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Asymmetric catalysis on industrial scale : challenges, approaches and solutions / / edited by Hans-Ulrich Blaser and Hans-Jürgen Federsel
Asymmetric catalysis on industrial scale : challenges, approaches and solutions / / edited by Hans-Ulrich Blaser and Hans-Jürgen Federsel
Edizione [2nd ed.]
Pubbl/distr/stampa Weinheim : , : Wiley-VCH, , [2010]
Descrizione fisica 1 online resource (582 p.)
Disciplina 547.1395
Soggetto topico Enantioselective catalysis
Asymmetric synthesis
Enantioselective catalysis - Industrial applications
Soggetto genere / forma Electronic books.
ISBN 1-282-78388-2
9786612783883
3-527-64216-1
3-527-63064-3
3-527-63063-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Asymmetric Catalysis on Industrial Scale; Contents; List of Contributors; Introduction; Part I New processes for Existing Active Compounds (APIs); 1 Some Recent Examples in Developing Biocatalytic Pharmaceutical Processes; 2 Enantioselective Hydrogenation: Applications in Process R&D of Pharmaceuticals; 3 Chiral Lactones by Asymmetric Hydrogenation - a Step Forward in (+)-Biotin Production; 4 Biocatalytic Asymmetric Oxidation for the Production of Bicyclic Proline Peptidomimetics
10 Development of Efficient Technical Processes for the Production of Enantiopure Amino Alcohols in the Pharmaceutical Industry11 The Asymmetric Hydrogenation of Enones - Access to a New L-Menthol Synthesis; 12 Eliminating Barriers in Large-Scale Asymmetric Synthesis; 13 Catalytic Asymmetric Ring Opening: A Transfer from Academia to Industry; 14 Asymmetric Baeyer-Villiger Reactions Using Whole-Cell Biocatalysts; 15 Large-Scale Applications of Hydrolases in Biocatalytic Asymmetric Synthesis; 16 Scale-Up Studies in Asymmetric Transfer Hydrogenation
17 2,2 ,5,5 -Tetramethyl-4,4 -bis(diphenylphoshino)-3,3 -bithiophene: A Very Efficient Chiral Ligand for Ru-Catalyzed Asymmetric Hydrogenations on the Multi-Kilograms Scale18 The Power of Whole-Cell Reaction: Efficient Production of Hydroxyproline, Sugar Nucleotides, Oligosaccharides, and Dipeptides; 19 Enantioselective Ketone Hydrogenation: from Research to Pilot Scale with Industrially Viable Ru-(Phosphine-Oxazoline) Complexes; Part III Processes for New Chemical Entities (NCEs); 20 Enabling Asymmetric Hydrogenation for the Design of Ef.cient Synthesis of Drug Substances
21 Scale-up of a Telescoped Enzymatic Hydrolysis Process for an Intermediate in the Synthesis of a Factor Xa Inhibitor22 An Efficient, Asymmetric Synthesis of Odanacatib, a Selective Inhibitor of Cathepsin K for the Treatment of Osteoporosis, Using an Enzyme-Mediated Dynamic Kinetic Resolution; 23 Biocatalytic Routes to the GPIIb/IIIa Antagonist Lotrafiban, SB 214857; 24 Discovery and Development of a Catalytic Asymmetric Conjugate Addition of Ketoesters to Nitroalkenes and Its Use in the Large-Scale Preparation of ABT-546
25 The Kagan Oxidation - Industrial-Scale Asymmetric Sulfoxidations in the Synthesis of Two Related NK1/NK2 Antagonists
Record Nr. UNINA-9910140344403321
Weinheim : , : Wiley-VCH, , [2010]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Asymmetric catalysis on industrial scale : challenges, approaches and solutions / / edited by Hans-Ulrich Blaser and Hans-Jürgen Federsel
Asymmetric catalysis on industrial scale : challenges, approaches and solutions / / edited by Hans-Ulrich Blaser and Hans-Jürgen Federsel
Edizione [2nd ed.]
Pubbl/distr/stampa Weinheim : , : Wiley-VCH, , [2010]
Descrizione fisica 1 online resource (582 p.)
Disciplina 547.1395
Soggetto topico Enantioselective catalysis
Asymmetric synthesis
Enantioselective catalysis - Industrial applications
ISBN 1-282-78388-2
9786612783883
3-527-64216-1
3-527-63064-3
3-527-63063-5
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Asymmetric Catalysis on Industrial Scale; Contents; List of Contributors; Introduction; Part I New processes for Existing Active Compounds (APIs); 1 Some Recent Examples in Developing Biocatalytic Pharmaceutical Processes; 2 Enantioselective Hydrogenation: Applications in Process R&D of Pharmaceuticals; 3 Chiral Lactones by Asymmetric Hydrogenation - a Step Forward in (+)-Biotin Production; 4 Biocatalytic Asymmetric Oxidation for the Production of Bicyclic Proline Peptidomimetics
10 Development of Efficient Technical Processes for the Production of Enantiopure Amino Alcohols in the Pharmaceutical Industry11 The Asymmetric Hydrogenation of Enones - Access to a New L-Menthol Synthesis; 12 Eliminating Barriers in Large-Scale Asymmetric Synthesis; 13 Catalytic Asymmetric Ring Opening: A Transfer from Academia to Industry; 14 Asymmetric Baeyer-Villiger Reactions Using Whole-Cell Biocatalysts; 15 Large-Scale Applications of Hydrolases in Biocatalytic Asymmetric Synthesis; 16 Scale-Up Studies in Asymmetric Transfer Hydrogenation
17 2,2 ,5,5 -Tetramethyl-4,4 -bis(diphenylphoshino)-3,3 -bithiophene: A Very Efficient Chiral Ligand for Ru-Catalyzed Asymmetric Hydrogenations on the Multi-Kilograms Scale18 The Power of Whole-Cell Reaction: Efficient Production of Hydroxyproline, Sugar Nucleotides, Oligosaccharides, and Dipeptides; 19 Enantioselective Ketone Hydrogenation: from Research to Pilot Scale with Industrially Viable Ru-(Phosphine-Oxazoline) Complexes; Part III Processes for New Chemical Entities (NCEs); 20 Enabling Asymmetric Hydrogenation for the Design of Ef.cient Synthesis of Drug Substances
21 Scale-up of a Telescoped Enzymatic Hydrolysis Process for an Intermediate in the Synthesis of a Factor Xa Inhibitor22 An Efficient, Asymmetric Synthesis of Odanacatib, a Selective Inhibitor of Cathepsin K for the Treatment of Osteoporosis, Using an Enzyme-Mediated Dynamic Kinetic Resolution; 23 Biocatalytic Routes to the GPIIb/IIIa Antagonist Lotrafiban, SB 214857; 24 Discovery and Development of a Catalytic Asymmetric Conjugate Addition of Ketoesters to Nitroalkenes and Its Use in the Large-Scale Preparation of ABT-546
25 The Kagan Oxidation - Industrial-Scale Asymmetric Sulfoxidations in the Synthesis of Two Related NK1/NK2 Antagonists
Record Nr. UNINA-9910830875203321
Weinheim : , : Wiley-VCH, , [2010]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Asymmetric heterogeneous supported catalysis [[electronic resource] ] : use of nitrogen-containing ligands / / Christine Saluzzo and Stephane Guillarme
Asymmetric heterogeneous supported catalysis [[electronic resource] ] : use of nitrogen-containing ligands / / Christine Saluzzo and Stephane Guillarme
Autore Saluzzo Christine
Pubbl/distr/stampa New York, : Nova Science Publishers, c2011
Descrizione fisica 1 online resource (185 p.)
Disciplina 541/.395
Altri autori (Persone) GuillarmeStéphane
Collana Polymer science and technology
Soggetto topico Asymmetric synthesis
Enantioselective catalysis
Ligands
Nitrogen compounds
Soggetto genere / forma Electronic books.
ISBN 1-61728-101-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910462369503321
Saluzzo Christine  
New York, : Nova Science Publishers, c2011
Materiale a stampa
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Asymmetric heterogeneous supported catalysis [[electronic resource] ] : use of nitrogen-containing ligands / / Christine Saluzzo and Stephane Guillarme
Asymmetric heterogeneous supported catalysis [[electronic resource] ] : use of nitrogen-containing ligands / / Christine Saluzzo and Stephane Guillarme
Autore Saluzzo Christine
Pubbl/distr/stampa New York, : Nova Science Publishers, c2011
Descrizione fisica 1 online resource (185 p.)
Disciplina 541/.395
Altri autori (Persone) GuillarmeStéphane
Collana Polymer science and technology
Soggetto topico Asymmetric synthesis
Enantioselective catalysis
Ligands
Nitrogen compounds
ISBN 1-61728-101-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910786822703321
Saluzzo Christine  
New York, : Nova Science Publishers, c2011
Materiale a stampa
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Asymmetric heterogeneous supported catalysis [[electronic resource] ] : use of nitrogen-containing ligands / / Christine Saluzzo and Stephane Guillarme
Asymmetric heterogeneous supported catalysis [[electronic resource] ] : use of nitrogen-containing ligands / / Christine Saluzzo and Stephane Guillarme
Autore Saluzzo Christine
Edizione [1st ed.]
Pubbl/distr/stampa New York, : Nova Science Publishers, c2011
Descrizione fisica 1 online resource (185 p.)
Disciplina 541/.395
Altri autori (Persone) GuillarmeStéphane
Collana Polymer science and technology
Soggetto topico Asymmetric synthesis
Enantioselective catalysis
Ligands
Nitrogen compounds
ISBN 1-61728-101-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intro -- ASYMMETRIC HETEROGENEOUS SUPPORTED CATALYSIS: USE OF NITROGEN-CONTAINING LIGANDS -- Library of Congress Cataloging-in-Publication Data -- Contents -- Preface -- Chapter 1: Introduction -- Chapter 2: Reduction of C=O and C=N Bond -- 2.1. Hydrogenation -- 2.2. Hydrogenation Transfer Reduction -- 2.2.1. 1,2-Diamine and Derivatives -- 2.2.2. Imprinting Technique for Hydrogen Transfer Reduction with 1,2-Diamines -- 2.2.3. Aminoalcohol as Ligand -- 2.2.4. Dialdimine Ligand as Ligand -- 2.3. Enantioselective Hydride Reduction -- 2.4. Hydrosilylation with Ligands as Pendent Group -- 2.5. Reduction of C=N bond -- Chapter 3: Cyclopropanation -- 3.1. Oxazolines Ligands -- 3.1.1. Insoluble Supported-Polymer Box a Ligands -- 3.1.2. Insoluble Supported-Polymer AzaBOX as Ligands -- 3.1.3. Insoluble Supported-Polymer PyBox as Ligands -- 3.1.4. Immobilization of PyBox on Natural Polymers -- 3.1.5. Soluble Supported-Polymer Box as Ligands -- 3.1.6. Soluble Supported-Polymer AzaBox as Ligands -- 3.2. Porphyrins -- 3.3. Miscellaneous -- Chapter 4: Cycloadditions and Heterocycloadditions -- 4.1. Supported Box Ligands -- 4.2. Supported Aminoalcohol and N-Sulfonylamino Acid-Derived Oxazaborolidine or Oxazaborolidinone -- 4.3. Supported Salen as Ligand -- Chapter 5: Addition of Organometallic Reagents to Aldehydes, Ketones and Imines -- 5.1. Supported Aminoalcohols as Ligands -- 5.2. Supported Sulfonamide -- and N-Sulfonylated Aminoalcohols -- 5.3. Supported Oxazoline -- or Oxazolidine as Ligands -- 5.4. Supported Salen as Chiral Ligands -- Chapter 6: Asymmetric (-Allylic Substitution -- Chapter 7: Dihydroxylation and Aminohydroxylation -- 7.1. Insoluble Supported Alkaloid as Ligand -- 7.2. Soluble Supported Alkaloid as Ligand -- Chapter 8: Epoxidation -- 8.1. Supported Salen as Ligand -- 8.2. Porphyrins -- 8.3. Soluble Polymers.
Chapter 9: Kinetic Resolution of Terminal Epoxides -- Chapter 10: Miscellaneous -- Chapter 11: Conclusion -- References -- Index.
Record Nr. UNINA-9910806234203321
Saluzzo Christine  
New York, : Nova Science Publishers, c2011
Materiale a stampa
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Chiral analysis : advances in spectroscopy, chromatography and emerging methods / / edited by Prasad L. Polavarapu
Chiral analysis : advances in spectroscopy, chromatography and emerging methods / / edited by Prasad L. Polavarapu
Edizione [Second edition.]
Pubbl/distr/stampa Amsterdam, Netherlands : , : Elsevier, , [2018]
Descrizione fisica 1 online resource (824 pages)
Disciplina 541.223
Soggetto topico Chirality
Enantioselective catalysis
ISBN 0-444-64028-2
0-444-64027-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Part one. Chirality in nature -- Chiral asymmetry in nature / Dilip Kondepudi -- Remote sensing of homochirality : a proxy for the detection of extraterrestrial life / C.H. Lucas Patty [and three others] -- Part two. Spectroscopic methods and analyses -- Light polarization and signal processing in chiroptical instrumentation / Kenneth W. Busch, Marianna A. Busch -- Chiroptical spectroscopic studies on soft aggregates and their interactions / Vijay Raghavan, Prasad L. Polavarapu -- Vibrational optical activity in chiral analysis / Laurence A. Nafie, Rina K. Dukor -- Raman optical activity / Saeideh Ostovar pour [and three others] -- Chiral molecular tools powerful for the preparation of enantiopure compounds and unambiguous determination of their absolute configurations by X-ray crystallography and/or ¹H MNR diamagnetic anistropy / Nobuyuki Harada -- Chiroptical probes for determination of absolute stereochemistry by circular dichroism exciton chirality method / Kuwahara Chunsuke, Ikeda Mari, Habata Yoichi -- Chiral analysis by NMR spectroscopy : chiral solvating agents / Federica Balzano, Gloria Uccello-Barretta, Federica Aiello -- Chiroptical spectroscopy of biofluids / Vladimír Setnička, Lucie Habartová -- Part three. Chromatographic and electromigration methods -- Chiral gas chromatography / Rahul A. Patil, Choyce A. Weatherly, Daniel W. Armstrong -- Chiral liquid chromatography / Muhammad F. Wahab [and three others] -- Enantioseparations by capillary electromigration techniques / Bezhan Chankvetadze -- Recent developments in chiral separations by supercritical fluid chromatography / Roberta Franzini [and four others] -- Chiral separation strategies in mass spectrometry : integration of chromatography, electrophoresis, and gas-phase mobility / James N. Dodds, Jody C. May, John A. McLean -- Part four. Emerging methods -- Cavity-based chiral polarimetry / Dimitris Sofikitis [and three others] -- Quantitative chiral analysis by molecular rotational spectroscopy / Brooks H. Pate [and seven others] -- Chiral rotational spectroscopy / Robert P. Cameron, Jörg B. Götte, Stephen M. Barnett -- Chiral analysis and separation using molecular rotation / Mirianas Chachisvilis.
Record Nr. UNINA-9910583072903321
Amsterdam, Netherlands : , : Elsevier, , [2018]
Materiale a stampa
Lo trovi qui: Univ. Federico II
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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
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Enantioselection in asymmetric catalysis / / Ilya Gridnev and Pavel A. Dub
Enantioselection in asymmetric catalysis / / Ilya Gridnev and Pavel A. Dub
Autore Gridnev Ilya <1963, >
Pubbl/distr/stampa Boca Raton : , : CRC Press, , [2017]
Descrizione fisica 1 online resource (247 pages) : illustrations
Disciplina 541/.395
Soggetto topico Enantioselective catalysis
Catalysis
Asymmetric synthesis
ISBN 1-315-35334-2
1-315-37041-7
1-4987-2655-0
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Chapter 1. Transition metal-catalyzed hydrogenation -- Chapter 2. Other enantioselective reactions catalyzed by transition metals -- Chapter 3. Mechanism of enantioselection in organocatalytic reactions.
Record Nr. UNINA-9910149364703321
Gridnev Ilya <1963, >  
Boca Raton : , : CRC Press, , [2017]
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