Meyer, Tjark Hannes

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[["dc.bibliographiccitation.firstpage","5443"],["dc.bibliographiccitation.issue","23"],["dc.bibliographiccitation.journal","Chemistry: a European Journal"],["dc.bibliographiccitation.lastpage","5447"],["dc.bibliographiccitation.volume","23"],["dc.contributor.author","Meyer, Tjark H."],["dc.contributor.author","Liu, Weiping"],["dc.contributor.author","Feldt, Milica"],["dc.contributor.author","Wuttke, Axel"],["dc.contributor.author","Mata, Ricardo A."],["dc.contributor.author","Ackermann, Lutz"],["dc.date.accessioned","2018-11-07T10:24:50Z"],["dc.date.accessioned","2020-05-12T10:18:08Z"],["dc.date.available","2018-11-07T10:24:50Z"],["dc.date.available","2020-05-12T10:18:08Z"],["dc.date.issued","2017"],["dc.description.abstract","C-H/C-C Functionalizations were achieved with the aid of a versatile manganese(I) catalyst. Thus, an organometallic manganese-catalyzed C-H activation set the stage for silver-free C-H/C-C transformations with ample substrate scope and excellent levels of chemo-, site-, and diastereo-selectivities. The robust nature of the manganese(I) catalysis regime was reflected by the first C-H/C-C functionalization on amino acids under racemization-free reaction conditions. Detailed experimental and computational mechanistic studies provided strong evidence for a facile C-H activation and a rate-determining C-C cleavage, with considerable contribution from London dispersion interactions."],["dc.identifier.doi","10.1002/chem.201701191"],["dc.identifier.isi","000399976700011"],["dc.identifier.pmid","28317205"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65168"],["dc.language.iso","en"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.relation.eissn","0947-6539"],["dc.relation.issn","1521-3765"],["dc.title","Manganese(I)-Catalyzed Dispersion-Enabled C−H/C−C Activation"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dspace.entity.type","Publication"]]

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