Please use this identifier to cite or link to this item: http://dx.doi.org/10.25673/103487
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dc.contributor.authorKappen, Jonas-
dc.contributor.authorManurung, Jeprianto-
dc.contributor.authorFuchs, Tristan-
dc.contributor.authorPhani Babu Vemulapalli, Sahithya-
dc.contributor.authorSchmitz, Lea M.-
dc.contributor.authorFrolov, Andrej-
dc.contributor.authorAgusta, Andria-
dc.contributor.authorMuellner-Riehl, Alexandra N.-
dc.contributor.authorGriesinger, Christian-
dc.contributor.authorFranke, Katrin-
dc.contributor.authorWessjohann, Ludger-
dc.date.accessioned2023-06-09T07:11:34Z-
dc.date.available2023-06-09T07:11:34Z-
dc.date.issued2023-
dc.identifier.urihttps://opendata.uni-halle.de//handle/1981185920/105439-
dc.identifier.urihttp://dx.doi.org/10.25673/103487-
dc.description.abstractThe previously undescribed natural product lumnitzeralactone (1), which represents a derivative of ellagic acid, was isolated from the anti-bacterial extract of the Indonesian mangrove species Lumnitzera racemosa Willd. The structure of lumnitzeralactone (1), a proton-deficient and highly challenging condensed aromatic ring system, was unambiguously elucidated by extensive spectroscopic analyses involving high-resolution mass spectrometry (HRMS), 1D 1H and 13C nuclear magnetic resonance spectroscopy (NMR), and 2D NMR (including 1,1-ADEQUATE and 1,n-ADEQUATE). Determination of the structure was supported by computer-assisted structure elucidation (CASE system applying ACD-SE), density functional theory (DFT) calculations, and a two-step chemical synthesis. Possible biosynthetic pathways involving mangrove-associated fungi have been suggested.eng
dc.language.isoeng-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc570-
dc.titleChallenging structure elucidation of lumnitzeralactone, an ellagic acid derivative from the mangrove Lumnitzera racemosaeng
dc.typeArticle-
local.versionTypepublishedVersion-
local.bibliographicCitation.journaltitleMarine drugs-
local.bibliographicCitation.volume21-
local.bibliographicCitation.issue4-
local.bibliographicCitation.pagestart1-
local.bibliographicCitation.pageend18-
local.bibliographicCitation.publishernameMDPI-
local.bibliographicCitation.publisherplaceBasel-
local.bibliographicCitation.doi10.3390/md21040242-
local.subject.keywordsLumnitzera racemosa; lumnitzeralactone; isolation; synthesis; structure elucidation; ellagic acid; anti-bacterial; NMR; 13C-1H ADEQUATE-
local.openaccesstrue-
dc.identifier.ppn1848495994-
local.bibliographicCitation.year2023-
cbs.sru.importDate2023-06-09T07:11:05Z-
local.bibliographicCitationEnthalten in Marine drugs - Basel : MDPI, 2003-
local.accessrights.dnbfree-
Appears in Collections:Open Access Publikationen der MLU

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