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dc.contributor.authorPomorski, Robert
dc.contributor.authorGarcía Valverde, María 
dc.contributor.authorQuesada Pato, Roberto 
dc.contributor.authorChmielewski, Michał J.
dc.date.accessioned2021-04-15T07:56:48Z
dc.date.available2021-04-15T07:56:48Z
dc.date.issued2021-03
dc.identifier.urihttp://hdl.handle.net/10259/5709
dc.description.abstractThioamide groups represent useful hydrogen-bonding motifs for the development of active transmembrane anion transporters. Using a 1,8-di(thioamido)carbazole scaffold the superior performance of thioamides compared with the parent amides has been demonstrated.en
dc.description.sponsorshipPolish National Science Centre for grant OPUS (2011/01/B/ST5/03900) and Consejer´ıa de Educaci´on de la Junta de Castilla y Le´on (project BU067P20)es
dc.format.mimetypeapplication/pdf
dc.language.isoenges
dc.publisherRoyal Society of Chemistryes
dc.relation.ispartofRSC Advances. 2021, V. 11, n. 20, p. 12249-12253es
dc.rightsAtribución-NoComercial 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.subject.otherQuímica orgánicaen
dc.subject.otherChemistry, Organicen
dc.titleTransmembrane anion transport promoted by thioamidesen
dc.typeinfo:eu-repo/semantics/article
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.relation.publisherversionhttps://doi.org/10.1039/D1RA01646F
dc.identifier.doi10.1039/d1ra01646f
dc.relation.projectIDinfo:eu-repo/grantAgreement/JCyL/BU067P20
dc.relation.projectIDinfo:eu-repo/grantAgreement/Polish National Science Centre/2011/01/B/ST5/03900
dc.identifier.essn2046-2069
dc.journal.titleRSC Advanceses
dc.volume.number11es
dc.issue.number20es
dc.page.initial12249es
dc.page.final12253es
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersion


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