Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/5588
DC FieldValueLanguage
dc.contributor.authorHafensteiner, B. D.en_us
dc.contributor.authorEscribano, M.en_us
dc.contributor.authorPetricci, Elenaen_us
dc.contributor.authorBaran, P. S.en_us
dc.date.accessioned2021-03-30T15:53:42Z-
dc.date.available2021-03-30T15:53:42Z-
dc.date.issued2009-
dc.identifier.issn0960-894Xen_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/5588-
dc.description6932en_US
dc.description.abstractA new method is reported for the synthesis of the α,β-unsaturated nitrone moiety characteristic of the stephacidin/avrainvillamide family of bioactive prenylated indole alkaloids. Application to the synthesis of stephacidin analogs and a potential biological probe are showcased.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofBIOORGANIC & MEDICINAL CHEMISTRY LETTERSen_US
dc.subjectClick-chemistry; Methodology; Oxidations; Synthesis; Antineoplastic Agents; Indole Alkaloids; Indoles; Nitrogen Oxides; Oxidation-Reduction; Biochemistry; Clinical Biochemistry; Molecular Biology; Molecular Medicine; Organic Chemistry; Drug Discovery3003 Pharmaceutical Science; 3003en_US
dc.titleAn improved synthesis of α,β-unsaturated nitrones relevant to the stephacidins and analogs thereofen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.bmcl.2009.04.045en_US
dc.identifier.pmid19423345en_US
dc.identifier.scopus2-s2.0-67649641698en_US
dc.identifier.isiWOS:000267762600025en_US
dc.relation.volume19en_US
dc.relation.issue14en_US
dc.description.firstpage3808en_US
dc.description.lastpage3810en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0002-9685-6342-
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