Literatura académica sobre el tema "Chiral ligand-exchange chromatography"
Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros
Consulte las listas temáticas de artículos, libros, tesis, actas de conferencias y otras fuentes académicas sobre el tema "Chiral ligand-exchange chromatography".
Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.
También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.
Artículos de revistas sobre el tema "Chiral ligand-exchange chromatography"
Schmid, Martin G. y Gerald Gübitz. "Chiral separation by ligand-exchange". Macedonian Journal of Chemistry and Chemical Engineering 30, n.º 2 (25 de diciembre de 2011): 127. http://dx.doi.org/10.20450/mjcce.2011.4.
Texto completoMathur, R., S. Bohra, V. Mathur, C. K. Narang y N. K. Mathur. "Chiral ligand exchange chromatography on polygalactomannan (Guaran)". Chromatographia 33, n.º 7-8 (abril de 1992): 336–38. http://dx.doi.org/10.1007/bf02275913.
Texto completoRizzi, Andreas M. "Efficiency in chiral high-performance ligand-exchange chromatography". Journal of Chromatography A 542 (enero de 1991): 221–37. http://dx.doi.org/10.1016/s0021-9673(01)88763-x.
Texto completoZhou, Jie, Suzhen Zhao, Guangjun Fu y Zhenzhong Zhang. "Isoleucine ionic liquids as additives to separate mandelic acid and their derivative enantiomers by HPLC". Anal. Methods 6, n.º 15 (2014): 5627–31. http://dx.doi.org/10.1039/c3ay41669k.
Texto completoTian, Minglei, Hyung Sang Row y Kyung Ho Row. "Chiral separation of ofloxacin enantiomers by ligand exchange chromatography". Monatshefte für Chemie - Chemical Monthly 141, n.º 3 (18 de febrero de 2010): 285–90. http://dx.doi.org/10.1007/s00706-010-0264-x.
Texto completoRemelli, M., P. Fornasari, F. Dondi y F. Pulidori. "Dynamic column-coating procedure for chiral ligand-exchange chromatography". Chromatographia 37, n.º 1-2 (julio de 1993): 23–30. http://dx.doi.org/10.1007/bf02272183.
Texto completoSanaie, Nooshafarin y Charles A. Haynes. "Modeling l-dopa purification by chiral ligand-exchange chromatography". AIChE Journal 53, n.º 3 (2007): 617–26. http://dx.doi.org/10.1002/aic.11111.
Texto completoXiong, Qing, Jing Jin, Liqiong Lv, Zhisi Bu y Shengqiang Tong. "Chiral ligand exchange countercurrent chromatography: Enantioseparation of amino acids". Journal of Separation Science 41, n.º 6 (6 de febrero de 2018): 1479–88. http://dx.doi.org/10.1002/jssc.201701117.
Texto completoNikolić, N., D. Veselinović, J. Vučina, H. Lingeman y K. Karljiković-Rajić. "Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime". Journal of Pharmaceutical and Biomedical Analysis 32, n.º 6 (agosto de 2003): 1159–66. http://dx.doi.org/10.1016/s0731-7085(03)00230-9.
Texto completoNatalini, Benedetto, Antonio Macchiarulo, Roccaldo Sardella, Alberto Massarotti y Roberto Pellicciari. "Descriptive structure-separation relationship studies in chiral ligand-exchange chromatography". Journal of Separation Science 31, n.º 13 (julio de 2008): 2395–403. http://dx.doi.org/10.1002/jssc.200800102.
Texto completoTesis sobre el tema "Chiral ligand-exchange chromatography"
Zaher, Mustapha. "Nouveaux sélecteurs chiraux à base d'aminoglycosides pour la séparation chirale par échange de ligands". Phd thesis, Grenoble, 2010. http://www.theses.fr/2010GRENV084.
Texto completoThe resolution of racemates is necessary in the pharmaceutical, chemical and food fields. The lipophilic derivatives of neamine have been used as a new class of ligands. The aim of this work was to study the enantioselective properties of the lipophilic derivatives of neamine by HPLC and CE. Many derivatives of neamine (4'- mono C18-neamine, 5-mono C18 -neamine, 6-mono C18-neamine, 3 ', 6-di C18-neamine, 4 ', 5-di C18-neamine, or 3′,6-di-O-2-methylnaphthalene-neamine), have been synthesized by our team and immobilized by dynamic coating on a chromatographic support (C18 type or porous graphitic carbon) and used successfully for the first time in LEC to discriminate various couples of enantiomers such as amino acids, nucleosides and dipeptides. However, certain hydrophobic molecules, such as tryptophan, are long retained and consequently not detectable. To overcome these problems, we have considered the property of the neamine 4'-mono C18 to form micelles allowing its use in LE-MEKC. The enantiomers of tryptophan are then separated in less than five minutes. The effects of various conditions (chiral selector concentration and electrolyte methanol content) on the migration time were evaluated. This method was also applied successfully to other hydrophobic enantiomers such as 1-methyl-tryptophan, 3, 5-diiodo-tyrosin and 1-naphtyl-alanine
Sanaie, Nooshafarin. "A molecular thermodynamic model for chiral drug purification using chiral ligand exchange chromatography". Thesis, 2006. http://hdl.handle.net/2429/18556.
Texto completoApplied Science, Faculty of
Chemical and Biological Engineering, Department of
Graduate
Capítulos de libros sobre el tema "Chiral ligand-exchange chromatography"
Lam, S. "Chiral ligand exchange chromatography". En Chiral Liquid Chromatography, 83–101. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0861-1_5.
Texto completoLam, S. "Chiral ligand exchange chromatography". En Chiral Liquid Chromatography, 83–101. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0699-3_5.
Texto completoBrückner, Hans, Barbara Sorsche, Ali Esna-Ashari y Rolf Jöster. "Chiral ligand-exchange chromatography of amino acid derivatives". En Amino Acids, 152–58. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_18.
Texto completoIanni, Federica, Lucia Pucciarini, Andrea Carotti, Roccaldo Sardella y Benedetto Natalini. "Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand Exchange". En Methods in Molecular Biology, 279–302. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9438-0_15.
Texto completoNatalini, Benedetto, Roccaldo Sardella y Federica Ianni. "Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand-Exchange". En Methods in Molecular Biology, 191–208. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-263-6_11.
Texto completoUdvarhelyi, P. M., D. C. Sunter y J. C. Watkins. "Separation and Assignment of the Stereoisomers of β-(p-Chlorophenyl) Glutamic Acid by Ligand Exchange Chromatography". En Recent Advances in Chiral Separations, 57–62. New York, NY: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-8282-9_8.
Texto completoDavankov, V. A. "Ligand-Exchange Chromatography of Chiral Compounds". En Complexation Chromatography, 197–246. CRC Press, 2020. http://dx.doi.org/10.1201/9781003066781-5.
Texto completoDavankov, V. A. "CHIRAL SEPARATIONS | Ligand Exchange Chromatography". En Encyclopedia of Separation Science, 2369–80. Elsevier, 2000. http://dx.doi.org/10.1016/b0-12-226770-2/03111-2.
Texto completo"Ligand Exchange-Based Chiral Stationary Phases". En Chiral Separations By Liquid Chromatography And Related Technologies, 247–80. CRC Press, 2003. http://dx.doi.org/10.1201/9780203911112.ch7.
Texto completo"Mechanistic Aspects and Applications of Chiral Ligand- Exchange Chromatography". En Advances in Chromatography, Volume 49, 80–143. CRC Press, 2016. http://dx.doi.org/10.1201/b10721-5.
Texto completo