Cobalt(II)-azabis(oxazoline)-catalyzed conjugate reduction of alpha,beta-unsaturated carbonyl compounds

Geiger, Christian and Kreitmeier, Peter and Reiser, Oliver (2005) Cobalt(II)-azabis(oxazoline)-catalyzed conjugate reduction of alpha,beta-unsaturated carbonyl compounds. ADVANCED SYNTHESIS & CATALYSIS, 347 (2-3). pp. 249-254. ISSN 1615-4150, 1615-4169

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Abstract

Azabis(oxazolines) prove to be superior ligands for the enantioselective, cobalt(II)-catalyzed conjugate reduction of alpha,beta-unsaturated carbonyl compounds with sodium borohydride. beta-Trisubstituted a,p-unsaturated esters and amides as well as gamma-butenolides are readily converted to their corresponding saturated counterparts with enantioselectivities up to 97% ee.

Item Type: Article
Uncontrolled Keywords: SEMICORRIN COBALT CATALYSTS; ENANTIOSELECTIVE REDUCTION; ASYMMETRIC CATALYSIS; CHIRAL LIGANDS; COMPLEXES; 1,4-REDUCTION; CARBOXAMIDES; BOROHYDRIDE; ESTERS; azabis(oxazolines); cobalt; conjugate reduction; transition metals; alpha,beta-unsaturated amides; alpha,beta-unsaturated esters
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: 28 May 2021 09:59
Last Modified: 28 May 2021 09:59
URI: https://pred.uni-regensburg.de/id/eprint/36492

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