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Asymmetric Catalysis. Part 149 [1]. Synthesis of New Chiral Tridentate Ligands for Enantioselective Catalysis
Authors:Henri Brunner  Christian Zettler  Manfred Zabel
Affiliation:(1) Institut für Anorganische Chemie, Universität Regensburg, D-93040 Regensburg, Germany, DE
Abstract:Summary. The synthesis of new chiral tridentate ligands is reported which coordinate transition metals in a meridional way. The ligands contain a pyridine ring, an oxazoline ring, and a strongly coordinating diphenylphosphanyl group. The methionine-derived ligand forms a copper complex, which has been studied by X-ray crystallography. The new ligands were tested in models of enantioselective catalyses, such as hydrogenation of ketopantolactone, hydrosilylation of acetophenone, and transfer hydrogenation of acetophenone.X-ray structure analysesReceived March 4, 2003; accepted March 4, 2003Published online August 18, 2003
Keywords:. Tridentate ligands   Chirality   Enantioselective catalysis   X-ray structure analysis.
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