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dc.contributor.authorTero, Tiia-Riikka
dc.contributor.authorSuhonen, Aku
dc.contributor.authorSalorinne, Kirsi
dc.contributor.authorCampos-Barbosa, Hélène
dc.contributor.authorNissinen, Maija
dc.date.accessioned2016-02-05T07:41:37Z
dc.date.available2016-02-05T07:41:37Z
dc.date.issued2013
dc.identifier.citationTero, T.-R., Suhonen, A., Salorinne, K., Campos-Barbosa, H., & Nissinen, M. (2013). The Missing Member of the Partially O-Alkylated Resorcinarene Family: Synthesis and Conformation of Methyl Tetramethoxy Resorcinarene. <i>Organic Letters</i>, <i>15</i>(5), 1096-1099. <a href="https://doi.org/10.1021/ol400118t" target="_blank">https://doi.org/10.1021/ol400118t</a>
dc.identifier.otherCONVID_22375514
dc.identifier.otherTUTKAID_56124
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/48632
dc.description.abstractAn improved Lewis acid catalyzed synthesis method for methyl tetramethoxy resorcinarene is described, which produced the missing lower rim methyl derivative of this partially O-alkylated resorcinarene family. Structural characterization by means of variable temperature NMR experiments and single crystal X-ray diffraction studies furthermore revealed that the resorcinarene core adopts different conformations in the solid state and in solution.
dc.language.isoeng
dc.publisherAmerican Chemical Society
dc.relation.ispartofseriesOrganic Letters
dc.relation.urihttp://dx.doi.org/10.1021/ol400118t
dc.subject.otherresorsinareeni
dc.subject.othertetrametoksiresorsinareeni
dc.subject.othersupramolekyylikemia
dc.subject.otherresorcinarene
dc.subject.othertetramethoxy resorcinarene
dc.titleThe Missing Member of the Partially O-Alkylated Resorcinarene Family: Synthesis and Conformation of Methyl Tetramethoxy Resorcinarene
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201602041453
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-02-04T13:15:18Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange1096-1099
dc.relation.issn1523-7060
dc.relation.numberinseries5
dc.relation.volume15
dc.type.versionacceptedVersion
dc.rights.copyright© 2013 American Chemical Society. This is a final draft version of an article whose final and definitive form has been published by ACS. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.subject.ysosupramolekulaarinen kemia
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
dc.relation.doi10.1021/ol400118t
dc.type.okmA1


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