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Green sustainable process for chemical and environmental engineering and science
Microwaves in Organic Synthesis provides an in-depth overview in the area of organic and pharmaceutical chemistry of the microwave technology in separation, purification and extraction of medicinal, biological, and organic compounds. This book methodically explores the application of microwaves in all types of organic synthesis. It includes stereoselectivity, regioselectivity, oxidation, reduction, protection, deprotection, addition, condensation, coupling, C-X bond formation, named reactions, heterocyclic, biological drugs, fluoro-organics and polymers. After a brief introduction discusses the main parameters which influence the process, and the limitations and advantages of the practical use of microwave in organic synthesis. This book is a vital resource on green chemistry technologies for students and academic researchers, R & D professionals, students and university professors working in the field of organic chemistry, medicinal chemistry and chemical engineering.
Intro -- Green Sustainable Process for Chemical and Environmental Engineering and Science: Organic Synthesis in Water and Supercriti... -- Copyright -- Contents -- Contributors -- Chapter 1: Polymer synthesis in water and supercritical water -- 1. Introduction -- 1.1. Water in industries -- 1.2. Supercritical fluids -- 1.3. Properties of water and supercritical water -- 2. Polymerization in water medium -- 2.1. Emulsion polymerization -- 2.2. Photoactivated polymerization -- 2.3. Dispersion polymerization -- 2.4. Controlled/``living ́́radical polymerization -- 2.5. Radical polymerization
5. Se-nucleophile -- 6. H-nucleophiles -- References -- Chapter 3: Cycloaddition reactions in water -- 1. Introduction -- 2. ``In-water ́́cycloaddition reactions -- 2.1. [4+2] Cycloaddition (Diels-Alder) reactions -- 2.2. Hydrophobicity effect on rate enhancement in water -- 2.2.1. Structure facilitated hydrophobic effect -- 2.3. Hydrogen-bonding effect on rate enhancement -- 2.4. Endo- vs exo-selectivity in intermolecular D-A reactions -- 2.5. Inverse electron demand D-A reactions in water -- 2.6. Asymmetric Diels-Alder reactions in water
2.7. Application to the total synthesis of natural products -- 2.8. Intramolecular Diels-Alder reactions in water -- 2.9. Aqueous intramolecular D-A reaction in the total synthesis -- 2.10. [3+2] Cycloaddition reactions in water -- 2.11. [4+3] Cycloaddition reaction -- 2.12. [2+2+2] Cycloadditions -- 2.13. [5+2] Cycloadditions -- 3. Cycloaddition reactions ``on-water ́́ -- 4. Concluding remarks -- Acknowledgments -- References -- Chapter 4: Hydrogenation reactions in water -- 1. Introduction -- 2. Types of hydrogenation -- 2.1. Catalytic hydrogenation -- 2.2. Transfer hydrogenation
2.3. Asymmetric hydrogenation -- 2.4. Asymmetric transfer hydrogenation -- 2.5. Electrocatalytic hydrogenation -- 2.6. Selective hydrogenation -- 2.6.1. Chemoselective hydrogenation -- 2.6.2. Diastereoselective hydrogenation -- 2.6.3. Regioselective hydrogenation -- 2.7. Other hydrogenation -- 3. Water as hydrogen donor -- 3.1. Synthesis of aliphatic compounds -- 3.2. Synthesis of aromatic compounds -- 3.3. Synthesis of carbonyl compounds -- 3.4. Synthesis of alcohols, ethers, sugars, nitro and nitril compounds -- 3.5. Synthesis of bio-oils, fossil fuel, and cellulose -- 4. Water as solvent
edited by Inamuddin, Rajender Boddula and Abdullah M. Asiri.