Enantioselective Organocatalyzed Reactions I, 2011
Enantioselective Oxidation, Reduction, Functionalization and Desymmetrization

Organocatalyzed ReactionsI and II presents a timely summary of organocatalysed reactions including: a) Enantioselective C-C bond formation processes e.g. Michael-addition, Mannich-reaction, Hydrocyanation (Strecker-reaction), aldol reaction, allylation, cycloadditions, aza-Diels-Alder reactions, benzoin condensation, Stetter reaction, conjugative Umpolung, asymmetric Friedel-Crafts reactions; b) Asymmetric enantioselective reduction processes e.g. Reductive amination of aldehydes or ketones, asymmetric transfer hydrogenation; c) Asymmetric enantioselective oxidation processes;
d) Asymmetric epoxidation, Bayer-Villiger oxidation; e) Enantioselective a-functionalization; f) A-alkylation of ketones, a-halogenation and a-oxidation of carbonyl compounds.

Organocatalysed Asymmetric Oxidation Reactions - Enantioselective Reductions Using Dihydropyridines - Organocatalyzed Enantioselective Protonation - Enantioselective á -Heterofunctionalization of  Carbonyl Compounds - Chiral Primary Amine Catalysis - Bifunctional Acid-Base Catalysis - Chalcogen-Based Organocatalysis

Dr. Rainer Mahrwald was born in 1950. He studied chemistry at MLU Halle and subsequently joined the „Manfred von Ardenne“ Research Institute in Dresden, where he led the synthetics group. He gained his doctorate under G. Wagner in Leipzig in 1979, and went on to the Institute of Organic Chemistry at the Academy of Science in Berlin, where he remained until 1990. Following a stay at the Philipps-University in Marburg, Dr. Mahrwald qualified as a lecturer at the Humboldt University Berlin, where he is now a lecturer.