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Organic Synthesis and Organic Reagents.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Chandra, Ramesh
Otros Autores: Singh, Snigdha, Singh, Aarushi
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Ashland : Arcler Press, 2020.
Temas:
Acceso en línea:Texto completo
Tabla de Contenidos:
  • Cover
  • Title Page
  • Copyright
  • ABOUT THE AUTHORS
  • TABLE OF CONTENTS
  • Glossary
  • List of Figures
  • List of Tables
  • List of Abbreviations
  • Preface
  • Chapter 1 Introduction to Organic Synthesis
  • 1.1. Introduction
  • 1.2. Birth of Organic Synthesis
  • 1.3. Organic Reactions
  • 1.4. Functional Groups
  • 1.5. Examples of Organic Synthesis At Work
  • 1.6. Digitization of Organic Synthesis
  • 1.7. Organic Synthesis And A 'Chemical Brain'
  • 1.8. Future Perspectives of Organic Synthesis
  • 1.9. Conclusion
  • References
  • Chapter 2 Acids, Bases, and Functional Group Exchange Reactions
  • 2.1. Introduction
  • 2.2. Bronsted Lowry Theory of Acids And Bases
  • 2.3. Lewis Concept of Acids And Bases
  • 2.4. Hard-Soft Acids And Bases
  • 2.5. Substitution Reaction
  • 2.6. General Features of Nucleophilic Substitution
  • 2.7. Elimination Reaction
  • 2.8. Addition Reaction
  • 2.9. Electrophilic Aromatic Substitution
  • 2.10. Conclusion
  • References
  • Chapter 3 Essential Reagents For Organic Synthesis
  • 3.1. Bis(Dibenzylideneacetone)Palladium(0) To N-Butyllithium
  • 3.2. N,N'-Carbonyl Diimidazole To Chlorotris (Triphenylphosphine)-Rhodium(I)
  • 3.3. (Diacetoxyiodo)Benzene To Dimethyldioxirane
  • 3.4. 1-Ethyl-3-(3'-Dimethylaminopropyl) Carbodiimide Hydrochloride
  • 3.5. N-Iodosuccinimide To 2-Iodoxybenzoic Acid
  • 3.6. Manganese Dioxide
  • 3.7. Osmium Tetroxide To Ozone
  • 3.8. Pinacolborane To Potassium Tert-Butoxide
  • 3.9. Ruthenium (II), Tris(2,2'-Bipyridine-.n1, .n1')-, (Oc-6-11)
  • 3.10. Tetrabutylammonium Fluoride To Trimethylsilyldiazomethane
  • 3.11. Conclusion
  • References
  • Chapter 4 Organometallic Reagents and Carbon Bonds
  • 4.1. Introduction
  • 4.2. Dipoles And Their Role In Reactions
  • 4.3. Organometallic Compounds
  • 4.4. Organolithium And Their Preparation
  • 4.5. Grignard Reagents And Their Preparation
  • 4.6. Organocopper Reagents
  • 4.7. Organozinc Reagents
  • 4.8. Conclusion
  • References
  • Chapter 5 Pericyclic Reactions, Photochemical Reactions, and Free-Radical Reactions
  • 5.1. Introduction
  • 5.2. Pericyclic Reactions
  • 5.3. Photochemical Reactions
  • 5.4. Free-Radical Reactions
  • 5.5. Conclusion
  • References
  • Chapter 6 Oxidation and Reduction
  • 6.1. Introduction
  • 6.2. The Concepts of Oxidation-Reduction
  • 6.3. Oxidation Reactions as a Loss of Electrons
  • 6.4. Electrolysis
  • 6.5. The Concept of Oxidation Number
  • 6.6. Redox Reactions
  • 6.7. Types of Redox Reactions
  • 6.8. Voltaic Cells
  • 6.9. Balancing of Redox Reactions
  • 6.10. Location of Oxidants And Reductants In The Periodic Table
  • 6.11. Conclusion
  • References
  • Chapter 7 Synthesis of Five- and Six-Membered Heterocyclic Compounds
  • 7.1. Introduction
  • 7.2. Basic Literature on Heterocyclic Compounds
  • 7.3. Comparison With Carbocyclic Compounds
  • 7.4. General Features Of Heterocyclic Compounds