01804nam1 22003733i 450 VEA006187620231121125919.020111215f ||||0itac50 baenggbz01i xxxe z01n˜The œillustrated Beatus˜a œcorpus of the illustrations of the Commentary on the ApocalypseJohn WilliamsLondonH. Millerv.34 cm.001BVE01448932001 ˜3: The œtenth and eleventh centuriesJohn Williams3001MIL06092362001 ˜5: The œtwelfth and thirteenth centuriesJohn Williams5001VEA00618752001 ˜1: œIntroductionJohn Williams1001VEA00618782001 ˜2: The œninth and tenth centuriesJohn Williams2001VEA01427682001 ˜4: The œeleventh and twelfth centuriesJohn Williams4Beato : di Liebana <santo> . Commentarius in ApocalypsinManoscritti miniatiFIRBVEC029006I745.67Disegno e arti decorative. Miniatura di manoscritti e libri20745.67Disegno e arti decorative. Miniatura di manoscritti e libri21Williams, John <1928-2015>PALV0506720701440294ITIT-0120111215IT-FR0084 IT-FR0017 Biblioteca Del Monumento Nazionale Di MontecassinoFR0084 v. 4Biblioteca umanistica Giorgio ApreaFR0017 VEA0061876Biblioteca umanistica Giorgio Aprea 52SALA BRAGAS.A. 83.5 52SALA BRAGAS.A. 83.4 52SALA BRAGAS.A. 83.3 52SALA BRAGAS.A. 83.2 52SALA BRAGAS.A. 83.15 25 52Illustrated Beatus3643188UNICAS05437nam 2200709Ia 450 991101913630332120200520144314.09786612301407978128230140512823014039780470186558047018655097804701880570470188057(CKB)1000000000376514(EBL)469913(OCoLC)609848406(SSID)ssj0000388223(PQKBManifestationID)11938150(PQKBTitleCode)TC0000388223(PQKBWorkID)10411435(PQKB)11327748(MiAaPQ)EBC469913(PPN)22224268X(Perlego)2773805(EXLCZ)99100000000037651420750817d1953 uy 0engur|n|---|||||txtccrCondensed pyridazine and pyrazine rings /J.C.E. SimpsonNew York Wiley19531 online resource (413 p.)Chemistry of heterocyclic compounds ;5Description based upon print version of record.9780470376201 0470376201 Includes bibliographical references and index.CONDENSED 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 SynthesisB . 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 Cinnolines1. 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 Rings4. 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-Substituent3Aryl-, 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 Perchlorates2. Derivatives of Compounds Containing a Methyl Group at C4 : 1-Methoxy-3-aryl-4-methylene-3,4-dihydrophthalazinesA 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. Chemistry of heterocyclic compounds ;5.Heterocyclic compoundsPyridazinesHeterocyclic compounds.Pyridazines.547.1547/.59/05Simpson J. C. E1841981MiAaPQMiAaPQMiAaPQBOOK9911019136303321Condensed pyridazine and pyrazine rings4421909UNINA