Homogeneous catalysis with renewables. ([2017])
- Record Type:
- Book
- Title:
- Homogeneous catalysis with renewables. ([2017])
- Main Title:
- Homogeneous catalysis with renewables
- Further Information:
- Note: Arno Behr, Andreas J. Vorholt.
- Authors:
- Behr, Arno
Vorholt, Andreas J - Contents:
- 1 Introduction; 1.1 Advantages of Homogeneous Catalysis in Derivatisation of Renewables; 1.2 Introduction into the Chemistry of Renewables; 1.3 Introduction into the Main Groups of Renewables; 1.3.1 Oleochemicals; 1.3.2 Terpenes; 1.3.3 Carbohydrates; 1.3.4 Lignin; 1.3.5 Peptides; 1.3.6 Carbon Dioxide; References; General literature; Oleochemicals; Terpenes; Carbohydrates; Lignin; Peptides; Carbon dioxide; 2 Hydrogenation of Renewables; 2.1 Introduction; 2.2 Hydrogenations of Carbon Dioxide; 2.2.1 Interconversion of CO2/Formic Acid as Hydrogen Storage; 2.2.2 Methanol; 2.3 Lignin. 2.4 Sugars2.5 Fats; 2.6 Conclusions; References; 3 Hydroformylation of Renewables; 3.1 Introduction; 3.1.1 Mechanisms; 3.1.2 Side Reactions; 3.1.3 Catalyst Development in Industrial Hydroformylation Processes; 3.2 Oleocompounds in Hydroformylation; 3.2.1 Catalyst Development; 3.2.2 Catalyst Recycling; 3.2.3 Applications; 3.3 Terpenes and Naturally Occurring Allylbenzenes; 3.3.1 Catalyst Development; 3.3.2 Catalyst Recycling; 3.4 Conclusions; References; 4 Amination of Renewables; 4.1 Introduction; 4.2 Carbohydrates; 4.2.1 5-Hydroxymethylfurfural (HMF); 4.2.2 Levulinic Acid. 4.2.3 Oils and Fats-Fatty Acid Esters4.2.4 Terpenes; 4.2.5 Myrcene; 4.2.6 Citronellal; 4.3 Conclusion; References; 5 Telomerisation of Renewables; 5.1 Introduction; 5.2 Telomerisation Using Renewable Dienes; 5.3 Telomerisation Using Renewable Nucleophiles; 5.3.1 Lignin-Derived Phenols; 5.3.2 Renewable Polyols; 5.3.2.1 Glycerol;1 Introduction; 1.1 Advantages of Homogeneous Catalysis in Derivatisation of Renewables; 1.2 Introduction into the Chemistry of Renewables; 1.3 Introduction into the Main Groups of Renewables; 1.3.1 Oleochemicals; 1.3.2 Terpenes; 1.3.3 Carbohydrates; 1.3.4 Lignin; 1.3.5 Peptides; 1.3.6 Carbon Dioxide; References; General literature; Oleochemicals; Terpenes; Carbohydrates; Lignin; Peptides; Carbon dioxide; 2 Hydrogenation of Renewables; 2.1 Introduction; 2.2 Hydrogenations of Carbon Dioxide; 2.2.1 Interconversion of CO2/Formic Acid as Hydrogen Storage; 2.2.2 Methanol; 2.3 Lignin. 2.4 Sugars2.5 Fats; 2.6 Conclusions; References; 3 Hydroformylation of Renewables; 3.1 Introduction; 3.1.1 Mechanisms; 3.1.2 Side Reactions; 3.1.3 Catalyst Development in Industrial Hydroformylation Processes; 3.2 Oleocompounds in Hydroformylation; 3.2.1 Catalyst Development; 3.2.2 Catalyst Recycling; 3.2.3 Applications; 3.3 Terpenes and Naturally Occurring Allylbenzenes; 3.3.1 Catalyst Development; 3.3.2 Catalyst Recycling; 3.4 Conclusions; References; 4 Amination of Renewables; 4.1 Introduction; 4.2 Carbohydrates; 4.2.1 5-Hydroxymethylfurfural (HMF); 4.2.2 Levulinic Acid. 4.2.3 Oils and Fats-Fatty Acid Esters4.2.4 Terpenes; 4.2.5 Myrcene; 4.2.6 Citronellal; 4.3 Conclusion; References; 5 Telomerisation of Renewables; 5.1 Introduction; 5.2 Telomerisation Using Renewable Dienes; 5.3 Telomerisation Using Renewable Nucleophiles; 5.3.1 Lignin-Derived Phenols; 5.3.2 Renewable Polyols; 5.3.2.1 Glycerol; 5.3.2.2 Sugars and Sugar-Derived Polyols; 5.3.3 Telomerisation with CO2; 5.4 Conclusion; References; 6 Oxidation of Renewables; 6.1 Introduction; 6.2 Fatty Acids and Fatty Acid Derivatives; 6.3 Terpenes and Terpene Alcohols; 6.4 Lignin and Phenylpropanoids. 6.5 ConclusionsReferences; 7 Tandem Reactions with Renewables; 7.1 Introduction; 7.2 Tandem Reactions with Metathesis; 7.2.1 Cross-Metathesis; 7.2.2 Intramolecular Ring-Closing Metathesis; 7.3 Tandem Reactions with Hydroformylations; 7.3.1 Hydroformylation/Hydrogenation; 7.3.2 Hydroformylation and C-O Bond Formation; 7.3.2.1 Intermolecular Hydroformylation/Acetalisation; 7.3.2.2 Intramolecular Hydroformylation/Lactolisation; 7.3.3 Hydroformylation and C-C Bond Formation; 7.3.3.1 Hydroformylation/Cyclisation; 7.3.3.2 Hydroformylation/Alkylation; 7.3.3.3 Hydroformylation/Aldol Condensation. 7.3.3.4 Hydroformylation/Acyloin reaction7.3.3.5 Hydroformylation/Arylation; 7.3.4 Hydroaminomethylation for C-N Bond Formation; 7.3.5 Alternative Syngas Resources for Hydroformylation; 7.3.5.1 Reverse Water-Gas Shift Reaction (RWGS); 7.3.5.2 Formic Acid Decomposition; 7.3.5.3 Polyol Degradation; 7.4 Defunctionalisation-Overcoming Over-Functionalisation; 7.4.1 Decarbonylative Dehydration; 7.4.2 Glycerol Degradation; 7.5 Isomerising Tandem Catalyses; 7.5.1 Isomerising Metathesis; 7.5.2 Isomerising Hydroformylation; 7.5.3 Isomerising Hydroboration; 7.5.4 Isomerising Trialkylsilylation. … (more)
- Publisher Details:
- Cham, Switzerland : Springer
- Publication Date:
- 2017
- Extent:
- 1 online resource
- Subjects:
- 660/.2995
Chemistry
Catalysis
SCIENCE -- Chemistry -- Industrial & Technical
TECHNOLOGY & ENGINEERING -- Chemical & Biochemical
Catalysis
Science -- Environmental Science
Industrial chemistry
Sustainability
Pollution & threats to the environment
Chemical engineering
Sustainable development
Environmental chemistry
Catalysis
Electronic books - Languages:
- English
- ISBNs:
- 9783319541617
3319541617 - Related ISBNs:
- 3319541595
9783319541594 - Notes:
- Note: Includes bibliographical references and index.
Note: Online resource; title from PDF title page (EBSCO, viewed June 8, 2017). - Access Rights:
- Legal Deposit; Only available on premises controlled by the deposit library and to one user at any one time; The Legal Deposit Libraries (Non-Print Works) Regulations (UK).
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- British Library HMNTS - ELD.DS.373527
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