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Asymmetric Organocatalysis in Natural Product Syntheses [electronic resource] / by Mario Waser.

By: Waser, Mario [author.].
Contributor(s): SpringerLink (Online service).
Material type: materialTypeLabelBookSeries: Progress in the Chemistry of Organic Natural Products: 96Publisher: Vienna : Springer Vienna : Imprint: Springer, 2012Description: XI, 197 p. 215 illus., 133 illus. in color. online resource.Content type: text Media type: computer Carrier type: online resourceISBN: 9783709111635.Subject(s): Chemistry | Chemistry, Organic | Biochemistry | Catalysis | Chemistry | Organic Chemistry | Medicinal Chemistry | CatalysisDDC classification: 547 Online resources: Click here to access online
Contents:
Enamine Catalysis -- Iminium Catalysis -- Combined Iminium-Enamine Catalyzed Approaches -- Single Occupied Molecular Orbital (SOMO) Catalysis -- Asymmetric Phase-Transfer Catalysis -- Chiral Brønsted Acids and Hydrogen Bonding Donors -- Chiral Brønsted and Lewis Bases.-Asymmetric Oxidations and Reductions.
In: Springer eBooksSummary: This book provides the reader with an illustrative overview concerning successful and widely used applications of organocatalysis in the field of natural product synthesis. The main focus will be on organocatalytic key-steps for each (multi-step) synthesis described, whereas other often particularly innovative transformations will be omitted, as this would be beyond the scope of this volume.
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Enamine Catalysis -- Iminium Catalysis -- Combined Iminium-Enamine Catalyzed Approaches -- Single Occupied Molecular Orbital (SOMO) Catalysis -- Asymmetric Phase-Transfer Catalysis -- Chiral Brønsted Acids and Hydrogen Bonding Donors -- Chiral Brønsted and Lewis Bases.-Asymmetric Oxidations and Reductions.

This book provides the reader with an illustrative overview concerning successful and widely used applications of organocatalysis in the field of natural product synthesis. The main focus will be on organocatalytic key-steps for each (multi-step) synthesis described, whereas other often particularly innovative transformations will be omitted, as this would be beyond the scope of this volume.

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