Onbehagen in de schriftcultuur [[electronic resource] ] : leesrevoluties in de negentiende en twintigste eeuw / / Adriaan van der Weel

• Record Nr.: UNINA9910480661503321
• Autore: Weel Adriaan van der
• Pubbl/distr/stampa: Amstserdam, : Leiden University Press, 2007
• ISBN: 1-281-99135-X; 9786611991357; 90-485-0999-8
• Descrizione fisica: 1 online resource (33 p.)
• Collana: LUP oraties
• Disciplina: 943.009045
• Soggetti: Book industries and trade - History - 19th century; Book industries and trade - History - 20th century; Books - History; Electronic books.
• Lingua di pubblicazione: Olandese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references (p. 31-32).
• Sommario/riassunto: Adriaan van der Weel beschrijft de opkomst van de grote commerciële markt voor vermaakslectuur in de negentiende eeuw. Hij presenteert hier een nieuwe, boekhistorische kijk op de processen van democratisering en emancipatie in de Nederlandse samenleving van de negentiende eeuw. Nederland leerde in de negentiende eeuw massaal lezen door allerlei onderwijsvernieuwingen en initiatieven om het volk te verheffen. Als gevolg daarvan ontstond een grote commerciële markt voor ontspanningslectuur. Over de manier waarop die tot stand kwam en functioneerde is weinig bekend. Dat die markt bediend werd doo

Name reactions in heterocyclic chemistry [[electronic resource] /] / edited by Jie-Jack Li

• Record Nr.: UNINA9910830429203321
• Pubbl/distr/stampa: Hoboken, N.J., : Wiley-Interscience, c2005
• ISBN: 1-280-27303-8; 9786610273034; 0-470-35202-7; 0-471-70414-8; 0-471-70415-6
• Descrizione fisica: 1 online resource (579 p.)
• Collana: Comprehensive Name Reactions ; ; v.3
• Altri autori (Persone): LiJie Jack
• Disciplina: 547.59; 547.590459
• Soggetti: Heterocyclic chemistry; Chemical reactions
• Lingua di pubblicazione: Inglese
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references and index.
• Nota di contenuto: Name Reactions in Heterocyclic Chemistry; Table of Contents; Foreword; Preface; Acronyms and abbreviations; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Epoxides and Aziridines; 1.1 Corey-Chaykovsky reaction; 1.2 Darzens glycidic ester condensation; 1.3 Hoch-Campbell aziridine synthesis; 1.4 Jacobsen-Katsuki epoxidation; 1.5 Paterno-Buchi reaction; 1.6 Sharpless-Katsuki epoxidation; 1.7 Wenker aziridine synthesis; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Barton-Zard reaction; 2.2 Knorr and Paal-Knorr pyrrole syntheses; 2.3 Hofmann-Loffler-Freytag reactionChapter 3 Indoles; 3.1 Bartoli indole synthesis; 3.2 Batcho-Leimgruber indole synthesis; 3.3 Bucherer carbazole synthesis; 3.4 Fischer indole synthesis; 3.5 Gassman indole synthesis; 3.6 Graebe-Ullman carbazole synthesis; 3.7 Hegedus indole synthesis; 3.8 Madelung indole synthesis; 3.9 Nenitzescu indole synthesis; 3.10 Reissert indole synthesis; Chapter 4 Furans; 4.1 Feist-Benary furan synthesis; 4.2 Paal-Knorr furan synthesis; Chapter 5 Thiophenes; 5.1 Fiesselmann thiophene synthesis; 5.2 Gewald ; aminothiophene synthesis; 5.3 Hinsberg synthesis of thiophene derivatives5.4 Paal thiophene synthesis; Chapter 6 Oxazoles and Isoxazoles; 6.1 Claisen isoxazole synthesis; 6.2 Cornforth rearrangement; 6.3 Erlenmeyer-Plochl azlactone synthesis; 6.4 Fischer oxazole synthesis; 6.5 Meyers oxazoline method; 6.6 Robinson-Gabriel synthesis; 6.7 van Leusen oxazole Synthesis; Chapter 7 Other Five-Membered Heterocycles; 7.1 Auwers flavone synthesis; 7.2 Bucherer-Bergs reaction; 7.3 Cook-Heilbron 5-amino-thiazole synthesis; 7.4 Hurd-Mori 1,2,3-thiadiazole synthesis; 7.5 Knorr pyrazole synthesis; PART 3 SIX-MEMBERED HETEROCYCLES; Chapter 8 Pyridines8.1 Preparation via condensation reactions; 8.1.1 Hantzsch (dihydro)-pyridine synthesis; 8.1.1.1 Description; 8.1.1.2 Historical perspective; 8.1.1.3 Mechanism; 8.1.1.4 Variations; 8.1.1.4.1 Guareschi-Thorpe pyridine synthesis; 8.1.1.4.2 Chichibabin (Tschitschibabin) pyridine synthesis; 8.1.1.4.3 Bohlmann-Rahtz pyridine synthesis; 8.1.1.4.4 Krohnke pyridine synthesis; 8.1.1.4.5 Petrenko-Kritschenko piperidone synthesis; 8.1.1.5 Improvements or modifications; 8.1.1.6 Experimental; 8.1.1.6.1 Three-component coupling; 8.1.1.6.2 Two-component coupling; 8.1.1.7 References; 8.2 Preparation via cycloaddition reactions8.2.1 Boger reaction; 8.3 Preparation via rearrangement reactions; 8.3.1 Boekelheide reaction; 8.3.2 Ciamician-Dennstedt rearrangement; 8.4 Zincke reaction; Chapter 9 Quinolines and Isoquinolines; 9.1 Bischler-Napieralski reaction; 9.2 Camps quinoline synthesis; 9.3 Combes quinoline synthesis; 9.4 Conrad-Limpach reaction; 9.5 Doebner quinoline synthesis; 9.6 Friedlander synthesis; 9.7 Gabriel-Colman rearrangement; 9.8 Gould-Jacobs reaction; 9.9 Knorr quinoline synthesis; 9.10 Meth-Cohn quinoline synthesis; 9.11 Pfitzinger quinoline synthesis; 9.12 Pictet-Gams isoquinoline synthesis
• Sommario/riassunto: Covers important name reactions relevant to heterocyclic chemistry The field of heterocyclic chemistry has long presented a special challenge for chemists. Because of the enormous amount and variety of information, it is often a difficult topic to cover for undergraduate and graduate chemistry students, even in simplified form. Yet the chemistry of heterocyclic compounds and methods for their synthesis form the bedrock of modern medicinal chemical and pharmaceutical research. Thus there is a great need for high quality, up-to-date, and authoritative books on heterocyclic synthesis helpful to