Details

Name Reactions in Heterocyclic Chemistry II


Name Reactions in Heterocyclic Chemistry II


Comprehensive Name Reactions, Band 6 1. Aufl.

von: Jie Jack Li, E. J. Corey

147,99 €

Verlag: Wiley
Format: PDF
Veröffentl.: 26.09.2011
ISBN/EAN: 9781118092859
Sprache: englisch
Anzahl Seiten: 688

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Beschreibungen

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 pyridines, quinolines, and isoquinolines Featuring contributions from the leading authorities in heterocyclic chemistry. Each section includes a description of the given reaction, as well as the relevant historical perspective, mechanism, variations and improvements, synthetic utilities, experimental details, and references to the current primary literature. The reactions covered in Name Reactions in Heterocyclic Chemistry have been widely adopted in all areas of organic synthesis, from the medicinal/pharmaceutical field, to agriculture, to fine chemicals, and the book brings the most cutting-edge knowledge to practicing synthetic chemists and students, along with the tools needed to synthesize new and useful molecules.
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 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.
Jie Jack Li is a Chemist at Bristol-Myers Squibb Company. He has authored or edited various books, including the first volume of Name Reactions in Heterocyclic Chemistry, Name Reactions for Functional Group Transformations, Name Reactions for Carbocyclic Ring Formations, and several others, all published by Wiley.
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 pyridines, quinolines, and isoquinolines Featuring contributions from the leading authorities in heterocyclic chemistry. Each section includes a description of the given reaction, as well as the relevant historical perspective, mechanism, variations and improvements, synthetic utilities, experimental details, and references to the current primary literature. The reactions covered in Name Reactions in Heterocyclic Chemistry have been widely adopted in all areas of organic synthesis, from the medicinal/pharmaceutical field, to agriculture, to fine chemicals, and the book brings the most cutting-edge knowledge to practicing synthetic chemists and students, along with the tools needed to synthesize new and useful molecules.

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