|
|
|
|
|
|
|
|
|
1. |
Record Nr. |
UNINA9910144284903321 |
|
|
Autore |
Brown D. J |
|
|
Titolo |
Quinazolines Supplement I [[electronic resource] /] / D.J. Brown |
|
|
|
|
|
Pubbl/distr/stampa |
|
|
New York, : J. Wiley, c1996 |
|
|
|
|
|
|
|
ISBN |
|
1-282-30612-X |
9786612306129 |
0-470-18795-6 |
0-470-18894-4 |
|
|
|
|
|
|
|
|
Descrizione fisica |
|
1 online resource (760 p.) |
|
|
|
|
|
|
Collana |
|
Chemistry of heterocyclic compounds ; ; v. 55 |
|
|
|
|
|
|
Disciplina |
|
547.593 |
547/.59/05 |
547/.593 |
|
|
|
|
|
|
|
|
Soggetti |
|
Quinazoline |
Heterocyclic compounds |
Electronic books. |
|
|
|
|
|
|
|
|
Lingua di pubblicazione |
|
|
|
|
|
|
Formato |
Materiale a stampa |
|
|
|
|
|
Livello bibliografico |
Monografia |
|
|
|
|
|
Note generali |
|
"An Interscience publication." |
|
|
|
|
|
|
Nota di bibliografia |
|
Includes bibliographical references (p. 607-681) and index. |
|
|
|
|
|
|
Nota di contenuto |
|
QUINAZOLINES; Contents; CHAPTER 1. PRIMARY SYNTHESES; 1.1 From a Single Benzene Substrate; 1.1.1 By Formation of the 1,2-Bond; 1.1.2 By Formation of the 1,Sa-Bond; 1.1.3 By Formation of the 2,3-Bond; 1.1.3.1. From o-Acylaminobenzamides; 1.1.3.2 From o-Acylaminobenzamide Oximes; 1.1.3.3 From o-(A1koxycarbonylamino)-benzamides; 1.1.3.4 From o-Ureidobenzamides; 1.1.3.5 From o-(Benzylideneamino)benz-amides; 1.1.3.6 From o-Acylaminobenzonitriles; 1.1.3.7 From o-(Substituted Methylene-amin0)benzonitriles; 1.1.3.8 From o-(Acylamino)benzaldehyde Hydrazones and Related Substrates |
1.1.3.9 From Miscellaneous Substrates1.1.4 By Formation of the 3,4-Bond; 1.1.4.1 From o-Ureidobenzoic Acids; 1.1.4.2 From o-Ureidobenzoic Esters; 1.1.4.3 From o-Ureidobenzoyl Chlorides or o-Ureidobenzamides; 1.1.4.4 From o-Ureidobenzonitriles; 1.1.4.5 From o- U reidobenzaldehyde Derivatives and Related Substrates; 1.1.4.6 From o-(Aminomethy1eneamino)-benzoic Acids, Esters, or Amides; 1.1.4.7 From Miscellaneous Substrates; 1.1.5 By Formation of the 4,4a- |
|
|
|
|
|
|
|
|
|
|
|
Bond; 1.2 From a Benzene Substrate and Ancillary Synthon(s); 1.2.1 Where the Synthon Supplies N1; 1.2.2 Where the Synthon Supplies C2 |
1.2.2.1 The Use of Carboxylic Acids and Related Synthons1.2.2.2 The Use of Carbonic Acid-Derived Synthons; 1.2.3 Where the Synthon Supplies N3; 1.2.3.1 With o-Acylaminobenzoic Acids as Substrates; 1.2.3.2 With o-Acylaminobenzoic Esters as Substrates; 1.2.3.3 With o-Acylaminobenzonitriles as Substrates; 1.2.3.4 With o-Acylaminobenzaldehydes or Related Ketones as Substrates; 1.2.3.5 With o-(Alkoxycarbony1amino)-benzoic Esters or Related Ketones as Substrates; 1.2.3.6 With o-(Substituted Methylene-amino)benzoic Esters or Related Ketones as Substrates |
1.2.3.7 With o-(Substituted Methylene-amin0)benzonitriles as Substrates1.2.3.8 With o-Isocyanatobenzoyl Chlorides as Substrates; 1.2.3.9 With o-Isocyanatobenzoic Esters and Related Ketones or Nitriles as Substrates; 1.2.3.10 With o-Cyanoamino- or o-Ureido-benzoic Esters and Related Ketones or Nitriles as Substrates; 1.2.3.11 With Miscellaneous Substrates; 1.2.4 Where the Synthon Supplies C4; 1.2.5 Where the Synthon(s) Supply N1 + C2; 1.2.6 Where the Synthon(s) Supply C2 + N3; 1.2.6.1 With o-Aminobenzoic Acids as Substrates; 1.2.6.2 With o-Aminobenzoic Esters as Substrates |
1.2.6.3 With o-Aminobenzarnides as Substrates1.2.6.4 With o-Arninobenzonitriles as Substrates; 1.2.6.5 With o-Aminobenzaldehydes or Related Ketones as Substrates; 1.2.6.6 With Miscellaneous o-Disubstitu-ted Benzenes as Substrates; 1.2.7 Where the Synthon(s) Supply N3 + C4; 1.2.7.1 With N-Acylanilines as Substrates; 1.2.7.2 With N-(α-Chloromethy1ene)ani-lines or Related Compounds as Substrates; 1.2.7.3 With Other Aniline Derivatives as Substrates; 1.2.8 Where the Synthon(s) Supply N1+C2 + N3; 1.2.8.1 With o-Halogeno or o-Alkoxyben-zonitriles as Substrates |
1.2.8.2 With o-Substituted Benzoic Esters or Related Compounds as Substrates |
|
|
|
|
|
|
Sommario/riassunto |
|
Primary Syntheses. Quinazoline, Alkylquinazolines, and Arylquinazolines. Halogenoquinazolines. Oxyquinazolines. Thioquinazolines. Nitro, Amino, and Related Quinazolines. Quinazolinecarboxylic Acids and Related Derivatives. Appendix. References. Index. |
|
|
|
|
|
|
|
| |