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dc.contributor.authorIsmael, Aya
dc.contributor.authorZeeshan, Muhammad
dc.contributor.authorHansen, Jørn H
dc.date.accessioned2022-08-11T09:16:36Z
dc.date.available2022-08-11T09:16:36Z
dc.date.issued2022-02-09
dc.description.abstractObjective: Synthesis of novel aromatic Lipoxin A4 lactone analogues. <p><p>Results: Novel para-substituted aromatic lactone analogues of Lipoxin A4 have been synthesized in a convergent manner with six steps in the longest linear sequence in 12–13% yields, employing 2-deoxy-d-ribose as a chiral pool starting material and the classical E-selective Wittig olefnation.en_US
dc.identifier.citationIsmael, Zeeshan, Hansen. Synthesis of aromatic lactone analogues of Lipoxin A4. BMC Research Notes. 2022;15(1)en_US
dc.identifier.cristinIDFRIDAID 2025352
dc.identifier.doi10.1186/s13104-022-05917-4
dc.identifier.issn1756-0500
dc.identifier.urihttps://hdl.handle.net/10037/26125
dc.language.isoengen_US
dc.publisherBMCen_US
dc.relation.journalBMC Research Notes
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2022 The Author(s)en_US
dc.titleSynthesis of aromatic lactone analogues of Lipoxin A4en_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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