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Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Autore Armarego W. L. F
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (564 p.)
Disciplina 547/.59/05
Altri autori (Persone) BrownD. J
Collana The chemistry of heterocyclic compounds
Soggetto topico Quinazoline
Heterocyclic compounds
Soggetto genere / forma Electronic books.
ISBN 1-282-30711-8
9786612307119
0-470-18691-7
0-470-18839-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto QUINAZOLINES; Contents; Tables; I. Introduction; 1. History; 2. Nomenclature; 3. The Dual Character of Quinazolines; 4. General Summary of Quinazoline Chemistry; A. Syntheses; a. Primary Syntheses; b. Secondary Syntheses; B. The Heightened Reactivity of 2- and 4-Alkyl Groups; C. Addition and Substitution Reactions, and Nucleophilic Metathesis; D. N-Oxides; E. Tautomerism; F. Oxidation and Reduction; G. Rearrangements; H. Biological Activity in Quinazolines; 5. Tables; Introduction; 6. References; II. Quinazoline; 1. Synthesis of Quinazoline; 2. Physical Properties
II.1. Quinazoline and 3-Alkyl Derivatives A. Theoretical Aspects; B. Spectra; a. Ultraviolet Spectra; b. Phosphorescence Spectra; c. Infrared Spectra; d. Proton Magnetic Resonance Spectra; e. Mass Spectra; C. Covalent Hydration; a. Covalent Hydration in Quinazoline; b. Effect of Substituents in the Pyrimidine Ring on Covalent Hydration; (i) Effect of substituents in position 4; (ii) Effect of saubstituenta in position 2; c. Effect Substituents in the Benzene Ring on Covalent Hydration; II.2. Electronic Effects and Hydration in 2-Substituted Quinazoline Cations
II.3. Ionization and Covalent Hydration of Quinazolines in Water at 20°II.4. Ionization Constants of Substituted Quinazolines in Water at 20°; D. Polarography; 3. Chemical Reactivity of Quinazoline; A. Hydrolysis, Oxidation, and Reduction; B. Electrophilic and Nucleophilic Substitution, and Alkylation; C. Addition Reactions; 4. References; III. C-Alkyl- and C-Arylquinazolines; 1. Methods of Preparation; A. Bischler's Synthesis; B. Oxidation of 3, 4-Dihydroquinazolines; C. Decarboxylation of Acids; D. From N'-ToIuene-p-sulphonylydrazino Derivatives; E. From Imidoyl Chlorides and Nitriles
F. From Aryl Diazonium Salts and NitrilesG. From 4-Chloro or 4-cyanoquinazolines and Grignard Reagents; H. From Chloro- or Cyanoquinazolines and Substances with an Active Methylene Group; I. Reidel's Synthesis; J. Miscellaneous; 2. Properties; A. Physical Properties; B. Chemical Properties; a. The Heightened Reactivity of 2- and 4-Methyl Groups; b. Oxidation and Reduction; c. Electrophilic Substitution; d. Alkylation; e. Reactivity of the Substituted Carbon Atoms Attached to C(2)and C(4); 3. Tables; III.1. 2-Alkyl- and Aryl- (including Heteroaryl-) quinazolines
III.2. 4-Alkyl- and Aryl- (including Heteroaryl-) quinazolineaIII.3. 2,4-Disubstituted Alkyl- and Arylquinazolines; III.4. Alkylquinazolines Substituted in the Benzene Ring; III.5. Alkyl- and Arylquinazolines Substituted in Both Rings; III.6. Miscellaneous Alkyl- and Arylquinazolines (including Quina-zolinium Salts}; 4. References; IV. Oxoquinazolines and 5-, 6-, 7-, and 8-Hydroxyquinazolines; 1. 2-Oxoquinazolines; A. Preparation; B. Properties; 2. 3,4- and 1,4-Dihydro-4-oxoquinasolines; A. Preparation of 3,4-Dihydro-4-oxoquinszolines; a. Niementowski's Synthesis
b. Cyclization of o-Amidobenzamides
Record Nr. UNINA-9910144282403321
Armarego W. L. F  
New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Autore Armarego W. L. F
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (564 p.)
Disciplina 547/.59/05
Altri autori (Persone) BrownD. J
Collana The chemistry of heterocyclic compounds
Soggetto topico Quinazoline
Heterocyclic compounds
ISBN 1-282-30711-8
9786612307119
0-470-18691-7
0-470-18839-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto QUINAZOLINES; Contents; Tables; I. Introduction; 1. History; 2. Nomenclature; 3. The Dual Character of Quinazolines; 4. General Summary of Quinazoline Chemistry; A. Syntheses; a. Primary Syntheses; b. Secondary Syntheses; B. The Heightened Reactivity of 2- and 4-Alkyl Groups; C. Addition and Substitution Reactions, and Nucleophilic Metathesis; D. N-Oxides; E. Tautomerism; F. Oxidation and Reduction; G. Rearrangements; H. Biological Activity in Quinazolines; 5. Tables; Introduction; 6. References; II. Quinazoline; 1. Synthesis of Quinazoline; 2. Physical Properties
II.1. Quinazoline and 3-Alkyl Derivatives A. Theoretical Aspects; B. Spectra; a. Ultraviolet Spectra; b. Phosphorescence Spectra; c. Infrared Spectra; d. Proton Magnetic Resonance Spectra; e. Mass Spectra; C. Covalent Hydration; a. Covalent Hydration in Quinazoline; b. Effect of Substituents in the Pyrimidine Ring on Covalent Hydration; (i) Effect of substituents in position 4; (ii) Effect of saubstituenta in position 2; c. Effect Substituents in the Benzene Ring on Covalent Hydration; II.2. Electronic Effects and Hydration in 2-Substituted Quinazoline Cations
II.3. Ionization and Covalent Hydration of Quinazolines in Water at 20°II.4. Ionization Constants of Substituted Quinazolines in Water at 20°; D. Polarography; 3. Chemical Reactivity of Quinazoline; A. Hydrolysis, Oxidation, and Reduction; B. Electrophilic and Nucleophilic Substitution, and Alkylation; C. Addition Reactions; 4. References; III. C-Alkyl- and C-Arylquinazolines; 1. Methods of Preparation; A. Bischler's Synthesis; B. Oxidation of 3, 4-Dihydroquinazolines; C. Decarboxylation of Acids; D. From N'-ToIuene-p-sulphonylydrazino Derivatives; E. From Imidoyl Chlorides and Nitriles
F. From Aryl Diazonium Salts and NitrilesG. From 4-Chloro or 4-cyanoquinazolines and Grignard Reagents; H. From Chloro- or Cyanoquinazolines and Substances with an Active Methylene Group; I. Reidel's Synthesis; J. Miscellaneous; 2. Properties; A. Physical Properties; B. Chemical Properties; a. The Heightened Reactivity of 2- and 4-Methyl Groups; b. Oxidation and Reduction; c. Electrophilic Substitution; d. Alkylation; e. Reactivity of the Substituted Carbon Atoms Attached to C(2)and C(4); 3. Tables; III.1. 2-Alkyl- and Aryl- (including Heteroaryl-) quinazolines
III.2. 4-Alkyl- and Aryl- (including Heteroaryl-) quinazolineaIII.3. 2,4-Disubstituted Alkyl- and Arylquinazolines; III.4. Alkylquinazolines Substituted in the Benzene Ring; III.5. Alkyl- and Arylquinazolines Substituted in Both Rings; III.6. Miscellaneous Alkyl- and Arylquinazolines (including Quina-zolinium Salts}; 4. References; IV. Oxoquinazolines and 5-, 6-, 7-, and 8-Hydroxyquinazolines; 1. 2-Oxoquinazolines; A. Preparation; B. Properties; 2. 3,4- and 1,4-Dihydro-4-oxoquinasolines; A. Preparation of 3,4-Dihydro-4-oxoquinszolines; a. Niementowski's Synthesis
b. Cyclization of o-Amidobenzamides
Record Nr. UNISA-996202924503316
Armarego W. L. F  
New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. di Salerno
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Autore Armarego W. L. F
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (564 p.)
Disciplina 547/.59/05
Altri autori (Persone) BrownD. J
Collana The chemistry of heterocyclic compounds
Soggetto topico Quinazoline
Heterocyclic compounds
ISBN 1-282-30711-8
9786612307119
0-470-18691-7
0-470-18839-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto QUINAZOLINES; Contents; Tables; I. Introduction; 1. History; 2. Nomenclature; 3. The Dual Character of Quinazolines; 4. General Summary of Quinazoline Chemistry; A. Syntheses; a. Primary Syntheses; b. Secondary Syntheses; B. The Heightened Reactivity of 2- and 4-Alkyl Groups; C. Addition and Substitution Reactions, and Nucleophilic Metathesis; D. N-Oxides; E. Tautomerism; F. Oxidation and Reduction; G. Rearrangements; H. Biological Activity in Quinazolines; 5. Tables; Introduction; 6. References; II. Quinazoline; 1. Synthesis of Quinazoline; 2. Physical Properties
II.1. Quinazoline and 3-Alkyl Derivatives A. Theoretical Aspects; B. Spectra; a. Ultraviolet Spectra; b. Phosphorescence Spectra; c. Infrared Spectra; d. Proton Magnetic Resonance Spectra; e. Mass Spectra; C. Covalent Hydration; a. Covalent Hydration in Quinazoline; b. Effect of Substituents in the Pyrimidine Ring on Covalent Hydration; (i) Effect of substituents in position 4; (ii) Effect of saubstituenta in position 2; c. Effect Substituents in the Benzene Ring on Covalent Hydration; II.2. Electronic Effects and Hydration in 2-Substituted Quinazoline Cations
II.3. Ionization and Covalent Hydration of Quinazolines in Water at 20°II.4. Ionization Constants of Substituted Quinazolines in Water at 20°; D. Polarography; 3. Chemical Reactivity of Quinazoline; A. Hydrolysis, Oxidation, and Reduction; B. Electrophilic and Nucleophilic Substitution, and Alkylation; C. Addition Reactions; 4. References; III. C-Alkyl- and C-Arylquinazolines; 1. Methods of Preparation; A. Bischler's Synthesis; B. Oxidation of 3, 4-Dihydroquinazolines; C. Decarboxylation of Acids; D. From N'-ToIuene-p-sulphonylydrazino Derivatives; E. From Imidoyl Chlorides and Nitriles
F. From Aryl Diazonium Salts and NitrilesG. From 4-Chloro or 4-cyanoquinazolines and Grignard Reagents; H. From Chloro- or Cyanoquinazolines and Substances with an Active Methylene Group; I. Reidel's Synthesis; J. Miscellaneous; 2. Properties; A. Physical Properties; B. Chemical Properties; a. The Heightened Reactivity of 2- and 4-Methyl Groups; b. Oxidation and Reduction; c. Electrophilic Substitution; d. Alkylation; e. Reactivity of the Substituted Carbon Atoms Attached to C(2)and C(4); 3. Tables; III.1. 2-Alkyl- and Aryl- (including Heteroaryl-) quinazolines
III.2. 4-Alkyl- and Aryl- (including Heteroaryl-) quinazolineaIII.3. 2,4-Disubstituted Alkyl- and Arylquinazolines; III.4. Alkylquinazolines Substituted in the Benzene Ring; III.5. Alkyl- and Arylquinazolines Substituted in Both Rings; III.6. Miscellaneous Alkyl- and Arylquinazolines (including Quina-zolinium Salts}; 4. References; IV. Oxoquinazolines and 5-, 6-, 7-, and 8-Hydroxyquinazolines; 1. 2-Oxoquinazolines; A. Preparation; B. Properties; 2. 3,4- and 1,4-Dihydro-4-oxoquinasolines; A. Preparation of 3,4-Dihydro-4-oxoquinszolines; a. Niementowski's Synthesis
b. Cyclization of o-Amidobenzamides
Record Nr. UNINA-9910643715403321
Armarego W. L. F  
New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Autore Armarego W. L. F
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (564 p.)
Disciplina 547/.59/05
Altri autori (Persone) BrownD. J
Collana The chemistry of heterocyclic compounds
Soggetto topico Quinazoline
Heterocyclic compounds
ISBN 1-282-30711-8
9786612307119
0-470-18691-7
0-470-18839-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto QUINAZOLINES; Contents; Tables; I. Introduction; 1. History; 2. Nomenclature; 3. The Dual Character of Quinazolines; 4. General Summary of Quinazoline Chemistry; A. Syntheses; a. Primary Syntheses; b. Secondary Syntheses; B. The Heightened Reactivity of 2- and 4-Alkyl Groups; C. Addition and Substitution Reactions, and Nucleophilic Metathesis; D. N-Oxides; E. Tautomerism; F. Oxidation and Reduction; G. Rearrangements; H. Biological Activity in Quinazolines; 5. Tables; Introduction; 6. References; II. Quinazoline; 1. Synthesis of Quinazoline; 2. Physical Properties
II.1. Quinazoline and 3-Alkyl Derivatives A. Theoretical Aspects; B. Spectra; a. Ultraviolet Spectra; b. Phosphorescence Spectra; c. Infrared Spectra; d. Proton Magnetic Resonance Spectra; e. Mass Spectra; C. Covalent Hydration; a. Covalent Hydration in Quinazoline; b. Effect of Substituents in the Pyrimidine Ring on Covalent Hydration; (i) Effect of substituents in position 4; (ii) Effect of saubstituenta in position 2; c. Effect Substituents in the Benzene Ring on Covalent Hydration; II.2. Electronic Effects and Hydration in 2-Substituted Quinazoline Cations
II.3. Ionization and Covalent Hydration of Quinazolines in Water at 20°II.4. Ionization Constants of Substituted Quinazolines in Water at 20°; D. Polarography; 3. Chemical Reactivity of Quinazoline; A. Hydrolysis, Oxidation, and Reduction; B. Electrophilic and Nucleophilic Substitution, and Alkylation; C. Addition Reactions; 4. References; III. C-Alkyl- and C-Arylquinazolines; 1. Methods of Preparation; A. Bischler's Synthesis; B. Oxidation of 3, 4-Dihydroquinazolines; C. Decarboxylation of Acids; D. From N'-ToIuene-p-sulphonylydrazino Derivatives; E. From Imidoyl Chlorides and Nitriles
F. From Aryl Diazonium Salts and NitrilesG. From 4-Chloro or 4-cyanoquinazolines and Grignard Reagents; H. From Chloro- or Cyanoquinazolines and Substances with an Active Methylene Group; I. Reidel's Synthesis; J. Miscellaneous; 2. Properties; A. Physical Properties; B. Chemical Properties; a. The Heightened Reactivity of 2- and 4-Methyl Groups; b. Oxidation and Reduction; c. Electrophilic Substitution; d. Alkylation; e. Reactivity of the Substituted Carbon Atoms Attached to C(2)and C(4); 3. Tables; III.1. 2-Alkyl- and Aryl- (including Heteroaryl-) quinazolines
III.2. 4-Alkyl- and Aryl- (including Heteroaryl-) quinazolineaIII.3. 2,4-Disubstituted Alkyl- and Arylquinazolines; III.4. Alkylquinazolines Substituted in the Benzene Ring; III.5. Alkyl- and Arylquinazolines Substituted in Both Rings; III.6. Miscellaneous Alkyl- and Arylquinazolines (including Quina-zolinium Salts}; 4. References; IV. Oxoquinazolines and 5-, 6-, 7-, and 8-Hydroxyquinazolines; 1. 2-Oxoquinazolines; A. Preparation; B. Properties; 2. 3,4- and 1,4-Dihydro-4-oxoquinasolines; A. Preparation of 3,4-Dihydro-4-oxoquinszolines; a. Niementowski's Synthesis
b. Cyclization of o-Amidobenzamides
Record Nr. UNINA-9910830530203321
Armarego W. L. F  
New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Fused pyrimidines . Part I Quinazolines [[electronic resource] /] / W.L.F. Armarego; edited by D.J. Brown
Autore Armarego W. L. F
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Interscience Publishers, 1967
Descrizione fisica 1 online resource (564 p.)
Disciplina 547/.59/05
Altri autori (Persone) BrownD. J
Collana The chemistry of heterocyclic compounds
Soggetto topico Quinazoline
Heterocyclic compounds
ISBN 1-282-30711-8
9786612307119
0-470-18691-7
0-470-18839-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto QUINAZOLINES; Contents; Tables; I. Introduction; 1. History; 2. Nomenclature; 3. The Dual Character of Quinazolines; 4. General Summary of Quinazoline Chemistry; A. Syntheses; a. Primary Syntheses; b. Secondary Syntheses; B. The Heightened Reactivity of 2- and 4-Alkyl Groups; C. Addition and Substitution Reactions, and Nucleophilic Metathesis; D. N-Oxides; E. Tautomerism; F. Oxidation and Reduction; G. Rearrangements; H. Biological Activity in Quinazolines; 5. Tables; Introduction; 6. References; II. Quinazoline; 1. Synthesis of Quinazoline; 2. Physical Properties
II.1. Quinazoline and 3-Alkyl Derivatives A. Theoretical Aspects; B. Spectra; a. Ultraviolet Spectra; b. Phosphorescence Spectra; c. Infrared Spectra; d. Proton Magnetic Resonance Spectra; e. Mass Spectra; C. Covalent Hydration; a. Covalent Hydration in Quinazoline; b. Effect of Substituents in the Pyrimidine Ring on Covalent Hydration; (i) Effect of substituents in position 4; (ii) Effect of saubstituenta in position 2; c. Effect Substituents in the Benzene Ring on Covalent Hydration; II.2. Electronic Effects and Hydration in 2-Substituted Quinazoline Cations
II.3. Ionization and Covalent Hydration of Quinazolines in Water at 20°II.4. Ionization Constants of Substituted Quinazolines in Water at 20°; D. Polarography; 3. Chemical Reactivity of Quinazoline; A. Hydrolysis, Oxidation, and Reduction; B. Electrophilic and Nucleophilic Substitution, and Alkylation; C. Addition Reactions; 4. References; III. C-Alkyl- and C-Arylquinazolines; 1. Methods of Preparation; A. Bischler's Synthesis; B. Oxidation of 3, 4-Dihydroquinazolines; C. Decarboxylation of Acids; D. From N'-ToIuene-p-sulphonylydrazino Derivatives; E. From Imidoyl Chlorides and Nitriles
F. From Aryl Diazonium Salts and NitrilesG. From 4-Chloro or 4-cyanoquinazolines and Grignard Reagents; H. From Chloro- or Cyanoquinazolines and Substances with an Active Methylene Group; I. Reidel's Synthesis; J. Miscellaneous; 2. Properties; A. Physical Properties; B. Chemical Properties; a. The Heightened Reactivity of 2- and 4-Methyl Groups; b. Oxidation and Reduction; c. Electrophilic Substitution; d. Alkylation; e. Reactivity of the Substituted Carbon Atoms Attached to C(2)and C(4); 3. Tables; III.1. 2-Alkyl- and Aryl- (including Heteroaryl-) quinazolines
III.2. 4-Alkyl- and Aryl- (including Heteroaryl-) quinazolineaIII.3. 2,4-Disubstituted Alkyl- and Arylquinazolines; III.4. Alkylquinazolines Substituted in the Benzene Ring; III.5. Alkyl- and Arylquinazolines Substituted in Both Rings; III.6. Miscellaneous Alkyl- and Arylquinazolines (including Quina-zolinium Salts}; 4. References; IV. Oxoquinazolines and 5-, 6-, 7-, and 8-Hydroxyquinazolines; 1. 2-Oxoquinazolines; A. Preparation; B. Properties; 2. 3,4- and 1,4-Dihydro-4-oxoquinasolines; A. Preparation of 3,4-Dihydro-4-oxoquinszolines; a. Niementowski's Synthesis
b. Cyclization of o-Amidobenzamides
Record Nr. UNINA-9910840726103321
Armarego W. L. F  
New York, : Interscience Publishers, 1967
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Autore Delia Thomas J
Pubbl/distr/stampa New York, : Interscience Publishers, 1992
Descrizione fisica 1 online resource (338 p.)
Disciplina 547.593
547.7/9
547/.59/05
547/.593
Altri autori (Persone) BrownD. J
ArmaregoW. L. F
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyrimidines
Heterocyclic compounds
Soggetto genere / forma Electronic books.
ISBN 1-282-30166-7
9786612301667
0-470-18690-9
0-470-18838-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES: Miscellaneous Fused Pyrimidines; Contents; CHAPTER I. PYRIDOPYRIMIDINES; 1. Introduction; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrido[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; B. Synthesis of Pyrido[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; C. Synthesis of Pyrido[3,4-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; D. Synthesis of Pyrido[2,3-d]pyrimidines; (1) From Pyrimidines; (a) Formation of Bond 4a-5; (b) Formation of Bond 5-6; (c) Formation of Bond 7-8; (d) Formation of Bond 8-8a; (2) From Pyridines
(a) Formation of Bond 8a-l(b) Formation of Bond 1-2; (c) Formation of Bond 2-3; (d) Formation of Bond 3-4; (e) Formation of Bond 4-4a; 3. Reactions; A. Of Pyrido[3,2-d]pyrimidines; B. Of Pyrido[4,3-d]pyrimidines; C. Of Pyrido[3,4-d]pyrimidines; D. Of Pyrido[2,3-d]pyrimidines; (1) With Nucleophiles; (2) With Electrophiles; (3) Reductions; (4) Oxidations; 4. Patent Literature; 5. Tables; Table 1. Derivatives of Pyrido[3,2-d]pyrimidine; Table 2. Derivatives of Pyrido[4,3-d]pyrimidines; Table 3. Derivatives of Pyrido[3,4-d]pyrimidines; Table 4. Derivatives of 2,4-Diaminopyrido[2,3-d]pyrimidines
Table 5. Derivatives of 2-Amino-4-hydroxypyrido[2,3-d]pyrimidinesTable 6. Derivatives of 2-Aminopyrido[2,3-d]pyrimidines; Table 7. Derivatives of 4-Aminopyrido[2,3-d]pyrimidines; Table 8. Derivatives of 2,4-Dihydroxypyrido[2,3-d]pyrimidines; Table 9. Derivatives of 2-Hydroxypyrido[2,3-d]pyrimidines; Table 10. Derivatives of 4-Hydroxypyrido[2,3-d]pyrimidines; Table 11. Derivatives of 4-Amino-2-mercaptopyrido[2,3-d]pyrimidines; Table 12. Derivatives of 4-Hydroxy-2-mercaptopyrido[2,3-d]pyrimidines; Table 13. Derivatives of 2-Mercapto- and 4-Mercaptopyrido[2,3-d]pyrimidines
Table 14. Derivatives of Pyrido[2,3-d]pyrimidines6. References; CHAPTER II. PYRANO- AND THIOPYRANOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; (3) From Nonheteroaromatic Precursors; B. Synthesis of Pyrano[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; C. Synthesis of Pyrano[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; D. Synthesis of Thiopyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Thiopyrans; E. Synthesis of Thiopyrano[3,4-d]pyrimidines
F. Synthesis of Thiopyrano[4,3-d]pyrimidines3. Reactions; A. With Nucleophilic Reagents; B. Other Reactions; 4. Patent Literature; 5. Tables; Table 1. The Pyrano[2,3-d]pyrimidines; Table 2. The Pyrano[4,3-d]pyrimidines; Table 3. Miscellaneous Pyranopyrimidines; Table 4. The Thiopyrano[2,3-d]pyrimidines; Table 5. The Thiopyrano[3,4-d]pyrimidines; 6. References; CHAPTER III. PYRIMIDOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrimido[4,5-d]pyrimidines; (1) From Pyrimidines with Amino Groups Adjacent to Hydrogen
(2) From Pyrimidines with Amino Groups Adjacent to Nitriles
Record Nr. UNINA-9910144282703321
Delia Thomas J  
New York, : Interscience Publishers, 1992
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Autore Delia Thomas J
Pubbl/distr/stampa New York, : Interscience Publishers, 1992
Descrizione fisica 1 online resource (338 p.)
Disciplina 547.593
547.7/9
547/.59/05
547/.593
Altri autori (Persone) BrownD. J
ArmaregoW. L. F
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyrimidines
Heterocyclic compounds
ISBN 1-282-30166-7
9786612301667
0-470-18690-9
0-470-18838-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES: Miscellaneous Fused Pyrimidines; Contents; CHAPTER I. PYRIDOPYRIMIDINES; 1. Introduction; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrido[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; B. Synthesis of Pyrido[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; C. Synthesis of Pyrido[3,4-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; D. Synthesis of Pyrido[2,3-d]pyrimidines; (1) From Pyrimidines; (a) Formation of Bond 4a-5; (b) Formation of Bond 5-6; (c) Formation of Bond 7-8; (d) Formation of Bond 8-8a; (2) From Pyridines
(a) Formation of Bond 8a-l(b) Formation of Bond 1-2; (c) Formation of Bond 2-3; (d) Formation of Bond 3-4; (e) Formation of Bond 4-4a; 3. Reactions; A. Of Pyrido[3,2-d]pyrimidines; B. Of Pyrido[4,3-d]pyrimidines; C. Of Pyrido[3,4-d]pyrimidines; D. Of Pyrido[2,3-d]pyrimidines; (1) With Nucleophiles; (2) With Electrophiles; (3) Reductions; (4) Oxidations; 4. Patent Literature; 5. Tables; Table 1. Derivatives of Pyrido[3,2-d]pyrimidine; Table 2. Derivatives of Pyrido[4,3-d]pyrimidines; Table 3. Derivatives of Pyrido[3,4-d]pyrimidines; Table 4. Derivatives of 2,4-Diaminopyrido[2,3-d]pyrimidines
Table 5. Derivatives of 2-Amino-4-hydroxypyrido[2,3-d]pyrimidinesTable 6. Derivatives of 2-Aminopyrido[2,3-d]pyrimidines; Table 7. Derivatives of 4-Aminopyrido[2,3-d]pyrimidines; Table 8. Derivatives of 2,4-Dihydroxypyrido[2,3-d]pyrimidines; Table 9. Derivatives of 2-Hydroxypyrido[2,3-d]pyrimidines; Table 10. Derivatives of 4-Hydroxypyrido[2,3-d]pyrimidines; Table 11. Derivatives of 4-Amino-2-mercaptopyrido[2,3-d]pyrimidines; Table 12. Derivatives of 4-Hydroxy-2-mercaptopyrido[2,3-d]pyrimidines; Table 13. Derivatives of 2-Mercapto- and 4-Mercaptopyrido[2,3-d]pyrimidines
Table 14. Derivatives of Pyrido[2,3-d]pyrimidines6. References; CHAPTER II. PYRANO- AND THIOPYRANOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; (3) From Nonheteroaromatic Precursors; B. Synthesis of Pyrano[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; C. Synthesis of Pyrano[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; D. Synthesis of Thiopyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Thiopyrans; E. Synthesis of Thiopyrano[3,4-d]pyrimidines
F. Synthesis of Thiopyrano[4,3-d]pyrimidines3. Reactions; A. With Nucleophilic Reagents; B. Other Reactions; 4. Patent Literature; 5. Tables; Table 1. The Pyrano[2,3-d]pyrimidines; Table 2. The Pyrano[4,3-d]pyrimidines; Table 3. Miscellaneous Pyranopyrimidines; Table 4. The Thiopyrano[2,3-d]pyrimidines; Table 5. The Thiopyrano[3,4-d]pyrimidines; 6. References; CHAPTER III. PYRIMIDOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrimido[4,5-d]pyrimidines; (1) From Pyrimidines with Amino Groups Adjacent to Hydrogen
(2) From Pyrimidines with Amino Groups Adjacent to Nitriles
Record Nr. UNISA-996202924903316
Delia Thomas J  
New York, : Interscience Publishers, 1992
Materiale a stampa
Lo trovi qui: Univ. di Salerno
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Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Autore Delia Thomas J
Pubbl/distr/stampa New York, : Interscience Publishers, 1992
Descrizione fisica 1 online resource (338 p.)
Disciplina 547.593
547.7/9
547/.59/05
547/.593
Altri autori (Persone) BrownD. J
ArmaregoW. L. F
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyrimidines
Heterocyclic compounds
ISBN 1-282-30166-7
9786612301667
0-470-18690-9
0-470-18838-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES: Miscellaneous Fused Pyrimidines; Contents; CHAPTER I. PYRIDOPYRIMIDINES; 1. Introduction; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrido[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; B. Synthesis of Pyrido[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; C. Synthesis of Pyrido[3,4-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; D. Synthesis of Pyrido[2,3-d]pyrimidines; (1) From Pyrimidines; (a) Formation of Bond 4a-5; (b) Formation of Bond 5-6; (c) Formation of Bond 7-8; (d) Formation of Bond 8-8a; (2) From Pyridines
(a) Formation of Bond 8a-l(b) Formation of Bond 1-2; (c) Formation of Bond 2-3; (d) Formation of Bond 3-4; (e) Formation of Bond 4-4a; 3. Reactions; A. Of Pyrido[3,2-d]pyrimidines; B. Of Pyrido[4,3-d]pyrimidines; C. Of Pyrido[3,4-d]pyrimidines; D. Of Pyrido[2,3-d]pyrimidines; (1) With Nucleophiles; (2) With Electrophiles; (3) Reductions; (4) Oxidations; 4. Patent Literature; 5. Tables; Table 1. Derivatives of Pyrido[3,2-d]pyrimidine; Table 2. Derivatives of Pyrido[4,3-d]pyrimidines; Table 3. Derivatives of Pyrido[3,4-d]pyrimidines; Table 4. Derivatives of 2,4-Diaminopyrido[2,3-d]pyrimidines
Table 5. Derivatives of 2-Amino-4-hydroxypyrido[2,3-d]pyrimidinesTable 6. Derivatives of 2-Aminopyrido[2,3-d]pyrimidines; Table 7. Derivatives of 4-Aminopyrido[2,3-d]pyrimidines; Table 8. Derivatives of 2,4-Dihydroxypyrido[2,3-d]pyrimidines; Table 9. Derivatives of 2-Hydroxypyrido[2,3-d]pyrimidines; Table 10. Derivatives of 4-Hydroxypyrido[2,3-d]pyrimidines; Table 11. Derivatives of 4-Amino-2-mercaptopyrido[2,3-d]pyrimidines; Table 12. Derivatives of 4-Hydroxy-2-mercaptopyrido[2,3-d]pyrimidines; Table 13. Derivatives of 2-Mercapto- and 4-Mercaptopyrido[2,3-d]pyrimidines
Table 14. Derivatives of Pyrido[2,3-d]pyrimidines6. References; CHAPTER II. PYRANO- AND THIOPYRANOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; (3) From Nonheteroaromatic Precursors; B. Synthesis of Pyrano[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; C. Synthesis of Pyrano[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; D. Synthesis of Thiopyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Thiopyrans; E. Synthesis of Thiopyrano[3,4-d]pyrimidines
F. Synthesis of Thiopyrano[4,3-d]pyrimidines3. Reactions; A. With Nucleophilic Reagents; B. Other Reactions; 4. Patent Literature; 5. Tables; Table 1. The Pyrano[2,3-d]pyrimidines; Table 2. The Pyrano[4,3-d]pyrimidines; Table 3. Miscellaneous Pyranopyrimidines; Table 4. The Thiopyrano[2,3-d]pyrimidines; Table 5. The Thiopyrano[3,4-d]pyrimidines; 6. References; CHAPTER III. PYRIMIDOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrimido[4,5-d]pyrimidines; (1) From Pyrimidines with Amino Groups Adjacent to Hydrogen
(2) From Pyrimidines with Amino Groups Adjacent to Nitriles
Record Nr. UNINA-9910830646803321
Delia Thomas J  
New York, : Interscience Publishers, 1992
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Fused pyrimidines . Part four Miscellaneous fused pyrimidines [[electronic resource] /] / Thomas J. Delia
Autore Delia Thomas J
Pubbl/distr/stampa New York, : Interscience Publishers, 1992
Descrizione fisica 1 online resource (338 p.)
Disciplina 547.593
547.7/9
547/.59/05
547/.593
Altri autori (Persone) BrownD. J
ArmaregoW. L. F
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyrimidines
Heterocyclic compounds
ISBN 1-282-30166-7
9786612301667
0-470-18690-9
0-470-18838-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES: Miscellaneous Fused Pyrimidines; Contents; CHAPTER I. PYRIDOPYRIMIDINES; 1. Introduction; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrido[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; B. Synthesis of Pyrido[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; C. Synthesis of Pyrido[3,4-d]pyrimidines; (1) From Pyrimidines; (2) From Pyridines; D. Synthesis of Pyrido[2,3-d]pyrimidines; (1) From Pyrimidines; (a) Formation of Bond 4a-5; (b) Formation of Bond 5-6; (c) Formation of Bond 7-8; (d) Formation of Bond 8-8a; (2) From Pyridines
(a) Formation of Bond 8a-l(b) Formation of Bond 1-2; (c) Formation of Bond 2-3; (d) Formation of Bond 3-4; (e) Formation of Bond 4-4a; 3. Reactions; A. Of Pyrido[3,2-d]pyrimidines; B. Of Pyrido[4,3-d]pyrimidines; C. Of Pyrido[3,4-d]pyrimidines; D. Of Pyrido[2,3-d]pyrimidines; (1) With Nucleophiles; (2) With Electrophiles; (3) Reductions; (4) Oxidations; 4. Patent Literature; 5. Tables; Table 1. Derivatives of Pyrido[3,2-d]pyrimidine; Table 2. Derivatives of Pyrido[4,3-d]pyrimidines; Table 3. Derivatives of Pyrido[3,4-d]pyrimidines; Table 4. Derivatives of 2,4-Diaminopyrido[2,3-d]pyrimidines
Table 5. Derivatives of 2-Amino-4-hydroxypyrido[2,3-d]pyrimidinesTable 6. Derivatives of 2-Aminopyrido[2,3-d]pyrimidines; Table 7. Derivatives of 4-Aminopyrido[2,3-d]pyrimidines; Table 8. Derivatives of 2,4-Dihydroxypyrido[2,3-d]pyrimidines; Table 9. Derivatives of 2-Hydroxypyrido[2,3-d]pyrimidines; Table 10. Derivatives of 4-Hydroxypyrido[2,3-d]pyrimidines; Table 11. Derivatives of 4-Amino-2-mercaptopyrido[2,3-d]pyrimidines; Table 12. Derivatives of 4-Hydroxy-2-mercaptopyrido[2,3-d]pyrimidines; Table 13. Derivatives of 2-Mercapto- and 4-Mercaptopyrido[2,3-d]pyrimidines
Table 14. Derivatives of Pyrido[2,3-d]pyrimidines6. References; CHAPTER II. PYRANO- AND THIOPYRANOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; (3) From Nonheteroaromatic Precursors; B. Synthesis of Pyrano[4,3-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; C. Synthesis of Pyrano[3,2-d]pyrimidines; (1) From Pyrimidines; (2) From Pyrans; D. Synthesis of Thiopyrano[2,3-d]pyrimidines; (1) From Pyrimidines; (2) From Thiopyrans; E. Synthesis of Thiopyrano[3,4-d]pyrimidines
F. Synthesis of Thiopyrano[4,3-d]pyrimidines3. Reactions; A. With Nucleophilic Reagents; B. Other Reactions; 4. Patent Literature; 5. Tables; Table 1. The Pyrano[2,3-d]pyrimidines; Table 2. The Pyrano[4,3-d]pyrimidines; Table 3. Miscellaneous Pyranopyrimidines; Table 4. The Thiopyrano[2,3-d]pyrimidines; Table 5. The Thiopyrano[3,4-d]pyrimidines; 6. References; CHAPTER III. PYRIMIDOPYRIMIDINES; 1. Nomenclature; 2. Methods of Synthesis of the Ring System; A. Synthesis of Pyrimido[4,5-d]pyrimidines; (1) From Pyrimidines with Amino Groups Adjacent to Hydrogen
(2) From Pyrimidines with Amino Groups Adjacent to Nitriles
Record Nr. UNINA-9910840726203321
Delia Thomas J  
New York, : Interscience Publishers, 1992
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part two [[electronic resource] /] / edited by D. J. Brown
Fused pyrimidines . Part two [[electronic resource] /] / edited by D. J. Brown
Autore Lister John H (John Henry)
Edizione [99th ed.]
Pubbl/distr/stampa New York, : Wiley-Interscience, 1971
Descrizione fisica 1 online resource (684 p.)
Disciplina 547.593
547/.59/05
547/.596
Altri autori (Persone) BrownD. J
Collana Chemistry of heterocyclic compounds
Soggetto topico Pyrimidines
Chemistry
ISBN 1-282-30164-0
9786612301643
0-470-18688-7
0-470-18836-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES: PURINES; Contents; Tables; I. Introduction to the Purines; 1. History; TABLE 1. Trivial Names of Purines; 2. Nomenclature and Notation; 3. The Basis of Purine Chemistry; A. The Electrophilic Character of the 2-, 6- and 8-Carbon Atoms; B. The Nucleophilic Character of the 8-Carbon Atom; C. Tautomeric Groups; 4. General Summary of Purine Chemistry; A. Electrophilic Substitution; (a) Nitration; (b) Diazo Coupling; (c) Halogenation; (d) Alkylation; B. Nucleophilic Substitution; (a) Halogen Replacement by Amino Groups; (b) Halogen Replacement by Methoxy and Other Alkoxy Groups
(c) Halogen Replacement by Oxo Group(d) Halogen Replacement by Alkylthio Groups; (e) Halogen Replacement by Thio Group; (f) Halogen Replacement by Thiocyanato and Cyano Groups; (g) Halogen Replacement by Sulpho Groups; (h) Replacement of Methoxy, Methylthio, and Methylsulphonyl Groups; C. Group Interconversion; (a) Interchange of Halogen Atoms; (b) Oxo- to Aminopurines; (c) Oxo- to Chloropurines; (d) Oxo- to Thiopurines; (e) Thio- (and Methylthio-) to Oxopurines; (f) Thio- (and Methylthio-) to Halogenopurines; (g) Thio- to Aminopurines; (h) Interchange of Amino Groups
(i) Amino- to Oxopurines(j) Amino- to Halogenopurines; D. Addition Reactions; (a) The Michael Reaction; (b) Quaternisation; (c) Formation of N-Oxides; (d) Addition of Water and Alcohols; E. Modification of Substituents; (a) Amino Groups; (b) Oxo Groups; (c) Thio Groups; (d) Methyl Groups; F. Reductive Reactions; (a) Nuclear Reduction; (b) Removal of Groups; (c) Reductive Modification of Groups; G. Oxidative Reactions; (a) Chemical Oxidation; (b) Free Radical Attack; (c) Enzymic Oxidation; 5. Physical Properties of Purines; A. Electronic Considerations; B. Ionisation Constants
C. Crystal StructureD. Dipole Moments; E. Polarography; F. Solubility and Melting Point; G. Spectra; Chapter II. Syntheses from Pyrimidines; 1. Use of 4,5-Diaminopyrimidines (The Traube Synthesis); A. History and General Application; B. Cyclisation with Formic Acid; C. Cyclisation with Dithioformic Acid; D. Cyclisation with Other Carboxylic Acids; E. Cyclisation with Acid Anhydride; F. Cyclisation with Acid Chlorides; G. Cyclisation with Orthoesters and Diethoxymethyl Acetate
TABLE 2. Cyclisation of 4,5-Diamino-6-dimethylamino-2-methylthiopyrimidine to 6-dimethylamino-2-methylthiopurine with OrthoestersH. Cyclisation with Formamide; I. Cyclisation with Other Amides; J. Cyclisation with NN-Dialkylamides and Phosphoryl Chloride; K. Cyclisation with Amidines; L. Cyclisation with Guanidines; M. Cyclisation with Urea; N. Cyclisation with Thiourea; O. Cyclisation with Cyanates, Isocyanates, and Derivatives; P. Cyclisation with lsothiocyanates; Q. Cyclisation with Carbon Dioxide; R. Cyclisation with Carbon Disulphide; S. Cyclisation with Phosgene
T. Cyclisation with Thiophosgene
Record Nr. UNINA-9910144283103321
Lister John H (John Henry)  
New York, : Wiley-Interscience, 1971
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui