Mostrar el registro sencillo del ítem

dc.contributor.authorÉcija, Patricia
dc.contributor.authorUriarte, Iciar
dc.contributor.authorSpada, Lorenzo
dc.contributor.authorDavis, Benjamin
dc.contributor.authorCaminati, Walther
dc.contributor.authorBasterretxea, Francisco José
dc.contributor.authorLesarri Gómez, Alberto Eugenio 
dc.contributor.authorCocinero, Alberto
dc.date.accessioned2017-06-09T19:04:55Z
dc.date.available2017-06-09T19:04:55Z
dc.date.issued2016
dc.identifier.citationChemComm, 2016, 52, 6241es
dc.identifier.issn1359-7345es
dc.identifier.urihttp://uvadoc.uva.es/handle/10324/23472
dc.description.abstractThe investigation of an isolated ribofuranose unit in the gas phase reveals the intrinsic conformational landscape of the biologically active sugar form.We report the rotational spectra of two conformers of methyl b-D-ribofuranoside in a supersonic jet expansion. Both conformers adopt a near twisted (3T2) ring conformation with the methoxy and hydroxymethyl substituents involved in various intramolecular hydrogen bonds.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.publisherRoyal Society of Chemistryes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.subjectQuímicaes
dc.titleFuranosic forms of sugars: conformational equilibrium of methyl beta-D-ribofuranosidees
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1039/c6cc01180bes
dc.identifier.publicationfirstpage6241es
dc.identifier.publicationlastpage6244es
dc.identifier.publicationtitleChemical Communicationses
dc.identifier.publicationvolume52es
dc.peerreviewedSIes
dc.description.projectMINECO-FEDER CTQ2015-68148-C2-Pes


Ficheros en el ítem

Thumbnail

Este ítem aparece en la(s) siguiente(s) colección(ones)

Mostrar el registro sencillo del ítem