| dc.contributor.author | Tero, Tiia-Riikka | |
| dc.contributor.author | Suhonen, Aku | |
| dc.contributor.author | Salorinne, Kirsi | |
| dc.contributor.author | Campos-Barbosa, Hélène | |
| dc.contributor.author | Nissinen, Maija | |
| dc.date.accessioned | 2016-02-05T07:41:37Z | |
| dc.date.available | 2016-02-05T07:41:37Z | |
| dc.date.issued | 2013 | |
| dc.identifier.citation | Tero, 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.other | CONVID_22375514 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/48632 | |
| dc.description.abstract | An 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.iso | eng | |
| dc.publisher | American Chemical Society | |
| dc.relation.ispartofseries | Organic Letters | |
| dc.relation.uri | http://dx.doi.org/10.1021/ol400118t | |
| dc.subject.other | resorsinareeni | |
| dc.subject.other | tetrametoksiresorsinareeni | |
| dc.subject.other | supramolekyylikemia | |
| dc.subject.other | resorcinarene | |
| dc.subject.other | tetramethoxy resorcinarene | |
| dc.title | The Missing Member of the Partially O-Alkylated Resorcinarene Family: Synthesis and Conformation of Methyl Tetramethoxy Resorcinarene | |
| dc.type | research article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201602041453 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Orgaaninen kemia | fi |
| dc.contributor.oppiaine | Nanoscience Center | fi |
| dc.contributor.oppiaine | Organic Chemistry | en |
| dc.contributor.oppiaine | Nanoscience Center | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.date.updated | 2016-02-04T13:15:18Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 1096-1099 | |
| dc.relation.issn | 1523-7060 | |
| dc.relation.numberinseries | 5 | |
| dc.relation.volume | 15 | |
| dc.type.version | acceptedVersion | |
| 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.accesslevel | openAccess | fi |
| dc.type.publication | article | |
| dc.subject.yso | supramolekulaarinen kemia | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p37759 | |
| dc.relation.doi | 10.1021/ol400118t | |
| dc.type.okm | A1 | |
