Applied biocatalysis : the chemist's enzyme toolbox /
"Biocatalysis has had a significant impact on the synthesis of active pharmaceutical ingredients (APIs) in recent years. The main driver for this is the ability to harness the regio- and stereoselectivity of enzymes to improve the efficiency of synthetic routes. For example, enzymes can offer d...
Clasificación: | Libro Electrónico |
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Otros Autores: | , |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Hoboken, NJ :
John Wiley & Sons, Inc.,
2021.
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Temas: | |
Acceso en línea: | Texto completo |
Tabla de Contenidos:
- Cover
- Title Page
- Copyright
- Contents
- Abbreviations
- Chapter 1 Directed Evolution of Enzymes Driving Innovation in API Manufacturing at GSK
- 1.1 Introduction
- 1.2 Drug Development Stages
- 1.3 Enzyme Panels
- 1.4 Enzyme Engineering
- 1.5 Case Studies
- 1.6 Outlook
- Chapter 2 Survey of Current Commercial Enzyme and Bioprocess Service Providers
- 2.1 Commercial Enzyme Suppliers/Distributors
- 2.2 Bioprocess Service Providers
- 2.3 Chemical Transformations of Selected Commercially Available Enzymes
- Chapter 3 Imine Reductases
- 3.1 Imine Reductase-Catalysed Enantioselective Reductive Amination for the Preparation of a Key Intermediate to Lysine-Specific Histone Demethylase 1 (LSD1) Inhibitor GSK2879552
- 3.2 Expanding the Collection of Imine Reductases Towards a Stereoselective Reductive Amination
- 3.3 Asymmetric Synthesis of the Key Intermediate of Dextromethorphan Catalysed by an Imine Reductase
- 3.4 Identification of Imine Reductases for Asymmetric Synthesis of 1-Aryl-tetrahydroisoquinolines
- 3.5 Preparation of Imine Reductases at 15 L Scale and Their Application in Asymmetric Piperazine Synthesis
- 5.4 Convenient Approach to the Biosynthesis of C2,C6-Disubstituted Purine Nucleosides Using E. coli Purine Nucleoside Phosphorylase and Arsenolysis
- 5.5 Production of L- and D-Phenylalanine Analogues Using Tailored Phenylalanine Ammonia-Lyases
- 5.6 Asymmetric Reductive Amination of Ketones Catalysed by Amine Dehydrogenases
- 5.7 Utilisation of Adenylating Enzymes for the Formation of N-Acyl Amides
- Chapter 6 Carbon-Carbon Bond Formation or Cleavage
- 6.1 An Improved Enzymatic Method for the Synthesis of (R)-Phenylacetyl Carbinol