Catalytic processes for API synthesis : from laboratory to industry /: from laboratory to industry. (2018)

• Record Type: Book
• Further Information: Note: Anthony J. Burke, Carolina Silva Marques, Nicholas Turner, Gesine Hermann.
• Authors: Burke, Anthony J (Anthony Joseph); Marques, Carolina Silva, 1981-; Turner, N. J (Nicholas J.); Hermann, Gesine J
• Contents: Foreword xi Preface xiii Abbreviations xvii 1 Catalysis and Prerequisites for the Modern Pharmaceutical Industry Landscape 1 1.1 Introduction 1 1.2 Key Historical Moments in Catalysis Development 2 1.3 Key Historical Developments in Catalysis for API Synthesis: Including Catalytic Asymmetric Synthesis 11 1.4 Catalytic Synthesis of APIs in the Twenty‐First Century: New Developments, Paradigm Shifts, and Future Challenges 20 1.5 Conclusions 26 References 26 2 Catalytic Process Design: The Industrial Perspective 31 2.1 Introduction 31 2.2 Process Design 32 2.2.1 Heterogeneous and Homogeneous Catalysts 32 2.2.2 Product Safety and Regulatory Requirements 36 2.2.3 Control of Residual Metals 37 2.2.3.1 Filtration and Adsorption 38 2.2.3.2 Extraction and Scavenging 38 2.2.3.3 Organic Solvent Nanofiltration (OSN) 41 2.2.4 Design of Experiment (DoE) 43 2.2.5 Catalyst Recycling 45 2.2.6 Scalability, Safety, and Environmental Aspects 46 2.3 Examples of Homogeneous and Heterogeneous Catalytic Reactions in API Manufacture 49 2.3.1 Batch Operations 49 2.3.2 Continuous‐Flow Operations 63 2.4 Conclusions 67 References 68 3 Hydrogenation, Hydroformylation, and Other Reductions 75 3.1 Introduction 75 3.2 Hydrogenation 75 3.2.1 Hydrogenation of Alkenes 77 3.2.1.1 Enamides 77 3.2.2 Hydrogenation of Carbonyl Groups 84 3.2.3 Hydrogenation of Imines 87 3.3 Transfer Hydrogenation 88 3.3.1 On Ketones 88 3.3.2 On Imines 92 3.4 Reductions with Oxazaborolidine Catalytic Systems 94 3.5 Hydroformylation 96 3.6 Reductions with Organocatalysts 103 3.7 Other Catalytic Reductions 104 3.7.1 Reduction of Nitro Units 104 3.7.2 Other Reductions 107 3.8 Conclusions 107 References 108 4 Oxidation: Nobel Prize Chemistry Catalysis 113 4.1 Introduction 113 4.2 Olefin Epoxidation 113 4.2.1 Metal‐based Electrophilic Methods 113 4.2.1.1 The Sharpless–Katsuki Asymmetric Epoxidation 113 4.2.1.2 The Jacobsen–Katsuki Asymmetric Epoxidation 116 4.2.2 Nucleophilic Methods 119 4.2.2.1 Nucleophilic Methods with Hydrogen Peroxide 119 4.2.3 Organocatalytic Methods 119 4.3 Olefin Dihydroxylation 121 4.4 Olefin Aminohydroxylation 125 4.5 Sulfur Oxidation 127 4.5.1 Synthesis of Sulfoxides – Use of Titanium, Molybdenum, and Vanadium Catalysts 127 4.5.2 Synthesis of Sulfones – Use of Tungsten Catalysts 132 4.6 Catalytic Oxidation of Carbonyls – Cu/Nitroxyl and Nitroxyl/NOx Catalytic Systems 133 4.7 Oxidative Dehydrogenations (ODs) 139 4.8 Conclusions 141 References 142 5 Catalytic Addition Reactions 147 5.1 Introduction 147 5.2 1, 2‐Additions 148 5.3 1, 4‐Additions 158 5.4 Conclusions 170 References 171 6 Catalytic Cross ‐Coupling Reactions – Nobel Prize Catalysis 175 6.1 Introduction 175 6.2 Heck–Mizoroki Reaction 176 6.3 The Suzuki–Miyaura Reaction 195 6.4 The Buchwald–Hartwig Reaction 210 6.5 The Sonogashira–Hagihara Reaction 224 6.6 The Allylic Substitution Reaction 234 6.7 C–H Activation Processes 239 6.8 Oxidative C─C Bond Formation 248 6.9 Conclusions 251 References 251 7 Catalytic Metathesis Reactions: Nobel Prize Catalysis 259 7.1 Introduction 259 7.2 Metathesis with Ru‐Based Catalysts 264 7.3 Mo‐Based Metathesis 283 7.4 Conclusions 286 References 286 8 Catalytic Cycloaddition Reactions: Coming Full Circle 291 8.1 Introduction 291 8.2 The “Classical” Catalytic Diels–Alder Reaction – Closing the Circle 291 8.3 The Catalytic Hetero‐Diels–Alder (hDA) Reaction 299 8.4 The Catalytic [3+2] Cycloaddition Reaction 302 8.4.1 1, 3‐Dipolar Azomethine Ylide Cycloadditions 302 8.4.2 [3+2] Cycloadditions with Carbonyl Ylides 307 8.4.3 The Azide Catalytic [3+2] Cycloaddition Reaction – The Dawn of Click Chemistry 308 8.5 Other Cycloaddition Reactions 312 8.5.1 [2+2] Cycloaddition 312 8.5.2 [2+2+2] Cycloaddition 313 8.5.3 [5+2] Cycloaddition 315 8.6 Conclusions 316 References 317 9 Catalytic Cyclopropanation Reactions 321 9.1 Introduction 321 9.2 Metal‐Catalyzed Processes 323 9.3 Conclusions 338 References 338 10 Catalytic C–H Insertion Reactions 341 10.1 Introduction 341 10.2 Metal‐Catalyzed Processes 342 10.3 Conclusions 356 References 357 11 Phase ‐Transfer Catalysis 359 11.1 Introduction 359 11.2 Achiral Phase‐Transfer Catalysis 360 11.3 Asymmetric Phase‐Transfer Catalysis 369 11.4 Conclusions 382 References 382 12 Biocatalysis 387 12.1 Introduction 387 12.2 Hydrolysis and Reverse Hydrolysis 388 12.3 Reduction 394 12.4 Oxidation 399 12.5 C─X Bond Formation 402 12.6 Conclusions 411 References 411 Index 415
• Edition: 1st
• Publisher Details: Weinheim : Wiley-VCH
• Publication Date: 2018
• Extent: 1 online resource
• Subjects: 660.2995; Catalysis
• Languages: English
• ISBNs: 9783527807260
• Related ISBNs: 9783527807246; 9783527807277
• Notes: Note: Description based on CIP data; resource not viewed.
• 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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