Stereoselective Organocatalysis
Bond Formation Methodologies and Activation Modes
- English
- ePUB (mobile friendly)
- Available on iOS & Android
About This Book
Sets forth an important group of environmentally friendly organic reactions
With contributions from leading international experts in organic synthesis, this book presents all the most important methodologies for stereoselective organocatalysis, fully examining both the activation mode as well as the type of bond formed. Clear explanations guide researchers through all the most important methods used to form key chemical bonds, including carbon-carbon (C–C), carbon-nitrogen (C–N), and carbon-halogen (C–X) bonds. Moreover, readers will discover how the use of non-metallic catalysts facilitates a broad range of important reactions that are environmentally friendly and fully meet the standards of green chemistry.
Stereoselective Organocatalysis begins with an historical overview and a review of activation modes in asymmetric organocatalysis. The next group of chapters is organized by bond type, making it easy to find bonds according to their applications. The first of these chapters takes a detailed look at the many routes to C–C bond formation. Next, the book covers:
- Organocatalytic C–N bond formation
- C–O bond formation
- C–X bond formation
- C–S, C–Se, and C–B bond formation
- Enantioselective organocatalytic reductions
- Cascade reactions forming both C–C bonds and C–heteroatom bonds
The final chapter is devoted to the use of organocatalysis for the synthesis of natural products. All the chapters in the book are extensively referenced, serving as a gateway to the growing body of original research reports and reviews in the field.
Based on the most recent findings and practices in organic synthesis, Stereoselective Organocatalysis equips synthetic chemists with a group of organocatalytic reactions that will help them design green reactions and overcome many challenges in organic synthesis.
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Table of contents
- Cover
- Title Page
- Copyright
- Preface
- Contributors
- Chapter 1: Introduction: A Historical Point of View
- Chapter 2: Activation Modes in Asymmetric Organocatalysis
- Chapter 3: C–C Bond Formation by Aldol Reaction
- Chapter 4: Examples of Metal-Free Direct Catalytic Asymmetric Mannich-Type Reactions Using Aminocatalysis
- Chapter 5: C–C Bond Formation by Michael Reaction
- Chapter 6: C–C Bond Formation by Diels–Alder and Other Pericyclic Reactions
- Chapter 7: N-Heterocyclic Carbene-Catalyzed C–C Bond Formation
- Chapter 8: α-Alkylation of Carbonyl Compounds
- Chapter 9: Other Reactions for C–C Bond Formation
- Chapter 10: Cascade Reactions Forming C–C Bonds
- Chapter 11: Organocatalytic C–N Bond Formation
- Chapter 12: C–O Bond Formation
- Chapter 13: Carbon–Halogen Bond Formation
- Chapter 14: C–Other Atom Bond Formation (S, Se, B)
- Chapter 15: Enantioselective Organocatalytic Reductions
- Chapter 16: Cascade Reactions Forming Both C–C Bond and C–Heteroatom Bond
- Chapter 17: Organocatalysis in the Synthesis of Natural Products
- Index