Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12779/3921
DC FieldValueLanguage
dc.contributor.authorBruno, Bottaen_us
dc.contributor.authorPaolo, Iacomaccien_us
dc.contributor.authorCristina Di, Giovannien_us
dc.contributor.authorGiuliano Delle, Monacheen_us
dc.contributor.authorEszter Gacs, Baitzen_us
dc.contributor.authorBotta, Maurizioen_us
dc.contributor.authorTafi, Andreaen_us
dc.contributor.authorCorelli, Federicoen_us
dc.contributor.authorDomenico, Misitien_us
dc.date.accessioned2021-03-30T14:36:23Z-
dc.date.available2021-03-30T14:36:23Z-
dc.date.issued1992-
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://hdl.handle.net/20.500.12779/3921-
dc.description49254en_US
dc.description.abstractTreatment of (E)-2,4-dimethoxycinnamic acid methyl ester with BF3.Et2O in CHCl3 at room temperature afforded in 75% yield two stereoisomeric C-alkylcalix[4]resorcinarenes, which were shown to be in the 1,2-alternate and flattened-cone configurations.en_US
dc.language.isoenen_US
dc.relationNoneen_US
dc.relation.ispartofJOURNAL OF ORGANIC CHEMISTRYen_US
dc.titleThe tetramerization of 2,4-dimethoxycinnamates. A novel route to calixarenesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jo00038a001en_US
dc.identifier.scopus2-s2.0-0000383822en_US
dc.identifier.isiWOS:A1992HX97100001en_US
dc.relation.volume57en_US
dc.description.firstpage3259en_US
dc.description.lastpage3261en_US
dc.description.thirdmissionNot applicableen_US
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeArticle-
item.fulltextNo Fulltext-
crisitem.author.orcid0000-0003-0456-6995-
crisitem.author.orcid0000-0003-4308-3531-
crisitem.author.orcid0000-0002-5750-4504-
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