Synthesis of two alnustone-like natural diarylheptanoids via 4+3 strategy

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dc.authorid25644181900
dc.authorid7005565474
dc.authorid26867642000
dc.authorid7006445126
dc.authorid6602849492
dc.authorid6701388846
dc.contributor.authorBurmao?lu S.
dc.contributor.authorÇelik H.
dc.contributor.authorGöiksu S.
dc.contributor.authorMaraş A.
dc.contributor.authorAltundaş R.
dc.contributor.authorSeçen H.
dc.date.accessioned20.04.201910:49:12
dc.date.accessioned2019-04-20T21:44:57Z
dc.date.available20.04.201910:49:12
dc.date.available2019-04-20T21:44:57Z
dc.date.issued2009
dc.departmentBayburt Üniversitesien_US
dc.description.abstractThe first total synthesis of (4E,6E)-1,7-bis(3,4-dihydroxyphenyl)-hepta-4, 6-dien-3-one and an alternative synthesis of (4E,6E)-1,7-bis(4-hydroxyphenyl)- hepta-4,6-dien-3-one, two natural diarylheptanoids, mainly based on Claisen-Schmidt condensation were described. The crucial steps of the syntheses were the condensation of OH-protected 4-aryl-2-butanones with OH-protected 3-aryl-acrylaldehydes by the in situ enamination and then deprotection of OH groups to give the corresponding natural diarylheptanoids. Copyright © Taylor & Francis Group, LLC.en_US
dc.identifier.doi10.1080/00397910802542036
dc.identifier.endpage1562
dc.identifier.issn0039-7911
dc.identifier.issue9
dc.identifier.scopus2-s2.0-67650069189en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage1549
dc.identifier.urihttps://dx.doi.org/10.1080/00397910802542036
dc.identifier.urihttps://hdl.handle.net/20.500.12403/979
dc.identifier.volume39
dc.identifier.wosWOS:000264825100005en_US
dc.identifier.wosqualityQ3en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofSynthetic Communicationsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1,7-Bis(3,4-dihydroxyphenyl)-hepta-4,6-dien-3-one
dc.subject1,7-bis(4-hydroxyphenyl)- hepta-4
dc.subject6-dien-3-one
dc.subjectClaisen-Schmidt condensation
dc.subjectdiarylheptanoid
dc.subjectin situ enamination
dc.subjectsynthesis
dc.subject1,7 bis(3,4 dihydroxyphenyl) hepta 4,6 dien 3 one
dc.subject1,7 bis(4 hydroxyphenyl) hepta 4,6 dien 3 one
dc.subjectalnustone
dc.subjectnatural product
dc.subjectunclassified drug
dc.subjectamination
dc.subjectarticle
dc.subjectClaisen condensation
dc.subjectdeprotection reaction
dc.subjectdrug structure
dc.subjectdrug synthesis
dc.subjectproton nuclear magnetic resonance
dc.subject1,7-Bis(3,4-dihydroxyphenyl)-hepta-4,6-dien-3-one
dc.subject1,7-bis(4-hydroxyphenyl)- hepta-4
dc.subject6-dien-3-one
dc.subjectClaisen-Schmidt condensation
dc.subjectdiarylheptanoid
dc.subjectin situ enamination
dc.subjectsynthesis
dc.subject1,7 bis(3,4 dihydroxyphenyl) hepta 4,6 dien 3 one
dc.subject1,7 bis(4 hydroxyphenyl) hepta 4,6 dien 3 one
dc.subjectalnustone
dc.subjectnatural product
dc.subjectunclassified drug
dc.subjectamination
dc.subjectarticle
dc.subjectClaisen condensation
dc.subjectdeprotection reaction
dc.subjectdrug structure
dc.subjectdrug synthesis
dc.subjectproton nuclear magnetic resonance
dc.titleSynthesis of two alnustone-like natural diarylheptanoids via 4+3 strategyen_US
dc.typeArticleen_US

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