E-Book, Englisch, 448 Seiten, E-Book
ISBN: 978-0-470-13143-5
Verlag: John Wiley & Sons
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
Published almost a decade ago, the first edition has served as theguide for research in this burgeoning field. Due to the cost,safety, efficiency, and environmental friendliness of water as asolvent, there are many new applications in industry and academiclaboratories. More than forty percent of this extensively updatedsecond edition covers new reactions. For ease of reference, it isorganized by functional groups. A core reference, ComprehensiveOrganic Reactions in Aqueous Media, Second Edition:
* Provides the most comprehensive coverage of aqueousorganicreactions available
* Covers the basic principles and theory and progresses toapplications
* Includes alkanes, alkenes, aromatics, electrophilicsubstitutions, carbonyls, alpha, beta-unsaturated carbonyls,carbon-nitrogen bonds, organic halides, pericyclic reactions,photochemical reactions, click chemistry, and multi-stepsyntheses?
* Provides examples of applications in industry
This is the premier reference for chemists and chemical engineersin industry or research, as well as for students in advanced-levelcourses.
Autoren/Hrsg.
Weitere Infos & Material
PREFACE TO THE SECOND EDITION.
1. INTRODUCTION.
1.1 The Structure and Forms of Water.
1.2 Properties of Water.
1.3 Solvation.
1.4 Hydrophobic Effect.
1.5 Salt Effect.
1.6 Water Under Extreme Conditions.
References.
2. ALKANES.
2.1 Oxygenation of Alkanes.
2.2 Halogenation of Alkanes.
2.3 Formation of Carbon-Carbon Bonds.
2.4 D/H Exchange of Alkanes in Water.
References.
3. ALKENES.
3.1 Reduction.
3.2 Electrophilic Additions.
3.3 Radical Reactions of Alkenes.
3.4 Carbene Reactions.
3.5 Alkene Isomerization.
3.6 Transition-Metal Catalyzed C-C FormationReactions.
3.7 Olefin Metathesis.
3.8 Reaction of Allylic C-H Bond.
4. ALKYNES.
4.1 Reaction of Terminal Alkynes.
4.2 Additions of C identical to C bonds.
4.3 Transition-Metal Catalyzed Cycloadditions.
4.4 Other Reactions.
References.
5. ALCOHOLS, PHENOLS, ETHERS, THIOLS, AND THIOETHERS.
5.1 Oxidation of Alcohols.
5.2 Substitutions/Elimination.
5.3 Addition of Alcohols, Phenols, and Thiols to Alkene andAlkyne Bonds.
5.4 Addition of Alcohols to C=O Bonds: Esterification and AcetalFormations.
5.5 Reaction of Ethers and Cyclic Ethers.
5.6 Reaction of Sulfur Compounds.
6. ORGANIC HALIDES.
6.1 General.
6.2 Reduction.
6.3 Elimination Reactions.
6.4 Nucleophilic Substitutions.
6.5 Reductive Coupling.
6.6 Carbonylation of Organic Halides.
6.7 Transition-Metal Catalyzed Coupling Reactions.
References.
7. AROMATIC COMPOUNDS.
7.1 General.
7.2 Substitution Reactions.
7.3 Oxidation Reactions.
7.4 Reductions.
References.
8. ALDEHDYE AND KETONES.
8.1 Reduction.
8.2 Oxidation.
8.3 Nucleophilic Addition: C-C Bond Formation.
8.4 Pinacol Coupling.
8.5 Other Reactions (Halogenation and Oxidation ofalpha-H).
References.
9. CARBOXYLIC ACIDS AND DERIVATIVES.
9.1 General.
9.2 Carboxylic Acids.
9.3 Carboxylic Acid Derivatives.
References.
10. CONJUGATED CARBONYL COMPOUNDS.
10.1 Reduction.
10.2 Epoxidation, Dihydroxylation, Hydroxyamination.
10.3 Conjugate Addition: Heteroatom.
10.4 C-C Bond Formation.
10.5 Other Reactions.
References.
11. NITROGEN COMPOUNDS.
11.1 Amines.
11.2 Imines.
11.3 Diazo Compounds.
11.4 Azides.
11.5 Nitro Compounds.
References.
12. PERICYCLIC REACTIONS.
12.1 Introduction.
12.2 Diels-Alder Reactions.
12.3 Sigmatropic Rearrangements.
12.4 Photochemical Cycloaddition Reactions.
References.
INDEX.