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dc.contributor.authorAchternbosch, Moritz-
dc.contributor.authorZibula, Lukas-
dc.contributor.authorSchmidt, Annika-
dc.contributor.authorKrieger, Waldemar-
dc.contributor.authorKockmann, Norbert-
dc.contributor.authorStrohmann, Carsten-
dc.date.accessioned2023-05-03T11:35:50Z-
dc.date.available2023-05-03T11:35:50Z-
dc.date.issued2022-12-27-
dc.identifier.urihttp://hdl.handle.net/2003/41360-
dc.identifier.urihttp://dx.doi.org/10.17877/DE290R-23203-
dc.description.abstractOrganolithium compounds have been used successfully in flow chemistry since the recent past. Most of the studies dealt with the use in halogen-lithium exchanges. So far, however, there has been a lack of use in substitution reactions. The use of flow microreactors makes the highly reactive organolithium compounds more controllable and thus creates new synthetic possibilities.en
dc.language.isoende
dc.relation.ispartofseriesJournal of flow chemistry;13(1)-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectOrganosilanesen
dc.subjectSubstitutionsen
dc.subjectSelectivityen
dc.subjectMicroreactoren
dc.subjectContinuous flowen
dc.subject.ddc540-
dc.titleSelective monosubstitution on a trichlorosilane with highly reactive organolithium compounds in a microflow reactoren
dc.typeTextde
dc.type.publicationtypearticlede
dcterms.accessRightsopen access-
eldorado.secondarypublicationtruede
eldorado.secondarypublication.primaryidentifierhttps://doi.org/10.1007/s41981-022-00254-wde
eldorado.secondarypublication.primarycitationAchternbosch, M., Zibula, L., Schmidt, A. et al. Selective monosubstitution on a trichlorosilane with highly reactive organolithium compounds in a microflow reactor. J Flow Chem 13, 9–12 (2023). https://doi.org/10.1007/s41981-022-00254-wde
Appears in Collections:Lehrstühle für Anorganische Chemie

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