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Sustainable Catalysis. Challenges and Practices for the Pharmaceutical and Fine Chemical Industries

  • ID: 2330602
  • Book
  • 440 Pages
  • John Wiley and Sons Ltd
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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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Foreword vii

Preface ix

Contributors xi

Abbreviations xiii

1 Catalytic Reduction of Amides Avoiding LiAlH4 or B2H6 1Deborah L. Dodds and David J. Cole–Hamilton

2 Hydrogenation of Esters 37Lionel A. Saudan

3 Synthesis of Chiral Amines Using Transaminases 63Nicholas J. Turner and Matthew D. Truppo

4 Development of a Sitagliptin Transaminase 75Jacob M. Janey

5 Direct Amide Formation Avoiding Poor Atom Economy Reagents 89Benjamin M. Monks and Andrew Whiting

6 Industrial Applications of Boric Acid and Boronic Acid–Catalyzed Direct Amidation Reactions 111Joanne E. Anderson, Jannine Cobb, Roman Davis, Peter J. Dunn, Russ N. Fitzgerald, and Alan J. Pettman

7 OH Activation for Nucleophilic Substitution 121Jonathan M.J. Williams

8 Application of a Redox–Neutral Alcohol Amination in the Kilogram–Scale Synthesis of a GlyT1 Inhibitor 139Martin A. Berliner

9 Olefin Metathesis: From Academic Concepts to Commercial Catalysts 163Justyna Czaban, Christian Torborg, and Karol Grela

10 Challenge and Opportunity in Scaling–up Metathesis Reaction: Synthesis of Ciluprevir (BILN 2061) 215Nathan Yee, Xudong Wei, and Chris Senanayake

11 C H Activation of Heteroaromatics 233Koji Hirano and Masahiro Miura

12 The Discovery of a New Pd/Cu Catalytic System for C H Arylation and Its Applications in a Pharmaceutical Process 269Jinkun Huang, Xiang Wang, and Johann Chan

13 Diarylprolinol Silyl Ethers: Development and Application as Organocatalysts 287Hiroaki Gotoh and Yujiro Hayashi

14 Organocatalysis for Asymmetric Synthesis: From Lab to Factory 317Feng Xu

15 Catalytic Variants of Phosphine Oxide–Mediated Organic Transformations 339Stephen P. Marsden

16 Formation of C C Bonds Via Catalytic Hydrogenation and Transfer Hydrogenation 363Joseph Moran and Michael J. Krische

Index 409

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Peter J. Dunn
K. K. (Mimi) Hii
Michael J. Krische
Michael T. Williams
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