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1. |
Record Nr. |
UNISA996556961703316 |
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Autore |
Meixner Sebastian |
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Titolo |
Kellers Welten : Territorien - Ordnungen - Zirkulationen |
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Pubbl/distr/stampa |
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Berlin/Boston : , : Walter de Gruyter GmbH, , 2023 |
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©2023 |
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ISBN |
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Edizione |
[1st ed.] |
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Descrizione fisica |
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1 online resource (294 pages) |
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Collana |
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Gottfried Kellers Moderne ; ; Band 3 |
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Soggetti |
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LITERARY CRITICISM / Modern / 19th Century |
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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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Sommario/riassunto |
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Gottfried Kellers Welten erscheint als dritter Band der Serie "Gottfried Kellers Moderne". Kellers Jahrhundert ist das der Industrialisierung, des Imperialismus und des Kolonialismus. Ob Martin Salander, der sein Vermögen in kolonialen Abenteuern erwirbt, Don Correa, der erst in Portugal und dann in Angola auf Brautschau geht, oder der Grüne Heinrich, der den Imaginationsraum Asien eröffnet: Kellers Texte vermessen die Grenzen zwischen ,Eigenem' und ,Fremdem', lokalisieren das Andere und zirkulieren ihre Figuren genauso wie Waren, Werte und Worte.Der Band leistet einen Beitrag zur internationalen Keller-Forschung, zur Erforschung des Poetischen Realismus und der klassischen Moderne. Er adressiert vor allem Forschende und Studierende, die neue Wege zu Autor und Werk suchen. |
This volume takes Gottfried Keller's century seriously as the century of industrialization, imperialism, and colonialism. Companies of international mercenaries, colonial adventures, transcontinental arranged marriages, and exotic imaginary spaces at the heart of Europe: Keller's texts create territories, orders, and circulations with their worlds, continuously renegotiating the borders between "ownness" and "strangeness." |
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2. |
Record Nr. |
UNINA9910830098803321 |
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Titolo |
Multicomponent reactions [[electronic resource] /] / edited by Jieping Zhu, Hugues Bienaymé |
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Pubbl/distr/stampa |
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Weinheim ; ; [Great Britain], : Wiley-VCH, c2005 |
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ISBN |
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1-280-51964-9 |
9786610519644 |
3-527-60511-8 |
3-527-60424-3 |
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Descrizione fisica |
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1 online resource (486 p.) |
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Classificazione |
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Altri autori (Persone) |
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BienayméHugues |
ZhuJieping |
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Disciplina |
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Soggetti |
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Catalysis |
Chemical reactions |
Chemistry, Organic |
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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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Description based upon print version of record. |
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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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Multicomponent Reactions; Contents; Preface; Contributors; 1 Asymmetric Isocyanide-based MCRs; 1.1 Introduction; 1.2 Racemization Issues; 1.3 Asymmetric Passerini Reactions; 1.3.1 Classical Passerini Reactions; 1.3.2 Passerini-type Reactions; 1.4 Asymmetric Intermolecular Ugi Reactions; 1.4.1 General Remarks; 1.4.2 Chiral Amines; 1.4.2.1 α-Methylbenzylamines; 1.4.2.2 Ferrocenylamines; 1.4.2.3 Glycosylamines; 1.4.2.4 Esters of α-amino Acids; 1.4.3 Chiral Isocyanides, Carboxylic Acids and Carbonyl Compounds; 1.4.4 Chiral Cyclic Imines; 1.5 Asymmetric Intramolecular Ugi Reactions |
1.5.1 With α-Amino Acids1.5.2 With Other Amino Acids; 1.5.3 With Keto Acids; 1.6 Other Asymmetric Isonitrile-based Multicomponent Reactions; 1.6.1 Tandem Ugi or Passerini Reaction/Intramolecular Diels-Alder (IMDA) Cyclizations; 1.6.2 Other Asymmetric Isonitrile-based Multicomponent Reactions; References; 2 Post-condensation Modifications of the Passerini and Ugi Reactions; 2.1 Convertible Isocyanides; 2.2 I-MCR Post-condensation Reactions in Synthesis of |
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Open-chain Products; 2.2.1 Passerini 3CR + O-Deacylation; 2.2.2 Passerini-3CR + N-Deprotection + O N Acyl Migration |
2.2.3 Ugi-4CR + Oxidation2.2.4 Ugi-4CR + Hydrolysis; 2.2.5 Ugi-4CR in Peptide Synthesis; 2.3 I-MCR Post-condensation Reactions in the Synthesis of Heterocycles; 2.3.1 Three-, Four-, and Five-membered Rings and their Benzo-fused Derivatives; 2.3.1.1 Oxiranes and β-Lactams by Passerini-3CR + O- or N-alkylation; 2.3.1.2 β-Lactams and Succinimides by Ugi-4CR + C-Alkylation; 2.3.1.3 Furans, Pyrroles, and Indoles by Passerini-3CR or Ugi-4CR and Knoevenagel Condensation; 2.3.1.4 Butenolides by Passerini-3CR and the Horner-Emmons-Wadsworth Reaction |
2.3.1.5 Pyrroles and γ-Lactams by Ugi-4CR and Hydrolysis2.3.1.6 Indazolinones by Ugi-4CR with N-deprotection and Aromatic Nucleophilic Substitution; 2.3.1.7 Oxazole Derivatives and Imidazoles by Passerini-3CR or Ugi-4CR and Davidson Cyclization; 2.3.1.8 2-Imidazolines, Imidazolidin-2-ones and Benzimidazoles by Ugi-4CR with N-Deprotection and Cyclization; 2.3.1.9 Spiroimidazolones and Spirothioimidohydantoins by Ugi-4CR and Further Transformations; 2.3.2 Six-membered Rings and Their Benzo-fused Systems; 2.3.2.1 Pyridine Derivatives by Ugi-4CR and Aldol-type Condensation |
2.3.2.2 Pyridazine Derivatives by Ugi-4CR and Knoevenagel Condensation2.3.2.3 Phthalazine Derivatives by Ugi-4CR with N-Deprotection and Cyclization; 2.3.2.4 Piperazines and Pyrazin-2-ones by Ugi-4CR and Cyclization; 2.3.2.5 Ketopiperazines, 2,5-Diketopiperazines and Quinoxalines by Ugi-4CR with N-Deprotection and Intramolecular Amide Bond Formation; 2.3.2.6 2,5-Diketopiperazines and Morpholines from Bifunctional Ugi-4CR Reagents; 2.3.3 Seven-membered Rings and Their Benzo-fused Systems; 2.3.3.1 Azepines by Ugi-4CR and Ring-closing Metathesis |
2.3.3.2 1,4-Benzodiazepine-5-ones by Ugi-4CR with N-Deprotection and Aromatic Nucleophilic Substitution |
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Sommario/riassunto |
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In the very first book on this hot topic, the expert editors and authors present a comprehensive overview of these elegant reactions. From the contents:Organoboron compoundsFree-radical mediated multicomponent coupling reactionsApplications in drug discoveryMetal catalyzed reactionsTotal synthesis of natural productsAsymmetric isocyanide-based reactionsThe Biginelli reactionAsymmetric isocyanide-based reactionsThe Domino-Knoevenagel-Hetero-Diels-Alder Re |
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