Ruthenium(II)-Catalyzed C-H Arylations of Arenes

Hubrich, Jonathan

dc.contributor.advisor	Ackermann, Lutz Prof. Dr.
dc.contributor.author	Hubrich, Jonathan
dc.date.accessioned	2016-10-10T08:15:02Z
dc.date.available	2016-10-10T08:15:02Z
dc.date.issued	2016-10-10
dc.identifier.uri	http://hdl.handle.net/11858/00-1735-0000-002B-7C15-6
dc.identifier.uri	http://dx.doi.org/10.53846/goediss-5885
dc.identifier.uri	http://dx.doi.org/10.53846/goediss-5885
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	Ruthenium(II)-Catalyzed C-H Arylations of Arenes	de
dc.type	doctoralThesis	de
dc.contributor.referee	Ackermann, Lutz Prof. Dr.
dc.date.examination	2016-09-30
dc.description.abstracteng	The goal of this work was to devise environmentally friendly and cost-effective novel concepts for the efficient synthesis of biaryl units as core structure in biologically active compounds, which are of great importance to the agrochemical and pharmaceutical industries. Transition metal-catalyzed direct functionalization processes of otherwise inert C‒H bonds emerged as a more sustainable alternative to the classically used cross-coupling reactions for the synthesis of biaryls. For this reason, the research was focused on the development of novel methods for efficient and selective direct C‒H transformations to construct biaryl scaffolds in an atom- and step-economical manner.	de
dc.contributor.coReferee	Breder, Alexander Dr.
dc.subject.eng	ruthenium	de
dc.subject.eng	arylation	de
dc.subject.eng	C-H activation	de
dc.subject.eng	bioactive compounds	de
dc.subject.eng	biaryl	de
dc.identifier.urn	urn:nbn:de:gbv:7-11858/00-1735-0000-002B-7C15-6-7
dc.affiliation.institute	Fakultät für Chemie	de
dc.subject.gokfull	Chemie (PPN62138352X)	de
dc.identifier.ppn	869904299

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Fakultät für Chemie (inkl. GAUSS) [701]

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