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Name Reactions for Carbocyclic Ring Formations

Comprehensive Name Reactions

Erschienen am 22.10.2010, 1. Auflage 2010
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Bibliografische Daten
ISBN/EAN: 9780470085066
Sprache: Englisch
Umfang: 772 S.
Einband: gebundenes Buch

Beschreibung

InhaltsangabeForeword. Preface. Contributing Authors. Chapter 1 Three-Membered Carbocycles. 1.1 Freund Reaction. 1.2 Kishner Cyclopropane Synthesis. 1.3 Kulinovich Cyclopropanol Synthesis. 1.4 SimmonsSmith Reaction. Chapter 2 Four-Membered Carbocycles. 2.1 Staudinger Ketene Cycloaddition. Chapter 3 Five-Membered Carbocycles. 3.1 Danheiser Annulation. 3.2 Dieckmann Condensation. 3.3 Favorskii Rearrangement. 3.4 Nazarov Cyclization. 3.5 PausonKhand Reaction. 3.6 WeissCook Reaction. Chapter 4 Six-Membered Carbocycles. 4.1 BardhanSengupta Pheantherene Synthesis. 4.2 Bergman Cyclization. 4.3 BogertCook Reaction. 4.4 Bradsher Cycloaddition and Bradsher Reaction. 4.5 Bradsher Reaction. 4.6 Darzens Synthesis of Tetralin Derivatives. 4.7 DielsAlder Reaction. 4.8 Dötz Benzannulation. 4.9 Elbs Reaction. 4.10 Fujimoto-Belleau Reaction. 4.11 Haworth Reaction. 4.12 Moore Cyclization. 4.13 MyersSaito Cyclization. 4.14 Robinson Annulation. 4.15 Scholl Reaction. Chapter 5 Large-Ring Carbocycles. 5.1 Buchner Reaction. 5.2 de Mayo Reaction. 5.3 Ringclosing Metathesis (RCM). 5.4 ThorpeZiegler Reaction. Chapter 6 Transformations of Carbocycles. 6.1 Blanc Chloromethylation Reaction. 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present. 6.3 HoubenHoesch Reaction. 6.4 KolbeSchmitt Reaction. 6.5 Vilsmeier-Haack Reaction. 6.6 von Richter Reaction. Appendices. 1 Contents Volume 1: Name Reactions in Heterocyclic Chemistry. 2 Contents Volume 2: Name Reactions for Functional Group Transformations. 3 Contents Volume 3: Name Reactions for Homologations--Part I. 4 Contents Volume 4: Name Reactions for Homologations--Part II. 5 Contents Volume 6: Name Reactions in Heterocyclic Chemistry--Part II. Subject Index.

Autorenportrait

JIE JACK LI is a chemist at Bristol-Myers Squibb Company in Wallingford, Connecticut. He has authored or edited various books, including Name Reactions in Heterocyclic Chemistry, Name Reactions for Functional Group Transformations, Name Reactions for Homologations, Parts I and II, Contemporary Drug Synthesis, The Art of Drug Synthesis, and Modern Drug Synthesis, all published by Wiley.

Leseprobe

Leseprobe

Inhalt

Foreword. Preface. Contributing Authors. Chapter 1 Three-Membered Carbocycles. 1.1 Freund Reaction. 1.2 Kishner Cyclopropane Synthesis. 1.3 Kulinovich Cyclopropanol Synthesis. 1.4 Simmons-Smith Reaction. Chapter 2 Four-Membered Carbocycles. 2.1 Staudinger Ketene Cycloaddition. Chapter 3 Five-Membered Carbocycles. 3.1 Danheiser Annulation. 3.2 Dieckmann Condensation. 3.3 Favorskii Rearrangement. 3.4 Nazarov Cyclization. 3.5 Pauson-Khand Reaction. 3.6 Weiss-Cook Reaction. Chapter 4 Six-Membered Carbocycles. 4.1 Bardhan-Sengupta Pheantherene Synthesis. 4.2 Bergman Cyclization. 4.3 Bogert-Cook Reaction. 4.4 Bradsher Cycloaddition and Bradsher Reaction. 4.5 Bradsher Reaction. 4.6 Darzens Synthesis of Tetralin Derivatives. 4.7 Diels-Alder Reaction. 4.8 Dötz Benzannulation. 4.9 Elbs Reaction. 4.10 Fujimoto-Belleau Reaction. 4.11 Haworth Reaction. 4.12 Moore Cyclization. 4.13 Myers-Saito Cyclization. 4.14 Robinson Annulation. 4.15 Scholl Reaction. Chapter 5 Large-Ring Carbocycles. 5.1 Buchner Reaction. 5.2 de Mayo Reaction. 5.3 Ring-closing Metathesis (RCM). 5.4 Thorpe-Ziegler Reaction. Chapter 6 Transformations of Carbocycles. 6.1 Blanc Chloromethylation Reaction. 6.2 Asymmetric Friedel-Crafts Reactions: Past to Present. 6.3 Houben-Hoesch Reaction. 6.4 Kolbe-Schmitt Reaction. 6.5 Vilsmeier-Haack Reaction. 6.6 von Richter Reaction. Appendices. 1 Contents Volume 1: Name Reactions in Heterocyclic Chemistry. 2 Contents Volume 2: Name Reactions for Functional Group Transformations. 3 Contents Volume 3: Name Reactions for Homologations--Part I. 4 Contents Volume 4: Name Reactions for Homologations--Part II. 5 Contents Volume 6: Name Reactions in Heterocyclic Chemistry--Part II. Subject Index.

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