Keywords:
Solvents.
;
Electronic books.
Description / Table of Contents:
These volumes are an essential primary resource that describe the properties of green solvents crucial to modern green chemistry. The books explore the hazards of regular solvents and the plethora of green solvent applications in analytical, organic and pharmaceutical chemistry.
Type of Medium:
Online Resource
Pages:
1 online resource (439 pages)
Edition:
1st ed.
ISBN:
9789400717121
URL:
https://ebookcentral.proquest.com/lib/geomar/detail.action?docID=971764
Language:
English
Note:
Intro -- Green Solvents I -- Preface -- Editors' bios -- Acknowledgments -- Contents -- Contributors -- Chapter 1: Green Solvents Fundamental and Industrial Applications -- 1.1 Introduction -- 1.2 Solvent-Free Reactions -- 1.2.1 Organic Synthesis -- 1.2.1.1 Protection/Deprotection Reactions -- 1.2.1.2 Tishchenko Reaction -- 1.2.1.3 Condensation Reactions -- 1.2.1.4 Aldol Reaction -- 1.2.1.5 Sonogashira Reaction -- 1.2.1.6 Metathesis Reactions -- 1.2.1.7 Diels-Alder Reactions -- 1.2.1.8 Heck Reaction -- 1.2.1.9 Mannich Reaction -- 1.2.1.10 Hydrogenation -- 1.2.1.11 Esterification -- 1.2.1.12 Meyers' Lactamization -- 1.2.1.13 Synthesis of 1,3,5-Triarylbenzene -- 1.2.1.14 Hydroaminovinylation of Olefins -- 1.2.1.15 Synthesis of Diynes -- 1.2.1.16 Synthesis of Lactic Acid -- 1.2.1.17 Synthesis of Thioglycosides -- 1.2.1.18 Synthesis of Lipidyl-Cyclodextrins -- 1.2.1.19 Synthesis of Unsaturated Ketones -- 1.2.1.20 Synthesis of Nitrotoluene -- 1.2.1.21 Synthesis of Quinazoline-2,4(1 H ,3 H)-Diones -- 1.2.1.22 Synthesis of Monomethine Indocyanine Dyes -- 1.2.1.23 Synthesis of Acetyl Salicylic Acid -- 1.2.1.24 Oxidation -- 1.2.1.25 Reduction -- 1.2.1.26 Synthesis of Heterocyclic Compounds -- 1.2.2 Inorganic and Materials Synthesis -- 1.2.3 Polymerization -- 1.3 Water -- 1.3.1 Organic Synthesis -- 1.3.1.1 Suzuki-Miyaura Reactions -- 1.3.1.2 Michael Reactions -- 1.3.1.3 Knoevenagel Reactions -- 1.3.1.4 Aldol Reactions -- 1.3.1.5 Telomerisation Reactions -- 1.3.1.6 Amination Reactions -- 1.3.1.7 Alkylation -- 1.3.1.8 Cycloaddition Reactions -- 1.3.1.9 Hydroxylation -- 1.3.1.10 Alkynylation -- 1.3.1.11 Condensation Reactions -- 1.3.1.12 Diels-Alder Reactions -- 1.3.1.13 Mannich Reactions -- 1.3.1.14 Condensation Reactions -- 1.3.1.15 Sonogashira-Hagihara Reaction -- 1.3.1.16 Hydrolysis -- 1.3.1.17 Aza-Friedel-Crafts Reaction.
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1.3.1.18 Cyanation of Aryl Iodides -- 1.3.1.19 Suzuki Reaction -- 1.3.1.20 Cycloaddition Reactions -- 1.3.1.21 Aminohalogenation Reaction -- 1.3.1.22 Photooxygenation of Furans -- 1.3.1.23 Electrooxidation -- 1.3.1.24 Synthesis of 1,8-Dioxo-9,10-Diaryldecahydroacridines -- 1.3.1.25 Oxidation -- 1.3.1.26 Reduction -- 1.3.1.27 Synthesis of Heterocyclic Compounds -- 1.3.2 Synthesis of Metal Nanoparticles -- 1.4 Supercritical Fluids -- 1.4.1 Extraction -- 1.4.2 Organic Synthesis -- 1.4.3 Materials Synthesis and Modifications -- 1.4.4 Solubility in Supercritical Carbon Dioxide (SC-CO 2) -- 1.5 Room Temperature Ionic Liquids (RTIL)s -- 1.5.1 Organic Synthesis -- 1.5.1.1 Enzymatic Reactions -- 1.5.1.2 Transesterification -- 1.5.1.3 Hydroesterificaton -- 1.5.1.4 Diels-Alder Reactions -- 1.5.1.5 Michael Reaction -- 1.5.1.6 Friedel-Crafts Reactions -- 1.5.1.7 Condensation Reactions -- 1.5.1.8 Cyclocondensation Reactions -- 1.5.1.9 Mannich Reaction -- 1.5.1.10 Hydrolysis -- 1.5.1.11 Dehydration -- 1.5.1.12 Epoxidation -- 1.5.1.13 Synthesis of Imidazoles -- 1.5.1.14 Synthesis of Diacetals and Diketals -- 1.5.1.15 Bonds Cleavage Reactions -- 1.5.1.16 Oligomerization -- 1.5.1.17 Synthesis of 5-Hydroxymethylfurfural and Furfural -- 1.5.1.18 Preparation of Biodiesel Fuel -- 1.5.1.19 Synthesis of Tributyl Citrate -- 1.5.1.20 Synthesis of Dimethyl Carbonate -- 1.5.1.21 Nitration of Aromatic Compounds -- 1.5.1.22 Alkylation and Acylation -- 1.5.1.23 Synthesis of Fatty Acid Esters of Steroids -- 1.5.1.24 Aldol Reaction -- 1.5.1.25 Synthesis of 1,4-Dibromo-Naphthalene -- 1.5.1.26 Heck and the Knoevenagel Reactions -- 1.5.1.27 Synthesis of Aromatic Chloroamines -- 1.5.1.28 Esterification -- 1.5.1.29 Hydrosilylation of Alkenes -- 1.5.1.30 Coupling Reactions -- 1.5.1.31 Synthesis of Cellulose Propionate -- 1.5.1.32 Synthesis of Hydroxy Ester.
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1.5.1.33 Sonogashira Reactions -- 1.5.1.34 Metathesis Reaction -- 1.5.1.35 Aziridination Reaction -- 1.5.1.36 Synthesis of [60] Fullerene -- 1.5.1.37 Methanolysis -- 1.5.1.38 Dimerization -- 1.5.1.39 Synthesis of Drugs -- 1.5.1.40 Oxidation -- 1.5.1.41 Synthesis of Heterocyclic Compounds -- 1.5.2 Materials Synthesis and Modifications -- 1.5.2.1 Synthesis of Nanoparticles -- 1.5.2.2 Synthesis of Silicas -- 1.5.2.3 Synthesis of Zeolites -- 1.5.2.4 Bioreactors -- 1.5.2.5 Synthesis of Tin Oxide Microspheres -- 1.5.2.6 Synthesis of ZnO Mesocrystals -- 1.5.2.7 Functionalization of Multiwalled Carbon Nanotubes (MWNTs) -- 1.5.2.8 Desulfurization of Diesel -- 1.5.2.9 Removal of Sulfur Dioxide -- 1.5.2.10 Decomposition -- 1.5.2.11 Carbonization -- 1.5.2.12 Synthesis of Hydrogels and Composite Hydrogels -- 1.5.2.13 Absorption -- 1.5.2.14 Corrosion Protection -- 1.5.2.15 Electrodeposition -- 1.5.2.16 Depolymerization -- 1.5.2.17 Inhibitor -- 1.5.2.18 Synthesis of Inorganic Materials -- 1.5.3 Polymerization -- 1.5.4 Extraction -- 1.5.5 Solubility -- 1.6 Perfluorinated Solvents -- 1.6.1 Extraction -- 1.6.2 Organic Synthesis -- 1.7 Conclusions -- References -- Chapter 2: Green Fluids Extraction and Purification of Bioactive Compounds from Natural Materials -- 2.1 Introduction -- 2.2 Isolation and Purification of 3,5-Diprenyl-4-Hydroxycinnamic Acid (DHCA) in Brazilian Propolis -- 2.2.1 Classical Solvent Extractions -- 2.2.2 Purification and Identification of 3,5-Diprenyl-4-Hydroxycinnamic Acid (DHCA) -- 2.2.3 Quantification of 3,5-Diprenyl-4-Hydroxycinnamic Acid (DHCA) -- 2.3 Green Fluid Extraction of 3,5-Diprenyl-4-Hydroxycinnamic Acid (DHCA) from Brazilian Propolis -- 2.3.1 Sensitivity Test of Supercritical Carbon Dioxide (SC-CO 2) Extractions -- 2.3.2 Response Surface Methodology (RSM): Designed Supercritical Carbon Dioxide (SC-CO 2) Extractions.
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2.4 Precipitation of Submicron Particles in Brazilian Propolis via Supercritical Carbon Dioxide (SC-CO 2) Antisolvent -- 2.4.1 Supercritical Carbon Dioxide (SC-CO 2) Micronization Process -- 2.4.2 Analysis of Micronized Precipitates -- 2.4.2.1 Determination of Particles Size, Distribution, and Morphology -- 2.4.2.2 Quantification of DHCA and Flavonoids -- 2.4.3 Experimental Results of Supercritical Carbon Dioxide (SC-CO 2) Antisolvent Micronization -- 2.4.3.1 Preliminary Experiment of Supercritical Carbon Dioxide (SC-CO 2) Precipitation -- 2.4.3.2 Response Surface Methodology (RSM): Designed Supercritical Carbon Dioxide (SC-CO 2) Precipitation -- 2.5 Biological Activity of Propolis Samples Produced by Supercritical Fluid Procedure -- 2.5.1 Cytotoxic Assay of Human Cells -- 2.5.1.1 Supercritical Carbon Dioxide (SC-CO 2) Extracts -- 2.5.1.2 Supercritical Carbon Dioxide (SC-CO 2) Precipitates -- 2.5.2 Antioxidative Ability Tests -- 2.5.2.1 2,2-Diphenyl-1-Picrylhydrazyl (DPPH) Free Radical -- 2.5.2.2 Low-Density Lipid Protein -- 2.6 Column Partition Fractionation of g -Oryzanols -- 2.6.1 Isolation and Identification of Two g -Oryzanols -- 2.6.2 Quantification of g -Oryzanols, Free Fatty Acids, and Triglycerides -- 2.6.3 Soxhlet Solvent Extractions -- 2.6.4 Purification of Rice Bran Oil Using Column Partition -- 2.7 Supercritical Carbon Dioxide (SC-CO 2) Extraction and Deacidification of Rice Bran Oil -- 2.7.1 Experimentally Designed Supercritical Carbon Dioxide (SC-CO 2) Extraction -- 2.7.2 Pilot-Scale Supercritical Carbon Dioxide (SC-CO 2) Extraction -- 2.7.3 Experimentally Designed Supercritical Carbon Dioxide (SC-CO 2) Deacidification -- 2.8 Conclusions -- References -- Chapter 3: Green Solvents for Biocatalysis -- 3.1 Introduction -- 3.2 Water -- 3.3 Supercritical fluids -- 3.4 Fluorous Solvents -- 3.4.1 Properties and Applications.
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3.4.2 Applications of Fluorous Biphasic Systems in Biocatalysis (FBS) -- 3.5 Ionic Liquids -- 3.5.1 Properties and Applications -- 3.5.2 Biocatalysis in Ionic Liquids -- 3.6 Conclusions -- References -- Chapter 4: Green Solvents for Pharmaceutical Industry -- 4.1 Pharmaceutical Green Chemistry -- 4.2 Organic Solvents in the Pharmaceutical Industry -- 4.3 Green Solvents Technology: A Potential Platform for the Pharmaceutical Industry -- 4.4 Acidic Ionic Liquids -- 4.5 Basic Ionic Liquids -- 4.6 Oxidation on Ionic Liquids -- 4.7 Chiral Ionic Liquids and Chiral Amino Acid Ionic Liquids -- 4.8 Supported Ionic Liquids -- 4.9 Microwave- and Ultrasound-Assisted Reactions Using Ionic Liquids -- 4.10 Recent Bioconversions on Ionic Liquids -- 4.11 Ionic Liquids for Analytical Spectroscopy -- References -- Chapter 5: Limonene as Green Solvent for Extraction of Natural Products -- 5.1 Introduction -- 5.2 Limonene: Origin, Applications, and Properties -- 5.3 Limonene as an Alternative Solvent for Soxhlet Extraction -- 5.4 Limonene as an Alternative Solvent for Dean-Stark Distillation -- 5.5 Limonene as an Alternative Solvent for Extraction of By-Products -- 5.6 Combining Green Extraction Technique and Green Solvent -- 5.7 Future Trends -- References -- Chapter 6: Glycerol as an Alternative Solvent for Organic Reactions -- 6.1 Introduction -- 6.2 Glycerol for Redox Reactions -- 6.3 Glycerol for Catalytic C-C Bond Formations -- 6.4 Glycerol for Biocatalysis -- 6.5 Glycerol for Micellar Catalytic Reactions -- 6.6 Other Catalytic Organic Reactions in Glycerol -- 6.7 Glycerol-Based Solvents -- References -- Chapter 7: Water as Reaction Medium in the Synthetic Processes Involving Epoxides -- 7.1 Introduction -- 7.2 Epoxides in the Synthesis of 1,2-Amino Alcohols in Water -- 7.3 Epoxides in the Synthesis 1,2-Diols, 1,2-Alkyloxy, and -Aryloxy Alcohols in Water.
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7.4 Epoxides in the Synthesis Hydroxy Sulfur Compounds.
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