Stereoselective Organocatalysis : Bond Formation Methodologies and Activation Modes

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 (CÂ-C), carbon-nitrogen (CÂ-N), and carbon-halogen (CÂ-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 CÂ-C bond formation. Next, the book covers: Organocatalytic CÂ-N bond formation CÂ-O bond formation CÂ-X bond formation CÂ-S, CÂ-Se, and CÂ-B bond formation Enantioselective organocatalytic reductions Cascade reactions forming both CÂ-C bonds and CÂ-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. [Publisher's Text]

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