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Name reactions in heterocyclic chemistry II

Author: Jie Jack Li; E J Corey
Publisher: Hoboken, N.J. : Wiley, ©2011.
Series: Comprehensive name reactions, v. 6.
Edition/Format:   Print book : EnglishView all editions and formats
Database:WorldCat
Summary:

Co-authored by Nobel Laureatte, E.J. Corey, this book builds on the first volume on this topic by presenting a comprehensive treatise on name reactions in heterocyclic chemistry.

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Document Type: Book
All Authors / Contributors: Jie Jack Li; E J Corey
ISBN: 9780470085080 0470085088
OCLC Number: 751821816
Description: xiii, 690 p. : ill. ; 25 cm.
Contents: Foreword. <p>Preface. <p>Contributing Authors. <p>PART 1 THREE- AND FOUR-MEMBERED HETEROCYCLES. <p>Chapter 1 Aziridines and Epoxides. <p>1.1 Blum Aziridine Synthesis. <p>1.2 Gabriel Heine Aziridine Isomerization. <p>1.3 Shi Epoxidation. <p>PART 2 FIVE-MEMBERED HETEROCYCLES. <p>Chapter 2 Pyrroles and Pyrrolidines. <p>2.1 Clauson Kass Pyrrole Synthesis. <p>2.2 Houben Hoech Acylation of Pyrroles. <p>2.3 Overman Pyrrolidine Synthesis. <p>2.4 Trofimov Synthesis of Pyrroles. <p>Chapter 3 Indoles. <p>3.1 Bischler Mohlau Indole Synthesis. <p>3.2 Borsche Drechsel Cyclization. <p>3.3 Buchwald Hartwig Indole Synthesis. <p>3.4 Cadogan Sundberg Indole Synthesis. <p>3.5 Fukuyama Indole Synthesis. <p>3.6 Gassman Oxindole Synthesis. <p>3.7 Larock Indole Synthesis. <p>3.8 Matinet Dioxindole Synthesis. <p>3.9 Mori Ban Indole Synthesis. <p>3.10 Sandmeyer Isatin Synthesis. <p>3.11 Sommelet Hauser Rearrangement. <p>3.12 Stolle Oxindole Synthesis. <p>Chapter 4 Furans and Oxazoles. <p>4.1 Nierenstein Reaction. <p>4.2 Davidson Oxazole Synthesis. <p>4.3 Fischer Oxazole Synthesis. <p>4.4 Japp Oxazole Synthesis. <p>4.5 Schollkopf Oxazole Synthesis. <p>Chapter 5 Other Five-Membered Heterocycles. <p>5.1 Bamberger Imidazole Cleavage. <p>5.2 Dimroth Triazole Synthesis. <p>5.3 Finnegan Tetrazole Synthesis. <p>5.4 Hantsch Thiazole Synthesis. <p>5.5 Huisgen Tetrazole Rearrangement. <p>5.6 Knorr Pyrazole Synthesis. <p>5.7 Pechmann Pyrazole Synthesis. <p>PART 3 SIX-MEMBERED HETEROCYCLES. <p>Chapter 6 Pyridines. <p>6.1 Baeyer Pyridine Synthesis. <p>6.2 Katrizky Reaction. <p>Chapter 7 Quinolines and Isoquinolines. <p>7.1 Betti reaction. <p>7.2 Bernthsen Acridine Synthesis. <p>7.3 Lehmstedt Tanasescu Reaction. <p>7.4 Niementowski Quinoline Synthesis. <p>7.5 Povarov Reaction. <p>Chapter 8 Six-Membered Heterocycles. <p>8.1 Balaban Nenitzescu Praill Reaction. <p>8.2 Borsche Cinnoline Synthesis. <p>8.3 Gutknecht Pyrazine Synthesis. <p>8.4 Niementowski Quinazoline Synthesis. <p>8.5 Pechmann Coumarin Synthesis. <p>8.6 Robinson Schopf Condensation. <p>8.7 Simonis Chromone Cyclization. <p>8.8 Wesseley Moser Rearrangement. <p>8.9 Widman Stoermer Cinnoline Synthesis. <p>8.10 Wichterle Reaction. <p>Chapter 9 Miscellaneous Name Reactions. <p>9.1 ANRORC Mechanism. <p>9.2 Boulton Katritzky Rearrangement. <p>9.3 Chichibabin Amination Reaction. <p>9.4 Dimroth Rearrangement. <p>9.5 Hantzsch Synthesis. <p>9.6 Ortoleva King Reaction. <p>Appendices. <p>Appendix 1, Table of Contents for Volume 1: Name Reactions inHeterocyclic Chemistry. <p>Appendix 2, Table of Contents for Volume 2: Name Reactionsfor Functional Group Transformations. <p>Appendix 3, Table of Contents for Volume 3: Name Reactionsfor Homologations-I. <p>Appendix 4, Table of Contents for Volume 4: Name Reactionsfor Homologations-II. <p>Appendix 5, Table of Contents for Volume 5: Name Reactionsfor Ring Formations.
Series Title: Comprehensive name reactions, v. 6.
Responsibility: edited by Jie Jack Li ; foreword by E.J. Corey.

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