Asymmetric catalysis. Part 127: Enantioselective desymmetrization of 2-n-butyl-4,7-dihydro-1,3-dioxepin with (eta(6)-arene)ruthenium(II) half-sandwich complexes

Brunner, Henri and Prommesberger, Markus (1998) Asymmetric catalysis. Part 127: Enantioselective desymmetrization of 2-n-butyl-4,7-dihydro-1,3-dioxepin with (eta(6)-arene)ruthenium(II) half-sandwich complexes. TETRAHEDRON-ASYMMETRY, 9 (18). pp. 3231-3239. ISSN 0957-4166

Full text not available from this repository. (Request a copy)

Abstract

(eta(6)-Arene)ruthenium half-sandwich complexes are highly active and stereoselective catalysts in the enantioselective desymmetrization of 2-n-butyl-4,7-dihydro-1,3-dioxepin to give 2-n-butyl-4,5-dihydro-1,3-dioxepin. Enantioselectivities up to 61% ee were achieved. The temperature and solvent dependence of the catalysis as well as the activation of the catalyst were investigated. (C) 1998 Elsevier Science Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: TRANSITION-METAL COMPLEXES; SCHIFF-BASE COMPLEXES; X-RAY STRUCTURE; DIASTEREOSELECTIVE SYNTHESIS; CRYSTAL-STRUCTURES; RUTHENIUM ATOM; LIGAND; STEREOCHEMISTRY
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: 16 Feb 2023 07:17
Last Modified: 16 Feb 2023 07:17
URI: https://pred.uni-regensburg.de/id/eprint/49491

Actions (login required)

View Item View Item