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This work reports two methods developed for the separation and determination of the enantiomers of the new alkaloid malacitanine (MLC) and the determination of the enantiomeric purity in mixtures. First, the isomers were separated using a Chirex 3020 (250 mm × 4.6 mm, 5 μm) chiral column with a mobile phase of cyclohexane-1,2-dichloroethane-ethanol-trifluoroacetic acid (64:30:6:0.6, v/v/v/v) at a flow rate of 1 mL/min and fluorimetric detection. Obtained retention times were 12.4 and 15.9 min (+ and -) with a resolution Rs of 1.13. Relative standard deviations (RSDs) were 2.5 and 2.4% at the 0.5-μg level (four determinations). Second, a nonenantioselective procedure for the determination of enantiomeric purity of MLC using a Lichrospher ® Si-60 (250 mm × 5 mm, 5 μm) normal phase with a mobile phase of 100% ethanol at a flow rate of 0.9 mL/min coupled to two detectors in series, fluorimetric and polarimetric. RSD of 3.3% was obtained. Calculated enantiomeric purity by chiral chromatography gave 48.6% (-)-MLC in the near racemic product. Using polarimetric signal of the nonseparated enantiomers and comparing the slopes of the calibration curves (enantiomers) from the racemic product gave 47.8% (-)-MLC content. A study of accuracy of (-)-MLC gave recoveries from 98.3 to 100.7%.
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http://dx.doi.org/10.1002/jssc.201200275 | DOI Listing |
J Org Chem
September 2025
School of Pharmaceutical Sciences, Nanjing Tech University, 30 South Puzhu Road, Nanjing 211816, China.
A new synthetic procedure was developed for the chiral synthons ()- and ()- that enabled us to complete the asymmetric total synthesis of entecavir, abacavir, and carbovir. This lipase-based procedure holds good potential for developing a green process for the industrial production of ()- and ()- with a high enantiomeric purity. The asymmetric synthesis of entecavir was powered by the highly challenging Michael addition-elimination reaction.
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Departamento de Química, Universidad Técnica Particular de Loja (UTPL), Calle París s/n y Praga, Loja 110107, Ecuador.
(Proteaceae) is a shrub native to subtropical and tropical regions of Central and South America. The EO extracted from was analyzed for its chemical composition and biological activities. GC analysis revealed that the essential oil has a chemically diverse composition, predominantly composed of oxygenated diterpenes (29.
View Article and Find Full Text PDFChirality
September 2025
Egyptian Drug Authority (EDA) formerly National Organization for Drug control and Research (NODCAR), Giza, Egypt.
The enantiomeric purity of Finerenone (FIN), a novel therapeutic for chronic kidney disease (CKD), is a critical quality attribute for ensuring patient safety. This study reports the first chiral HPLC method for the simultaneous determination of FIN and its enantiomer, developed and validated using a rigorous analytical quality by design (AQbD) framework. The method employs a CHIRALPAK AD-H column with an isocratic mobile phase of n-hexane: ethanol (62:38, v/v).
View Article and Find Full Text PDFNat Commun
August 2025
Key Laboratory for Advanced Materials and Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai, China.
Chiral purity is crucial in life sciences, emphasizing the importance of precise enantiomeric identification and the development of analytical techniques. Here, we design functional dyes with visual chiral recognition capabilities by introducing recognition units 2-amino-1,2-diphenylethanol into vibration-induced emission molecules. The unambiguous differentiation in luminescent colors upon binding to enantiomers facilitates the efficient recognition of enantiomers and the analysis of enantiomeric excess.
View Article and Find Full Text PDFRSC Adv
August 2025
Department of Chemistry, Faculty of Science, Chiang Mai University 239 Huay Kaew Road Chiang Mai 50200 Thailand
1,1'-bi-2-naphthols (BINOLs) and their derivatives have been extensively studied over the years. Enantiopure BINOLs are crucial in asymmetric synthesis, circularly polarized luminescent dyes, and charge transfer host systems. Several methods, including asymmetric oxidative coupling, enzymatic resolution, and chemical resolution, have been explored to prepare enantiopure BINOLs.
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