NMR studies and crystal structure determinations of CF3 group-containing bieyelie phenolates

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dc.bibliographicCitation.firstPage423eng
dc.bibliographicCitation.issue4eng
dc.bibliographicCitation.journalTitleZeitschrift für Naturforschung - Section B Journal of Chemical Scienceseng
dc.bibliographicCitation.volume64eng
dc.contributor.authorMamat, C.
dc.contributor.authorReinke, H.
dc.contributor.authorLanger, P.
dc.date.accessioned2020-08-13T10:35:50Z
dc.date.available2020-08-13T10:35:50Z
dc.date.issued2009
dc.description.abstractThree new CF3-substituted bicyclic salicylate derivatives were synthesized by the TiCl4-mediated cyclization of trifluoromethyl- containing ketones with l,3-bis(silyl enol ethers) and characterized by NMR and IR, spectroscopy, mass spectrometry and elemental analysis. The crystal structures of the bicyclic derivatives have been determined by single crystal X-ray analysis. All structures exhibit hydrogen bonding. © 2009 Verlag der Zeitschrift für Naturforschung.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://doi.org/10.34657/4170
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/5541
dc.language.isoengeng
dc.publisherBerlin : de Gruytereng
dc.relation.doihttps://doi.org/10.1515/znb-2009-0411
dc.relation.issn0932-0776
dc.rights.licenseCC BY-NC-ND 3.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/3.0/eng
dc.subject.ddc540eng
dc.subject.other19F NMR Spectroscopyeng
dc.subject.otherCF3 salicylateseng
dc.subject.otherX-Ray crystallographyeng
dc.subject.other[3+3] cyclizationeng
dc.titleNMR studies and crystal structure determinations of CF3 group-containing bieyelie phenolateseng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccesseng
wgl.contributorLIKATeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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