Keywords:
Heterocyclic compounds.
;
Electronic books.
Type of Medium:
Online Resource
Pages:
1 online resource (413 pages)
Edition:
1st ed.
ISBN:
9780470188057
Series Statement:
Chemistry of Heterocyclic Compounds: a Series of Monographs ; v.10
URL:
https://ebookcentral.proquest.com/lib/geomar/detail.action?docID=469913
Language:
English
Note:
CONDENSED PYRIDAZINE AND PYRAZINE RINGS (Cianolines, Phthalazines, and Quinoxalines) -- Contents -- J. C. E. Simpson, 1908-1952 -- Preface -- PART I. Cinnolines -- I . General Introduction to Cinnoline Derivatives. Preparation and Properties of Cinnoline -- 1. General Introduction to Cinnoline Derivatives -- 2. Preparation and Properties of Cinnoline -- II. 4-Aryl-, 4-Aeyl-, and 4-Carboxycinnolines -- 1. 4-Arylcinnolines -- 2. 4-Acylcinnolines -- 3. 4-Carboxycinnolines (Cinnoline-4-carboxylic Acids) -- III. 4-Methylcinnolines -- IV. 4-Hydroxycinnolines -- 1. Methods of Preparation -- A . Richter Synthesis -- B . Pfannstiel and Janecke Synthesis -- C. Borsehe Synthesis -- 2. Properties -- A. 4-Hydroxycinnolines Other Than 4-Hydroxycinnoline-3-carboxylic Acids -- B. 4-Hydroxycinnoline-3-carboxylic Acids -- V. 4-Chloro-, 4-Alkoxy-, and 4-Phenoxycinnolines -- 1. 4-Chlorocinnolines -- 2. 4-Alkoxycinnoline -- 3. 4-Phenoxycinnoline -- VI. 4-Aminocinnolines -- 1. Primary Amino Compounds -- 2. Secondary Amino Compounds -- A. 4-Arylaminocinnolines -- B. 4-Dialkylaminoalkylaminocinnolines -- C. 4-Hydroxylamino-7-acetylcinnolineoxime -- VII. Cinnoline Quaternary Salts -- A. Preparation -- B. Structure -- C. Reactions -- VIII . Reduced Cinnolines -- 1. Reduced Cinnolines with Nonoxygenated Rings -- A . Dihydrocinnolines -- B . Tetrahydrocinnoline -- C . Hexahydrocinnolines -- 2 . Reduced Cinnolines with Oxygenated Rings -- A . Reduced 3- and 4-Hydroxycinnolines -- B . 1-Methyl -4-keto-1,4-dihydrocinnolines -- C . Methyl 4-Keto-4,6-dihydrocinnolyl-6-nitronates -- D . 3-Acetoxy-2-aryl-6-keto-2,6-dihydrocinnolines -- E. 2-Pheny1-3-keto-hydroxy-2,3,5,6,7,8-hexahydrocinnoline -- IX . Cinnolines Containing Additional Fused Rings -- 1. 3,4--Benzocinnolines -- 2. Tetrahydro-3,4-benzocinnolines -- 3. Other Cinnolines with Additional Aromatic Rings.
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4. Cinnolines Containing Bridged Rings -- 5. Cinnolinea Containing Fused Heterocyclic Rings -- PART II . Phthalazines -- X . Phthalazines Unsubstituted in the Hetero Ring -- 1. Phthalazine -- 2. 5,6-Dihydroxyphthalazine -- XI . 1-Alkyl-, 1-Aryl-, and 1,4-Diarylphthalazines -- 1. 1-Alkyl- and 1-Arylphthalazines -- 2 . 1,4-Diarylphthalazines -- XIl. 1-Hydroxyphthalazines -- A. Preparation -- B . Properties. -- Xlll. Alkyl, Aryl, and Acyl Derivatives of 4-(1-)Hydroxyphthalazines -- 1. O-Derivatives -- 2. N-Derivatives (3-Substituted-4-keto-3,4-hydrophthalazines) -- A . Compounds without a 1-Substituent -- 3Aryl-, 3-Alkyl-, and 3-Aralky-4-keto-3,4-dihydrophthalazines -- B . Compounds with a 1-Substituent -- 3. Derivatives of Unknown Structure -- XIV. 1-Hydroxy-3-aryl-3,4-dihydrophthalazine- 4-acetic Acids -- A . Preparation -- B . Properties -- XV. 3-Aryl-1-ketophthalazines -- A . Preparation -- B. Properties and Reactions -- XVI . Methylated Derivatives of 3-Aryl-1-ketophthalazines -- 1. Derivatives of Compounds Containing a Hydrogen Atom at C4 -- A. 1.Methoxy-4-alkoxy-3-aryl-3,4-dihydrophthalazines -- B. 1-Methoxy-3-arylphthalazinium Perchlorates -- 2. Derivatives of Compounds Containing a Methyl Group at C4 : 1-Methoxy-3-aryl-4-methylene-3,4-dihydrophthalazines -- XVII. 1.4.Dihydroxyphthalazines -- A. Preparation -- B . Properties -- C. Chemiluminescence of Phthalazine Derivatives -- XVIII. Monoalkyl and Monoacyl Derivatives of 1,4-DihydroxyphthaIazines -- 1. O-Derivatives -- 2. X-Derivatives (1-Hydrosy-3-substituted-4-keto-3,4-dihydrophthalazines) -- A. Compounds Containing No Substituent in the Benzene Ring -- B. Compounds Containing a Substituent in the Benzene Ring -- 3. Derivatives of Unknown Structure -- XIX. Dialkyl and Diacyl Derivatives of 1,4-Dihydroxyphthalazines -- 1. 1,4-Derivatives.
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2. 1,3-Derivatives (1-Alkoxy- and 1-Acetoxy-3substituted-4-keto-3,4-dihydrophthalazines -- A. Preparation -- B . Properties -- C. Structure of Alkoxy Compounds -- 3. 2,3-Derivatives -- 4. Derivatives of Unknown Structure -- XX. 1-Halogeno- and 1,4-Dihalogenophthalazines -- 1. 1-Halogenophthalazines -- 2. 1,4-Dihalogenophthalnzines -- XXI. 1-Aminophthalazines -- XXII. Reduced Phthalazines -- 1. 3,4-Dihydrophthalazines -- 2. 1.2,3,4-Tetrahydrophthalazines -- XXIII. Condensed Phthalazines and Azaphthalazines -- 1. 1',2'-3,4-Benziminazolo-3,4-dihydrophthalazines -- 2. Compounds Prepared from 1,4-Diketones -- 3. Miscellaneous Compounds -- 4. Azaphthalazines -- PART III. Quinoxalines -- XXIV. Preparation of Quinoxalines from Primary Aromatic o-Diamines and 1,2-Dicarbonyl Compounds -- XXV. Quinoxalines Unsubstituted in the Hetero Ring -- Quinoxaline -- 6,6'--Diquinoxalyl -- XXVI. Quinoxaline N-Oxides -- A. Preparation -- B. Properties -- XXVII. 2-Hydroxy- and 2,3-Dihydroxyquinoxalines -- 1. 2-Hydroxyquinosalines -- A. Compounds Containing No Additional Sulmtituent in the Hetero Ring -- B. Compounds Containing an additional (C2) Substituent in the Hctero Ring -- Methylation of Hydroxyquinosalines -- 2. 2,3-Dihydroxyquinosnlines -- XXVIII. Quinoxaline-2-aldehydes -- A. Preparation -- B. Properties -- C. 3-Hvdroxyquinosuline-2-aldehyde -- XXIX. Quinoxaline-2-carboxylic and -2,3-dicarboxylic acids -- 1. Quinoxaline-2-carboxylic Acids -- 2. Quinoxaline-2,3-dicarboxylic Acids -- XXX. 2-Chloro- and 2,3-Dichloroquinoxalines -- 1. 2-Chloroquinosaline -- 2. 2,3-Dihalogenoquinoxalines -- A. 2,3-DichIoroquirioxalines -- B. 2,3,-DibromoquinoxaIine -- XXXI. 2-Amino- and 2,3-Diaminoquinoxalines -- 1. 2-Aminoquinoxalines -- A. Primary Amino Compounds -- B. Secondary Amino Compounds -- C. 2-Sulfondmidoquinoxalines -- D. Tertiary Amino Compound. -- 2. Diaminoquinoxalines.
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A. Diprimary Amino Compounds -- 2,3-Diamonoquinoxaline -- 2,3-Diaminoquinoxaline-6-arsonic Acid -- B. Primary-Secondary Amino Campounds -- C. Disecondary Amino Compounds -- XXXII . 2-Alkoxy-, 2,3-Dialkoxy-, and 2,3-Diaryloxyquinoxalines -- 1. 2-Alkoxyquinoxalines -- 2. 2,3-Dialkoxy- and 2,3-Diaryloxyquinoxalines -- XXXIII. 2-Methyl- and 2,3-Dimethylquinoxalines -- 1. 2-Methylquinoxalines -- 2. 2,3-Dimethylquinoxalines -- XXXIV. Quinoxaline Quaternary Salts -- A . Preparation -- B . Properties -- C . Decomposition by Alkali -- D . Quinoxaline Cyanines -- XXXV . Formation of Quinoxalines from Compounds Containing a Furan Ring -- 1. Conversion of 5-Hydroxy-2,5-diphenyl-4-keto-4,5-dihydrofurans and Related Compounds into Quinoxalines -- 2. Conversion of Coumaran-3-ones into Quinoxalines -- A. 2-Hydroxy- and 2-Bromocoumaran-3-ones -- B. Coumaran-2,3-diones -- XXXVI. 2-Polyhydroxyalkylquinoualines -- 1. Synthesis -- 2. Properties and Reactions -- A . General -- B. Decoposition by Alkali -- C. Reactions with Phenylhydrazine -- XXXVII. Reduced Quinoxalines -- 1. 1,2- and 1,4-Dihydroquinoxalines -- A. Compounds Containing No Hydroxyl or Carbonyl Group in the Hetero Ring -- B. Compounds Containing a Hydroxyl or Carbonyl Group in the Hetero Ring -- (a) 1-Substituted-2-keto-1,2-dihydroquinoxalines -- (b) 1,2- and 1,4-Dihydroquinoxalines Having Hydroxyl Groups at C2 or C3 -- 2. 1,2,3,4-Tetrahydroquinoxalines -- A. 1,2,3,4-Tetrahydroquinoxalines Containing No Oxygen Atom attached to the Hetero Ring -- Preparation -- Properties -- Stereoisomerism of 1,2,3,4-Tetrahydroquinoxalines -- 1,4-Endoalkylene-1,2,3,4-tetrahydroquinoxalines -- B. 1,2,3,4-Tetrahydroquinoxalines Containing an Oxygen Atom Attached to the Hetero Ring -- XXXVIII. Condensed Quinoxalines -- 1. Quinoxalines Condensed with Carboxyclic Rings -- A. 5,6-Benzoquinoxalines -- B. 5,6,7,8-Dibenzoquinoxalines.
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C. Glucazidone and Derivatives -- D. Other Condensed Quinoxalines -- 2. Quinoxalines Condensed with Nitrogenous Heterocyclic Rings -- A. Pyrroloquinoxalines -- B. Pyridoquinoxalines -- C. Pyrazoloquinoxalines (Flavazoles) -- D. Glyoxalinoquinoxalines -- E. Triazoloquinoxalines -- F. Pyridamquinoxalines -- XXXIX. Azaquinoxalines -- Appendix I. Ultraviolet Absorption Spectra of Cinnoline and Quinoxaline Derivatives -- Appendix II . Basic Strengths of Cinnoline, Phthalazine, and Quinoxaline Derivatives -- Appendix III . Antibacterial and Parasiticidal Activities of Cinnoline and Quinoxaline Derivatives -- Index.
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