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Rhenium and Manganese-Catalyzed Selective Alkenylation of Indoles

dc.contributor.authorWang, Chengming
dc.contributor.authorRueping, Magnus
dc.date.accessioned2018-04-19T10:45:31Z
dc.date.available2018-04-19T10:45:31Z
dc.date.issued2018-04-25
dc.identifier.citationWang C, Rueping M (2018) Rhenium and Manganese-Catalyzed Selective Alkenylation of Indoles. ChemCatChem. Available: http://dx.doi.org/10.1002/cctc.201800553.
dc.identifier.issn1867-3880
dc.identifier.doi10.1002/cctc.201800553
dc.identifier.urihttp://hdl.handle.net/10754/627568
dc.description.abstractAn efficient rhenium-catalyzed regioselective C-H bond alkenylation of indoles is reported. The protocol operates well for internal as well as terminal alkynes, affording products in good to excellent yields. Furthermore, a manganese catalyzed, acid free, regioselective C2-alkenylation of indoles with internal alkynes is described. The directing groups can be easily removed after the reaction and the resulting products can be used as valuable building blocks for the synthesis of diverse heterocyclic compounds.
dc.publisherWiley
dc.relation.urlhttps://onlinelibrary.wiley.com/doi/abs/10.1002/cctc.201800553
dc.rightsArchived with thanks to ChemCatChem
dc.titleRhenium and Manganese-Catalyzed Selective Alkenylation of Indoles
dc.typeArticle
dc.contributor.departmentChemical Science Program
dc.contributor.departmentKAUST Catalysis Center (KCC)
dc.contributor.departmentPhysical Science and Engineering (PSE) Division
dc.identifier.journalChemCatChem
dc.eprint.versionPublisher's Version/PDF
dc.contributor.institutionGERMANY
dc.contributor.institutionRWTH Aachen; Institure of Organic Chemistry; Landoltweg 1 52074 Aachen GERMANY
kaust.personRueping, Magnus
dc.date.published-online2018-04-25
dc.date.published-print2018-06-21


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