Halogenated pyridines can be used as interesting starting materials in a wide range of organic synthesis methods. Substituted pyridine compounds are used generally as starting materials in the nucleophilic substitution reactions and have unique scaffolds for the construction of other heterocyclic an
Perhalopyridines: Synthesis and Synthetic Utility
โ Scribed by Ranjbar-Karimi R., Poorfreidoni A.
- Publisher
- Bentham Books
- Year
- 2020
- Tongue
- English
- Leaves
- 256
- Category
- Library
No coin nor oath required. For personal study only.
โฆ Synopsis
Halogenated pyridines can be used as interesting starting materials in a wide range of organic synthesis methods. Substituted pyridine compounds are used generally as starting materials in the nucleophilic substitution reactions and have unique scaffolds for the construction of other heterocyclic and macrocyclic compounds. They also have important medicinal properties. Due to synthetic difficulties in the synthesis of the highly substituted pyridine derivatives from pyridine itself, perhalopyridines have a special importance in this regard. This book covers the synthetic reactions and applications of perhalopyridines. An introductory chapter introduces the reader to the physical and chemical properties of halopyridines, followed by 3 chapters which focus on pentafluoropyridine, pentachloropyridine and pentabromopyridine, respectively. The focused chapters provide information about synthetic methods and relevant nucleophilic reactions for each of the listed perhalopyridines and their derivatives. The book is a quick reference on perhalopyridines for students of applied chemistry, organic chemistry and chemical engineering.
โฆ Table of Contents
Cover
Perhalopyridines: Synthesis and Synthetic Utility
Copyright
End User License Agreement
Contents
Preface
Foreword
Abbreviations
Chapter 1. Properties of Perhalopyridines
1. Physical and Chemical Properties
2. Spectroscopy
3. Reactions
References
Chapter 2. Perfluoropyridines
1. Introduction
2. Synthesis of Pentafluoropyridine
3. Reaction Mechanism
4. Reaction of Pentafluoropyridine with Various Mono Dentate Nucleophiles
4.1. Reaction of S-centered Nucleophile with Pentafluoropyridine
4.2. Reaction of O-centered Nucleophile with Pentafluoropyridine
4.3. Reaction of C-centered Nucleophile with Pentafluoropyridine
4.4. Reaction of N-centered Nucleophile with Pentafluoropyridine
4.5. Reaction of Pentafluoropyridine 3 with Halogenating Reagents (Cl, Br, I)
4.6. Reduction of Perfluorinated Pyridines
5. Reaction of Perfluoropyridines with Various Multidentate Nucleophiles
5.1. Synthesis of Perfluorinated Heterocyles
5.2. Synthesis of Fluorinated Ring-fused Heterocyles
6. Organometallic Compounds of Perfluoro-Heteroaromatics
7. Photochemical Reactions of Fluorinated Pyridines
8. Copolymerization of Pentafluoropyridine
9. The Pentafluoropyridine Cation C5F5N+
10. Salts of Perfluoropyridine
11. Synthesis of Macrocyclic Compounds from Polyfluoropyridines
12. Pentafluoropyridine in Medicinal Chemistry and Biochemistry
References
Chapter 3. Perchloropyridines
1. Introduction
2. Synthesis of Pentachloropyridine
2.1. By Straight Chlorination
2.2. By Ring-closing Method
2.3. Synthesis of Pentachloropyridine-1-15N-2,6-13C2
3. Nucleophilic Reactions of Perchloropyridines
3.1. Reaction of Pentachloropyridine with Various Mono Dentate Nucleophiles
3.1.1. Reaction of N-centered Nucleophile with Pentachloropyridine
3.1.2. Reaction of S-centered Nucleophile with Pentachloropyridine
3.1.3. Reaction of C-centered Nucleophile with Perchloropyridines
3.2. Reaction of Perchloropyridines with Bidentate Nucleophiles
4. Cross-Coupling reactions of Perchloropyridines
5. Bromination of Pentachloropyridine
6. Oxidation of Polychloropyridines
7. Reduction of Polychloropyridines
8. Alkylation of Polychloropyridines
9. Photochemical Reactions of Polychloropyridines
10. Organometallic Reagents of Perchloropyridine
References
Chapter 4. Perbromopyridines
1. Synthesis of Pentabromopyridine
2. Nucleophilic Reactions of Pentabromopyridine
2.1. Reaction of O-centered Nucleophile with Pentabromopyridine
2.2. Reaction of N-centered Nucleophile with Pentabromopyridine
2.3. Reaction of S-centered Nucleophile with Pentabromopyridine
3. Organometalic Reagent of Polybromopyridines
4. Salts of Pentabromopyridine
5. Oxidation of Pentabromopyridine
6. Photochemical Reactions of Pentabromopyridine
7. Synthesis and Reactions of 2,4,6-tribromo-3,5-difluoropyridine
8. Synthesis and Reactions of 3,5-dibromo-2,6-dichloropyridine
References
Subject Index
Cover back
๐ SIMILAR VOLUMES
Imidazole and Benzimidazole Synthesis is a comprehensive survey of the known methods of syntheses and ring modification. It brings together the multitude of synthesis of the imidazole ring in a systemic way interms of specific bond formation, and recommends the most attractive synthetic approaches.
<em>Refining Sound</em> is a practical roadmap to the complexities of creating sounds on modern synthesizers. Perhaps the most difficult aspect of learning to create sounds on a synthesizer is understanding what all the individual synthesizer components contribute to the complex finished sound. Auth
<span><b>Natural and Synthetic Fiber Reinforced Composites</b> <p><b>Discover a comprehensive exploration of fiber reinforced polymers by an expert team of editors </b> </p><p>Fiber reinforced polymer (FRP) composites offer several unique properties that make them ideal for use in a wide range of in
ExLi4EvA, 2016. โ 512 p. โ ISBN: 9535122665; 9535122657<div class="bb-sep"></div>This book provides a basic overview of general knowledges of this topic in order to provide the comprehensive survey from a scientific and technological perspective. <br/>Apatite-type minerals and their synthetic analog