LEADER 05321nam 2200649Ia 450 001 9910144289203321 005 20170814190100.0 010 $a1-282-30140-3 010 $a9786612301407 010 $a0-470-18655-0 010 $a0-470-18805-7 035 $a(CKB)1000000000376514 035 $a(EBL)469913 035 $a(OCoLC)609848406 035 $a(SSID)ssj0000388223 035 $a(PQKBManifestationID)11938150 035 $a(PQKBTitleCode)TC0000388223 035 $a(PQKBWorkID)10411435 035 $a(PQKB)11327748 035 $a(MiAaPQ)EBC469913 035 $a(PPN)22224268X 035 $a(EXLCZ)991000000000376514 100 $a20750817d1953 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCondensed pyridazine and pyrazine rings$b[electronic resource] /$fJ.C.E. Simpson 210 $aNew York $cWiley$d1953 215 $a1 online resource (413 p.) 225 1 $aChemistry of heterocyclic compounds ;$v5 300 $aDescription based upon print version of record. 311 $a0-470-37620-1 320 $aIncludes bibliographical references and index. 327 $aCONDENSED PYRIDAZINE AND PYRAZINE RINGS (Cianolines, Phthalazines, and Quinoxalines); J. C. E. Simpson, 1908-1952; Preface; Contents; 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 327 $aB . Pfannstiel and Janecke SynthesisC. 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 327 $a1. Reduced Cinnolines with Nonoxygenated RingsA . 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 327 $a4. Cinnolines Containing Bridged Rings5. 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 327 $a3Aryl-, 3-Alkyl-, and 3-Aralky-4-keto-3,4-dihydrophthalazinesB . 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 327 $a2. Derivatives of Compounds Containing a Methyl Group at C4 : 1-Methoxy-3-aryl-4-methylene-3,4-dihydrophthalazines 330 $aA volume in the Chemistry of Heterocyclic Compounds series, this book provides a summary of the chemistry of each of the six naphthyridine systems along with tables of known simple derivatives with original references. Each of the six naphthyridine systems are described in valuable detail and coverage includes: Primary synthetic methods from non-naphthyridine substrates; Chemistry and properties of the parent heterocycle and its simple alkyl derivatives; Formation and reactions of halogeno derivatives; formation and reactions of hydroxy, oxo, alkoxy, and related derivatives. 410 0$aChemistry of heterocyclic compounds ;$v5. 606 $aHeterocyclic compounds 606 $aPyridazines 615 0$aHeterocyclic compounds. 615 0$aPyridazines. 676 $a547.1 676 $a547/.59/05 700 $aSimpson$b J. C. E$0960849 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910144289203321 996 $aCondensed pyridazine and pyrazine rings$92178175 997 $aUNINA