Asymmetric Organocatalysis in Natural Product Syntheses (eBook)

Artikelnummer: 978-3-7091-1163-5
Einband: PDF
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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.
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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VerlagSpringer Vienna
EinbandPDF
Erscheinungsjahr2012
Seitenangabe197 S.
AusgabekennzeichenEnglisch
AbbildungenXI, 197 p.
Masse8'188 KB
PlattformPDF
ReiheProgress in the Chemistry of Organic Natural Products
AutorWaser, Mario

Alle Bände der Reihe "Progress in the Chemistry of Organic Natural Products"

Über den Autor Mario Waser

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.

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