Name reactions in heterocyclic chemistry II

Name reactions in heterocyclic chemistry II

Li, Jie Jack
Corey, E.J.

130,60 €(IVA inc.)

ÍNDICE: Foreword. Preface. Contributing Authors. PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES. Chapter 1 Aziridines and Epoxides. 1.1 Blum Aziridine Synthesis. 1.2 GabrielHeine Aziridine Isomerization. 1.3 Shi Epoxidation. PART 2 FIVE-MEMBERED HETEROCYCLES. Chapter 2 Pyrroles and Pyrrolidines. 2.1 ClausonKass Pyrrole Synthesis. 2.2 HoubenHoech Acylation of Pyrroles. 2.3 Overman Pyrrolidine Synthesis. 2.4 Trofimov Synthesis of Pyrroles. Chapter 3 Indoles. 3.1 BischlerMöhlau Indole Synthesis. 3.2 BorscheDrechsel Cyclization. 3.3 BuchwaldHartwig Indole Synthesis. 3.4 CadoganSundberg Indole Synthesis. 3.5 Fukuyama Indole Synthesis. 3.6 Gassman Oxindole Synthesis. 3.7 Larock Indole Synthesis. 3.8 Matinet Dioxindole Synthesis. 3.9 MoriBan Indole Synthesis. 3.10 Sandmeyer Isatin Synthesis. 3.11 SommeletHauser 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 Hantsch 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 Reaction. Chapter 7 Quinolines and Isoquinolines. 7.1 Betti reaction. 7.2 Bernthsen Acridine Synthesis. 7.3 LehmstedtTanasescu Reaction. 7.4 Niementowski Quinoline Synthesis. 7.5 Povarov Reaction. Chapter 8 Six-Membered Heterocycles. 8.1 BalabanNenitzescuPraill Reaction. 8.2 Borsche Cinnoline Synthesis. 8.3 Gutknecht Pyrazine Synthesis. 8.4 Niementowski Quinazoline Synthesis. 8.5 Pechmann Coumarin Synthesis. 8.6 RobinsonSchöpf Condensation. 8.7 Simonis Chromone Cyclization. 8.8 WesseleyMoser Rearrangement. 8.9 WidmanStoermer Cinnoline Synthesis. 8.10 Wichterle Reaction. Chapter 9 Miscellaneous Name Reactions. 9.1 ANRORC Mechanism. 9.2 BoultonKatritzky Rearrangement. 9.3 Chichibabin Amination Reaction. 9.4 Dimroth Rearrangement. 9.5 Hantzsch Synthesis. 9.6 OrtolevaKing Reaction. Appendices. 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.

  • ISBN: 978-0-470-08508-0
  • Editorial: John Wiley & Sons
  • Encuadernacion: Cartoné
  • Páginas: 688
  • Fecha Publicación: 12/08/2011
  • Nº Volúmenes: 1
  • Idioma: Inglés