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Index
Cover
Related Titles
Title Page
Copyright
Table of Contents
Preface to the First Edition
1 Background
2 Organization of the Book and Directions for Its Use
References
Preface to the Second Edition
Reference
Acknowledgments
About the Authors
Abbreviations and Symbols
Chapter 1: C–C Bond Formation
1.1 Nucleophilic Addition to Aldehydes, Ketones, Carboxylic Acid Derivatives (Esters, Anhydrides), and α,β-Unsaturated Carbonyl Compounds; Carbonyl Olefination
1.2 Alkylation of Aldehydes/Ketones, Carboxylic Acids, and β-Dicarbonyl Compounds
1.3 Reactions of the Aldol and Mannich Type
1.4 Electrophilic and Nucleophilic Acylation
1.5 Reactions of Alkenes Via Carbenium Ions
1.6 Transition-Metal-Catalyzed Reactions
1.7 Pericyclic Reactions
1.8 Radical Reactions
Chapter 2: Oxidation and Reduction
2.1 Epoxidation of C=C Bonds
2.2 Dihydroxylation of C=C Bonds
2.3 Oxidation of Alcohols to Carbonyl Compounds
2.4 Enantioselective Reduction of Ketones
2.5 Biomimetic Reductive Amination
2.6 Enantioselective Wacker Oxidation
Chapter 3: Heterocyclic Compounds
3.1 Three- and Four-Membered Heterocycles
3.2 Five-Membered Heterocycles
3.3 Six-Membered Heterocycles
3.4 Condensed Heterocycles
3.5 Other Heterocyclic Systems, Heterocyclic Dyes
Chapter 4: Selected Natural Products
4.1 Isoprenoids
4.2 Carbohydrates
4.3 Amino Acids and Peptides
4.4 Nucleotides and Oligonucleotides
Chapter 5: Domino Reactions
5.1 Domino Reactions in Synthetic Methodology
5.2 Domino Reactions in the Synthesis of Alkaloids
5.3 Domino Reactions in the Synthesis of Isoprenoids
5.4 Domino Reactions for the Synthesis of Chromans and Dioxins
5.5 Domino Reactions in the Synthesis of Chiroptical Switches
Index of Reactions
Index of Products
Subject Index
End User License Agreement
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