Chemistry of Heterocyclic Compounds: Pyridazine and Pyrazine Rings: (Cinnolines, Phthalazines, and Quinoxalines), Volume 5

Content: Chapter I General Introduction to Cinnoline Derivatives. Preparation and Properties of Cinnoline (pages 1–5): Chapter II 4?Aryl?, 4?Acyl?, and 4?Carboxy?Cinnolines (pages 6–12): Chapter III 4?Methylcinnolines (pages 13–15): Chapter IV 4?Hydroxycinnolines (pages 16–28): Chapter V 4?Chloro?, 4?Alkoxy?, and 4?Phenoxycinnolines (pages 29–34): Chapter VI 4?Aminocinnolines (pages 35–38): Chapter VII Cinnoline Quaternary Salts (pages 39–45): Chapter VIII Reduced Cinnolines (pages 46–51): Chapter IX Cinnolines Containing Additional Fused Rings (pages 52–65): Chapter X Phthalazines Unsubstituted in the Hetero Ring (pages 67–71): Chapter XI 1?Alkyl?, 1?Aryl?, and 1,4?Diarylphthalazines (pages 72–77): Chapter XII 1?Hydroxyphthalazines (pages 78–83): Chapter XIII Alkyl, Aryl, and Acyl Derivatives of 4?(1?)Hydroxyphthalazines (pages 84–105): Chapter XIV 1?Hydroxy?3?Aryl?3,4?Dihydrophthalazine?4?Acetic Acids (pages 106–118): Chapter XV 3?Aryl?1?Ketophthalazines (pages 119–129): Chapter XVI Methylated Derivatives of 3?Aryl?1?Ketophthalazines (pages 130–139): Chapter XVII 1,4?Dihydroxyphthalazines (pages 140–156): Chapter XVIII Monoalkyl and Monoacyl Derivatives of 1,4?Dihydroxyphthalazines (pages 157–167): Chapter XIX Dialkyl and Diacyl Derivatives of 1,4?Dihydroxyphthalazines (pages 168–177): Chapter XX 1?Halogeno? and 1,4?Dihalogenophathalazines (pages 178–182): Chapter XXI 1?Aminophthalazines (pages 183–185): Chapter XXII Reduced Phthalazines (pages 186–190): Chapter XXIII Condensed Phthalazines and Azaphthalazines (pages 191–200): Chapter XXIV Preparation of Quinoxalines from Primary Aromatic O?Diamines and 1,2?Dicarbonyl Compounds (pages 201–227): Chapter XXV Quinoxalines Unsubstituted in the Hetero Ring (pages 228–231): Chapter XXVI Quinoxaline N?Oxides (pages 232–234): Chapter XXVII 2?Hydroxy? and 2,3?Dihydroxyquinoxalines (pages 235–245): Chapter XXVIII Quinoxaline?2?Aldehydes (pages 246–249): Chapter XXIX Quinoxaline?2?Carboxylic and ?2,3?Dicarboxylic Acids (pages 250–257): Chapter XXX 2?Chloro? and 2,3?Dichloroquinoxalines (pages 258–262): Chapter XXXI 2?Amino? and 2,3?Diaminoquinoxalines (pages 263–269): Chapter XXXII 2?Alkoxy?, 2,3?Dialkoxy?, and 2,3?Diaryloxyquinoxalines (pages 270–272): Chapter XXXIII 2?Methyl? and 2,3?Dimethylquinoxalines (pages 273–285): Chapter XXXIV Quinoxaline Quaternary Salts (pages 286–292): Chapter XXXV Formation of Quinoxalines from Compounds Containing a Furan Ring (pages 293–299): Chapter XXXVI 2?Polyhydroxyalkaylquinoxalines (pages 300–309): Chapter XXXVII Reduced Quinoxalines (pages 310–331): Chapter XXXVIII Condensed Quinoxalines (pages 332–355): Chapter XXXIX Azaquinoxalines (pages 356–357): The Chemistry of Heterocyclic Compounds, since its inception, has been recognized as a cornerstone of heterocyclic chemistry. Each volume attempts to discuss all aspects – properties, synthesis, reactions, physiological and industrial significance – of a specific ring system. To keep the series up-to-date, supplementary volumes covering the recent literature on each individual ring system have been published. Many ring systems (such as pyridines and oxazoles) are treated in distinct books, each consisting of separate volumes or parts dealing with different individual topics. With all authors are recognized authorities, the Chemistry of Heterocyclic Chemistry is considered worldwide as the indispensable resource for organic, bioorganic, and medicinal chemists. A volume in the Chemistry of Heterocyclic Compounds series, this book provides a summary of the chemistry of each of the six naphthyridine systems along with tables of known simple derivatives with original references. Each of the six naphthyridine systems are described in valuable detail and coverage includes: Primary synthetic methods from non-naphthyridine substrates; Chemistry and properties of the parent heterocycle and its simple alkyl derivatives; Formation and reactions of halogeno derivatives; formation and reactions of hydroxy, oxo, alkoxy, and related derivatives