
Sustainable Catalysis
Challenges and Practices for the Pharmaceutical and Fine Chemical Industries
- English
- ePUB (mobile friendly)
- Available on iOS & Android
Sustainable Catalysis
Challenges and Practices for the Pharmaceutical and Fine Chemical Industries
About this book
Opens the door to the sustainable production of pharmaceuticals and fine chemicals
Driven by both public demand and government regulations, pharmaceutical and fine chemical manufacturers are increasingly seeking to replace stoichiometric reagents used in synthetic transformations with catalytic routes in order to develop greener, safer, and more cost-effective chemical processes. This book supports the discovery, development, and implementation of new catalytic methodologies on a process scale, opening the door to the sustainable production of pharmaceuticals and fine chemicals.
Pairing contributions from leading academic and industrial researchers, Sustainable Catalysis focuses on key areas that are particularly important for the fine chemical and pharmaceutical industries, including chemo-, bio-, and organo-catalytic approaches to C–H, C–N, and C–C bond-forming reactions. Chapters include academic overviews of current innovations and industrial case studies at the process scale, providing new insights into green catalytic methodologies from proof-of-concept to their applications in the synthesis of target organic molecules.
Sustainable Catalysis provides the foundation needed to develop sustainable green synthetic procedures, with coverage of such emerging topics as:
- Catalytic reduction of amides avoiding LiAlH4 or B2H6
- Synthesis of chiral amines using transaminases
- Industrial applications of boric acid and boronic acid catalyzed direct amidation reactions
- C–H activation of heteroaromatics
- Organocatalysis for asymmetric synthesis
Offering a balanced perspective on current limitations, challenges, and solutions, Sustainable Catalysis is recommended for synthetic organic chemists seeking to develop new methodologies and for industrial chemists dedicated to large-scale process development.
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Information
Table of contents
- Cover
- Title Page
- Copyright
- Foreword
- Preface
- Contributors
- Abbreviations
- Chapter 1: Catalytic Reduction of Amides Avoiding Lialh4 or B2H6
- Chapter 2: Hydrogenation of Esters
- Chapter 3: Synthesis of Chiral Amines Using Transaminases
- Chapter 4: Development of a Sitagliptin Transaminase
- Chapter 5: Direct Amide Formation Avoiding Poor Atom Economy Reagents
- Chapter 6: Industrial Applications of Boric Acid and Boronic Acid-Catalyzed Direct Amidation Reactions
- Chapter 7: OH Activation for Nucleophilic Substitution
- Chapter 8: Application of a Redox-Neutral Alcohol Amination in the Kilogram-Scale Synthesis of a GlyT1 Inhibitor
- Chapter 9: Olefin Metathesis: From Academic Concepts to Commercial Catalysts
- Chapter 10: Challenge and Opportunity in Scaling-up Metathesis Reaction: Synthesis of Ciluprevir (Biln 2061)
- Chapter 11: C–H Activation of Heteroaromatics
- Chapter 12: The Discovery of a New Pd/Cu Catalytic System for C–H Arylation and Its Applications in a Pharmaceutical Process
- Chapter 13: Diarylprolinol Silyl Ethers: Development and Application as Organocatalysts
- Chapter 14: Organocatalysis for Asymmetric Synthesis: From Lab to Factory
- Chapter 15: Catalytic Variants of Phosphine Oxide-Mediated Organic Transformations
- Chapter 16: Formation of C–C Bonds Via Catalytic Hydrogenation and Transfer Hydrogenation
- Index