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dc.contributor.authorÁlvarez, Rosa-
dc.contributor.authorJimeno, M. Luisa-
dc.contributor.authorTomas-Gil, Francisco J.-
dc.contributor.authorPérez Pérez, María Jesús-
dc.contributor.authorCamarasa Rius, María José-
dc.date.accessioned2011-05-19T10:23:27Z-
dc.date.available2011-05-19T10:23:27Z-
dc.date.issued1997-
dc.identifier.citationNucleosides, Nucleotides and Nucleic Acids 16(7 & 9) : 1399 - 1402 (1997)es_ES
dc.identifier.issn0732-8311-
dc.identifier.urihttp://hdl.handle.net/10261/35852-
dc.description.abstractThe conformational properties in solution of the prototype compound TSAO-T (1) and its two analogues 2 and 3 have been determined by H and C NMR techniques. The three compounds showed a sugar ring conformation rare among HIV-inhibitory nucleosides, probably due to the presence, at the 3'-position of the spiro moietyes_ES
dc.language.isoenges_ES
dc.publisherTaylor & Francises_ES
dc.rightsclosedAccesses_ES
dc.titleConformational studies of 3'-spironucleosides (TSAO-T and analogues) by NMR spectroscopyes_ES
dc.typeArtículoes_ES
dc.identifier.doi10.1080/07328319708006191-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1080/07328319708006191es_ES
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