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto IMIDAZOLE and Its Derivatives; Preface; Contents; Section 1 CHEMISTRY OF CLASSES AND DERIVATIVES; I. General Properties and Structure of the Imidazoles; A. Nomenclature; B. Physical Properties; 1. Introduction; 2. Boiling and Melting Points; 3. Solubility; 4. Molecular Weight and Degree of Association; 5. Viscosity; 6. Dipole Moments; 7. Spectroscopic Properties; (a) Ultraviolet Absorption Spectra; (b) Raman Spectra; (c) Chemiluminescence; 8. Miscellaneous Physical Properties; C. Chemical Properties; 1. Basic Strength; 2. Pseudoacidic Character; 3. Chemical Stability and Aromatic Character
D. Structural Considerations1. The Classical Imidazole Formula; 2. Current Views; E. Tautomeric Character; II. The Alkyl- and Arylimidazoles; A. Synthetic Procedures; 1. Introduction; 2. The Radziszewski Synthesis; 3. The Weidenhagen Synthesis; 4. Formation from Carbohydrates; 5. Formation from 2(3H)-Imidazolethiones and Dithiohydantoins; 6. Formation from Imidazolecarboxylic Acids; 7. Formation from 2-Imidazolines; 8. Miscellaneous Procedures; B. Properties and Chemical Behavior; 1. General Properties; 2. Acylation; 3. Alkylation
III. The Oxo- and Hydroxyimidazoles and Their Sulfur AnaloguesA. The Oxoimidazoles; 1. Imidazolecarboxaldehydes; 2. Imidazole Ketones; 3. Imidazolones and Thiones; (a) Nomenclature; (b) Structural Considerations Regarding the 2(3H)-Imidazolones and Thiones; (c) 2(3H)-Imidazolones; (d) 2(3H)-Imidazolethiones; (e) 2(5H)-Imidazolones; (f) 4(5H) (or 5(4H))-Imidazolones; B. The Hydroxyalkylimidazoles; 1. Monohydroxyalkylimidazoles; (a) Hydroxymethylimidazoles; (b) 4(or 5)-(2-Hydroxyethyl)Imidazole; 2. Polyhydroxyalkylimidazoles; (a) 4(or 5)-Polyhydroxyalkylimidazoles
(b)) l-PolyhydroxyalkylimidazolesIV. The Halogenoimidazoles; A. Bromoimidazoles; 1. Preparative Methods; 2. Properties; B. Chloroimidazoles; C. Chloroalkylimidazoles; D. Iodoimidazoles; 1. Preparative Methods; 2. Properties; V. The Nitro-, Arylazo-, and Aminoimidazoles; A. Nitroimidazoles; 1. Synthetic Methods and Orientation of the Nitro Group; 2. Properties; B. Arylazoimidazoles; 1. Formation and Orientation of the Arylazo Group; 2. Application of the Diazo Test to the Identification and Estimation of Imidazoles; 3. Properties; C. Aminoimidazoles; 1. 2-Aminoimidazoles
2. 4(or 5)-AminoimidazolesD. Histamine; 1. Discovery, Distribution in Nature, and Pharmacological Effects; 2. Isolation from Natural Materials; 3. Quantitative Estimation of Histamine; (a) Biological Methods; (b) Colorimetric Methods; 4. Formation by Microorganisms; 5. Preparative Methods; 6. Physical and Chemical Properties; 7. Structural Analogues of Histamine; (a) Position Isomers; (b) Ring-Substitution Products; (c) N-Monoalkyl- and N-Dialkylhistamine Derivatives; (d) Histamine Analogues Possessing Longer or Shorter Aliphatic Side Chains; 8. Pharmacological Specificity
VI. The Imidazolecarboxylic and Sulfonic Acids
Record Nr. UNISA-996202936603316
Hofmann Klaus <1911-1995.>  
New York, : Interscience, 1953
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Autore Hofmann Klaus <1911-1995.>
Pubbl/distr/stampa New York, : Interscience, 1953
Descrizione fisica 1 online resource (470 p.)
Disciplina 547.59
547/.59/05
Collana Chemistry of heterocyclic compounds
Soggetto topico Imidazoles
Imidazoles - Derivatives
ISBN 1-282-30139-X
9786612301391
0-470-18654-2
0-470-18804-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto IMIDAZOLE and Its Derivatives; Preface; Contents; Section 1 CHEMISTRY OF CLASSES AND DERIVATIVES; I. General Properties and Structure of the Imidazoles; A. Nomenclature; B. Physical Properties; 1. Introduction; 2. Boiling and Melting Points; 3. Solubility; 4. Molecular Weight and Degree of Association; 5. Viscosity; 6. Dipole Moments; 7. Spectroscopic Properties; (a) Ultraviolet Absorption Spectra; (b) Raman Spectra; (c) Chemiluminescence; 8. Miscellaneous Physical Properties; C. Chemical Properties; 1. Basic Strength; 2. Pseudoacidic Character; 3. Chemical Stability and Aromatic Character
D. Structural Considerations1. The Classical Imidazole Formula; 2. Current Views; E. Tautomeric Character; II. The Alkyl- and Arylimidazoles; A. Synthetic Procedures; 1. Introduction; 2. The Radziszewski Synthesis; 3. The Weidenhagen Synthesis; 4. Formation from Carbohydrates; 5. Formation from 2(3H)-Imidazolethiones and Dithiohydantoins; 6. Formation from Imidazolecarboxylic Acids; 7. Formation from 2-Imidazolines; 8. Miscellaneous Procedures; B. Properties and Chemical Behavior; 1. General Properties; 2. Acylation; 3. Alkylation
III. The Oxo- and Hydroxyimidazoles and Their Sulfur AnaloguesA. The Oxoimidazoles; 1. Imidazolecarboxaldehydes; 2. Imidazole Ketones; 3. Imidazolones and Thiones; (a) Nomenclature; (b) Structural Considerations Regarding the 2(3H)-Imidazolones and Thiones; (c) 2(3H)-Imidazolones; (d) 2(3H)-Imidazolethiones; (e) 2(5H)-Imidazolones; (f) 4(5H) (or 5(4H))-Imidazolones; B. The Hydroxyalkylimidazoles; 1. Monohydroxyalkylimidazoles; (a) Hydroxymethylimidazoles; (b) 4(or 5)-(2-Hydroxyethyl)Imidazole; 2. Polyhydroxyalkylimidazoles; (a) 4(or 5)-Polyhydroxyalkylimidazoles
(b)) l-PolyhydroxyalkylimidazolesIV. The Halogenoimidazoles; A. Bromoimidazoles; 1. Preparative Methods; 2. Properties; B. Chloroimidazoles; C. Chloroalkylimidazoles; D. Iodoimidazoles; 1. Preparative Methods; 2. Properties; V. The Nitro-, Arylazo-, and Aminoimidazoles; A. Nitroimidazoles; 1. Synthetic Methods and Orientation of the Nitro Group; 2. Properties; B. Arylazoimidazoles; 1. Formation and Orientation of the Arylazo Group; 2. Application of the Diazo Test to the Identification and Estimation of Imidazoles; 3. Properties; C. Aminoimidazoles; 1. 2-Aminoimidazoles
2. 4(or 5)-AminoimidazolesD. Histamine; 1. Discovery, Distribution in Nature, and Pharmacological Effects; 2. Isolation from Natural Materials; 3. Quantitative Estimation of Histamine; (a) Biological Methods; (b) Colorimetric Methods; 4. Formation by Microorganisms; 5. Preparative Methods; 6. Physical and Chemical Properties; 7. Structural Analogues of Histamine; (a) Position Isomers; (b) Ring-Substitution Products; (c) N-Monoalkyl- and N-Dialkylhistamine Derivatives; (d) Histamine Analogues Possessing Longer or Shorter Aliphatic Side Chains; 8. Pharmacological Specificity
VI. The Imidazolecarboxylic and Sulfonic Acids
Record Nr. UNINA-9910830143603321
Hofmann Klaus <1911-1995.>  
New York, : Interscience, 1953
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Imidazole and its derivatives . Part I [[electronic resource] /] / Klaus Hofmann
Autore Hofmann Klaus <1911-1995.>
Pubbl/distr/stampa New York, : Interscience, 1953
Descrizione fisica 1 online resource (470 p.)
Disciplina 547.59
547/.59/05
Collana Chemistry of heterocyclic compounds
Soggetto topico Imidazoles
Imidazoles - Derivatives
ISBN 1-282-30139-X
9786612301391
0-470-18654-2
0-470-18804-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto IMIDAZOLE and Its Derivatives; Preface; Contents; Section 1 CHEMISTRY OF CLASSES AND DERIVATIVES; I. General Properties and Structure of the Imidazoles; A. Nomenclature; B. Physical Properties; 1. Introduction; 2. Boiling and Melting Points; 3. Solubility; 4. Molecular Weight and Degree of Association; 5. Viscosity; 6. Dipole Moments; 7. Spectroscopic Properties; (a) Ultraviolet Absorption Spectra; (b) Raman Spectra; (c) Chemiluminescence; 8. Miscellaneous Physical Properties; C. Chemical Properties; 1. Basic Strength; 2. Pseudoacidic Character; 3. Chemical Stability and Aromatic Character
D. Structural Considerations1. The Classical Imidazole Formula; 2. Current Views; E. Tautomeric Character; II. The Alkyl- and Arylimidazoles; A. Synthetic Procedures; 1. Introduction; 2. The Radziszewski Synthesis; 3. The Weidenhagen Synthesis; 4. Formation from Carbohydrates; 5. Formation from 2(3H)-Imidazolethiones and Dithiohydantoins; 6. Formation from Imidazolecarboxylic Acids; 7. Formation from 2-Imidazolines; 8. Miscellaneous Procedures; B. Properties and Chemical Behavior; 1. General Properties; 2. Acylation; 3. Alkylation
III. The Oxo- and Hydroxyimidazoles and Their Sulfur AnaloguesA. The Oxoimidazoles; 1. Imidazolecarboxaldehydes; 2. Imidazole Ketones; 3. Imidazolones and Thiones; (a) Nomenclature; (b) Structural Considerations Regarding the 2(3H)-Imidazolones and Thiones; (c) 2(3H)-Imidazolones; (d) 2(3H)-Imidazolethiones; (e) 2(5H)-Imidazolones; (f) 4(5H) (or 5(4H))-Imidazolones; B. The Hydroxyalkylimidazoles; 1. Monohydroxyalkylimidazoles; (a) Hydroxymethylimidazoles; (b) 4(or 5)-(2-Hydroxyethyl)Imidazole; 2. Polyhydroxyalkylimidazoles; (a) 4(or 5)-Polyhydroxyalkylimidazoles
(b)) l-PolyhydroxyalkylimidazolesIV. The Halogenoimidazoles; A. Bromoimidazoles; 1. Preparative Methods; 2. Properties; B. Chloroimidazoles; C. Chloroalkylimidazoles; D. Iodoimidazoles; 1. Preparative Methods; 2. Properties; V. The Nitro-, Arylazo-, and Aminoimidazoles; A. Nitroimidazoles; 1. Synthetic Methods and Orientation of the Nitro Group; 2. Properties; B. Arylazoimidazoles; 1. Formation and Orientation of the Arylazo Group; 2. Application of the Diazo Test to the Identification and Estimation of Imidazoles; 3. Properties; C. Aminoimidazoles; 1. 2-Aminoimidazoles
2. 4(or 5)-AminoimidazolesD. Histamine; 1. Discovery, Distribution in Nature, and Pharmacological Effects; 2. Isolation from Natural Materials; 3. Quantitative Estimation of Histamine; (a) Biological Methods; (b) Colorimetric Methods; 4. Formation by Microorganisms; 5. Preparative Methods; 6. Physical and Chemical Properties; 7. Structural Analogues of Histamine; (a) Position Isomers; (b) Ring-Substitution Products; (c) N-Monoalkyl- and N-Dialkylhistamine Derivatives; (d) Histamine Analogues Possessing Longer or Shorter Aliphatic Side Chains; 8. Pharmacological Specificity
VI. The Imidazolecarboxylic and Sulfonic Acids
Record Nr. UNINA-9910841670203321
Hofmann Klaus <1911-1995.>  
New York, : Interscience, 1953
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui