2026-04-19T15:45:38Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/57092021-11-02T12:01:26Zcom_10259_3924com_10259_5086com_10259_2604col_10259_3925
Pomorski, Robert
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García Valverde, María
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500
Quesada Pato, Roberto
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500
Chmielewski, Michał J.
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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
ORIGINAL
Pomorski-rsca_2021.pdf
Pomorski-rsca_2021.pdf
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https://riubu.ubu.es/bitstream/10259/5709/1/Pomorski-rsca_2021.pdf
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LICENSE
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10259/5709
oai:riubu.ubu.es:10259/5709
2021-11-02 13:01:26.638
Repositorio Institucional de la Universidad de Burgos
bubrep@ubu.es
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