Bechtoldt, Alexander

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[["dc.bibliographiccitation.firstpage","264"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","267"],["dc.bibliographiccitation.volume","55"],["dc.contributor.author","Bechtoldt, Alexander"],["dc.contributor.author","Tirler, Carina"],["dc.contributor.author","Raghuvanshi, Keshav"],["dc.contributor.author","Warratz, Svenja"],["dc.contributor.author","Kornhaass, Christoph"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T10:19:30Z"],["dc.date.available","2018-11-07T10:19:30Z"],["dc.date.issued","2016"],["dc.description.abstract","Ruthenium(II) oxidase catalysis by direct dioxygencoupled turnover enabled step-economical oxidative C-H alkenylation reactions at ambient pressure. Versatile ruthenium(II) biscarboxylate catalysts displayed ample substrate scope and proved applicable to weakly coordinating and removable directing groups. The twofold C-H functionalization strategy was characterized by exceedingly mild reaction conditions as well as excellent positional selectivity."],["dc.identifier.doi","10.1002/anie.201507801"],["dc.identifier.isi","000368065300032"],["dc.identifier.pmid","26489871"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/41673"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.title","Ruthenium Oxidase Catalysis for Site-Selective C-H Alkenylations with Ambient O-2 as the Sole Oxidant"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","6929"],["dc.bibliographiccitation.issue","24"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","6932"],["dc.bibliographiccitation.volume","55"],["dc.contributor.author","Kumar, N. Y. Phani"],["dc.contributor.author","Bechtoldt, Alexander"],["dc.contributor.author","Raghuvanshi, Keshav"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T10:12:54Z"],["dc.date.available","2018-11-07T10:12:54Z"],["dc.date.issued","2016"],["dc.description.abstract","Ruthenium(II) bis(carboxylate)s proved highly effective for two decarboxylative C-H alkenylation strategies. The decarboxylation proceeded efficiently at rather low temperatures. The unique versatility of the decarboxylative ruthenium(II) catalysis is reflected in the oxidative olefinations with alkenes as well as the redox-neutral hydroarylations of alkynes."],["dc.identifier.doi","10.1002/anie.201600490"],["dc.identifier.isi","000377921400023"],["dc.identifier.pmid","26996920"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/40326"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","Wiley-v C H Verlag Gmbh"],["dc.relation.issn","1521-3773"],["dc.relation.issn","1433-7851"],["dc.title","Ruthenium(II)-Catalyzed Decarboxylative C-H Activation: Versatile Routes to meta-Alkenylated Arenes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dspace.entity.type","Publication"]]