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SCIDIR_on1194673219 |
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cr cnu---unuuu |
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200910s2020 ne o 001 0 eng d |
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|a OPELS
|b eng
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|e pn
|c OPELS
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|a GBC0E9035
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|a 019960447
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|a 9780128195390
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|a 0128195398
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|a 9780128226704
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|a 0128226706
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|z 9780128198483
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|a (OCoLC)1194673219
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|a QD262
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|a 660.29
|2 23
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|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.
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|a Sustainable organic synthesis
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|a Amsterdam :
|b Elsevier,
|c 2020.
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|a 1 online resource
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Includes index.
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|a Print version record.
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|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.
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|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
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|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
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|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
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|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
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|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
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|a Organic compounds
|x Synthesis.
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650 |
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|a Green chemistry.
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|a Compos�es organiques
|x Synth�ese.
|0 (CaQQLa)201-0020323
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|a Chimie verte.
|0 (CaQQLa)201-0337434
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|a Green chemistry.
|2 fast
|0 (OCoLC)fst00912867
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|a Organic compounds
|x Synthesis.
|2 fast
|0 (OCoLC)fst01047668
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|a Inamuddin,
|d 1980-
|e editor.
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700 |
1 |
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|a Boddula, Rajender,
|e editor.
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700 |
1 |
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|a Asiri, Abdullah M.,
|e editor.
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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
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856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128195390
|z Texto completo
|