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Chemical Transformations of Carbon Dioxide / Xiao-Feng Wu, Matthias Beller editors
Chemical Transformations of Carbon Dioxide / Xiao-Feng Wu, Matthias Beller editors
Edizione [Cham : Springer, 2018]
Pubbl/distr/stampa VIII, 253 p., : ill. ; 24 cm
Descrizione fisica Pubblicazione in formato elettronico
Disciplina 660(Ingegneria chimica e tecnologie connesse)
540(Chimica generale)
547(Chimica organica)
541.395(Catalisi)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-SUN0125636
VIII, 253 p., : ill. ; 24 cm
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
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Chemistry of Thioamides / Toshiaki Murai editor
Chemistry of Thioamides / Toshiaki Murai editor
Pubbl/distr/stampa Singapore, : Springer, 2019
Descrizione fisica VII, 238 p. : ill. ; 24 cm
Disciplina 540(Chimica generale)
547(Chimica organica)
541.395(Catalisi)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN0126185
Singapore, : Springer, 2019
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
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Chemistry of Thioamides / Toshiaki Murai editor
Chemistry of Thioamides / Toshiaki Murai editor
Edizione [Singapore : Springer, 2019]
Pubbl/distr/stampa VII, 238 p., : ill. ; 24 cm
Descrizione fisica Pubblicazione in formato elettronico
Disciplina 540(Chimica generale)
547(Chimica organica)
541.395(Catalisi)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-SUN0126185
VII, 238 p., : ill. ; 24 cm
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
Chiral catalyst immobilization and recycling [[electronic resource] /] / edited by D.E. De Vos, I.F.J. Vankelecom, P.A. Jacobs
Chiral catalyst immobilization and recycling [[electronic resource] /] / edited by D.E. De Vos, I.F.J. Vankelecom, P.A. Jacobs
Pubbl/distr/stampa Weinheim ; ; New York, : Wiley-VCH, c2000
Descrizione fisica 1 online resource (342 p.)
Disciplina 541.395
547.1395
Altri autori (Persone) VosD. E. de (Dirk E.)
VankelecomI. F. J (Ivo F. J.)
JacobsPeter A
Soggetto topico Enantioselective catalysis
Catalysts
Soggetto genere / forma Electronic books.
ISBN 1-281-76408-6
9786611764081
3-527-61314-5
3-527-61315-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chiral Catalvst Immobilization and Recycling; Contents; 1 Enantioselective Heterogeneous Catalysis: Academic and Industrial Challenges; 1.1 Introduction; 1.2 The Industrial Process in General and the Specific Prerequisites for Chiral Catalysts; 1. 2.1 Characteristics of the Manufacture of Enantiomerically Pure Products; 1.2.2 Process Development: Critical Factors for the Application of (Heterogeneous) Enantioselective Catalysts; 1. 2.3 Important Criteria for Enantioselective Catalysts; 1.3 The General Challenges; 1.3.1 For Academia; 1.3.2 For Industry
1.4 Chiral Heterogeneous Catalysts: State of the Art and Future Challenges1.4.1 Heterogeneous Catalysts Modified with a Chiral Auxiliary; 1.4.1.1 Metallic Catalysts on Chiral Supports; 1.4.1.2 Metallic Catalysts Modified with a Low Molecular Weight Chiral Auxiliary; 1.4.1.3 Metal Oxide Catalysts Modified with a Chiral Auxiliary having Low Molecular Weight; 1.4.2 Immobilized and Functionalized Homogeneous Catalysts; 1.4.2.1 lmmobilized Homogeneous Catalysts; 1.4.2.2 Alternative Methods Using Functionalized Ligands; 1.4.3 Catalysts with No Known Heterogeneous or Homogeneous Precedent
1.4.3.1 Insoluble Polypeptides and Gels1.4.3.2 Artificial Catalytic Antibodies; 1.5 Conclusions; References; 2 Catalyst Immobilization on Inorganic Supports; 2.1 Introduction; 2.2 General Considerations; 2.3 Supports; 2.4 Improved Activity of Heterogeneous Complexes; 2.5 Practical Examples; 2.5.1 Covalent Attachment; 2.5.2 Adsorption or Ion-Pair Formation; 2.5.3 Encapsutation; 2.5.4 Entrapment; 2.5.5 Supported Liquid Phase (SLP); 2.5.6 Modification of an Achiral Heterogeneous Catalyst with a Chiral Auxiliary; 2.5.7 Achiral Metal Catalysts on Chiral Supports; References
3 Organic Polymers as a Catalyst Recovery Vehicle3.1 General Introduction; 3.2 Alkene Hydrogenation; 3.3 Carbonyl and Imine Reduction; 3.4 Carbon-Carbon Bond Formation; 3.5 Carbonyl Alkylation; 3.6 Diels-Alder Reactions; 3.7 Enolate Chemistry; 3.8 Strecker Chemistry; 3.9 Asymmetric Dihydroxylation; 3.10 Epoxidation and Epoxide Ring Opening; 3.11 Acylation Catalysts; 3.12 Conclusion; References; 4 Liquid Biphasic Enantioselective Catalysis; 4.1 Introduction; 4.2 Hydrogenation; 4.3 Hydroformylation; 4.4 Oxidation; 4.5 Lewis Acid-Catalyzed Reactions; 4.6 Enzymatic Reactions; 4.7 Summary
References5 Immobilized Enzymes in Enantioselective Organic Synthesis; 5.1 Introduction; 5.2 Immobilization; 5.2.1 Methods of Immobilization; 5.2.1.1 Enzymes; 5.2.1.2 Carriers; 5.2.1.3 Binding Enzymes to Carriers; 5.2.1.4 Cross-Linked Enzyme Crystals; 5.2.2 Activity Assay; 5.2.3 Activity Balance; 5.2.4 Cost of Immobilization; 5.3 Operation; 5.3.1 Reactors; 5.3.2 Operational Stability; 5.4 Summary; References; 6 Enantioselective Hydrogenation Catalyzed by Platinum Group Metals Modified by Natural Alkaloids; 6.1 Historical Perspective
6.2 Enantioselective Hydrogenation of Activated Ketones over Platinum
Record Nr. UNINA-9910144279303321
Weinheim ; ; New York, : Wiley-VCH, c2000
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral catalyst immobilization and recycling [[electronic resource] /] / edited by D.E. De Vos, I.F.J. Vankelecom, P.A. Jacobs
Chiral catalyst immobilization and recycling [[electronic resource] /] / edited by D.E. De Vos, I.F.J. Vankelecom, P.A. Jacobs
Pubbl/distr/stampa Weinheim ; ; New York, : Wiley-VCH, c2000
Descrizione fisica 1 online resource (342 p.)
Disciplina 541.395
547.1395
Altri autori (Persone) VosD. E. de (Dirk E.)
VankelecomI. F. J (Ivo F. J.)
JacobsPeter A
Soggetto topico Enantioselective catalysis
Catalysts
ISBN 1-281-76408-6
9786611764081
3-527-61314-5
3-527-61315-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chiral Catalvst Immobilization and Recycling; Contents; 1 Enantioselective Heterogeneous Catalysis: Academic and Industrial Challenges; 1.1 Introduction; 1.2 The Industrial Process in General and the Specific Prerequisites for Chiral Catalysts; 1. 2.1 Characteristics of the Manufacture of Enantiomerically Pure Products; 1.2.2 Process Development: Critical Factors for the Application of (Heterogeneous) Enantioselective Catalysts; 1. 2.3 Important Criteria for Enantioselective Catalysts; 1.3 The General Challenges; 1.3.1 For Academia; 1.3.2 For Industry
1.4 Chiral Heterogeneous Catalysts: State of the Art and Future Challenges1.4.1 Heterogeneous Catalysts Modified with a Chiral Auxiliary; 1.4.1.1 Metallic Catalysts on Chiral Supports; 1.4.1.2 Metallic Catalysts Modified with a Low Molecular Weight Chiral Auxiliary; 1.4.1.3 Metal Oxide Catalysts Modified with a Chiral Auxiliary having Low Molecular Weight; 1.4.2 Immobilized and Functionalized Homogeneous Catalysts; 1.4.2.1 lmmobilized Homogeneous Catalysts; 1.4.2.2 Alternative Methods Using Functionalized Ligands; 1.4.3 Catalysts with No Known Heterogeneous or Homogeneous Precedent
1.4.3.1 Insoluble Polypeptides and Gels1.4.3.2 Artificial Catalytic Antibodies; 1.5 Conclusions; References; 2 Catalyst Immobilization on Inorganic Supports; 2.1 Introduction; 2.2 General Considerations; 2.3 Supports; 2.4 Improved Activity of Heterogeneous Complexes; 2.5 Practical Examples; 2.5.1 Covalent Attachment; 2.5.2 Adsorption or Ion-Pair Formation; 2.5.3 Encapsutation; 2.5.4 Entrapment; 2.5.5 Supported Liquid Phase (SLP); 2.5.6 Modification of an Achiral Heterogeneous Catalyst with a Chiral Auxiliary; 2.5.7 Achiral Metal Catalysts on Chiral Supports; References
3 Organic Polymers as a Catalyst Recovery Vehicle3.1 General Introduction; 3.2 Alkene Hydrogenation; 3.3 Carbonyl and Imine Reduction; 3.4 Carbon-Carbon Bond Formation; 3.5 Carbonyl Alkylation; 3.6 Diels-Alder Reactions; 3.7 Enolate Chemistry; 3.8 Strecker Chemistry; 3.9 Asymmetric Dihydroxylation; 3.10 Epoxidation and Epoxide Ring Opening; 3.11 Acylation Catalysts; 3.12 Conclusion; References; 4 Liquid Biphasic Enantioselective Catalysis; 4.1 Introduction; 4.2 Hydrogenation; 4.3 Hydroformylation; 4.4 Oxidation; 4.5 Lewis Acid-Catalyzed Reactions; 4.6 Enzymatic Reactions; 4.7 Summary
References5 Immobilized Enzymes in Enantioselective Organic Synthesis; 5.1 Introduction; 5.2 Immobilization; 5.2.1 Methods of Immobilization; 5.2.1.1 Enzymes; 5.2.1.2 Carriers; 5.2.1.3 Binding Enzymes to Carriers; 5.2.1.4 Cross-Linked Enzyme Crystals; 5.2.2 Activity Assay; 5.2.3 Activity Balance; 5.2.4 Cost of Immobilization; 5.3 Operation; 5.3.1 Reactors; 5.3.2 Operational Stability; 5.4 Summary; References; 6 Enantioselective Hydrogenation Catalyzed by Platinum Group Metals Modified by Natural Alkaloids; 6.1 Historical Perspective
6.2 Enantioselective Hydrogenation of Activated Ketones over Platinum
Record Nr. UNINA-9910830973703321
Weinheim ; ; New York, : Wiley-VCH, c2000
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral catalyst immobilization and recycling [[electronic resource] /] / edited by D.E. De Vos, I.F.J. Vankelecom, P.A. Jacobs
Chiral catalyst immobilization and recycling [[electronic resource] /] / edited by D.E. De Vos, I.F.J. Vankelecom, P.A. Jacobs
Pubbl/distr/stampa Weinheim ; ; New York, : Wiley-VCH, c2000
Descrizione fisica 1 online resource (342 p.)
Disciplina 541.395
547.1395
Altri autori (Persone) VosD. E. de (Dirk E.)
VankelecomI. F. J (Ivo F. J.)
JacobsPeter A
Soggetto topico Enantioselective catalysis
Catalysts
ISBN 1-281-76408-6
9786611764081
3-527-61314-5
3-527-61315-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chiral Catalvst Immobilization and Recycling; Contents; 1 Enantioselective Heterogeneous Catalysis: Academic and Industrial Challenges; 1.1 Introduction; 1.2 The Industrial Process in General and the Specific Prerequisites for Chiral Catalysts; 1. 2.1 Characteristics of the Manufacture of Enantiomerically Pure Products; 1.2.2 Process Development: Critical Factors for the Application of (Heterogeneous) Enantioselective Catalysts; 1. 2.3 Important Criteria for Enantioselective Catalysts; 1.3 The General Challenges; 1.3.1 For Academia; 1.3.2 For Industry
1.4 Chiral Heterogeneous Catalysts: State of the Art and Future Challenges1.4.1 Heterogeneous Catalysts Modified with a Chiral Auxiliary; 1.4.1.1 Metallic Catalysts on Chiral Supports; 1.4.1.2 Metallic Catalysts Modified with a Low Molecular Weight Chiral Auxiliary; 1.4.1.3 Metal Oxide Catalysts Modified with a Chiral Auxiliary having Low Molecular Weight; 1.4.2 Immobilized and Functionalized Homogeneous Catalysts; 1.4.2.1 lmmobilized Homogeneous Catalysts; 1.4.2.2 Alternative Methods Using Functionalized Ligands; 1.4.3 Catalysts with No Known Heterogeneous or Homogeneous Precedent
1.4.3.1 Insoluble Polypeptides and Gels1.4.3.2 Artificial Catalytic Antibodies; 1.5 Conclusions; References; 2 Catalyst Immobilization on Inorganic Supports; 2.1 Introduction; 2.2 General Considerations; 2.3 Supports; 2.4 Improved Activity of Heterogeneous Complexes; 2.5 Practical Examples; 2.5.1 Covalent Attachment; 2.5.2 Adsorption or Ion-Pair Formation; 2.5.3 Encapsutation; 2.5.4 Entrapment; 2.5.5 Supported Liquid Phase (SLP); 2.5.6 Modification of an Achiral Heterogeneous Catalyst with a Chiral Auxiliary; 2.5.7 Achiral Metal Catalysts on Chiral Supports; References
3 Organic Polymers as a Catalyst Recovery Vehicle3.1 General Introduction; 3.2 Alkene Hydrogenation; 3.3 Carbonyl and Imine Reduction; 3.4 Carbon-Carbon Bond Formation; 3.5 Carbonyl Alkylation; 3.6 Diels-Alder Reactions; 3.7 Enolate Chemistry; 3.8 Strecker Chemistry; 3.9 Asymmetric Dihydroxylation; 3.10 Epoxidation and Epoxide Ring Opening; 3.11 Acylation Catalysts; 3.12 Conclusion; References; 4 Liquid Biphasic Enantioselective Catalysis; 4.1 Introduction; 4.2 Hydrogenation; 4.3 Hydroformylation; 4.4 Oxidation; 4.5 Lewis Acid-Catalyzed Reactions; 4.6 Enzymatic Reactions; 4.7 Summary
References5 Immobilized Enzymes in Enantioselective Organic Synthesis; 5.1 Introduction; 5.2 Immobilization; 5.2.1 Methods of Immobilization; 5.2.1.1 Enzymes; 5.2.1.2 Carriers; 5.2.1.3 Binding Enzymes to Carriers; 5.2.1.4 Cross-Linked Enzyme Crystals; 5.2.2 Activity Assay; 5.2.3 Activity Balance; 5.2.4 Cost of Immobilization; 5.3 Operation; 5.3.1 Reactors; 5.3.2 Operational Stability; 5.4 Summary; References; 6 Enantioselective Hydrogenation Catalyzed by Platinum Group Metals Modified by Natural Alkaloids; 6.1 Historical Perspective
6.2 Enantioselective Hydrogenation of Activated Ketones over Platinum
Record Nr. UNINA-9910841240203321
Weinheim ; ; New York, : Wiley-VCH, c2000
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chiral Lewis Acids / Koichi Mikami editor
Chiral Lewis Acids / Koichi Mikami editor
Pubbl/distr/stampa Cham, : Springer, 2018
Descrizione fisica XIII, 220 p. : ill. ; 24 cm
Disciplina 540(Chimica generale)
546(Chimica inorganica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-VAN0125273
Cham, : Springer, 2018
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
Chiral Lewis Acids / Koichi Mikami editor
Chiral Lewis Acids / Koichi Mikami editor
Edizione [Cham : Springer, 2018]
Pubbl/distr/stampa XIII, 220 p., : ill. ; 24 cm
Descrizione fisica Pubblicazione in formato elettronico
Disciplina 540(Chimica generale)
546(Chimica inorganica)
541.395(Catalisi)
547.05(Chimica dei composti metallorganici)
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNICAMPANIA-SUN0125273
XIII, 220 p., : ill. ; 24 cm
Materiale a stampa
Lo trovi qui: Univ. Vanvitelli
Opac: Controlla la disponibilità qui
Chirale metallkomplexe der lanthanoide mit amidinat- und pyrrolyl-liganden und deren anwendung als katalysatoren in der intramolekularen hydroaminierung / / Tobias Stephan Brunner
Chirale metallkomplexe der lanthanoide mit amidinat- und pyrrolyl-liganden und deren anwendung als katalysatoren in der intramolekularen hydroaminierung / / Tobias Stephan Brunner
Autore Brunner Tobias Stephan
Pubbl/distr/stampa Göttingen, [Germany] : , : Cuvillier Verlag, , 2016
Descrizione fisica 1 online resource (128 pages) : illustrations, tables
Disciplina 541.395
Soggetto topico Catalysis
ISBN 3-7369-8229-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ger
Record Nr. UNINA-9910794973303321
Brunner Tobias Stephan  
Göttingen, [Germany] : , : Cuvillier Verlag, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Chirale metallkomplexe der lanthanoide mit amidinat- und pyrrolyl-liganden und deren anwendung als katalysatoren in der intramolekularen hydroaminierung / / Tobias Stephan Brunner
Chirale metallkomplexe der lanthanoide mit amidinat- und pyrrolyl-liganden und deren anwendung als katalysatoren in der intramolekularen hydroaminierung / / Tobias Stephan Brunner
Autore Brunner Tobias Stephan
Pubbl/distr/stampa Göttingen, [Germany] : , : Cuvillier Verlag, , 2016
Descrizione fisica 1 online resource (128 pages) : illustrations, tables
Disciplina 541.395
Soggetto topico Catalysis
ISBN 3-7369-8229-1
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione ger
Record Nr. UNINA-9910824099603321
Brunner Tobias Stephan  
Göttingen, [Germany] : , : Cuvillier Verlag, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui