E-Book, Englisch, Band 2, 704 Seiten, E-Book
Reihe: Comprehensive Name Reactions
ISBN: 978-1-118-09284-2
Verlag: John Wiley & Sons
Format: EPUB
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
Name Reactions in Heterocyclic Chemistry II presents acomprehensive treatise on name reactions in heterocyclic chemistry,one of the most exciting--and important--fields withinorganic chemistry today.
The book not only covers fresh ground, but also providesextensive 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 pyridines, quinolines, andisoquinolines
Featuring contributions from the leading authorities inheterocyclic chemistry. Each section includes a description of thegiven reaction, as well as the relevant historical perspective,mechanism, variations and improvements, synthetic utilities,experimental details, and references to the current primaryliterature.
The reactions covered in Name Reactions in HeterocyclicChemistry have been widely adopted in all areas of organicsynthesis, from the medicinal/pharmaceutical field, to agriculture,to fine chemicals, and the book brings the most cutting-edgeknowledge to practicing synthetic chemists and students, along withthe tools needed to synthesize new and useful molecules.
Weitere Infos & Material
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-Hoech 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 Synthesis.
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 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 Lehmstedt-Tanasescu 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.
Appendices.
Appendix 1, Table of Contents for Volume 1: Name Reactions inHeterocyclic Chemistry.
Appendix 2, Table of Contents for Volume 2: Name Reactionsfor Functional Group Transformations.
Appendix 3, Table of Contents for Volume 3: Name Reactionsfor Homologations-I.
Appendix 4, Table of Contents for Volume 4: Name Reactionsfor Homologations-II.
Appendix 5, Table of Contents for Volume 5: Name Reactionsfor Ring Formations.
