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Glucose- und Galactose-Oximether in der enantioselektiven Katalyse

URN to cite this document: urn:nbn:de:bvb:355-opus-1124

Schönherr, Maximilian (2002) Glucose- und Galactose-Oximether in der enantioselektiven Katalyse. PhD, Universität Regensburg

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Abstract (German)

Die Darstellung von Aminooxy-substituerter Glucose und Galactose wird beschrieben. Diese Verbindungen werden mit geeigneten Carbonylverbindungen zu Oximethern kondensiert und bilden neue Liganden für die homogene Katalyse. Sie sind im Gegensatz zu Iminen äußerst hydrolysestabil. Die hergestellten Liganden wurden in verschiedenen Katalysesystemen getestet. Von einem Glucose-P,N-Liganden konnte ein ...

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Translation of the abstract (English)

The synthesis of aminooxy-substituted glucose and galactose is described. They are condensated with suitable carbonyl-bearing compounds to give oxime ethers stable towards hydrolysis as new ligands for homogenous catalysis. The ligands were tested in different catalytic systems. The structure of a Palladium-allyl-complex with one of the ligands was ...

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Item Type:Thesis of the University of Regensburg (PhD)
Date:24 October 2002
Referee:Henri Brunner
Date of exam:4 September 2002
Institutions:Chemistry and Pharmacy > Institut für Anorganische Chemie > Emeriti > Prof. Dr. Henri Brunner
Keywords:Wasserlöslichkeit , Palladium , Katalyse , Enantioselektivität , Ligand , Oximether , palladium , catalysis , enantioselective , ligands , oxime ether
Subjects:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Yes
Owner: Universitätsbibliothek Regensburg
Deposited On:21 Oct 2009 13:44
Last Modified:13 Mar 2014 11:10
Item ID:9955
Owner Only: item control page

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