Diastereospecific enantiodivergent allylation of pyrazolones as an entry to β‐aminoamides

dc.contributor.authorWannenmacher, Nick
dc.contributor.authorHeberle, Martin
dc.contributor.authorYu, Xin
dc.contributor.authorDemircan, Aysegül
dc.contributor.authorWanner, Daniel M.
dc.contributor.authorPfeffer, Camilla
dc.contributor.authorPeters, René
dc.date.accessioned2024-08-13T14:53:01Z
dc.date.available2024-08-13T14:53:01Z
dc.date.issued2022de
dc.date.updated2023-11-14T00:09:33Z
dc.description.abstractA diastereospecific enantiodivergent allylation of pyrazolones is reported which is catalyzed by a planar chiral pentaphenylferrocene based palladacycle. With the same catalyst batch both product enantiomers were selectively available. The method is applicable to structurally diverse substrates and gave products with enantiomeric excesses between 85 and 94%. In addition, we could show that pyrazolones are transformable into β‐aminoamides.en
dc.description.sponsorshipChina Scholarship Council (CSC)de
dc.description.sponsorshipanalytical service of the Institute of Organic Chemistry at the University of Stuttgartde
dc.identifier.issn1615-4169
dc.identifier.other1898542473
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:bsz:93-opus-ds-148280de
dc.identifier.urihttp://elib.uni-stuttgart.de/handle/11682/14828
dc.identifier.urihttp://dx.doi.org/10.18419/opus-14809
dc.language.isoende
dc.relation.uridoi:10.1002/adsc.202200185de
dc.rightsinfo:eu-repo/semantics/openAccessde
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/de
dc.subject.ddc540de
dc.titleDiastereospecific enantiodivergent allylation of pyrazolones as an entry to β‐aminoamidesen
dc.typearticlede
ubs.fakultaetChemiede
ubs.institutInstitut für Organische Chemiede
ubs.publikation.seiten3396-3403de
ubs.publikation.sourceAdvanced synthesis & catalysis 364 (2022), S. 3396-3403de
ubs.publikation.typZeitschriftenartikelde

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