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Record Nr. |
UNINA9910511638903321 |
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Titolo |
Textual strategies in ancient war narrative : : Thermopylae, Cannae and beyond / / edited by Lidewij van Gils, Irene J.F. de Jong, Caroline Kroon |
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Pubbl/distr/stampa |
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Leiden ; ; Boston : , : Brill, , 2018 |
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ISBN |
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90-04-38334-4 |
90-04-38333-6 |
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Descrizione fisica |
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1 online resource (409 pages) |
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Collana |
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Amsterdam studies in classical philology ; ; volume 29 |
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Disciplina |
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Soggetti |
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War in literature |
Thermopylae, Battle of, Greece, 480 B.C |
Cannae, Battle of, Italy, 216 B.C |
Electronic books. |
Greece History, Military |
Rome History, Military |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Nota di bibliografia |
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Includes bibliographical references and index. |
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Nota di contenuto |
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Front Matter -- Copyright Page -- Preface -- Notes on Contributors -- Introduction / Lidewij van Gils , Irene de Jong and Caroline Kroon -- Thermopylae -- Thermopylae: Herodotus versus the Legend / Hans van Wees -- A Narratological Comparison of Herodotus and Diodorus on Thermopylae / Mathieu de Bakker -- Narrative and Identity in Thermopylae (Herodotus 7.201–7.239) / Antonis Tsakmakis -- Herodotus’ Handling of (Narratological) Time in the Thermopylae Passage / Irene de Jong -- Herodotus and Thucydides: Distance and Immersion / Rutger Allan -- Cannae -- Livy on Cannae: a Literary Overview / Stephen Oakley -- Discourse-Linguistic Strategies in Livy’s Account of the Battle at Cannae / Lidewij van Gils and Caroline Kroon -- Who Knows What Will Happen Next? Livy’s fraus Punica from a Literary Point of View / Dennis Pausch -- Livy’s Use of Spatial References in the Cannae Episode: from Structure to Strategy / Lidewij van Gils -- ET RATIO ET RES: Characterization of Roman Conduct through Speech Representation in the Battle of Cannae / Michel Buijs -- Words When It’s Time for Action: Representations of Speech and |
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Thought in the Battles of Cannae and Zama / Suzanne Adema -- Beyond Thermopylae and Cannae -- Thermopylae and Cannae: How One Battle Narrative Enriches Another / Mathieu de Bakker and Michiel van der Keur -- The Great and the Small: Thermopylae and Sphacteria / Adriaan Rademaker -- Force, Frequency and Focalisation: the Function of Similes in the Battle-Narrative of Vergil, Aeneid 10 / Stephen Harrison -- Parallel Plotlines: the Function of Similes in the Battle Narrative of Vergil, Aeneid 10 (2) / Michiel van der Keur -- Back Matter -- Index. |
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Sommario/riassunto |
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In this collected volume fourteen experts in the fields of Classics and Ancient History study the textual strategies used by Herodotus and Livy when recounting the disastrous battles at Thermopylae and Cannae. Literary, linguistic and historical approaches are used (often in combination) in order to enhance and enrich the interpretation of the accounts, which for obvious reasons confronted the authors with a special challenge. Chapters drawing a comparison with other battle narratives and with other genres help to establish genre-specific elements in ancient historiography, and draw attention to the particular techniques employed by Herodotus and Livy in their war narratives. |
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2. |
Record Nr. |
UNINA9911019638503321 |
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Autore |
Brown D. J |
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Titolo |
The naphthyridines / / D.J. Brown |
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Pubbl/distr/stampa |
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Hoboken, N.J., : Wiley, c2008 |
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ISBN |
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9786611373887 |
9781281373885 |
1281373885 |
9780470181164 |
0470181168 |
9780470181157 |
047018115X |
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Descrizione fisica |
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1 online resource (448 p.) |
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Collana |
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The chemistry of heterocyclic compounds ; ; 63 |
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Disciplina |
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547.59 |
547/.59/05 |
547/.593 |
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Soggetti |
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Pyridine - Derivatives |
Chemistry |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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"An Interscience publication." |
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Nota di bibliografia |
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Includes bibliographical references (p. 295-336) and index. |
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Nota di contenuto |
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THE NAPHTHYRIDINES; Contents; CHAPTER 1 PRIMARY SYNTHESES OF 1,5-NAPHTHYRIDINES; 1.1 From a Single Aliphatic Substrate; 1.2 From a Single Pyridine Substrate; 1.2.1 By Formation of the N1,C2-Bond; 1.2.2 By Formation of the C3,C4-Bond; 1.2.3 By Formation of the C4,C4a-Bond; 1.3 From a Pyridine Substrate with One Synthon; 1.3.1 Where the Synthon Supplies One Atom; 1.3.2 Where the Synthon Supplies Two Atoms; 1.3.3 Where the Synthon Supplies Three Atoms; 1.4 From a Pyridine Substrate and Two Synthons; 1.5 From Other Heterocyclic Substrates |
CHAPTER 2 1,5-NAPHTHYRIDINE, ALKYL-1,5- NAPHTHYRIDINES, AND ARYL-1,5- NAPHTHYRIDINES2.1 1,5-Naphthyridine; 2.1.1 Preparation of 1,5-Naphthyridine; 2.1.2 Properties of 1,5-Naphthyridine; 2.1.3 Reactions of 1,5-Naphthyridine; 2.2 Alkyl- and Aryl-1,5-Naphthyridines; 2.2.1 Preparation of Alkyl- and Aryl-1,5- |
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Naphthyridines; 2.2.2 Reactions of Alkyl- and Aryl-1,5-Naphthyridines; CHAPTER 3 HALOGENO-1,5-NAPHTHYRIDINES; 3.1 Preparation of Halogeno-1,5-Naphthyridines; 3.1.1 By Direct Halogenation; 3.1.2 By Halogenolysis of 1,5-Naphthyridinones or the Like |
3.1.3 By the Meissenheimer Reaction on 1,5-Naphthyridine N-Oxides3.1.4 By Miscellaneous Procedures; 3.2 Reactions of Halogeno-1,5-Naphthyridines; 3.2.1 Alcoholysis or Phenolysis of Halogeno-1, 5-Naphthyridines; 3.2.2 Aminolysis of Halogeno-1,5-Naphthyridines; 3.2.3 Other Reactions of Halogeno-1,5-Naphthyridines; CHAPTER 4 OXY-1,5-NAPHTHYRIDINES; 4.1 Tautomeric 1,5-Naphthyridinones and Extranuclear Hydroxy-1,5-Naphthyridines; 4.1.1 Preparation of Tautomeric 1,5-Naphthyridinones and the Like; 4.1.2 Reactions of Tautomeric 1,5-Naphthyridinones and the Like |
4.2 Alkoxy- and Aryloxy-1,5-Naphthyridines4.3 Nontautomeric 1,5-Naphthyridinones; 4.4 1,5-Naphthyridine N-Oxides; CHAPTER 5 THIO-1,5-NAPHTHYRIDINES; CHAPTER 6 NITRO-, AMINO-, AND RELATED 1,5-NAPHTHYRIDINES; 6.1 Nitro-1,5-Naphthyridines; 6.1.1 Preparation of Nitro-1,5-Naphthyridines; 6.1.2 Reactions of Nitro-1,5-Naphthyridines; 6.2 Amino- and (Substituted-Amino)-1,5-Naphthyridines; 6.2.1 Preparation of Amino-1,5-Naphthyridines; 6.2.2 Reactions of Amino-1,5-Naphthyridines; CHAPTER 7 1,5-NAPHTHYRIDINECARBOXYLIC ACIDS AND RELATED DERIVATIVES; 7.1 1,5-Naphthyridinecarboxylic Acids |
7.2 1,5-Naphthyridinecarboxylic Esters7.3 1,5-Naphthyridinecarboxamides, Carbonitriles, Carbaldehydes, and Ketones; CHAPTER 8 PRIMARY SYNTHESES OF 1,6-NAPHTHYRIDINES; 8.1 By Condensation of Two or More Aliphatic Substrates/Synthons; 8.2 From a Single Pyridine Substrate; 8.3 From a Pyridine Substrate with One Synthon; 8.3.1 Where the Synthon Supplies One Ring Atom; 8.3.2 Where the Synthon Supplies Two Ring Atoms; 8.3.3 Where the Synthon Supplies Three or More Ring Atoms; 8.4 From a Pyridine Substrate with Two or More Synthons; 8.5 From Other Heterocyclic Systems |
CHAPTER 9 1,6-NAPHTHYRIDINE, ALKYL-1,6- NAPHTHYRIDINES, AND ARYL-1,6- NAPHTHYRIDINES |
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Sommario/riassunto |
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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. |
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