The importance of complex stability for asymmetric copper-catalyzed cyclopropanations in [emim][OTf] ionic liquid: the bis(oxazoline)-azabis(oxazoline) case

Fraile, J. M. and Garcia, J. I. and Herrerias, C. I. and Mayoral, J. A. and Reiser, Oliver and Vaultier, M. (2004) The importance of complex stability for asymmetric copper-catalyzed cyclopropanations in [emim][OTf] ionic liquid: the bis(oxazoline)-azabis(oxazoline) case. TETRAHEDRON LETTERS, 45 (36). pp. 6765-6768. ISSN 0040-4039,

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Abstract

Azabis(oxazoline)-Cu complexes are more stable than their analogues based on bis(oxazoline) ligands. This increased stability leads to improved recoverability (up to eight times) when these systems are used in an ionic liquid medium. The solution of the chiral catalyst can even be reused in different enantioselective cyclopropanation reactions and still lead to high enantiomeric excess (>90%). (C) 2004 Elsevier Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: DIELS-ALDER REACTIONS; PHOSPHINE-LIGANDS; SOLVENT; HYDROFORMYLATION; HYDROGENATION; DIHYDROXYLATION; IMMOBILIZATION; SELECTIVITIES; CATALYSIS/; MECHANISM; asymmetric catalysis; ionic liquids
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Oliver Reiser
Depositing User: Dr. Gernot Deinzer
Date Deposited: 02 Jul 2021 05:01
Last Modified: 02 Jul 2021 05:01
URI: https://pred.uni-regensburg.de/id/eprint/37319

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