Asymmetric Catalysis. Part 149 [1]. Synthesis of New Chiral Tridentate Ligands for Enantioselective Catalysis |
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Authors: | Henri Brunner Christian Zettler Manfred Zabel |
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Affiliation: | (1) Institut für Anorganische Chemie, Universität Regensburg, D-93040 Regensburg, Germany, DE |
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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 |
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Keywords: | . Tridentate ligands Chirality Enantioselective catalysis X-ray structure analysis. |
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