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Iron- and Ruthenium-Catalyzed Site-Selective C–C Forming Direct C–H Functionalizations

dc.contributor.advisorAckermann, Lutz Prof. Dr.
dc.contributor.authorGraczyk, Karolina
dc.date.accessioned2015-04-09T08:27:48Z
dc.date.available2015-04-09T08:27:48Z
dc.date.issued2015-04-09
dc.identifier.urihttp://hdl.handle.net/11858/00-1735-0000-0022-5FA5-4
dc.identifier.urihttp://dx.doi.org/10.53846/goediss-5014
dc.language.isoengde
dc.publisherNiedersächsische Staats- und Universitätsbibliothek Göttingende
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject.ddc540de
dc.titleIron- and Ruthenium-Catalyzed Site-Selective C–C Forming Direct C–H Functionalizationsde
dc.typedoctoralThesisde
dc.contributor.refereeAckermann, Lutz Prof. Dr.
dc.date.examination2015-03-23
dc.description.abstractengDuring the last decades, C‒C bond forming reactions have been established as one of the most important tools for modern organic synthesis for the functionalization of otherwise difficult to activate compounds. The inexpensive iron and ruthenium catalysts were suitable for sustainable syntheses through C–H bond functionalization for the preparation of functionalized heterocycles in oxidative couplings as well as alkylation and arylation reactions of otherwise inert C–H bonds. The target molecules are useful intermediates in synthetic organic and medicinal chemistry as well as material sciences.de
dc.contributor.coRefereeDiederichsen, Ulf Prof. Dr.
dc.subject.engC-H Functionalizationde
dc.subject.engIronde
dc.subject.engRutheniumde
dc.subject.engOxidative Annulationde
dc.subject.engC-C Formingde
dc.subject.engSustainable Chemistryde
dc.identifier.urnurn:nbn:de:gbv:7-11858/00-1735-0000-0022-5FA5-4-1
dc.affiliation.instituteFakultät für Chemiede
dc.subject.gokfullChemie  (PPN62138352X)de
dc.identifier.ppn821890972


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