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 | ||
|
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 | ||
|
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 | ||
|