Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/3037
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dc.contributor.authorDjordjević, Irisen_US
dc.contributor.authorVajs, Vlatkaen_US
dc.contributor.authorBulatović, Vanjaen_US
dc.contributor.authorMenković, Nebojšaen_US
dc.contributor.authorTešević, Veleen_US
dc.contributor.authorMacura, Slobodanen_US
dc.contributor.authorJanaćković, Peđaen_US
dc.contributor.authorMilosavljević, Slobodanen_US
dc.date.accessioned2019-10-30T15:14:57Z-
dc.date.available2019-10-30T15:14:57Z-
dc.date.issued2004-01-01-
dc.identifier.issn0031-9422-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/3037-
dc.description.abstractQuantitative 1H NMR measurements revealed Δ 11(13) sesquiterpene γ-lactones as the main constituents (≥ 1% per weight of dried plant material) in the crude extracts of the aerial parts of Amphoricarpos neumayeri ssp. neumayeri and ssp. murbeckii from mountains Orjen and Visitor (Montenegro), respectively. Preparative silica gel chromatography afforded thirteen guai-11(13)-en-12,6α-olides, named amphoricarpolides (1-13), with the same relative (1αH,4βH,5αH, 7βH) configuration of the basic skeleton. The common structural feature of lactones 2-13 was 3β,15-dioxygenation pattern. The only exception was 1 (3-deoxyamphoricarpolide), containing a single oxygen substituent (15-OH). Eight of them exhibited an additional oxygen substituent, 9β-OH (5 and 6), 2α-OH (8-12), or 2α-OAc (13). Compound 7 was epoxydated at 10α(14)-position, whereas the remaining lactones contained a 10(14) double bond. © 2004 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.relation.ispartofPhytochemistryen_US
dc.subjectAmphoricarpolidesen_US
dc.subjectAmphoricarpos neumayerien_US
dc.subjectAsteraceaeen_US
dc.subjectGuaianolidesen_US
dc.subjectSesquiterpene lactonesen_US
dc.titleGuaianolides from two subspecies of Amphoricarpos neumayeri from Montenegroen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.phytochem.2004.07.014-
dc.identifier.pmid15381005-
dc.identifier.scopus2-s2.0-4544342932-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/4544342932-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
crisitem.author.deptChair of Plant Morphology and Systematics-
crisitem.author.orcid0000-0002-0236-0013-
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