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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.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

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