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dc.contributor.authorSeymen, Andreas-
dc.contributor.authorOpper, Ulrike-
dc.contributor.authorVoß, Andreas-
dc.contributor.authorBrieger, Lukas-
dc.contributor.authorOtte, Felix-
dc.contributor.authorUnkelbach, Christian-
dc.contributor.authorO'Shea, Donal F.-
dc.contributor.authorStrohmann, Carsten-
dc.date.accessioned2021-07-16T12:54:59Z-
dc.date.available2021-07-16T12:54:59Z-
dc.date.issued2020-08-26-
dc.identifier.urihttp://hdl.handle.net/2003/40320-
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-22195-
dc.description.abstractInsights gained from a comparison of aminometalation reactions with lithium amides, potassium amides and mixed lithium/potassium amides are presented. A combination of structural characterization, DFT calculations and electrophile reactions of aminometalated intermediates has shown the advantages of using a mixed metal strategy. While potassium amides fail to add, the lithium amides are uncontrollable and eliminated, yet the mixed K/Li amides deliver the best of both systems. Aminopotassiation proceeds to form the alkylpotassium species which has enhanced stability over its lithium counterpart allowing for its isolation and thereby its further characterization.en
dc.language.isoende
dc.relation.ispartofseriesAngewandte Chemie International Edition;Vol. 59. 2020, Issue 50, pp 22500-22504-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectAlkali metalsen
dc.subjectAminometalationen
dc.subjectCarbanionsen
dc.subjectPotassiumen
dc.subjectSynergistic effectsen
dc.subject.ddc540-
dc.titleAminopotassiation by mixed K/Li amidesen
dc.title.alternativea synthetic path to difficult to access phenethylamine derivatesen
dc.typeTextde
dc.type.publicationtypearticlede
dcterms.accessRightsopen access-
eldorado.secondarypublicationtruede
eldorado.secondarypublication.primaryidentifierhttps://doi.org/10.1002/anie.202009318de
eldorado.secondarypublication.primarycitationAngewandte Chemie International Edition. Vol. 59. 2020, Issue 50, pp 22500-22504de
Appears in Collections:Lehrstühle für Anorganische Chemie

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