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 | ||
|
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-9910830142903321 |
Lister John H (John Henry) | ||
New York, : Wiley-Interscience, 1971 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|