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Novel stilbene-based Fischer base analog of leuco-TAM - (2E,2 ' Z)-{2-(4-(E)-styrylphenyl) propane-1,3-diylidene}bis(1,3,3-trimethylin doline) - derivatives: synthesis and structural consideration by 1D NMR and 2D NMR spectroscopy

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dc.contributor.authorKeum, Sam-Rok-
dc.contributor.authorLim, Hyun-Woo-
dc.date.accessioned2021-09-04T03:31:54Z-
dc.date.available2021-09-04T03:31:54Z-
dc.date.created2021-06-18-
dc.date.issued2016-02-
dc.identifier.issn0749-1581-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/89685-
dc.description.abstractWe report the synthesis of a series of novel stilbene-based (St) Fischer base analogs of leuco-triarylmethane (LTAM) dyes by treating Fischer base with (E)-4-styrylbenzaldehyde derivatives. All St-LTAM molecules examined herein are characterized by 1D and 2D NMR. They were found to exhibit ZE configuration and isomerize to their diastereomers EE and ZZ in 2-3h. They exhibit type I behavior of diastereomeric isomerization. Copyright (C) 2015 John Wiley & Sons, Ltd.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-BLACKWELL-
dc.subjectMALACHITE GREEN-
dc.subjectTRIARYLMETHANE DYES-
dc.subjectDIASTEREOMERIC ISOMERIZATION-
dc.subjectANTIINFLAMMATORY ACTIVITY-
dc.subjectTRIPHENYLMETHANE DYES-
dc.subjectLEUCOMALACHITE GREEN-
dc.subjectMOLECULAR-STRUCTURE-
dc.subjectUNUSUAL STABILITY-
dc.subjectORGANIC-SOLVENTS-
dc.subjectTUMOR-CELLS-
dc.titleNovel stilbene-based Fischer base analog of leuco-TAM - (2E,2 ' Z)-{2-(4-(E)-styrylphenyl) propane-1,3-diylidene}bis(1,3,3-trimethylin doline) - derivatives: synthesis and structural consideration by 1D NMR and 2D NMR spectroscopy-
dc.typeArticle-
dc.contributor.affiliatedAuthorKeum, Sam-Rok-
dc.identifier.doi10.1002/mrc.4359-
dc.identifier.scopusid2-s2.0-85000350948-
dc.identifier.wosid000370051400006-
dc.identifier.bibliographicCitationMAGNETIC RESONANCE IN CHEMISTRY, v.54, no.2, pp.143 - 150-
dc.relation.isPartOfMAGNETIC RESONANCE IN CHEMISTRY-
dc.citation.titleMAGNETIC RESONANCE IN CHEMISTRY-
dc.citation.volume54-
dc.citation.number2-
dc.citation.startPage143-
dc.citation.endPage150-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaSpectroscopy-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.relation.journalWebOfScienceCategorySpectroscopy-
dc.subject.keywordPlusMALACHITE GREEN-
dc.subject.keywordPlusTRIARYLMETHANE DYES-
dc.subject.keywordPlusDIASTEREOMERIC ISOMERIZATION-
dc.subject.keywordPlusANTIINFLAMMATORY ACTIVITY-
dc.subject.keywordPlusTRIPHENYLMETHANE DYES-
dc.subject.keywordPlusLEUCOMALACHITE GREEN-
dc.subject.keywordPlusMOLECULAR-STRUCTURE-
dc.subject.keywordPlusUNUSUAL STABILITY-
dc.subject.keywordPlusORGANIC-SOLVENTS-
dc.subject.keywordPlusTUMOR-CELLS-
dc.subject.keywordAuthorNMR-
dc.subject.keywordAuthorH-1-
dc.subject.keywordAuthorCOSY-
dc.subject.keywordAuthorHMBC-
dc.subject.keywordAuthorHETCOR-
dc.subject.keywordAuthorNOESY-
dc.subject.keywordAuthorFischer base analogs of leuco-TAM dyes-
dc.subject.keywordAuthordiastereomeric isomerization-
dc.subject.keywordAuthorHeck reaction-
dc.subject.keywordAuthorphotochemotherapy agents-
dc.subject.keywordAuthormalachite green-
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