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Green sustainable process for chemical and environmental engineering and science. Sustainable organic synthesis /

Green Sustainable Process for Chemical and Environmental Engineering and Science: Sustainable Organic Synthesis provides an in-depth overview in the area of organic, pharmaceutical, engineering and environmental sciences, with a focus on the purification and extraction of fine chemicals, alternative...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Inamuddin, 1980- (Editor ), Boddula, Rajender (Editor ), Asiri, Abdullah M. (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam : Elsevier, 2020.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Green sustainable process for chemical and environmental engineering and science.  |p Sustainable organic synthesis /  |c edited by Dr. Inamuddin, Rajender Boddula, Abdullah M. Asiri. 
246 3 0 |a Sustainable organic synthesis 
264 1 |a Amsterdam :  |b Elsevier,  |c 2020. 
300 |a 1 online resource 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Includes index. 
588 0 |a Print version record. 
520 |a Green Sustainable Process for Chemical and Environmental Engineering and Science: Sustainable Organic Synthesis provides an in-depth overview in the area of organic, pharmaceutical, engineering and environmental sciences, with a focus on the purification and extraction of fine chemicals, alternative green solvents, medicinal, analytical drugs, and bioactive compounds utilizing green chemistry protocols. It also focuses on the nanocatalysis, biocatalysis, solvent-free, recyclable organocatalysis, solid-supported reagents, heterogeneous polymer reusable catalysis, and CO2 conversion to commercial chemicals, utilizing industrial strategies such as flow-reactor, microwave, ultrasonics, ball-mill, photochemical and electrochemical methods. --  |c Provided by publisher. 
505 0 |a Intro -- Green Sustainable Process for Chemical and Environmental Engineering and Science: Microwaves in Organic Synthesis -- Copyright -- Contents -- Contributors -- Chapter 1: Microwave catalysis in organic synthesis -- 1. Introduction -- 1.1. History -- 1.2. Early development in utilization of microwave heating for organic synthesis -- 2. Factors influencing microwave heating in organic reactions -- 2.1. Microwave heating mechanism -- 2.1.1. Dipolar polarization mechanism -- 2.1.2. Ionic conduction mechanism -- 2.2. Dielectric properties and loss tangent -- 2.3. Superheating effect 
505 8 |a 2.4. Interaction of microwaves with different materials -- 3. Comparison of microwave with conventional heating -- 4. Microwave-assisted catalytic organic reactions -- 4.1. Coupling reactions -- 4.1.1. Suzuki reaction (or Suzuki-Miyaura coupling) -- 4.1.2. Stille coupling reaction -- 4.1.3. Sonogashira coupling -- 4.1.4. Heck reaction -- 4.2. Microwave-assisted heterocyclic chemistry -- 4.2.1. Nitrogen-containing heterocycles -- 4.2.2. Oxygen-containing heterocycles -- 4.2.3. Sulfur-containing heterocycles -- 4.3. Multicomponent reactions -- 4.3.1. Hantzsch reaction -- 4.3.2. Ugi reaction 
505 8 |a 4.3.3. Biginelli reaction -- 4.3.4. Mannich reaction -- 4.3.5. Strecker reaction -- 4.4. Alkylation reactions -- 4.4.1. N-Alkylation -- 4.4.2. C-Alkylation -- 4.4.3. O-Alkylation -- 4.5. Esterification and transesterification reactions -- 5. Microwave reactors -- 6. Current challenges in microwave-assisted synthesis -- 6.1. Energy efficiency -- 6.2. Scale-up of microwave-assisted organic reactions -- 7. Conclusion -- References -- Chapter 2: Microwave-assisted CN formation reactions -- 1. Introduction -- 2. N-Arylations, N-alkylations, and related reactions 
505 8 |a 2.1. Palladium-catalyzed processes-Buchawald-Hartwig amination -- 2.2. Copper-catalyzed reactions-The Ullmann coupling -- 2.3. Application of other metal catalysts -- 2.4. Metal-free transformations -- 2.5. The Petasis borono-Mannich reaction -- 2.6. Three-component propargylations -- 3. Amidations -- 3.1. Direct amidations -- 3.2. Amidation by reacting esters and amines -- 3.3. Transamidations -- 3.4. Oxidative amidations -- 3.5. Miscellaneous processes -- 4. Ring-forming reactions -- 4.1. Rings with one nitrogen atom -- 4.1.1. Synthesis of three- and four-membered rings 
505 8 |a 4.1.2. Synthesis of five-membered rings -- 4.1.3. Six-membered and larger rings -- 4.1.4. Condensed rings: Indoles and structural isomers -- 4.1.5. Condensed rings: Quinolines and isoquinolines -- 4.1.6. Molecules with multiple rings -- 4.2. Ring systems with two nitrogen atoms -- 4.2.1. Synthesis of diazoles -- 4.2.2. Six-membered rings -- 4.2.3. Condensed rings -- 4.2.4. Molecules with multiple rings -- 4.3. Rings with three and four nitrogen atoms -- 4.3.1. Synthesis of azoles -- Synthesis of 1,2,3-triazoles -- Synthesis of 1,2,4-triazoles -- Synthesis of tetrazoles 
650 0 |a Organic compounds  |x Synthesis. 
650 0 |a Green chemistry. 
650 6 |a Compos�es organiques  |x Synth�ese.  |0 (CaQQLa)201-0020323 
650 6 |a Chimie verte.  |0 (CaQQLa)201-0337434 
650 7 |a Green chemistry.  |2 fast  |0 (OCoLC)fst00912867 
650 7 |a Organic compounds  |x Synthesis.  |2 fast  |0 (OCoLC)fst01047668 
700 0 |a Inamuddin,  |d 1980-  |e editor. 
700 1 |a Boddula, Rajender,  |e editor. 
700 1 |a Asiri, Abdullah M.,  |e editor. 
776 0 8 |i Print version:  |t Green sustainable process for chemical and environmental engineering and science. Sustainable organic synthesis.  |d Amsterdam : Elsevier, 2020  |w (OCoLC)1175020981 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128195390  |z Texto completo