Synthesis and complementary self-association of novel lipophilic π-conjugated nucleoside oligomers

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dc.contributor.author Camacho García, J.
dc.contributor.author López-Pérez, Ana M.
dc.contributor.author González-Rodríguez, David
dc.contributor.other UAM. Departamento de Química Orgánica es_ES
dc.date.accessioned 2015-04-21T08:42:05Z
dc.date.available 2015-04-21T08:42:05Z
dc.date.issued 2015-04-21
dc.identifier.citation Organic and Biomolecular Chemistry 13.15 (2015): 4506-4513 en_US
dc.identifier.issn 1477-0520 (print) es_ES
dc.identifier.issn 1477-0539 (on line) es_ES
dc.identifier.uri http://hdl.handle.net/10486/665317
dc.description The following article appeared in Organic and Biomolecular Chemistry 13.15 (2015): 4506-4513 and may be found at http://dx.doi.org/10.1039/c5ob00098j, reproduced by permission of The Royal Society of Chemistry en_US
dc.description.abstract A series of lipophilic nucleosides comprising natural and non-natural bases that are π-conjugated to a short oligophenylene-ethynylene fragment has been synthesized. These bases comprise guanosine, isoguanosine, and 2-aminoadenosine as purine heterocycles, and cytidine, isocytosine and uridine as complementary pyrimidine bases. The hydrogen-bonding dimerization and association processes between complementary bases were also studied by 1H NMR and absorption spectroscopy in order to obtain the relevant association constants en_US
dc.description.sponsorship Funding from the European Research Council (ERC-StG 279548) and MINECO (CTQ2011-23659) is gratefully acknowledged en_US
dc.format.extent 8 pag. es_ES
dc.format.mimetype application/pdf en
dc.language.iso eng en
dc.publisher Royal Society of Chemistry en_US
dc.relation.ispartof Organic and Biomolecular Chemistry en_US
dc.rights © 2015 The Royal Society of Chemistry en_US
dc.title Synthesis and complementary self-association of novel lipophilic π-conjugated nucleoside oligomers en_US
dc.type article en
dc.subject.eciencia Química es_ES
dc.date.embargoend 2016-02-25
dc.relation.publisherversion http://dx.doi.org/10.1039/c5ob00098j es_ES
dc.identifier.doi 10.1039/c5ob00098j es_ES
dc.identifier.publicationfirstpage 4506 es_ES
dc.identifier.publicationissue 15 es_ES
dc.identifier.publicationlastpage 4513 es_ES
dc.identifier.publicationvolume 13 es_ES
dc.relation.projectID info:eu-repo/grantAgreement/EC/FP7/279548 en_US
dc.type.version info:eu-repo/semantics/acceptedVersion en_US
dc.rights.accessRights openAccess en


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