Enantioselective catalysis. Part 119: New chiral 2-(2-pyridinyl)oxazoline ligands containing an additional optically active substituent in the pyridine system

Brunner, Henri and Störiko, Reinhard and Nuber, Bernhard (1998) Enantioselective catalysis. Part 119: New chiral 2-(2-pyridinyl)oxazoline ligands containing an additional optically active substituent in the pyridine system. TETRAHEDRON-ASYMMETRY, 9 (3). pp. 407-422. ISSN 0957-4166

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Abstract

The synthesis of novel chiral nitrogen ligands and their precursors is described. They consist of an optically active oxazoline bound to pyridine in the 2-position. In addition, another optically active substituent is attached to the pyridine ring. The effect of the two independent stereogenic units in one ligand was studied in the Rh(I)-catalysed enantioselective hydrosilylation of acetophenone with diphenylsilane. (C) 1998 Elsevier Science Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: ASYMMETRIC HYDROSILYLATION; KETONES; OLEFINS; ACETOPHENONE; COMPLEXES
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Anorganische Chemie > Alumni or Retired Professors > Prof. Dr. Henri Brunner
Depositing User: Dr. Gernot Deinzer
Date Deposited: 28 Feb 2023 09:09
Last Modified: 28 Feb 2023 09:09
URI: https://pred.uni-regensburg.de/id/eprint/50086

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