2003
DOI: 10.1016/s0731-7085(02)00697-0
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Enantiomeric separation of β-blockers by HPLC using (R)-1-naphthylglycine and 3,5-dinitrobenzoic acid as chiral stationary phase

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Cited by 31 publications
(15 citation statements)
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“…These show enantiorecognition abilities toward a broad spectrum of chiral compounds, due to the higher-order structure of the chiral polysaccharide derivative polymers [32,33]. Many chemically different classes of chiral compounds can be resolved by these selectors [34][35][36][37][38][39][40][41].…”
Section: Screening Strategies In High-performance Liquid Chromatographymentioning
confidence: 99%
“…These show enantiorecognition abilities toward a broad spectrum of chiral compounds, due to the higher-order structure of the chiral polysaccharide derivative polymers [32,33]. Many chemically different classes of chiral compounds can be resolved by these selectors [34][35][36][37][38][39][40][41].…”
Section: Screening Strategies In High-performance Liquid Chromatographymentioning
confidence: 99%
“…The interactions of antagonists with the CSP are shown in Fig. 1; both enantiomers of the drugs produce different interactions with the CSP because of the different conformation [16,17].…”
Section: Enantioseparation By Liquid Chromatographymentioning
confidence: 99%
“…Prior to the prevalent use of LC-MS techniques, various analytical methods, such as capillary electrophoresis (Awadallah et al, 2003), gas chromatography (Kim et al, 2001) and HPLC with an ultraviolet (Zhang et al, 2003;Ruiz-Angel et al, 2002;Modamio et al, 1996), fluorescence (Buhring and Garbe, 1986;Eastwood et al, 1990;Suzuki et al, 1993) or diode array detector (Caudron et al, 2004), have been developed to determine bisoprolol in formulation and biological samples.…”
Section: Bisoprolol Hemifumarate (±)-1-{p-[(2-isopropoxyethoxy) Methyl]mentioning
confidence: 99%