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    Biocatalysis in Asymmetric Synthesis

    Biocatalysis in Asymmetric Synthesis by Gonzalo, Gonzalo De; Alcántara, Andrés R.;

    Sorozatcím: Foundations and Frontiers in Enzymology;

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        65 751 Ft (62 620 Ft + 5% áfa)
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    A termék adatai:

    • Kiadó Academic Press
    • Megjelenés dátuma 2024. május 8.

    • ISBN 9780443190575
    • Kötéstípus Puhakötés
    • Terjedelem520 oldal
    • Méret 234x190 mm
    • Súly 450 g
    • Nyelv angol
    • 610

    Kategóriák

    Hosszú leírás:

    Biocatalysis in Asymmetric Synthesis, a new volume in the Foundations and Frontiers of Enzymology series, offers an applied discussion on synthesizing biological catalysts using asymmetric synthesis for varying applications. Here, global experts in the field analyze a wide variety of biocatalysts and their physical states, process conditions for their asymmetric synthesis, solvents required during synthesis, and even downstream procedures for the recovery of final products. The book adopts an interdisciplinary approach, merging fundamental biology and its synthetic applications across industries with a wide range of practical examples, from directed evolution to biotransformation and production of novel enzymes and non-conventional catalysts. Throughout the book, the impact and application of biocatalysis in sustainable processing is considered in-depth. This book will also help non-experts in biocatalysis to apply this knowledge in their own research, providing a thorough overview of the ways asymmetric biocatalytic approaches may be adapted for different disciplines and downstream products.

    Több

    Tartalomjegyzék:

    List of contributors
    About the editors
    Preface

    1. Introduction to asymmetric synthesis employing biocatalysts
    Andrés R. Alcántara and Gonzalo de Gonzalo

    1.1 Introduction
    1.2 Type of enzymatic processes for generating asymmetry
    1.3 Biocatalysts preparations
    1.4 Novel-to-nature enzymatic processes
    1.5 Enzymes in multicatalytic systems
    1.6 Outlook
    References

    2. Biocatalysis and Green Chemistry: assessing the greenness of enzymatic processes
    Andrés R. Alcántara and Pablo Domínguez de María

    2.1 Introduction
    2.2 Green Chemistry metrics
    2.3 Green Chemistry in biocatalysis for practitioners: defining the boundaries of a biocatalytic reaction
    2.4 Conclusions
    References

    3. Study of stereocontrol in enzymatic reactions using atomic models and computational methods
    Daniel Platero-Rochart and Pedro A. Sánchez-Murcia

    3.1 Introduction
    3.2 Relevant features for stereocontrol in enzymes
    3.3 Studying the stereocontrol in enzyme catalysis using atomic models
    3.4 Some final considerations for a step-by-step protocol for simulation of enzyme activity
    References

    4. Control of the activity and enantioselectivity in biocatalyzed procedures: immobilization, medium engineering, and protein engineering
    Zhongyao Tang, Fahmi Ihza Alghiffary and Tomoko Matsuda

    4.1 Introduction
    4.2 Immobilization of enzymes
    4.3 Medium engineering
    4.4 Protein engineering
    4.5 Conclusions and future perspectives
    References

    5. Hydrolases and their application in asymmetric synthesis
    Georgina Sandoval

    5.1 Hydrolases
    5.2 Low/nonaqueous solvents as media for asymmetric synthesis by hydrolases
    5.3 Asymmetric synthesis catalyzed by key lipases
    5.4 Proteases (peptidases)
    5.5 Other hydrolases in asymmetric synthesis
    5.6 Tools to discover and improve hydrolases
    5.7 Conclusions
    References

    6. Biocatalysis for the selective reduction of carbonyl groups
    Gonzalo de Gonzalo and Antonio Franconetti

    6.1 Introduction
    6.2 Examples of the application of alcohol dehydrogenases in asymmetric synthesis
    6.3 Dynamic processes catalyzed by alcohol dehydrogenases
    6.4 Alcohol dehydrogenases in deracemization protocols
    6.5 Use of alcohol dehydrogenases in multienzymatic systems
    6.6 Conclusions
    References

    7. Synthesis of chiral amines employing imine reductases and reductive aminases
    Juan Mangas-Sánchez

    7.1 Introduction
    7.2 Imine reductases: structural and mechanistic aspects
    7.3 Cyclic imine reductions
    7.4 Imine reductase/RedAm-mediated reductive aminations
    7.5 Conclusions and perspectives
    References

    8. Biocatalyzed CarbonCarbon bond formation in enantioselective synthesis
    Daniela Gamenara and Gustavo A. Seoane

    8.1 Introduction
    8.2 Enzymatic aldol reactions. Enzymes involved. Classification
    8.3 Synthetic applications
    8.4 Perspectives and concluding remarks
    References

    9. Synthesis of chiral compounds through biooxidations
    Caterina Martin, Hugo L. van Beek, Ivana Maric, Gonzalo de Gonzalo and Nikola Loncar ?

    9.1 Introduction
    9.2 Dehydrogenases
    9.3 Oxidases
    9.4 Peroxidases
    9.5 Monooxygenases
    9.6 Peroxygenases
    9.7 Conclusion and perspectives
    References

    10. Asymmetric biocatalysis in nonconventional media: neat conditions, eutectic solvents, and supercritical conditions
    Ningning Zhang and Selin Kara

    10.1 Introduction
    10.2 Neat conditions
    10.3 Eutectic solvents
    10.4 Supercritical conditions
    10.5 Summary and perspectives
    References

    11. Multienzyme-catalyzed processes in asymmetric synthesis: state of the art and future trends
    Eduardo Macedo de Melo, Christiane Claassen, William Finnigan, Rodrigo O.M.A. de Souza and Dörte Rother

    11.1 Introduction
    11.2 Process design and optimization
    11.3 Recent developments and future trends
    11.4 Summary
    References

    12. Development of asymmetric biotransformations: flow biocatalysis, photobiocatalysis, and microwave biocatalysis
    Lucia Tamborini, Francesco Molinari and Andrea Pinto

    12.1 Introduction
    12.2 Flow biocatalysis
    12.3 Photobiocatalysis
    12.4 Microwave biocatalysis
    12.5 Conclusions
    References

    13. Industrial asymmetric biocatalysis
    Roland Wohlgemuth

    13.1 Introduction
    13.2 Asymmetric biocatalysis in manufacturing chiral intermediates and building blocks
    13.3 Asymmetric biocatalysis in manufacturing chiral pharmaceutical intermediates and active pharmaceutical ingredients
    13.4 Biocatalytic synthesis of chiral metabolites
    13.5 Biocatalytic synthesis of chiral flavor ingredients
    13.6 Biocatalytic synthesis of chiral fragrance ingredients
    13.7 Biocatalytic synthesis of chiral cosmetic ingredients
    13.8 Biocatalytic synthesis of chiral agrochemicals
    13.9 Asymmetric biocatalysis in manufacturing chiral monomers
    13.10 Biocatalytic synthesis of chiral oligomers and polymers
    13.11 Conclusions
    References

    14. Patents based on biocatalytic methods for the synthesis of valuable chiral compounds
    Nadia Guajardo

    14.1 Motivation for the biocatalytic synthesis of chiral compounds
    14.2 Methodologies for the synthesis of chiral compound employing wild-type enzymes
    14.3 Patented methodologies for the synthesis of chiral compounds employing modified enzymes
    14.4 Concluding remarks
    References
    Index

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    Gonzalo, Gonzalo De; Alcántara, Andrés R.; (ed.)

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