Asymmetric Organocatalysis in Natural Product Syntheses (eBook)

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2012 | 2012
XI, 197 Seiten
Springer Wien (Verlag)
978-3-7091-1163-5 (ISBN)

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Asymmetric Organocatalysis in Natural Product Syntheses - Mario Waser
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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.

Mario Waser was born in Steyr, Austria in 1977. After studying chemistry at the Johannes Kepler University (JKU) Linz, Austria, he finished his Ph.D. thesis in 2005 in the group of Prof. Dr. Heinz Falk, working on the synthesis of second-generation hypericin-based photosensitizers. After a postdoctoral stay in the group of Prof. Dr. Alois Fürstner at the Max-Planck Institut für Kohlenforschung (Mülheim, Germany), investigating the first total syntheses of iejimalide B and iejimalide A, he spent two years as a research and development chemist for DSM Linz. Since the summer of 2009 he has held the position of Assistant Professor at JKU Linz, where he is currently working on his habilitation. Dr. Waser's main research interests are focused in the field of synthetic organic chemistry with a special emphasis on ammonium ylide-mediated (dia)-stereoselective reactions and the design of new tartaric acid-derived organocatalysts.

Mario Waser was born in Steyr, Austria in 1977. After studying chemistry at the Johannes Kepler University (JKU) Linz, Austria, he finished his Ph.D. thesis in 2005 in the group of Prof. Dr. Heinz Falk, working on the synthesis of second-generation hypericin-based photosensitizers. After a postdoctoral stay in the group of Prof. Dr. Alois Fürstner at the Max-Planck Institut für Kohlenforschung (Mülheim, Germany), investigating the first total syntheses of iejimalide B and iejimalide A, he spent two years as a research and development chemist for DSM Linz. Since the summer of 2009 he has held the position of Assistant Professor at JKU Linz, where he is currently working on his habilitation. Dr. Waser’s main research interests are focused in the field of synthetic organic chemistry with a special emphasis on ammonium ylide-mediated (dia)-stereoselective reactions and the design of new tartaric acid-derived organocatalysts.

1 Introduction.- 2 Enamine Catalysis.- Aldol Reactions.- Mannich Reactions.- a-Heterofunctionalizations.- Conjugate Additions.- Dienamine Catalysis.- Combined Enamine-Catalyzed Approaches and Cascade Reactions.- Synopsis.- 3 Iminium Catalysis.- Pericyclic Reactions.- Conjugate Additions.- Iminium-Catalyzed Organocascade Reactions.- Synopsis.- 4 Combined Iminium-Enamine Catalyzed Approaches.- Cascade Reactions Using a Single Organocatalyst.- Organocascade Catalysis Using a Combination of Different Catalysts.- Synopsis.- 5 Singly Occupied Molecular Orbital (SOMO) Catalysis.- Friedel-Crafts Reactions.- Epoxide Formation.- Synopsis.- 6 Asymmetric Phase-Transfer Catalysis.- Asymmetric a-Alkylations.- Phase-Transfer Catalyzed Michael Additions.- Alkylative Dearomatization-Annulation Reaction.- Synopsis.- 7 Chiral Brønsted Acids and Hydrogen Bonding Donors.- Chiral Phosphoric Acids.- Chiral Diols.- Chiral (Thio)-Ureas.- Bifunctional Brønsted Acid-Base Active (Thio)-Ureas.- Synopsis.- 8 Chiral Brønsted and Lewis Bases.- Cinchona Alkaloids.- Phosphine Catalysis.- Carbene Catalysis.- Synopsis.- 9 Asymmetric Oxidations and Reductions.- Organocatalytic Oxidations.- Organocatalytic Reductions.- Synopsis.- 10 Conclusions.

Erscheint lt. Verlag 30.7.2012
Reihe/Serie Progress in the Chemistry of Organic Natural Products
Zusatzinfo XI, 197 p.
Verlagsort Vienna
Sprache englisch
Themenwelt Naturwissenschaften Chemie Organische Chemie
Technik
Schlagworte Chiral Brønsted Acids • Enamine Catalysis • Iminium Catalysis • Single Occupied Molecular Orbital (SOMO) catalysis
ISBN-10 3-7091-1163-3 / 3709111633
ISBN-13 978-3-7091-1163-5 / 9783709111635
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