Name reactions in heterocyclic chemistry

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

資料種別:

図書

出版情報:

Hoboken : Wiley, c2011

形態:

xiii, 690 p. ; 24 cm

シリーズ名:

Wiley series on comprehensive name reactions <BB04789723>

著者名:

ISBN:

9780470085080 [0470085088] (2)

書誌ID:

BB06852886

子書誌情報

フルテキスト

所蔵情報

他の版・巻

書誌詳細

注記:

Includes bibliographical references
Subject index: p. 663-690

主題:

Chemical reactions; Heterocyclic chemistry

言語:

英語

目次情報:

Foreword

Preface

Contributing Authors

Three- And Four-Membered Heterocycles / Part 1：

Aziridines and Epoxides / Chapter 1：

Blum Aziridine Synthesis / 1.1：

Gabriel–Heine Aziridine Isomerization / 1.2：

Shi Epoxidation / 1.3：

Five-Membered Heterocycles / Part 2：

Pyrroles and Pyrrolidines / Chapter 2：

Clauson–Kass Pyrrole Synthesis / 2.1：

Houben–Hoech Acylation of Pyrroles / 2.2：

Overman Pyrrolidine Synthesis / 2.3：

Trofimov Synthesis of Pyrroles / 2.4：

Indoles / Chapter 3：

Bischler–Möhlau Indole Synthesis / 3.1：

Borsche–Drechsel Cyclization / 3.2：

Buchwald–Hartwig Indole Synthesis / 3.3：

Cadogan–Sundberg Indole Synthesis / 3.4：

Fukuyama Indole Synthesis / 3.5：

Gassman Oxindole Synthesis / 3.6：

Larock Indole Synthesis / 3.7：

Matinet Dioxindole Synthesis / 3.8：

Mori–Ban Indole Synthesis / 3.9：

Sandmeyer Isatin Synthesis / 3.10：

Sommelet–Hauser Rearrangement / 3.11：

Stollé Oxindole Synthesis / 3.12：

Furans and Oxazoles / Chapter 4：

Nierenstein Reaction / 4.1：

Davidson Oxazole Synthesis / 4.2：

Fischer Oxazole Synthesis / 4.3：

Japp Oxazole Synthesis / 4.4：

Schöllkopf Oxazole Synthesis / 4.5：

Other Five-Membered Heterocycles / Chapter 5：

Bamberger Imidazole Cleavage / 5.1：

Dimroth Triazole Synthesis / 5.2：

Finnegan Tetrazole Synthesis / 5.3：

Hantsch Thiazole Synthesis / 5.4：

Huisgen Tetrazole Rearrangement / 5.5：

Knorr Pyrazole Synthesis / 5.6：

Pechmann Pyrazole Synthesis / 5.7：

Six-Membered Heterocycles / Part 3：

Pyridines / Chapter 6：

Baeyer Pyridine Synthesis / 6.1：

Katrizky Reaction / 6.2：

Quinolines and Isoquinolines / Chapter 7：

Betti reaction / 7.1：

Bernthsen Acridine Synthesis / 7.2：

Lehmstedt–Tanasescu Reaction / 7.3：

Niementowski Quinoline Synthesis / 7.4：

Povarov Reaction / 7.5：

Balaban–Nenitzescu–Praill Reaction / Chapter 8：

Borsche Cinnoline Synthesis / 8.2：

Gutknecht Pyrazine Synthesis / 8.3：

Niementowski Quinazoline Synthesis / 8.4：

Pechmann Coumarin Synthesis / 8.5：

Robinson–Schöpf Condensation / 8.6：

Simonis Chromone Cyclization / 8.7：

Wesseley–Moser Rearrangement / 8.8：

Widman–Stoermer Cinnoline Synthesis / 8.9：

Wichterle Reaction / 8.10：

Miscellaneous Name Reactions / Chapter 9：

ANRORC Mechanism / 9.1：

Boulton–Katritzky Rearrangement / 9.2：

Chichibabin Amination Reaction / 9.3：

Dimroth Rearrangement / 9.4：

Hantzsch Synthesis / 9.5：

Ortoleva–King Reaction / 9.6：

Appendices

Table of Contents for Volume 1: Name Reactions in Heterocyclic Chemistry / Appendix 1：

Table of Contents for Volume 2: Name Reactions for Functional Group Transformations / Appendix 2：

Table of Contents for Volume 3: Name Reactions for Homologations-I / Appendix 3：

Table of Contents for Volume 4: Name Reactions for Homologations-II / Appendix 4：

Table of Contents for Volume 5: Name Reactions for Ring Formations / Appendix 5：

Foreword

Preface

Contributing Authors

Three- And Four-Membered Heterocycles / Part 1：

Aziridines and Epoxides / Chapter 1：

Blum Aziridine Synthesis / 1.1：

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