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1,1'-binaphthyl-based chiral materials [[electronic resource] ] : our journey / / Lin Pu
1,1'-binaphthyl-based chiral materials [[electronic resource] ] : our journey / / Lin Pu
Autore Pu Lin <1965->
Pubbl/distr/stampa London, : Imperial College Press, c2010
Descrizione fisica 1 online resource (346 p.)
Disciplina 547
Soggetto topico Chirality
Asymmetric synthesis
Molecular theory
Soggetto genere / forma Electronic books.
ISBN 1-282-75993-0
9786612759932
1-84816-412-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preface; Contents; References; 1. Introduction About 1,1 -Binaphthyls; References; 2. Main Chain Chiral-Conjugated Polymers; 2.1. Introduction About Chiral-Conjugated Polymers; 2.2. Binaphthyl-Based Polyarylenevinylenes; 2.3. Binaphthyl-Based Polyarylenes; 2.4. Binaphthyl-Based Polyaryleneethynylenes; 2.5. Binaphthyl-Thiophene Copolymers; 2.5.1. Copolymerization of Binaphthyl and Oligothiophene Monomers; 2.5.2. Electroluminescence Study; 2.6. Copolymers of BINAM and Thiophene-Containing Conjugated Linkers; 2.7. Polybinaphthyls Without Conjugated Linkers
2.7.1. Using Nickel Complexes to Promote Polymerization212.7.2. Synthesis of the Binaphthyl-Based Polydendrimers by Using Ni Complexes to Promote Polymerization23; 2.7.3. Using the Suzuki Coupling Reaction for Polymerization21b; 2.7.4. Electroluminescence Study of the Polybinaphthyls26; 2.8. Propeller-Like Polybinaphthyls; 2.8.1. Synthesis of the Propeller-Like Polymers Derived from BINOL27,28; 2.8.2. Synthesis of the Propeller-Like Polymers Derived from BINAM31; 2.8.3. Study of the Non-linear Optical Properties of the Propeller-Like Polymers32; 2.9. Dipole-Oriented Propeller-Like Polymers
2.10. Binaphthyl-Based Polysalophens2.11. Helical Ladder Polybinaphthyls; References; 3. Polybinaphthyls in Asymmetric Catalysis; 3.1. Introduction about Chiral Polymers in Asymmetric Catalysis; 3.2. Synthesis of Major-Groove Poly(BINOL)s; 3.2.1. Synthesis of Polybinaphthyls with Various Protecting Groups5; 3.2.2. Hydrolysis of the Polybinaphthyls to Generate Poly(BINOL)s5; 3.2.3. Synthesis of Poly(BINOL)s Containing Alkyl-Substituted Phenylene Linkers6; 3.3. Application of the Major-Groove Poly(BINOL)s to Catalyze the Mukaiyama Aldol Reaction
3.4. Application of the Major-Groove Poly(BINOL)s to Catalyze the Hetero-Diels-Alder Reaction3.5. Using the Ti(IV) Complex of the Major-Groove Poly(BINOL) to Catalyze the Diethylzinc Addition to Aldehydes; 3.6. Synthesis of the Minor-Groove Poly(BINOL)s; 3.7. Application of the Major- and Minor-Groove Poly(BINOL)s to Catalyze the Asymmetric Organozinc Addition to Aldehydes; 3.7.1. Asymmetric Diethylzinc Addition to Aldehydes Catalyzed by the Poly(BINOL)s; 3.7.2. Study of the Reactions of the Minor-Groove Poly(BINOL) and a Few Monomeric BINOL Derivatives with Diethylzinc
3.7.3. Synthesis of the Monomeric Model Compound of the Minor-Groove Poly(BINOL) to Catalyze the Dialkylzinc Addition to Aldehydes10b,c3.7.4. Converting the Highly Enantioselective Mono(BINOL) Catalyst to a Highly Enantioselective Poly(BINOL) Catalyst for the Asymmetric Organozinc Additions10; 3.8. Asymmetric Reduction of Prochiral Ketones Catalyzed by the Chiral BINOL Monomer and Polymer Catalysts; 3.9. Asymmetric Epoxidation of α, β-UnsaturatedKetones Catalyzed by the Minor- and Major-GroovePoly(BINOL)s
3.9.1. Asymmetric Epoxidation of α,β-Unsaturated Ketonesin the Presence of a Stoichiometric Amount of theMajor-Groove Poly(BINOL)s, Diethylzincand Oxygen
Record Nr. UNINA-9910456159103321
Pu Lin <1965->  
London, : Imperial College Press, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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1,1'-binaphthyl-based chiral materials [[electronic resource] ] : our journey / / Lin Pu
1,1'-binaphthyl-based chiral materials [[electronic resource] ] : our journey / / Lin Pu
Autore Pu Lin <1965->
Pubbl/distr/stampa London, : Imperial College Press, c2010
Descrizione fisica 1 online resource (346 p.)
Disciplina 547
Soggetto topico Chirality
Asymmetric synthesis
Molecular theory
ISBN 1-282-75993-0
9786612759932
1-84816-412-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Preface; Contents; References; 1. Introduction About 1,1 -Binaphthyls; References; 2. Main Chain Chiral-Conjugated Polymers; 2.1. Introduction About Chiral-Conjugated Polymers; 2.2. Binaphthyl-Based Polyarylenevinylenes; 2.3. Binaphthyl-Based Polyarylenes; 2.4. Binaphthyl-Based Polyaryleneethynylenes; 2.5. Binaphthyl-Thiophene Copolymers; 2.5.1. Copolymerization of Binaphthyl and Oligothiophene Monomers; 2.5.2. Electroluminescence Study; 2.6. Copolymers of BINAM and Thiophene-Containing Conjugated Linkers; 2.7. Polybinaphthyls Without Conjugated Linkers
2.7.1. Using Nickel Complexes to Promote Polymerization212.7.2. Synthesis of the Binaphthyl-Based Polydendrimers by Using Ni Complexes to Promote Polymerization23; 2.7.3. Using the Suzuki Coupling Reaction for Polymerization21b; 2.7.4. Electroluminescence Study of the Polybinaphthyls26; 2.8. Propeller-Like Polybinaphthyls; 2.8.1. Synthesis of the Propeller-Like Polymers Derived from BINOL27,28; 2.8.2. Synthesis of the Propeller-Like Polymers Derived from BINAM31; 2.8.3. Study of the Non-linear Optical Properties of the Propeller-Like Polymers32; 2.9. Dipole-Oriented Propeller-Like Polymers
2.10. Binaphthyl-Based Polysalophens2.11. Helical Ladder Polybinaphthyls; References; 3. Polybinaphthyls in Asymmetric Catalysis; 3.1. Introduction about Chiral Polymers in Asymmetric Catalysis; 3.2. Synthesis of Major-Groove Poly(BINOL)s; 3.2.1. Synthesis of Polybinaphthyls with Various Protecting Groups5; 3.2.2. Hydrolysis of the Polybinaphthyls to Generate Poly(BINOL)s5; 3.2.3. Synthesis of Poly(BINOL)s Containing Alkyl-Substituted Phenylene Linkers6; 3.3. Application of the Major-Groove Poly(BINOL)s to Catalyze the Mukaiyama Aldol Reaction
3.4. Application of the Major-Groove Poly(BINOL)s to Catalyze the Hetero-Diels-Alder Reaction3.5. Using the Ti(IV) Complex of the Major-Groove Poly(BINOL) to Catalyze the Diethylzinc Addition to Aldehydes; 3.6. Synthesis of the Minor-Groove Poly(BINOL)s; 3.7. Application of the Major- and Minor-Groove Poly(BINOL)s to Catalyze the Asymmetric Organozinc Addition to Aldehydes; 3.7.1. Asymmetric Diethylzinc Addition to Aldehydes Catalyzed by the Poly(BINOL)s; 3.7.2. Study of the Reactions of the Minor-Groove Poly(BINOL) and a Few Monomeric BINOL Derivatives with Diethylzinc
3.7.3. Synthesis of the Monomeric Model Compound of the Minor-Groove Poly(BINOL) to Catalyze the Dialkylzinc Addition to Aldehydes10b,c3.7.4. Converting the Highly Enantioselective Mono(BINOL) Catalyst to a Highly Enantioselective Poly(BINOL) Catalyst for the Asymmetric Organozinc Additions10; 3.8. Asymmetric Reduction of Prochiral Ketones Catalyzed by the Chiral BINOL Monomer and Polymer Catalysts; 3.9. Asymmetric Epoxidation of α, β-UnsaturatedKetones Catalyzed by the Minor- and Major-GroovePoly(BINOL)s
3.9.1. Asymmetric Epoxidation of α,β-Unsaturated Ketonesin the Presence of a Stoichiometric Amount of theMajor-Groove Poly(BINOL)s, Diethylzincand Oxygen
Record Nr. UNINA-9910780725203321
Pu Lin <1965->  
London, : Imperial College Press, c2010
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Advances in asymmetric autocatalysis and related topics / / editors, Gyula Palyi, Robert Kurdi, Claudia Zucchi
Advances in asymmetric autocatalysis and related topics / / editors, Gyula Palyi, Robert Kurdi, Claudia Zucchi
Pubbl/distr/stampa London, England : , : Academic Press, , 2017
Descrizione fisica 1 online resource (376 pages) : illustrations (some color)
Disciplina 547.2
Collana National Academy of Sciences, Literature and Arts (Modena) ;
Soggetto topico Asymmetric synthesis
Autocatalysis
ISBN 0-12-812825-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910583032303321
London, England : , : Academic Press, , 2017
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Autore Rueping Magnus
Edizione [1st ed.]
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Descrizione fisica 1 online resource (303 pages)
Disciplina 541.395
Soggetto topico Catalysis
Asymmetric synthesis
ISBN 3-527-69479-X
3-527-69478-1
3-527-69477-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Introduction -- 1.1 Book Structure and Notation -- 1.2 Catalyst Preparation -- 1.3 Metal Impurities -- References -- Chapter 2 Reactions of Imines -- 2.1 Nucleophilic Addition Reactions -- 2.1.1 C-Nucleophiles -- 2.1.2 N-Nucleophiles -- 2.1.3 O-Nucleophiles -- 2.1.4 P-Nucleophiles -- 2.2 Mannich Reactions -- 2.3 Strecker Reactions -- 2.4 Biginelli Reactions -- 2.5 Friedel-Crafts Reactions -- 2.5.1 Indole Coupling Partners with Aldimines -- 2.5.2 Indole Coupling Partners to Ketimines -- 2.5.3 Non-Indole Aromatic Partners -- 2.5.4 Pictet-Spengler Reactions -- 2.6 Transfer Hydrogenations -- 2.6.1 Imine Partners -- 2.6.2 α-Imino Ester Partners -- 2.6.3 N-Heterocycles -- 2.6.4 Cascade Processes -- 2.6.5 Miscellaneous Reactions -- 2.7 Pericyclic Reactions -- 2.7.1 Aza-Diels-Alder/Povarov -- 2.7.2 1,3-Dipolar Cycloaddition -- 2.7.3 Electrocyclizations and Sigmatropic Rearrangements -- 2.8 Radical Reactions -- References -- Chapter 3 Reactions of Generated Imine Intermediates -- 3.1 Enamines -- 3.1.1 Nucleophilic Addition Reactions -- 3.1.2 Transfer Hydrogenation -- 3.2 Indoles Containing Leaving Groups -- 3.2.1 Nucleophilic Addition Reactions -- 3.2.2 Friedel-Crafts Reactions -- 3.3 N-Acetals and Aminals -- 3.3.1 Nucleophilic Addition Reactions -- 3.3.2 Friedel-Crafts Reactions -- 3.3.3 Transfer Hydrogenation -- 3.4 Miscellaneous Formation -- References -- Chapter 4 Reactions of Carbonyls -- 4.1 Nucleophilic Addition Reactions -- 4.1.1 C-Nucleophiles -- 4.1.2 N-, O-, and P-Nucleophiles -- 4.2 Aldol Reactions -- 4.3 Pericyclic Reactions -- 4.4 Reductions -- References -- Chapter 5 Reactions of Generated Carbonyl Intermediates -- 5.1 Enol Ethers -- 5.2 Acetals -- 5.3 Phenols Containing Leaving Groups -- References -- Chapter 6 Reactions of Alkenes -- 6.1 Nucleophilic Addition Reactions.
6.2 Friedel-Crafts Reactions -- 6.3 Pericyclic Reactions -- 6.4 Cascades -- References -- Chapter 7 Reactions of Other Substrates -- 7.1 Aziridines -- 7.2 O-Heterocycles and Ethers -- 7.3 Hydrazines and Hydrazones -- 7.4 Azo/Diazo Substrates -- 7.5 Halogens -- 7.5.1 Fluorine -- 7.5.2 Bromine -- 7.6 Oxidizing Agents -- 7.7 Miscellaneous Substrates -- References -- Experimental Protocols -- Appendix A: Catalyst Frequency -- Appendix B: Overview of Phosphoric Acids (PA) -- Appendix C: Overview of N-Phosphoramide Acids (NPA) -- Appendix D: Overview of SPINOL Phosphoric Acids (SPA) -- Appendix E: Overview of All Other Brønsted Acids (BA) -- Index -- EULA.
Record Nr. UNINA-9910137225903321
Rueping Magnus  
Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Asymmetric bronsted acid catalysis / / Magnus Rueping, Dixit Parmar, and Erli Sugiono
Autore Rueping Magnus
Edizione [1st ed.]
Pubbl/distr/stampa Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Descrizione fisica 1 online resource (303 pages)
Disciplina 541.395
Soggetto topico Catalysis
Asymmetric synthesis
ISBN 3-527-69479-X
3-527-69478-1
3-527-69477-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright -- Contents -- Preface -- Chapter 1 Introduction -- 1.1 Book Structure and Notation -- 1.2 Catalyst Preparation -- 1.3 Metal Impurities -- References -- Chapter 2 Reactions of Imines -- 2.1 Nucleophilic Addition Reactions -- 2.1.1 C-Nucleophiles -- 2.1.2 N-Nucleophiles -- 2.1.3 O-Nucleophiles -- 2.1.4 P-Nucleophiles -- 2.2 Mannich Reactions -- 2.3 Strecker Reactions -- 2.4 Biginelli Reactions -- 2.5 Friedel-Crafts Reactions -- 2.5.1 Indole Coupling Partners with Aldimines -- 2.5.2 Indole Coupling Partners to Ketimines -- 2.5.3 Non-Indole Aromatic Partners -- 2.5.4 Pictet-Spengler Reactions -- 2.6 Transfer Hydrogenations -- 2.6.1 Imine Partners -- 2.6.2 α-Imino Ester Partners -- 2.6.3 N-Heterocycles -- 2.6.4 Cascade Processes -- 2.6.5 Miscellaneous Reactions -- 2.7 Pericyclic Reactions -- 2.7.1 Aza-Diels-Alder/Povarov -- 2.7.2 1,3-Dipolar Cycloaddition -- 2.7.3 Electrocyclizations and Sigmatropic Rearrangements -- 2.8 Radical Reactions -- References -- Chapter 3 Reactions of Generated Imine Intermediates -- 3.1 Enamines -- 3.1.1 Nucleophilic Addition Reactions -- 3.1.2 Transfer Hydrogenation -- 3.2 Indoles Containing Leaving Groups -- 3.2.1 Nucleophilic Addition Reactions -- 3.2.2 Friedel-Crafts Reactions -- 3.3 N-Acetals and Aminals -- 3.3.1 Nucleophilic Addition Reactions -- 3.3.2 Friedel-Crafts Reactions -- 3.3.3 Transfer Hydrogenation -- 3.4 Miscellaneous Formation -- References -- Chapter 4 Reactions of Carbonyls -- 4.1 Nucleophilic Addition Reactions -- 4.1.1 C-Nucleophiles -- 4.1.2 N-, O-, and P-Nucleophiles -- 4.2 Aldol Reactions -- 4.3 Pericyclic Reactions -- 4.4 Reductions -- References -- Chapter 5 Reactions of Generated Carbonyl Intermediates -- 5.1 Enol Ethers -- 5.2 Acetals -- 5.3 Phenols Containing Leaving Groups -- References -- Chapter 6 Reactions of Alkenes -- 6.1 Nucleophilic Addition Reactions.
6.2 Friedel-Crafts Reactions -- 6.3 Pericyclic Reactions -- 6.4 Cascades -- References -- Chapter 7 Reactions of Other Substrates -- 7.1 Aziridines -- 7.2 O-Heterocycles and Ethers -- 7.3 Hydrazines and Hydrazones -- 7.4 Azo/Diazo Substrates -- 7.5 Halogens -- 7.5.1 Fluorine -- 7.5.2 Bromine -- 7.6 Oxidizing Agents -- 7.7 Miscellaneous Substrates -- References -- Experimental Protocols -- Appendix A: Catalyst Frequency -- Appendix B: Overview of Phosphoric Acids (PA) -- Appendix C: Overview of N-Phosphoramide Acids (NPA) -- Appendix D: Overview of SPINOL Phosphoric Acids (SPA) -- Appendix E: Overview of All Other Brønsted Acids (BA) -- Index -- EULA.
Record Nr. UNINA-9910830359603321
Rueping Magnus  
Weinheim, [Germany] : , : Wiley-VCH Verlag GmbH & Co. KGaA, , 2016
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Asymmetric Catalysis
Asymmetric Catalysis
Pubbl/distr/stampa [Place of publication not identified] : , : De Gruyter Open
Soggetto topico Asymmetric synthesis
Organic compounds - Synthesis
Catalysis
Soggetto genere / forma Periodicals.
Soggetto non controllato Organic Chemistry
Formato Materiale a stampa
Livello bibliografico Periodico
Lingua di pubblicazione eng
Record Nr. UNINA-9910894978703321
[Place of publication not identified] : , : De Gruyter Open
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
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
Opac: Controlla la disponibilità qui
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
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
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
Lo trovi qui: Univ. Federico II
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