Cargando…
Unambiguous Assignment of the (1)H- and (13)C-NMR Spectra of Propafenone and a Thiophene Analogue
Full and unambiguous asssignment of all (1)H- and (13)C-NMR resonances of the free bases as well as the hydrochloride salts of the antiarrhythmic agent propafenone and a thiophene analogue in different solutions (DMSO-d(6), CDCl(3)) is reported.
Autor principal: | Holzer, Wolfgang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2001
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6236368/ http://dx.doi.org/10.3390/61000796 |
Ejemplares similares
-
Complete Assignment of the (1)H and (13)C NMR Spectra of Carthamin Potassium Salt Isolated from Carthamus tinctorius L.
por: Sasaki, Maiko, et al.
Publicado: (2021) -
Microstructure of Copolymers of Norbornene Based on Assignments of (13)C NMR Spectra: Evolution of a Methodology
por: Boggioni, Laura, et al.
Publicado: (2018) -
Ligand-induced structural transitions combined with paramagnetic ions facilitate unambiguous NMR assignments of methyl groups in large proteins
por: Mühlberg, Lars, et al.
Publicado: (2022) -
Π-Stacking Signature in NMR Solution
Spectra of Thiophene-Based Conjugated Polymers
por: Parenti, Francesca, et al.
Publicado: (2017) -
Univariate Statistical Analysis as a Guide to (1)H-NMR Spectra Signal Assignment by Visual Inspection
por: Zhu, Chenglin, et al.
Publicado: (2019)