Green sustainable process for chemical and environmental engineering and science : organic synthesis in water and supercritical water /

Green Sustainable Process for Chemical and Environmental Engineering and Science: Organic Synthesis in Water and Supercritical Water provides an in-depth review of purification and extraction methods for medicinal, analytical, engineering and bioactive compounds utilizing green chemistry protocols.

Bibliographic Details
Corporate Author:	ScienceDirect (Online service)
Other Authors:	Inamuddin, 1980- (Editor), Boddula, Rajender (Editor), Asiri, Abdullah M. (Editor)
Format:	eBook
Language:	English
Published:	Amsterdam, Netherlands : Elsevier, 2020.
Subjects:	Green chemistry. Chimie verte. Green chemistry Electronic books.
Online Access:	Connect to the full text of this electronic book

Table of Contents:

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
4.1. Synthesis of aliphatic compounds
4.2. Synthesis of aromatic compounds
4.3. Synthesis of carbonyl compounds
4.4. Synthesis of alcohols, ethers, sugars, nitro, and nitril compounds
5. Conclusion
References
Chapter 5: Magnetically separable nanocatalyzed synthesis of bioactive heterocycles in water
1. Introduction
2. Synthesis of nitrogen-containing heterocycles
2.1. Synthesis of N-substituted pyrroles
2.2. Synthesis of 1,4-dihydropyridines
2.3. Synthesis of hexahydroquinoline carboxylates
2.4. Synthesis of quinolines
2.5. Synthesis of acridine-1,8(2H,5H)-diones
2.6. Synthesis of benzo[d]imidazoles
2.7. Synthesis of imidazo[1,2-a]pyridines
2.8. Synthesis of quinoxalines
2.9. Synthesis of 1,2,3-triazoles.
5. Factors affecting CC coupling reactions in water
5.1. Catalyst
5.2. Bimetallic catalysts
5.3. Base and concentration effect
5.4. Light water/heavy water
5.5. Energy source
5.6. Additives and transfer agents
6. Specific CC coupling reactions
6.1. Mizoroki-Heck reaction
6.2. Hiyama reaction
6.3. Suzuki-Miyaura reaction
6.4. Sonogashira-Hagihara reaction
6.5. Stille reaction
6.6. Negishi reaction
7. Applications in synthesis
7.1. Derivatization of biomolecules
7.2. Bioactive molecules
8. Conclusions
References
Index.