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dc.contributor.authorAngelucci, Francesco
dc.contributor.authorCirillo, Davide
dc.contributor.authorBjørsvik, Hans-René
dc.date.accessioned2023-01-23T12:42:59Z
dc.date.available2023-01-23T12:42:59Z
dc.date.created2022-09-14T18:03:37Z
dc.date.issued2022
dc.identifier.issn1434-193X
dc.identifier.urihttps://hdl.handle.net/11250/3045327
dc.description.abstractA selective and high-rate Ru-catalyzed cross-metathesis reaction of alkenes with vinylimidazole is disclosed. Cross-metathesis is known to operate less efficiently on N-heterocycles, but through optimization by means of statistical experimental design and multiple regression, optimal reaction conditions were identified that allowed for consistent high-yields without the need of overly complicated set-ups or additives. The method was tested on a series of terminal alkene reagents with a variety of different functional groups and it provides the corresponding target molecules in good to high yields.en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleImidazole Backbone Functionalization with Olefin Cross-Metathesisen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2022 the authorsen_US
dc.source.articlenumbere202200437en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1002/ejoc.202200437
dc.identifier.cristin2051775
dc.source.journalEuropean Journal of Organic Chemistryen_US
dc.identifier.citationEuropean Journal of Organic Chemistry. 2022, 2022 (22), e202200437.en_US
dc.source.volume2022en_US
dc.source.issue22en_US


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal