Rogge, Torben

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[["dc.bibliographiccitation.firstpage","5828"],["dc.bibliographiccitation.issue","20"],["dc.bibliographiccitation.journal","Angewandte Chemie International Edition"],["dc.bibliographiccitation.lastpage","5832"],["dc.bibliographiccitation.volume","57"],["dc.contributor.author","Qiu, Youai"],["dc.contributor.author","Kong, Wei-Jun"],["dc.contributor.author","Struwe, Julia"],["dc.contributor.author","Sauermann, Nicolas"],["dc.contributor.author","Rogge, Torben"],["dc.contributor.author","Scheremetjew, Alexej"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2020-12-10T14:05:32Z"],["dc.date.available","2020-12-10T14:05:32Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1002/anie.201803342"],["dc.identifier.issn","1433-7851"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/69569"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Electrooxidative Rhodium-Catalyzed C−H/C−H Activation: Electricity as Oxidant for Cross-Dehydrogenative Alkenylation"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","15430"],["dc.bibliographiccitation.journal","Nature Communications"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Li, Jie"],["dc.contributor.author","Korvorapun, Korkit"],["dc.contributor.author","De Sarkar, Suman"],["dc.contributor.author","Rogge, Torben"],["dc.contributor.author","Burns, David J."],["dc.contributor.author","Warratz, Svenja"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T10:22:45Z"],["dc.date.available","2018-11-07T10:22:45Z"],["dc.date.issued","2017"],["dc.description.abstract","The full control of positional selectivity is of prime importance in C-H activation technology. Chelation assistance served as the stimulus for the development of a plethora of ortho-selective arene functionalizations. In sharp contrast, meta-selective C-H functionalizations continue to be scarce, with all ruthenium-catalysed transformations currently requiring difficult to remove or modify nitrogen-containing heterocycles. Herein, we describe a unifying concept to access a wealth of meta-decorated arenes by a unique arene ligand effect in proximity-induced ruthenium(II) C-H activation catalysis. The transformative nature of our strategy is mirrored by providing a step-economical entry to a range of meta-substituted arenes, including ketones, acids, amines and phenols-key structural motifs in crop protection, material sciences, medicinal chemistry and pharmaceutical industries."],["dc.identifier.doi","10.1038/ncomms15430"],["dc.identifier.isi","000402961800001"],["dc.identifier.pmid","28598411"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14905"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42331"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Nature Publishing Group"],["dc.relation.issn","2041-1723"],["dc.rights.access","openAccess"],["dc.subject.ddc","540"],["dc.title","Ruthenium(II)-catalysed remote C-H alkylations as a versatile platform to meta-decorated arenes"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

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[["dc.bibliographiccitation.firstpage","12840"],["dc.bibliographiccitation.issue","91"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","12843"],["dc.bibliographiccitation.volume","54"],["dc.contributor.author","Dias, Gleiston G."],["dc.contributor.author","Rogge, Torben"],["dc.contributor.author","Kuniyil, Rositha"],["dc.contributor.author","Jacob, Claus"],["dc.contributor.author","Menna-Barreto, Rubem F. S."],["dc.contributor.author","da Silva Júnior, Eufrânio N."],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2020-12-10T18:11:20Z"],["dc.date.available","2020-12-10T18:11:20Z"],["dc.date.issued","2018"],["dc.identifier.doi","10.1039/C8CC07572G"],["dc.identifier.eissn","1364-548X"],["dc.identifier.issn","1359-7345"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/73969"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-354"],["dc.title","Ruthenium-catalyzed C–H oxygenation of quinones by weak O-coordination for potent trypanocidal agents"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","3668"],["dc.bibliographiccitation.issue","30"],["dc.bibliographiccitation.journal","Chemical Communications"],["dc.bibliographiccitation.lastpage","3671"],["dc.bibliographiccitation.volume","57"],["dc.contributor.author","Shen, Zhigao"],["dc.contributor.author","Maksso, Isaac"],["dc.contributor.author","Kuniyil, Rositha"],["dc.contributor.author","Rogge, Torben"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2021-06-01T10:50:53Z"],["dc.date.available","2021-06-01T10:50:53Z"],["dc.date.issued","2021"],["dc.description.abstract","Herein, we report on selectivity control in C–H activations with alkylidenecyclopropanes (ACPs) for the chemo-selective assembly of cyclopropanes or dienes. Thus, unprecedented rhodaelectro-catalyzed C–H activations were realized with diversely decorated ACPs with a wide substrate scope and electricity as the sole oxidant."],["dc.identifier.doi","10.1039/D0CC08123J"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/86814"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-425"],["dc.relation.eissn","1364-548X"],["dc.relation.issn","1359-7345"],["dc.title","Rhodaelectro-catalyzed chemo-divergent C–H activations with alkylidenecyclopropanes for selective cyclopropylations"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.journal","Synlett"],["dc.contributor.author","Rogge, Torben"],["dc.contributor.author","Müller, Thomas"],["dc.contributor.author","Simon, Hendrik"],["dc.contributor.author","Hou, Xiaoyan"],["dc.contributor.author","Wagschal, Simon"],["dc.contributor.author","Broggini, Diego"],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2021-07-05T14:57:27Z"],["dc.date.available","2021-07-05T14:57:27Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract A triazole-directed direct C–H arylation of arenes with electron-deficient aryl halides or a synthetically useful pyrimidyl chloride was achieved through ruthenium catalysis. Our novel strategy provides operationally simple and environmentally benign access to highly functionalized hetarenes, avoiding the use of strong organometallic bases. Detailed studies revealed a significant effect of the phosphine ligand, thereby permitting the reaction to occur with excellent levels of chemo- and position selectivity."],["dc.description.abstract","Abstract A triazole-directed direct C–H arylation of arenes with electron-deficient aryl halides or a synthetically useful pyrimidyl chloride was achieved through ruthenium catalysis. Our novel strategy provides operationally simple and environmentally benign access to highly functionalized hetarenes, avoiding the use of strong organometallic bases. Detailed studies revealed a significant effect of the phosphine ligand, thereby permitting the reaction to occur with excellent levels of chemo- and position selectivity."],["dc.identifier.doi","10.1055/a-1495-6994"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/87647"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-441"],["dc.relation.eissn","1437-2096"],["dc.relation.issn","0936-5214"],["dc.title","Triazole-Enabled Ruthenium(II) Carboxylate-Catalyzed C–H Arylation with Electron-Deficient Aryl Halides"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]