top

  Info

  • Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.

  Info

  • Utilizzare questo link per rimuovere la selezione effettuata.

Biblioteca

MARC Lista (tabellare)
Cinnolines and phthalazines [[electronic resource] ] : supplement II / / D.J. Brown
Cinnolines and phthalazines [[electronic resource] ] : supplement II / / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2005
Descrizione fisica 1 online resource (499 p.)
Disciplina 547.2
547.593
Altri autori (Persone) CastleRaymond N <1916-> (Raymond Nielson)
Collana Chemistry of heterocyclic compounds
Soggetto topico Pyridazines
Organic compounds - Synthesis
Chirality
Soggetto genere / forma Electronic books.
ISBN 1-280-23559-4
9786610235599
0-470-31848-1
0-471-74412-3
0-471-74411-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CINNOLINES AND PHTHALAZINES Supplement II; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES OF CINNOLINES; 1.1 From a Single Carbocyclic Substrate; 1.1.1 By Formation of the N1-C8a Bond; 1.1.2 By Formation of the N1-N2 Bond; 1.1.3 By Formation of the N2-C3 Bond; 1.1.4 By Formation of the C3-C4 Bond; 1.1.5 By Formation of the C4-C4a Bond; 1.2 From a Carbocyclic Substrate and One Synthon; 1.2.1 When the Synthon Supplies N2 of the Cinnoline; 1.2.2 When the Synthon Supplies N1 + N2 of the Cinnoline; 1.2.3 When the Synthon Supplies N2 + C3 of the Cinnoline
1.2.4 When the Synthon Supplies C3 + C4 of the Cinnoline1.2.5 When the Synthon Supplies N1 + N2 + C3 + C4 of the Cinnoline; 1.3 From a Pyridazine Substrate; 1.4 From Other Heteromonocyclic Substrates; 1.5 From Heterobicyclic Substrates; 1.6 From Heteropolycyclic Substrates; 1.7 Glance Index to Typical Cinnolines Derivatives Available by Primary Syntheses; CHAPTER 2 CINNOLINE, ALKYLCINNOLINES, AND ARYLCINNOLINES; 2.1 Cinnoline; 2.1.1 Preparation of Cinnoline and Hydrocinnolines; 2.1.2 Physical Properties of Cinnoline; 2.1.3 Reactions of Cinnoline; 2.2 Alkyl- and Arylcinnolines
2.2.1 Preparation of Alkyl- and Arylcinnolines2.2.2 Reactions of Alkyl- and Arylcinnolines; CHAPTER 3 HALOGENOCINNOLINES; 3.1 Preparation of Halogenocinnolines; 3.2 Reactions of Halogenocinnolines; CHAPTER 4 OXYCINNOLINES; 4.1 Tautomeric Cinnolinones; 4.1.1 Preparation of Tautomeric Cinnolinones; 4.1.2 Reactions of Tautomeric Cinnolinones; 4.1.2.1 Alkylation of Tautomeric Cinnolinones; 4.1.2.2 Other Reactions of Tautomeric Cinnolinones; 4.2 Other Oxycinnolines; CHAPTER 5 THIOCINNOLINES; 5.1 Cinnolinethiones; 5.2 Other Thiocinnolines; CHAPTER 6 NITRO-, AMINO-, AND RELATED CINNOLINES
6.1 Nitrocinnolines6.2 Aminocinnolines and Related Compounds; 6.2.1 Preparation of Amino-, Hydrazino-, and Arylazocinnolines; 6.2.2 Reactions of Amino- and Hydrazinocinnolines; CHAPTER 7 CINNOLINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 Cinnolinecarboxylic Acids; 7.1.1 Preparation of Cinnolinecarboxylic Acids; 7.1.2 Reactions of Cinnolinecarboxylic Acids; 7.2 Cinnolinecarboxylic Esters; 7.3 Cinnolinecarboxamides and Cinnolinecarbohydrazides; 7.4 Cinnolinecarbonitriles; 7.5 Cinnoline Aldehydes and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF PHTHALAZINES
8.1 From a Single Benzene Derivative as Substrate8.1.1 By Formation of the C1-C8a Bond; 8.1.2 By Formation of the C1-N2 Bond; 8.2 From a Benzene Derivative as Substrate and One Synthon; 8.2.1 Where the Synthon Supplies C1 of the Phthalazine; 8.2.2 Where the Synthon Supplies N2 + N3 of the Phthalazine; 8.2.2.1 Using 1,2-Dialkylbenzenes as Substrates; 8.2.2.2 Using 1-Alkyl-2-ketobenzenes as Substrates; 8.2.2.3 Using 1-Alkyl-2-halogenoformylbenzenes as Substrates; 8.2.2.4 Using 1,2-Dialdehydrobenzenes as Substrates; 8.2.2.5 Using 1-Aldehydo-2-ketobenzenes as Substrates
8.2.2.6 Using 1-Aldehydo-2-carboxybenzenes as Substrates
Record Nr. UNINA-9910143556303321
Brown D. J  
Hoboken, N.J., : Wiley, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cinnolines and phthalazines [[electronic resource] ] : supplement II / / D.J. Brown
Cinnolines and phthalazines [[electronic resource] ] : supplement II / / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2005
Descrizione fisica 1 online resource (499 p.)
Disciplina 547.2
547.593
Altri autori (Persone) CastleRaymond N <1916-> (Raymond Nielson)
Collana Chemistry of heterocyclic compounds
Soggetto topico Pyridazines
Organic compounds - Synthesis
Chirality
ISBN 1-280-23559-4
9786610235599
0-470-31848-1
0-471-74412-3
0-471-74411-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CINNOLINES AND PHTHALAZINES Supplement II; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES OF CINNOLINES; 1.1 From a Single Carbocyclic Substrate; 1.1.1 By Formation of the N1-C8a Bond; 1.1.2 By Formation of the N1-N2 Bond; 1.1.3 By Formation of the N2-C3 Bond; 1.1.4 By Formation of the C3-C4 Bond; 1.1.5 By Formation of the C4-C4a Bond; 1.2 From a Carbocyclic Substrate and One Synthon; 1.2.1 When the Synthon Supplies N2 of the Cinnoline; 1.2.2 When the Synthon Supplies N1 + N2 of the Cinnoline; 1.2.3 When the Synthon Supplies N2 + C3 of the Cinnoline
1.2.4 When the Synthon Supplies C3 + C4 of the Cinnoline1.2.5 When the Synthon Supplies N1 + N2 + C3 + C4 of the Cinnoline; 1.3 From a Pyridazine Substrate; 1.4 From Other Heteromonocyclic Substrates; 1.5 From Heterobicyclic Substrates; 1.6 From Heteropolycyclic Substrates; 1.7 Glance Index to Typical Cinnolines Derivatives Available by Primary Syntheses; CHAPTER 2 CINNOLINE, ALKYLCINNOLINES, AND ARYLCINNOLINES; 2.1 Cinnoline; 2.1.1 Preparation of Cinnoline and Hydrocinnolines; 2.1.2 Physical Properties of Cinnoline; 2.1.3 Reactions of Cinnoline; 2.2 Alkyl- and Arylcinnolines
2.2.1 Preparation of Alkyl- and Arylcinnolines2.2.2 Reactions of Alkyl- and Arylcinnolines; CHAPTER 3 HALOGENOCINNOLINES; 3.1 Preparation of Halogenocinnolines; 3.2 Reactions of Halogenocinnolines; CHAPTER 4 OXYCINNOLINES; 4.1 Tautomeric Cinnolinones; 4.1.1 Preparation of Tautomeric Cinnolinones; 4.1.2 Reactions of Tautomeric Cinnolinones; 4.1.2.1 Alkylation of Tautomeric Cinnolinones; 4.1.2.2 Other Reactions of Tautomeric Cinnolinones; 4.2 Other Oxycinnolines; CHAPTER 5 THIOCINNOLINES; 5.1 Cinnolinethiones; 5.2 Other Thiocinnolines; CHAPTER 6 NITRO-, AMINO-, AND RELATED CINNOLINES
6.1 Nitrocinnolines6.2 Aminocinnolines and Related Compounds; 6.2.1 Preparation of Amino-, Hydrazino-, and Arylazocinnolines; 6.2.2 Reactions of Amino- and Hydrazinocinnolines; CHAPTER 7 CINNOLINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 Cinnolinecarboxylic Acids; 7.1.1 Preparation of Cinnolinecarboxylic Acids; 7.1.2 Reactions of Cinnolinecarboxylic Acids; 7.2 Cinnolinecarboxylic Esters; 7.3 Cinnolinecarboxamides and Cinnolinecarbohydrazides; 7.4 Cinnolinecarbonitriles; 7.5 Cinnoline Aldehydes and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF PHTHALAZINES
8.1 From a Single Benzene Derivative as Substrate8.1.1 By Formation of the C1-C8a Bond; 8.1.2 By Formation of the C1-N2 Bond; 8.2 From a Benzene Derivative as Substrate and One Synthon; 8.2.1 Where the Synthon Supplies C1 of the Phthalazine; 8.2.2 Where the Synthon Supplies N2 + N3 of the Phthalazine; 8.2.2.1 Using 1,2-Dialkylbenzenes as Substrates; 8.2.2.2 Using 1-Alkyl-2-ketobenzenes as Substrates; 8.2.2.3 Using 1-Alkyl-2-halogenoformylbenzenes as Substrates; 8.2.2.4 Using 1,2-Dialdehydrobenzenes as Substrates; 8.2.2.5 Using 1-Aldehydo-2-ketobenzenes as Substrates
8.2.2.6 Using 1-Aldehydo-2-carboxybenzenes as Substrates
Record Nr. UNINA-9910830721503321
Brown D. J  
Hoboken, N.J., : Wiley, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Cinnolines and phthalazines [[electronic resource] ] : supplement II / / D.J. Brown
Cinnolines and phthalazines [[electronic resource] ] : supplement II / / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2005
Descrizione fisica 1 online resource (499 p.)
Disciplina 547.2
547.593
Altri autori (Persone) CastleRaymond N <1916-> (Raymond Nielson)
Collana Chemistry of heterocyclic compounds
Soggetto topico Pyridazines
Organic compounds - Synthesis
Chirality
ISBN 1-280-23559-4
9786610235599
0-470-31848-1
0-471-74412-3
0-471-74411-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto CINNOLINES AND PHTHALAZINES Supplement II; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES OF CINNOLINES; 1.1 From a Single Carbocyclic Substrate; 1.1.1 By Formation of the N1-C8a Bond; 1.1.2 By Formation of the N1-N2 Bond; 1.1.3 By Formation of the N2-C3 Bond; 1.1.4 By Formation of the C3-C4 Bond; 1.1.5 By Formation of the C4-C4a Bond; 1.2 From a Carbocyclic Substrate and One Synthon; 1.2.1 When the Synthon Supplies N2 of the Cinnoline; 1.2.2 When the Synthon Supplies N1 + N2 of the Cinnoline; 1.2.3 When the Synthon Supplies N2 + C3 of the Cinnoline
1.2.4 When the Synthon Supplies C3 + C4 of the Cinnoline1.2.5 When the Synthon Supplies N1 + N2 + C3 + C4 of the Cinnoline; 1.3 From a Pyridazine Substrate; 1.4 From Other Heteromonocyclic Substrates; 1.5 From Heterobicyclic Substrates; 1.6 From Heteropolycyclic Substrates; 1.7 Glance Index to Typical Cinnolines Derivatives Available by Primary Syntheses; CHAPTER 2 CINNOLINE, ALKYLCINNOLINES, AND ARYLCINNOLINES; 2.1 Cinnoline; 2.1.1 Preparation of Cinnoline and Hydrocinnolines; 2.1.2 Physical Properties of Cinnoline; 2.1.3 Reactions of Cinnoline; 2.2 Alkyl- and Arylcinnolines
2.2.1 Preparation of Alkyl- and Arylcinnolines2.2.2 Reactions of Alkyl- and Arylcinnolines; CHAPTER 3 HALOGENOCINNOLINES; 3.1 Preparation of Halogenocinnolines; 3.2 Reactions of Halogenocinnolines; CHAPTER 4 OXYCINNOLINES; 4.1 Tautomeric Cinnolinones; 4.1.1 Preparation of Tautomeric Cinnolinones; 4.1.2 Reactions of Tautomeric Cinnolinones; 4.1.2.1 Alkylation of Tautomeric Cinnolinones; 4.1.2.2 Other Reactions of Tautomeric Cinnolinones; 4.2 Other Oxycinnolines; CHAPTER 5 THIOCINNOLINES; 5.1 Cinnolinethiones; 5.2 Other Thiocinnolines; CHAPTER 6 NITRO-, AMINO-, AND RELATED CINNOLINES
6.1 Nitrocinnolines6.2 Aminocinnolines and Related Compounds; 6.2.1 Preparation of Amino-, Hydrazino-, and Arylazocinnolines; 6.2.2 Reactions of Amino- and Hydrazinocinnolines; CHAPTER 7 CINNOLINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 Cinnolinecarboxylic Acids; 7.1.1 Preparation of Cinnolinecarboxylic Acids; 7.1.2 Reactions of Cinnolinecarboxylic Acids; 7.2 Cinnolinecarboxylic Esters; 7.3 Cinnolinecarboxamides and Cinnolinecarbohydrazides; 7.4 Cinnolinecarbonitriles; 7.5 Cinnoline Aldehydes and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF PHTHALAZINES
8.1 From a Single Benzene Derivative as Substrate8.1.1 By Formation of the C1-C8a Bond; 8.1.2 By Formation of the C1-N2 Bond; 8.2 From a Benzene Derivative as Substrate and One Synthon; 8.2.1 Where the Synthon Supplies C1 of the Phthalazine; 8.2.2 Where the Synthon Supplies N2 + N3 of the Phthalazine; 8.2.2.1 Using 1,2-Dialkylbenzenes as Substrates; 8.2.2.2 Using 1-Alkyl-2-ketobenzenes as Substrates; 8.2.2.3 Using 1-Alkyl-2-halogenoformylbenzenes as Substrates; 8.2.2.4 Using 1,2-Dialdehydrobenzenes as Substrates; 8.2.2.5 Using 1-Aldehydo-2-ketobenzenes as Substrates
8.2.2.6 Using 1-Aldehydo-2-carboxybenzenes as Substrates
Record Nr. UNINA-9910877610403321
Brown D. J  
Hoboken, N.J., : Wiley, c2005
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part three Pteridines [[electronic resource] /] / D.J. Brown
Fused pyrimidines . Part three Pteridines [[electronic resource] /] / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa New York, : Wiley & Sons, c1988
Descrizione fisica 1 online resource (762 p.)
Disciplina 547.593
547/.59/05
547/.593
Collana Chemistry of heterocyclic compounds
Soggetto topico Pteridines
Pyrimidines
ISBN 1-282-30165-9
9786612301650
0-470-18689-5
0-470-18837-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES; Contents; List of Tables; CHAPTER I. INTRODUCTION TO THE PTERIDINES; 1. History; 2. Nomenclature; 3. The Basis of Pteridine Chemistry; 4. A General Summary of Pteridine Chemistry; A. Electrophilic Reactions; B. Direct Nucleophilic Substitutions; C. Nucleophilic Metatheses; (1) Replacement of Halogeno Substituents; (a) By Amino or Substituted-Amino Groups; (b) By Hydroxy-Oxo Substituents; (c) By Alkoxy or Aryloxy Groups; (d) By Mercapto- Thioxo Substituents; (e) By Alkylthio or Arylthio Groups; (f) By Sulfo Groups; (g) By Other Groups; (2) Replacement of Alkoxy Groups
(3) Replacement of Alkylthio Groups(4) Replacement of Sulfo Groups; (5) Replacement of Alkylsulfonyl Groups; D. Other Metatheses; (1) Pteridinones to Chloropteridines; (2) Pteridinones to Pteridinethiones; (3) Pteridinethiones to Pteridinones; (4) Pteridinones to Pteridinamines; (5) Pteridinethiones to Pteridinamines or Pteridinimines; (6) Pteridinamines or Pteridinimines to Pteridinones; E. Addition Reactions; (1) Covalent Hydration and Similar Additions; (2) Addition of Phenyllithium; F. Oxidative Reactions; (1) Nuclear Oxidation; (2) Formation of N-Oxides
(3) Oxidative Modification of Groups(a) C- Methyl to C-Formyl; (b) C-Alkyl to C-Acyl; (c) Alkyl to Carboxy; (d) Hydroxyalkyl to Formyl; (e) Hydroxyalkyl to Carboxy; (f) C-Formyl to Carboxy; (g) C-Acyl to Carboxy; (h) Pteridinethiones to Dipteridinyl Disulfides; (i) Thioxo to Sulfeno, Sulfino, or Sulfo; (j) Alkylthio to Alkylsulfinyl or Alkylsulfonyl; G. Reductive Reactions; (1) Nuclear Reduction; (2) Reductive Removal of Groups; (3) Reductive Modification of Groups; (a) C-Formyl to Hydroxymethyl; (b) Carboxy or Alkoxycarbonyl to Hydroxymethyl; (c) C-Acyl to Hydroxyalkyl or Alkyl
(d) Cyano to Aminomethyl(e) Sulfo, Sulfino, or Sulfeno to Thioxo; H. Other Substituent Modifications; (1) Modification of Alkyl Groups; (2) Modification of Oxo Substituents; (3) Modification of Thioxo Substituents; (4) Modification of Amino Groups; (a) Amino to Acylamino; (b) Amino to Alkylideneamino; (c) Amino to Alkylamino; (d) Transamination; (5) Modification of Carboxy and Related Groups; (a) Carboxy to Related Groups; (b) Alkoxycarbonyl to Related Groups; (c) Carbamoyl to Related Groups; (d) Cyano to Related Groups; (e) C-Formyl to Related Groups; (f) C-Acyl to Related Groups
I. DecarboxylationJ. Homolytic C-Acylation; K. Degradation to Pyrazines or Pyrimidines; (1) Degradation of Pteridine; (2) Degradation of Pteridinones; (3) Degradation of Pteridinamines and Pteridinimines; (4) Degradation of Pteridine N-Oxides; 5. Physical Properties of Pteridines; CHAPTER II. PRIMARY SYNTHESES FROM PYRIMIDINES; 1. The Gabriel and Colman Synthesis from 4,5- Pyrimidinediamines and α-Dicarbonyl Compounds; A. Use of the α-Dialdehyde, Glyoxal; B. Use of α-Aldehydoketones; (1) Simple Cases; (2) Cases with One Functional Group; (3) Cases with Two Functional Groups
(a) The 6- or 7-Alkyl-2-amino-4(3H)-pteridinones
Record Nr. UNINA-9910144282903321
Brown D. J  
New York, : Wiley & Sons, c1988
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part three Pteridines [[electronic resource] /] / D.J. Brown
Fused pyrimidines . Part three Pteridines [[electronic resource] /] / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa New York, : Wiley & Sons, c1988
Descrizione fisica 1 online resource (762 p.)
Disciplina 547.593
547/.59/05
547/.593
Collana Chemistry of heterocyclic compounds
Soggetto topico Pteridines
Pyrimidines
ISBN 1-282-30165-9
9786612301650
0-470-18689-5
0-470-18837-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES; Contents; List of Tables; CHAPTER I. INTRODUCTION TO THE PTERIDINES; 1. History; 2. Nomenclature; 3. The Basis of Pteridine Chemistry; 4. A General Summary of Pteridine Chemistry; A. Electrophilic Reactions; B. Direct Nucleophilic Substitutions; C. Nucleophilic Metatheses; (1) Replacement of Halogeno Substituents; (a) By Amino or Substituted-Amino Groups; (b) By Hydroxy-Oxo Substituents; (c) By Alkoxy or Aryloxy Groups; (d) By Mercapto- Thioxo Substituents; (e) By Alkylthio or Arylthio Groups; (f) By Sulfo Groups; (g) By Other Groups; (2) Replacement of Alkoxy Groups
(3) Replacement of Alkylthio Groups(4) Replacement of Sulfo Groups; (5) Replacement of Alkylsulfonyl Groups; D. Other Metatheses; (1) Pteridinones to Chloropteridines; (2) Pteridinones to Pteridinethiones; (3) Pteridinethiones to Pteridinones; (4) Pteridinones to Pteridinamines; (5) Pteridinethiones to Pteridinamines or Pteridinimines; (6) Pteridinamines or Pteridinimines to Pteridinones; E. Addition Reactions; (1) Covalent Hydration and Similar Additions; (2) Addition of Phenyllithium; F. Oxidative Reactions; (1) Nuclear Oxidation; (2) Formation of N-Oxides
(3) Oxidative Modification of Groups(a) C- Methyl to C-Formyl; (b) C-Alkyl to C-Acyl; (c) Alkyl to Carboxy; (d) Hydroxyalkyl to Formyl; (e) Hydroxyalkyl to Carboxy; (f) C-Formyl to Carboxy; (g) C-Acyl to Carboxy; (h) Pteridinethiones to Dipteridinyl Disulfides; (i) Thioxo to Sulfeno, Sulfino, or Sulfo; (j) Alkylthio to Alkylsulfinyl or Alkylsulfonyl; G. Reductive Reactions; (1) Nuclear Reduction; (2) Reductive Removal of Groups; (3) Reductive Modification of Groups; (a) C-Formyl to Hydroxymethyl; (b) Carboxy or Alkoxycarbonyl to Hydroxymethyl; (c) C-Acyl to Hydroxyalkyl or Alkyl
(d) Cyano to Aminomethyl(e) Sulfo, Sulfino, or Sulfeno to Thioxo; H. Other Substituent Modifications; (1) Modification of Alkyl Groups; (2) Modification of Oxo Substituents; (3) Modification of Thioxo Substituents; (4) Modification of Amino Groups; (a) Amino to Acylamino; (b) Amino to Alkylideneamino; (c) Amino to Alkylamino; (d) Transamination; (5) Modification of Carboxy and Related Groups; (a) Carboxy to Related Groups; (b) Alkoxycarbonyl to Related Groups; (c) Carbamoyl to Related Groups; (d) Cyano to Related Groups; (e) C-Formyl to Related Groups; (f) C-Acyl to Related Groups
I. DecarboxylationJ. Homolytic C-Acylation; K. Degradation to Pyrazines or Pyrimidines; (1) Degradation of Pteridine; (2) Degradation of Pteridinones; (3) Degradation of Pteridinamines and Pteridinimines; (4) Degradation of Pteridine N-Oxides; 5. Physical Properties of Pteridines; CHAPTER II. PRIMARY SYNTHESES FROM PYRIMIDINES; 1. The Gabriel and Colman Synthesis from 4,5- Pyrimidinediamines and α-Dicarbonyl Compounds; A. Use of the α-Dialdehyde, Glyoxal; B. Use of α-Aldehydoketones; (1) Simple Cases; (2) Cases with One Functional Group; (3) Cases with Two Functional Groups
(a) The 6- or 7-Alkyl-2-amino-4(3H)-pteridinones
Record Nr. UNINA-9910830071703321
Brown D. J  
New York, : Wiley & Sons, c1988
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Fused pyrimidines . Part three Pteridines / / D.J. Brown
Fused pyrimidines . Part three Pteridines / / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa New York, : Wiley & Sons, c1988
Descrizione fisica 1 online resource (762 p.)
Disciplina 547.593
547/.59/05
547/.593
Collana Chemistry of heterocyclic compounds
Soggetto topico Pteridines
Pyrimidines
ISBN 1-282-30165-9
9786612301650
0-470-18689-5
0-470-18837-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto FUSED PYRIMIDINES; Contents; List of Tables; CHAPTER I. INTRODUCTION TO THE PTERIDINES; 1. History; 2. Nomenclature; 3. The Basis of Pteridine Chemistry; 4. A General Summary of Pteridine Chemistry; A. Electrophilic Reactions; B. Direct Nucleophilic Substitutions; C. Nucleophilic Metatheses; (1) Replacement of Halogeno Substituents; (a) By Amino or Substituted-Amino Groups; (b) By Hydroxy-Oxo Substituents; (c) By Alkoxy or Aryloxy Groups; (d) By Mercapto- Thioxo Substituents; (e) By Alkylthio or Arylthio Groups; (f) By Sulfo Groups; (g) By Other Groups; (2) Replacement of Alkoxy Groups
(3) Replacement of Alkylthio Groups(4) Replacement of Sulfo Groups; (5) Replacement of Alkylsulfonyl Groups; D. Other Metatheses; (1) Pteridinones to Chloropteridines; (2) Pteridinones to Pteridinethiones; (3) Pteridinethiones to Pteridinones; (4) Pteridinones to Pteridinamines; (5) Pteridinethiones to Pteridinamines or Pteridinimines; (6) Pteridinamines or Pteridinimines to Pteridinones; E. Addition Reactions; (1) Covalent Hydration and Similar Additions; (2) Addition of Phenyllithium; F. Oxidative Reactions; (1) Nuclear Oxidation; (2) Formation of N-Oxides
(3) Oxidative Modification of Groups(a) C- Methyl to C-Formyl; (b) C-Alkyl to C-Acyl; (c) Alkyl to Carboxy; (d) Hydroxyalkyl to Formyl; (e) Hydroxyalkyl to Carboxy; (f) C-Formyl to Carboxy; (g) C-Acyl to Carboxy; (h) Pteridinethiones to Dipteridinyl Disulfides; (i) Thioxo to Sulfeno, Sulfino, or Sulfo; (j) Alkylthio to Alkylsulfinyl or Alkylsulfonyl; G. Reductive Reactions; (1) Nuclear Reduction; (2) Reductive Removal of Groups; (3) Reductive Modification of Groups; (a) C-Formyl to Hydroxymethyl; (b) Carboxy or Alkoxycarbonyl to Hydroxymethyl; (c) C-Acyl to Hydroxyalkyl or Alkyl
(d) Cyano to Aminomethyl(e) Sulfo, Sulfino, or Sulfeno to Thioxo; H. Other Substituent Modifications; (1) Modification of Alkyl Groups; (2) Modification of Oxo Substituents; (3) Modification of Thioxo Substituents; (4) Modification of Amino Groups; (a) Amino to Acylamino; (b) Amino to Alkylideneamino; (c) Amino to Alkylamino; (d) Transamination; (5) Modification of Carboxy and Related Groups; (a) Carboxy to Related Groups; (b) Alkoxycarbonyl to Related Groups; (c) Carbamoyl to Related Groups; (d) Cyano to Related Groups; (e) C-Formyl to Related Groups; (f) C-Acyl to Related Groups
I. DecarboxylationJ. Homolytic C-Acylation; K. Degradation to Pyrazines or Pyrimidines; (1) Degradation of Pteridine; (2) Degradation of Pteridinones; (3) Degradation of Pteridinamines and Pteridinimines; (4) Degradation of Pteridine N-Oxides; 5. Physical Properties of Pteridines; CHAPTER II. PRIMARY SYNTHESES FROM PYRIMIDINES; 1. The Gabriel and Colman Synthesis from 4,5- Pyrimidinediamines and α-Dicarbonyl Compounds; A. Use of the α-Dialdehyde, Glyoxal; B. Use of α-Aldehydoketones; (1) Simple Cases; (2) Cases with One Functional Group; (3) Cases with Two Functional Groups
(a) The 6- or 7-Alkyl-2-amino-4(3H)-pteridinones
Record Nr. UNINA-9910876592203321
Brown D. J  
New York, : Wiley & Sons, c1988
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The naphthyridines [[electronic resource] /] / D.J. Brown
The naphthyridines [[electronic resource] /] / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2008
Descrizione fisica 1 online resource (448 p.)
Disciplina 547.59
547/.59/05
547/.593
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyridine - Derivatives
Chemistry
Soggetto genere / forma Electronic books.
ISBN 1-281-37388-5
9786611373887
0-470-18116-8
0-470-18115-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE NAPHTHYRIDINES; Contents; CHAPTER 1 PRIMARY SYNTHESES OF 1,5-NAPHTHYRIDINES; 1.1 From a Single Aliphatic Substrate; 1.2 From a Single Pyridine Substrate; 1.2.1 By Formation of the N1,C2-Bond; 1.2.2 By Formation of the C3,C4-Bond; 1.2.3 By Formation of the C4,C4a-Bond; 1.3 From a Pyridine Substrate with One Synthon; 1.3.1 Where the Synthon Supplies One Atom; 1.3.2 Where the Synthon Supplies Two Atoms; 1.3.3 Where the Synthon Supplies Three Atoms; 1.4 From a Pyridine Substrate and Two Synthons; 1.5 From Other Heterocyclic Substrates
CHAPTER 2 1,5-NAPHTHYRIDINE, ALKYL-1,5- NAPHTHYRIDINES, AND ARYL-1,5- NAPHTHYRIDINES2.1 1,5-Naphthyridine; 2.1.1 Preparation of 1,5-Naphthyridine; 2.1.2 Properties of 1,5-Naphthyridine; 2.1.3 Reactions of 1,5-Naphthyridine; 2.2 Alkyl- and Aryl-1,5-Naphthyridines; 2.2.1 Preparation of Alkyl- and Aryl-1,5-Naphthyridines; 2.2.2 Reactions of Alkyl- and Aryl-1,5-Naphthyridines; CHAPTER 3 HALOGENO-1,5-NAPHTHYRIDINES; 3.1 Preparation of Halogeno-1,5-Naphthyridines; 3.1.1 By Direct Halogenation; 3.1.2 By Halogenolysis of 1,5-Naphthyridinones or the Like
3.1.3 By the Meissenheimer Reaction on 1,5-Naphthyridine N-Oxides3.1.4 By Miscellaneous Procedures; 3.2 Reactions of Halogeno-1,5-Naphthyridines; 3.2.1 Alcoholysis or Phenolysis of Halogeno-1, 5-Naphthyridines; 3.2.2 Aminolysis of Halogeno-1,5-Naphthyridines; 3.2.3 Other Reactions of Halogeno-1,5-Naphthyridines; CHAPTER 4 OXY-1,5-NAPHTHYRIDINES; 4.1 Tautomeric 1,5-Naphthyridinones and Extranuclear Hydroxy-1,5-Naphthyridines; 4.1.1 Preparation of Tautomeric 1,5-Naphthyridinones and the Like; 4.1.2 Reactions of Tautomeric 1,5-Naphthyridinones and the Like
4.2 Alkoxy- and Aryloxy-1,5-Naphthyridines4.3 Nontautomeric 1,5-Naphthyridinones; 4.4 1,5-Naphthyridine N-Oxides; CHAPTER 5 THIO-1,5-NAPHTHYRIDINES; CHAPTER 6 NITRO-, AMINO-, AND RELATED 1,5-NAPHTHYRIDINES; 6.1 Nitro-1,5-Naphthyridines; 6.1.1 Preparation of Nitro-1,5-Naphthyridines; 6.1.2 Reactions of Nitro-1,5-Naphthyridines; 6.2 Amino- and (Substituted-Amino)-1,5-Naphthyridines; 6.2.1 Preparation of Amino-1,5-Naphthyridines; 6.2.2 Reactions of Amino-1,5-Naphthyridines; CHAPTER 7 1,5-NAPHTHYRIDINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 1,5-Naphthyridinecarboxylic Acids
7.2 1,5-Naphthyridinecarboxylic Esters7.3 1,5-Naphthyridinecarboxamides, Carbonitriles, Carbaldehydes, and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF 1,6-NAPHTHYRIDINES; 8.1 By Condensation of Two or More Aliphatic Substrates/Synthons; 8.2 From a Single Pyridine Substrate; 8.3 From a Pyridine Substrate with One Synthon; 8.3.1 Where the Synthon Supplies One Ring Atom; 8.3.2 Where the Synthon Supplies Two Ring Atoms; 8.3.3 Where the Synthon Supplies Three or More Ring Atoms; 8.4 From a Pyridine Substrate with Two or More Synthons; 8.5 From Other Heterocyclic Systems
CHAPTER 9 1,6-NAPHTHYRIDINE, ALKYL-1,6- NAPHTHYRIDINES, AND ARYL-1,6- NAPHTHYRIDINES
Record Nr. UNINA-9910145293303321
Brown D. J  
Hoboken, N.J., : Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The naphthyridines [[electronic resource] /] / D.J. Brown
The naphthyridines [[electronic resource] /] / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2008
Descrizione fisica 1 online resource (448 p.)
Disciplina 547.59
547/.59/05
547/.593
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyridine - Derivatives
Chemistry
ISBN 1-281-37388-5
9786611373887
0-470-18116-8
0-470-18115-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE NAPHTHYRIDINES; Contents; CHAPTER 1 PRIMARY SYNTHESES OF 1,5-NAPHTHYRIDINES; 1.1 From a Single Aliphatic Substrate; 1.2 From a Single Pyridine Substrate; 1.2.1 By Formation of the N1,C2-Bond; 1.2.2 By Formation of the C3,C4-Bond; 1.2.3 By Formation of the C4,C4a-Bond; 1.3 From a Pyridine Substrate with One Synthon; 1.3.1 Where the Synthon Supplies One Atom; 1.3.2 Where the Synthon Supplies Two Atoms; 1.3.3 Where the Synthon Supplies Three Atoms; 1.4 From a Pyridine Substrate and Two Synthons; 1.5 From Other Heterocyclic Substrates
CHAPTER 2 1,5-NAPHTHYRIDINE, ALKYL-1,5- NAPHTHYRIDINES, AND ARYL-1,5- NAPHTHYRIDINES2.1 1,5-Naphthyridine; 2.1.1 Preparation of 1,5-Naphthyridine; 2.1.2 Properties of 1,5-Naphthyridine; 2.1.3 Reactions of 1,5-Naphthyridine; 2.2 Alkyl- and Aryl-1,5-Naphthyridines; 2.2.1 Preparation of Alkyl- and Aryl-1,5-Naphthyridines; 2.2.2 Reactions of Alkyl- and Aryl-1,5-Naphthyridines; CHAPTER 3 HALOGENO-1,5-NAPHTHYRIDINES; 3.1 Preparation of Halogeno-1,5-Naphthyridines; 3.1.1 By Direct Halogenation; 3.1.2 By Halogenolysis of 1,5-Naphthyridinones or the Like
3.1.3 By the Meissenheimer Reaction on 1,5-Naphthyridine N-Oxides3.1.4 By Miscellaneous Procedures; 3.2 Reactions of Halogeno-1,5-Naphthyridines; 3.2.1 Alcoholysis or Phenolysis of Halogeno-1, 5-Naphthyridines; 3.2.2 Aminolysis of Halogeno-1,5-Naphthyridines; 3.2.3 Other Reactions of Halogeno-1,5-Naphthyridines; CHAPTER 4 OXY-1,5-NAPHTHYRIDINES; 4.1 Tautomeric 1,5-Naphthyridinones and Extranuclear Hydroxy-1,5-Naphthyridines; 4.1.1 Preparation of Tautomeric 1,5-Naphthyridinones and the Like; 4.1.2 Reactions of Tautomeric 1,5-Naphthyridinones and the Like
4.2 Alkoxy- and Aryloxy-1,5-Naphthyridines4.3 Nontautomeric 1,5-Naphthyridinones; 4.4 1,5-Naphthyridine N-Oxides; CHAPTER 5 THIO-1,5-NAPHTHYRIDINES; CHAPTER 6 NITRO-, AMINO-, AND RELATED 1,5-NAPHTHYRIDINES; 6.1 Nitro-1,5-Naphthyridines; 6.1.1 Preparation of Nitro-1,5-Naphthyridines; 6.1.2 Reactions of Nitro-1,5-Naphthyridines; 6.2 Amino- and (Substituted-Amino)-1,5-Naphthyridines; 6.2.1 Preparation of Amino-1,5-Naphthyridines; 6.2.2 Reactions of Amino-1,5-Naphthyridines; CHAPTER 7 1,5-NAPHTHYRIDINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 1,5-Naphthyridinecarboxylic Acids
7.2 1,5-Naphthyridinecarboxylic Esters7.3 1,5-Naphthyridinecarboxamides, Carbonitriles, Carbaldehydes, and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF 1,6-NAPHTHYRIDINES; 8.1 By Condensation of Two or More Aliphatic Substrates/Synthons; 8.2 From a Single Pyridine Substrate; 8.3 From a Pyridine Substrate with One Synthon; 8.3.1 Where the Synthon Supplies One Ring Atom; 8.3.2 Where the Synthon Supplies Two Ring Atoms; 8.3.3 Where the Synthon Supplies Three or More Ring Atoms; 8.4 From a Pyridine Substrate with Two or More Synthons; 8.5 From Other Heterocyclic Systems
CHAPTER 9 1,6-NAPHTHYRIDINE, ALKYL-1,6- NAPHTHYRIDINES, AND ARYL-1,6- NAPHTHYRIDINES
Record Nr. UNINA-9910830429103321
Brown D. J  
Hoboken, N.J., : Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The naphthyridines / / D.J. Brown
The naphthyridines / / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa Hoboken, N.J., : Wiley, c2008
Descrizione fisica 1 online resource (448 p.)
Disciplina 547.59
547/.59/05
547/.593
Collana The chemistry of heterocyclic compounds
Soggetto topico Pyridine - Derivatives
Chemistry
ISBN 1-281-37388-5
9786611373887
0-470-18116-8
0-470-18115-X
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE NAPHTHYRIDINES; Contents; CHAPTER 1 PRIMARY SYNTHESES OF 1,5-NAPHTHYRIDINES; 1.1 From a Single Aliphatic Substrate; 1.2 From a Single Pyridine Substrate; 1.2.1 By Formation of the N1,C2-Bond; 1.2.2 By Formation of the C3,C4-Bond; 1.2.3 By Formation of the C4,C4a-Bond; 1.3 From a Pyridine Substrate with One Synthon; 1.3.1 Where the Synthon Supplies One Atom; 1.3.2 Where the Synthon Supplies Two Atoms; 1.3.3 Where the Synthon Supplies Three Atoms; 1.4 From a Pyridine Substrate and Two Synthons; 1.5 From Other Heterocyclic Substrates
CHAPTER 2 1,5-NAPHTHYRIDINE, ALKYL-1,5- NAPHTHYRIDINES, AND ARYL-1,5- NAPHTHYRIDINES2.1 1,5-Naphthyridine; 2.1.1 Preparation of 1,5-Naphthyridine; 2.1.2 Properties of 1,5-Naphthyridine; 2.1.3 Reactions of 1,5-Naphthyridine; 2.2 Alkyl- and Aryl-1,5-Naphthyridines; 2.2.1 Preparation of Alkyl- and Aryl-1,5-Naphthyridines; 2.2.2 Reactions of Alkyl- and Aryl-1,5-Naphthyridines; CHAPTER 3 HALOGENO-1,5-NAPHTHYRIDINES; 3.1 Preparation of Halogeno-1,5-Naphthyridines; 3.1.1 By Direct Halogenation; 3.1.2 By Halogenolysis of 1,5-Naphthyridinones or the Like
3.1.3 By the Meissenheimer Reaction on 1,5-Naphthyridine N-Oxides3.1.4 By Miscellaneous Procedures; 3.2 Reactions of Halogeno-1,5-Naphthyridines; 3.2.1 Alcoholysis or Phenolysis of Halogeno-1, 5-Naphthyridines; 3.2.2 Aminolysis of Halogeno-1,5-Naphthyridines; 3.2.3 Other Reactions of Halogeno-1,5-Naphthyridines; CHAPTER 4 OXY-1,5-NAPHTHYRIDINES; 4.1 Tautomeric 1,5-Naphthyridinones and Extranuclear Hydroxy-1,5-Naphthyridines; 4.1.1 Preparation of Tautomeric 1,5-Naphthyridinones and the Like; 4.1.2 Reactions of Tautomeric 1,5-Naphthyridinones and the Like
4.2 Alkoxy- and Aryloxy-1,5-Naphthyridines4.3 Nontautomeric 1,5-Naphthyridinones; 4.4 1,5-Naphthyridine N-Oxides; CHAPTER 5 THIO-1,5-NAPHTHYRIDINES; CHAPTER 6 NITRO-, AMINO-, AND RELATED 1,5-NAPHTHYRIDINES; 6.1 Nitro-1,5-Naphthyridines; 6.1.1 Preparation of Nitro-1,5-Naphthyridines; 6.1.2 Reactions of Nitro-1,5-Naphthyridines; 6.2 Amino- and (Substituted-Amino)-1,5-Naphthyridines; 6.2.1 Preparation of Amino-1,5-Naphthyridines; 6.2.2 Reactions of Amino-1,5-Naphthyridines; CHAPTER 7 1,5-NAPHTHYRIDINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 1,5-Naphthyridinecarboxylic Acids
7.2 1,5-Naphthyridinecarboxylic Esters7.3 1,5-Naphthyridinecarboxamides, Carbonitriles, Carbaldehydes, and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF 1,6-NAPHTHYRIDINES; 8.1 By Condensation of Two or More Aliphatic Substrates/Synthons; 8.2 From a Single Pyridine Substrate; 8.3 From a Pyridine Substrate with One Synthon; 8.3.1 Where the Synthon Supplies One Ring Atom; 8.3.2 Where the Synthon Supplies Two Ring Atoms; 8.3.3 Where the Synthon Supplies Three or More Ring Atoms; 8.4 From a Pyridine Substrate with Two or More Synthons; 8.5 From Other Heterocyclic Systems
CHAPTER 9 1,6-NAPHTHYRIDINE, ALKYL-1,6- NAPHTHYRIDINES, AND ARYL-1,6- NAPHTHYRIDINES
Record Nr. UNINA-9910877095803321
Brown D. J  
Hoboken, N.J., : Wiley, c2008
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
The pyrazines . Supplement I [[electronic resource] /] / D.J. Brown
The pyrazines . Supplement I [[electronic resource] /] / D.J. Brown
Autore Brown D. J
Pubbl/distr/stampa New York, : John Wiley & Sons, c2002
Descrizione fisica 1 online resource (575 p.)
Disciplina 547.59
547/.59/05
547/.593
Collana Chemistry of heterocyclic compounds
Soggetto topico Pyridazines
Heterocyclic compounds
Soggetto genere / forma Electronic books.
ISBN 1-280-36683-4
9786610366835
0-470-31459-1
0-471-46143-1
0-471-24429-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto THE PYRAZINES Supplement I; The Chemistry of Heterocyclic Compounds Introduction to the Series; Preface; Contents; CHAPTER 1 PRIMARY SYNTHESES FROM ALIPHATIC OR CARBOCYCLIC SYNTHONS; 1.1 From a Single Six-Atom Synthon; 1.1.1 By Completion of the N-C2 Bond; 1.1.1.1 From Appropriate w-Unsaturated Azaalkylamines; 1.1.1.2 From Appropriate w-Halogeno(azaalkylamines); 1.1.1.3 From Appropriate a,w-Diamino(azaalkanes); 1.1.1.4 From Appropriate w-Amino(azaalkanols); 1.1.1.5 From Appropriate w-Amino(azaalkanals); 1.1.1.6 From Appropriate w-Amino(azaalkanones)
1.1.1.7 From Appropriate w-Amino(azaalkanoic Acids)1.1.1.8 From Appropriate w-Amino(azaalkanoic Esters); 1.1.1.9 From Appropriate w-Amino(azaalkanamides); 1.1.1.10 From Appropriate w-Amino(azaalkanenitriles); 1.1.2 By Completion of the C2-C3 Bond; 1.2 From Two Synthons; 1.2.1 By Using a One-Atom and a Five-Atom Synthon; 1.2.1.1 Where the One-Atom Synthon Supplies N1; 1.2.1.2 Where the One-Atom Synthon Supplies C2; 1.2.2 By Using a Two-Atom and a Four-Atom Synthon; 1.2.2.1 Where the Two-Atom Synthon Supplies N1 + C2; 1.2.2.2 Where the Two-Atom Synthon Supplies C2 + C3
1.2.3 By Using Two Three-Atom Synthons1.2.3.1 Where Identical Synthons Provide N1 + C2 + C3 and N4 + C5 + C6; 1.2.3.2 Where Different Synthons Provide N1 + C2 + C3 and N4 + C5 + C6; 1.2.3.3 Where the Synthons Provide N1 + C2 + C6 and C3 + N4 + C5; 1.3 From Three Synthons; 1.4 From Four or More Synthons; 1.4.1 Where Synthons Provide N1, C2 + C3, N4, C5 + C6; 1.4.2 Where Synthons Provide N1 + C2, C3 + N4, C5, C6; 1.4.3 Where Synthons Provide N1 + C2, C3, N4 + C5, C6; 1.5 Appendix: Glance Index to Typical Pyrazine Derivatives Available from Aliphatic or Carbocyclic Synthons
CHAPTER 2 PRIMARY SYNTHESES FROM OTHER HETEROCYCLIC SYSTEMS2.1 Pyrazines from Other Heteromonocyclic Systems; 2.1.1 Azepines as Substrates; 2.1.2 Azetes as Substrates; 2.1.3 Azirines as Substrates; 2.1.4 Azocines as Substrates; 2.1.5 1,2-Diazepines as Substrates; 2.1.6 1,4-Diazepines as Substrates; 2.1.7 Furans as Substrates; 2.1.8 Imidazoles as Substrates; 2.1.9 Isoxazoles as Substrates; 2.1.10 Oxazoles as Substrates; 2.1.11 Oxirenes as Substrates; 2.1.12 Pyridazines as Substrates; 2.1.13 Pyridines as Substrates; 2.1.14 Pyrroles as Substrates; 2.1.15 1,2,5-Selenadiazoles as Substrates
2.1.16 1,2,5-Thiadiazoles as Substrates2.1.17 Thiirenes as Substrates; 2.2 Pyrazines from Heterobicyclic Systems; 2.2.1 1, 2-Diazabicyclo[2.2.0]hexanes as Substrates; 2.2.2 2,4,-Diazabicyclo[3.1.0]hexanes as Substrates; 2.2.3 2,3-Dioxa-5,7-diazabicyclo-[2.2.2]octanes as Substrates; 2.2.4 Furo[2,3-b]pyrazines as Substrates; 2.2.5 Imidazo[1,2-a]pyrazines as Substrates; 2.2.6 Indoles as Substrates; 2.2.7 Isoxazolo[2,3-a]pyrazines as Substrates; 2.2.8 Isoxazolo[4,5-b]pyrazines as Substrates; 2.2.9 Pteridines as Substrates; 2.2.10 Pyrazino[2,3-d][1,3]oxazines as Substrates
2.2.11 Pyrazino[2,3-e][1,3,4]thiadiazines as Substrates
Record Nr. UNINA-9910143176203321
Brown D. J  
New York, : John Wiley & Sons, c2002
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui