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oai:riubu.ubu.es:10259/57092021-11-02T12:01:26Zcom_10259_3924com_10259_5086com_10259_2604col_10259_3925

Pomorski, Robert García Valverde, María Quesada Pato, Roberto Chmielewski, Michał J. 2021-04-15T07:56:48Z 2021-04-15T07:56:48Z 2021-03 http://hdl.handle.net/10259/5709 10.1039/d1ra01646f 2046-2069 Thioamide 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. Polish 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) application/pdf eng Royal Society of Chemistry RSC Advances. 2021, V. 11, n. 20, p. 12249-12253 https://doi.org/10.1039/D1RA01646F info:eu-repo/grantAgreement/JCyL/BU067P20 info:eu-repo/grantAgreement/Polish National Science Centre/2011/01/B/ST5/03900 Atribución-NoComercial 4.0 Internacional http://creativecommons.org/licenses/by-nc/4.0/ info:eu-repo/semantics/openAccess Química orgánica Chemistry, Organic Transmembrane anion transport promoted by thioamides info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion RSC Advances 11 20 12249 12253