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Unique cyclolignan’s architecture obtained via acid catalyzed cyclization/intramolecular Friedel-Crafts tandem reaction

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dc.abstract.enWe examine the cyclization of chiral bis-benzylidenesuccinate 6 (precursor to podophyllotoxin-related cyclolignans) in different conditions. Under acid catalysis, a new type of cyclolignan was obtained via cyclization/intramolecular Friedel-Crafts tandem reaction. The structure of the product was confirmed by spectroscopic data and X-ray diffraction. Also, a plausible mechanism of this transformation was proposed.
dc.affiliationUniwersytet Warszawski
dc.contributor.authorLisiecki, Kamil
dc.contributor.authorKrawczyk, Krzysztof K.
dc.contributor.authorCzarnocki, Zbigniew
dc.date.accessioned2024-01-26T11:19:33Z
dc.date.available2024-01-26T11:19:33Z
dc.date.copyright2020-06-05
dc.date.issued2020
dc.description.accesstimeAT_PUBLICATION
dc.description.financePublikacja bezkosztowa
dc.description.number7
dc.description.versionFINAL_PUBLISHED
dc.description.volume2020
dc.identifier.doi10.24820/ARK.5550190.P011.207
dc.identifier.issn1551-7004
dc.identifier.urihttps://repozytorium.uw.edu.pl//handle/item/124215
dc.identifier.weblinkhttp://dx.doi.org/10.24820/ark.5550190.p011.207
dc.languageeng
dc.pbn.affiliationchemical sciences
dc.relation.ispartofArkivoc
dc.relation.pages46-55
dc.rightsCC-BY
dc.sciencecloudnosend
dc.subject.enCyclolignans
dc.subject.encyclization
dc.subject.enL-prolinol
dc.subject.entandem reaction
dc.titleUnique cyclolignan’s architecture obtained via acid catalyzed cyclization/intramolecular Friedel-Crafts tandem reaction
dc.typeJournalArticle
dspace.entity.typePublication