C–H Activation by Ruthenium(II), Cobalt(III) and Manganese(I) Catalysis

Zell, Daniel

dc.contributor.advisor	Ackermann, Lutz Prof. Dr.
dc.contributor.author	Zell, Daniel
dc.date.accessioned	2017-07-07T08:12:19Z
dc.date.available	2017-07-07T08:12:19Z
dc.date.issued	2017-07-07
dc.identifier.uri	http://hdl.handle.net/11858/00-1735-0000-0023-3E9C-2
dc.identifier.uri	http://dx.doi.org/10.53846/goediss-6385
dc.language.iso	eng	de
dc.publisher	Niedersächsische Staats- und Universitätsbibliothek Göttingen	de
dc.rights.uri	http://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc	540	de
dc.title	C–H Activation by Ruthenium(II), Cobalt(III) and Manganese(I) Catalysis	de
dc.type	doctoralThesis	de
dc.contributor.referee	Ackermann, Lutz Prof. Dr.
dc.date.examination	2017-07-04
dc.description.abstracteng	C–H functionalizations have expanded the toolbox of organic chemistry and found widespread applications in the synthesis of complex and bioactive molecules. Within this thesis, several new synthetic transformations by powerful ruthenium(II) and earth-abundant cobalt(III) and manganese(I) catalysis were developed. Detailed studies provided fundamental mechanistic insights and set the stage for the design of highly stereoselective catalytic systems.	de
dc.contributor.coReferee	Breder, Alexander Dr.
dc.subject.eng	C–H Activation	de
dc.subject.eng	Catalysis	de
dc.subject.eng	Stereoselective Synthesis	de
dc.subject.eng	3d Transition Metals	de
dc.identifier.urn	urn:nbn:de:gbv:7-11858/00-1735-0000-0023-3E9C-2-1
dc.affiliation.institute	Fakultät für Chemie	de
dc.subject.gokfull	Chemie (PPN62138352X)	de
dc.identifier.ppn	893112909

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Fakultät für Chemie (inkl. GAUSS) [701]

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