Ruthenium(II)-Catalyzed C-N, C-O and C-C Formations by C-H Activation

dc.contributor.advisor	Ackermann, Lutz Prof. Dr.
dc.contributor.author	Raghuvanshi, Keshav
dc.date.accessioned	2017-02-16T09:41:38Z
dc.date.available	2017-02-16T09:41:38Z
dc.date.issued	2017-02-16
dc.identifier.uri	http://hdl.handle.net/11858/00-1735-0000-002B-7D4C-2
dc.identifier.uri	http://dx.doi.org/10.53846/goediss-6135
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-N, C-O and C-C Formations by C-H Activation	de
dc.type	doctoralThesis	de
dc.contributor.referee	Ackermann, Lutz Prof. Dr.
dc.date.examination	2017-02-06
dc.description.abstracteng	Ruthenium catalyzed C-N, C-O and C-C formation is achieved by C-H activation. access to primary aminoketones leds to synthetic synthons for different heterocycles. removable and reusability was shown first time in C-O bond formation via ruthenium catalysis. Cheapest solo oxidanr molecular di-oxygen was used to be a sacrificial oxidant in oxidative alkenylation reaction to lead fully decorated phenol derivatives.	de
dc.contributor.coReferee	Koszinowski, Konrad Prof. Dr.
dc.subject.eng	Ruthenium, C‒N, C‒O and C‒C bond, C‒H Activation, C‒H functionalization	de
dc.identifier.urn	urn:nbn:de:gbv:7-11858/00-1735-0000-002B-7D4C-2-3
dc.affiliation.institute	Fakultät für Chemie	de
dc.subject.gokfull	Chemie (PPN62138352X)	de
dc.identifier.ppn	880357983

Name:Binder1.pdf

Size:6.017Mb

Format:PDF