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NMR investigations on catalysts and conformations in organo- and photocatalytic reactions, and characterization of electrolytes and supramolecular switchable container molecules

URN to cite this document: urn:nbn:de:bvb:355-epub-234770

Fleischmann, Matthias (2012) NMR investigations on catalysts and conformations in organo- and photocatalytic reactions, and characterization of electrolytes and supramolecular switchable container molecules. PhD, Universität Regensburg

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Abstract (English)

Over the last decade the field of organocatalysis, i.e. the use of small organic molecules as catalysts, has grown to a prospering area of general concepts and widely useful reactions connected with a vast increase of the research activities. Various generic activation modes, such as H-bond, counterion, enamine, iminium, SOMO or photoredox catalysis, have been identified and successfully applied ...

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Translation of the abstract (German)

Im Laufe der letzten 10 Jahre ist die Organokatalyse, d. h. die Katalyse mit kleinen organischen Molekülen als Katalysatoren, zu einem blühenden Gebiet mit allgemeinen Konzepten und breit anwendbaren Reaktionen gewachsen, verbunden mit einem enormen Anstieg der Forschungsaktivitäten. Einige grundlegende Aktivierungsmodi, wie Wasserstoffbrücken-, Gegenion-, Enamin-, Iminium-, SOMO- oder ...

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Item Type:Thesis of the University of Regensburg (PhD)
Date:7 September 2012
Referee:Prof. Dr. Ruth M. Gschwind and Dr. Kirsten Zeitler and Prof. Dr. Manfred Scheer
Date of exam:19 August 2011
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Arbeitskreis Prof. Dr. Ruth Gschwind
Keywords:NMR, peptides, organocatalysis, photocatalysis, DOSY, supramolecular chemistry, container molecules
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:07 Sep 2012 06:00
Last Modified:13 Mar 2014 19:11
Item ID:23477
Owner Only: item control page

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