Name reactions in heterocyclic chemistry II / / edited by Jie Jack Li ; foreword by E.J. Corey

• Pubblicazione: Hoboken, N.J., : Wiley, c2011
• Edizione: 1st ed.
• Descrizione fisica: 1 online resource (706 p.)
• Disciplina: 547.2
• Soggetto topico: Heterocyclic chemistry; Chemical reactions
• Altri autori: LiJie Jack CoreyE. J
• 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 II; Contents; Foreword; Preface; Contributing Authors; PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES; Chapter 1 Aziridines and Epoxides; 1.1 Blum Aziridine Synthesis; 1.2 Gabriel-Heine Aziridine Isomerization; 1.3 Shi Epoxidation; PART 2 FIVE-MEMBERED HETEROCYCLES; Chapter 2 Pyrroles and Pyrrolidines; 2.1 Clauson-Kass Pyrrole Synthesis; 2.2 Houben-Hoesch Acylation of Pyrroles; 2.3 Overman Pyrrolidine Synthesis; 2.4 Trofimov Synthesis of Pyrroles; Chapter 3 Indoles; 3.1 Bischler-Möhlau Indole Synthesis; 3.2 Borsche-Drechsel Cyclization ; 3.3 Buchwald-Hartwig Indole Synthesis 3.4 Cadogan-Sundberg Indole Synthesis; 3.5 Fukuyama Indole Synthesis; 3.6 Gassman Oxindole Synthesis; 3.7 Larock Indole Synthesis; 3.8 Matinet Dioxindole Reaction; 3.9 Mori-Ban Indole Synthesis; 3.10 Sandmeyer Isatin Synthesis; 3.11 Sommelet-Hauser Rearrangement; 3.12 Stollé Oxindole Synthesis; Chapter 4 Furans and Oxazoles; 4.1 Nierenstein Reaction; 4.2 Davidson Oxazole Synthesis; 4.3 Fischer Oxazole Synthesis; 4.4 Japp Oxazole Synthesis; 4.5 Schöllkopf Oxazole Synthesis; Chapter 5 Other Five-Membered Heterocycles; 5.1 Bamberger Imidazole Cleavage ; 5.2 Dimroth Triazole Synthesis 5.3 Finnegan Tetrazole Synthesis; 5.4 Hantzsch Thiazole Synthesis; 5.5 Huisgen Tetrazole Rearrangement; 5.6 Knorr Pyrazole Synthesis; 5.7 Pechmann Pyrazole Synthesis; PART 3 SIX-MEMBERED HETEROCYCLES; Chapter 6 Pyridines; 6.1 Baeyer Pyridine Synthesis; 6.2 Katrizky Pyridine Synthesis; Chapter 7 Quinolines and Isoquinolines; 7.1 Betti Reaction; 7.2 Bernthsen Acridine Synthesis; 7.3 Lehmstedt- Tănăsescu Reaction; 7.4 Niementowski Quinoline Synthesis; 7.5 Povarov Reaction; Chapter 8 Six-Membered Heterocycles; 8.1 Balaban-Nenitzescu-Praill Reaction ; 8.2 Borsche Cinnoline Synthesis 8.3 Gutknecht Pyrazine Synthesis; 8.4 Niementowski Quinazoline Synthesis; 8.5 Pechmann Coumarin Synthesis; 8.6 Robinson-Schöpf Condensation; 8.7 Simonis Chromone Cyclization; 8.8 Wesseley-Moser Rearrangement; 8.9 Widman-Stoermer Cinnoline Synthesis; 8.10 Wichterle Reaction; Chapter 9 Miscellaneous Name Reactions; 9.1 ANRORC Mechanism; 9.2 Boulton-Katritzky Rearrangement; 9.3 Chichibabin Amination Reaction; 9.4 Dimroth Rearrangement; 9.5 Hantzsch Synthesis; 9.6 Ortoleva-King Reaction; Appendixes ; Appendix 1, Table of Contents for Volume 1 : Name Reactions in Heterocyclic Chemistry Appendix 2, Table of Contents for Volume 2: Name Reactions for Functional Group Transformations; Appendix 3, Table of Contents for Volume 3: Name Reactions for Homologations-I; Appendix 4, Table of Contents for Volume 4: Name Reactions for Homologations-II; Appendix 5, Table of Contents for Volume 5: Name Reactions for Ring Formations; Subject Index
• Sommario/riassunto: The up-to-DATE guide to name reactions in heterocyclic chemistry Name Reactions in Heterocyclic Chemistry II presents a comprehensive treatise on name reactions in heterocyclic chemistry, one of the most exciting-and important-fields within organic chemistry today. The book not only covers fresh ground, but also provides extensive information on new and/or expanded reactions in: Three- and four-membered heterocycles Five-membered heterocycles (pyrroles and pyrrolidines, indoles, furans, thiophenes, and oxazoles) Six-membered heterocycles, including pyrid
• Titolo autorizzato: Name reactions in heterocyclic chemistry II
• ISBN: 1-283-28270-4; 9786613282705; 1-118-09284-8; 1-118-09285-6; 1-118-09282-1
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910817213403321
• Lo trovi qui: Univ. Federico II
• Serie: Comprehensive name reactions ; ; v. 6.