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Asymmetric Synthesis with Chemical and Biological Methods

Asymmetric Synthesis with Chemical and Biological Methods

Dieter Enders (Editor), Karl-Erich Jaeger (Editor), Günter Helmchen (Foreword by)

ISBN: 978-3-527-31473-7

Apr 2007

470 pages

Out of stock

$282.00

Description

Edited by two of the leading researchers in the field, this book provides a deep, interdisciplinary insight into stoichiometric and catalytic reactions in this continuously expanding area. A plethora of top German scientists with an international reputation covers various aspects, from classical organic chemistry to process development, and from the theoretical background to biological methods using enzymes. Throughout the focus is on the development of new synthetic methods in asymmetric synthesis, the synthesis of natural and bioactive compounds and the latest developments in both chemical and biological methods of catalysis, as well as the investigation of special technical and biotechnical aspects.
STOICHIOMETRIC ASYMMETRIC SYNTHESIS
Development of Novel Enantioselective Synthetic Methods
Asymmetric Synthesis of Natural Products Employing the SAMP/RAMP-Hydrazone Methodology
Asymmetric Synthesis Based on Sulfonimidoyl-Substituted Allyltitanium Complexes
The ""Daniphos"" Ligands: Synthesis and Catalytic Applications
New Chiral Ligands Based on Substituted Heterometallocenes

CATALYTIC ASYMMETRIC SYNTHESIS WITH CHEMICAL METHODS
Sulfoximines as Ligands in Asymmetric Metal Catalysis
Catalyzed Asymmetric Aryl Transfer Reactions
Substituted [2.2]-Paracyclophane Derivatives as Efficient Ligands for Asymmetric 1,2- and 1,4-Addition Reactions
Palladium-Catalyzed Allylic Alkylation of Sulfur and Oxygen Nucleophiles -
Asymmetric Synthesis, Kinetic Resolution and Dynamic Kinetic Resolution
The QUINAPHOS Ligand Family and its Application in Asymmetric Synthesis
Immobilization of Transition Metal Complexes and their Application to Enantioselective Catalysis

CATALYTIC ASYMMETRIC SYNTHESIS WITH BIOLOGICAL METHODS
Directed Evolution to Increase the Substrate Range of Benzoylformate Decarboxylase from Pseudomonas Putida
C-C Bonding Microbial Enzymes: Thiamine Diphosphate-Dependent Enzymes and Class I Aldolases
Enzymes for Carboligation -
2-Ketoacid Decarboxylases and Hydroxynitrile Lyases
Preparative Syntheses of Chiral Alcohols using (R)-specific Alcohol Dehydrogenases from Lactobacillus strains
Biocatalytic C-C Bond Formation in Asymmetric Synthesis
Exploring and Broadening the Biocatalytic Properties of Recombinant Sucrose Synthase 1 for the Synthesis of Sucrose Analogues
Flexible Asymmetric Redox Reactions and C-C Bond Formation by Bioorganic Synthetic Strategies

REACTION TECHNOLOGY IN ASYMMETRIC SYNTHESIS
Reaction Engineering in Asymmetric Synthesis
Biocatalyzed Asymmetric Syntheses Using Gel-Stabilized Aqueous-Organic Two-Phase Systems
Reasonable contribution to the literature and indeed is a fantastic testimony to SFB 280 and its many talent participants. (Journal of the American Chemical Society, July 9, 2008)