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dc.contributor.authorHåheim, Katja Stangeland
dc.contributor.authorLund, Bjarte Aarmo
dc.contributor.authorSydnes, Magne Olav
dc.date.accessioned2024-03-21T14:32:41Z
dc.date.available2024-03-21T14:32:41Z
dc.date.issued2023-02-23
dc.description.abstractA large number of diversely functionalized analogs of the bioactive natural products neocryptolepine and isocryptolepine have been prepared from a series of 3-bromoquinoline derivatives. The neocryptolepines were obtained by a Pd<sup>0</sup>-catalyzed C−C bond coupling followed by C−N bond formation in yields up to 80 %, whereas the indoloquinolines were prepared by a Suzuki-Miyaura cross-coupling followed by azidation-photochemical cyclization in yields ranging from traces to 95 % yield.en_US
dc.identifier.citationHåheim KS, Lund BAL, Sydnes MO. Regiodivergent Synthesis of 11H-Indolo[3,2-c]quinolines and Neocryptolepine from a Common Starting Material. European Journal of Organic Chemistry. 2023;26
dc.identifier.cristinIDFRIDAID 2133534
dc.identifier.doi10.1002/ejoc.202300137
dc.identifier.issn1434-193X
dc.identifier.issn1099-0690
dc.identifier.urihttps://hdl.handle.net/10037/33222
dc.language.isoengen_US
dc.publisherWileyen_US
dc.relation.journalEuropean Journal of Organic Chemistry
dc.relation.urihttps://doi.org/10.1002/ejoc.202300137
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0en_US
dc.rightsAttribution-NonCommercial 4.0 International (CC BY-NC 4.0)en_US
dc.titleRegiodivergent Synthesis of 11H-Indolo[3,2-c]quinolines and Neocryptolepine from a Common Starting Materialen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)