Добірка наукової літератури з теми "Chiral ligand-exchange chromatography"
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Статті в журналах з теми "Chiral ligand-exchange chromatography"
Schmid, Martin G., and Gerald Gübitz. "Chiral separation by ligand-exchange." Macedonian Journal of Chemistry and Chemical Engineering 30, no. 2 (December 25, 2011): 127. http://dx.doi.org/10.20450/mjcce.2011.4.
Повний текст джерелаMathur, R., S. Bohra, V. Mathur, C. K. Narang, and N. K. Mathur. "Chiral ligand exchange chromatography on polygalactomannan (Guaran)." Chromatographia 33, no. 7-8 (April 1992): 336–38. http://dx.doi.org/10.1007/bf02275913.
Повний текст джерелаRizzi, Andreas M. "Efficiency in chiral high-performance ligand-exchange chromatography." Journal of Chromatography A 542 (January 1991): 221–37. http://dx.doi.org/10.1016/s0021-9673(01)88763-x.
Повний текст джерелаZhou, Jie, Suzhen Zhao, Guangjun Fu, and Zhenzhong Zhang. "Isoleucine ionic liquids as additives to separate mandelic acid and their derivative enantiomers by HPLC." Anal. Methods 6, no. 15 (2014): 5627–31. http://dx.doi.org/10.1039/c3ay41669k.
Повний текст джерелаTian, Minglei, Hyung Sang Row, and Kyung Ho Row. "Chiral separation of ofloxacin enantiomers by ligand exchange chromatography." Monatshefte für Chemie - Chemical Monthly 141, no. 3 (February 18, 2010): 285–90. http://dx.doi.org/10.1007/s00706-010-0264-x.
Повний текст джерелаRemelli, M., P. Fornasari, F. Dondi, and F. Pulidori. "Dynamic column-coating procedure for chiral ligand-exchange chromatography." Chromatographia 37, no. 1-2 (July 1993): 23–30. http://dx.doi.org/10.1007/bf02272183.
Повний текст джерелаSanaie, Nooshafarin, and Charles A. Haynes. "Modeling l-dopa purification by chiral ligand-exchange chromatography." AIChE Journal 53, no. 3 (2007): 617–26. http://dx.doi.org/10.1002/aic.11111.
Повний текст джерелаXiong, Qing, Jing Jin, Liqiong Lv, Zhisi Bu, and Shengqiang Tong. "Chiral ligand exchange countercurrent chromatography: Enantioseparation of amino acids." Journal of Separation Science 41, no. 6 (February 6, 2018): 1479–88. http://dx.doi.org/10.1002/jssc.201701117.
Повний текст джерелаNikolić, N., D. Veselinović, J. Vučina, H. Lingeman, and K. Karljiković-Rajić. "Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime." Journal of Pharmaceutical and Biomedical Analysis 32, no. 6 (August 2003): 1159–66. http://dx.doi.org/10.1016/s0731-7085(03)00230-9.
Повний текст джерелаNatalini, Benedetto, Antonio Macchiarulo, Roccaldo Sardella, Alberto Massarotti, and Roberto Pellicciari. "Descriptive structure-separation relationship studies in chiral ligand-exchange chromatography." Journal of Separation Science 31, no. 13 (July 2008): 2395–403. http://dx.doi.org/10.1002/jssc.200800102.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаThe 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.
Повний текст джерелаApplied Science, Faculty of
Chemical and Biological Engineering, Department of
Graduate
Частини книг з теми "Chiral ligand-exchange chromatography"
Lam, S. "Chiral ligand exchange chromatography." In Chiral Liquid Chromatography, 83–101. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0861-1_5.
Повний текст джерелаLam, S. "Chiral ligand exchange chromatography." In Chiral Liquid Chromatography, 83–101. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0699-3_5.
Повний текст джерелаBrückner, Hans, Barbara Sorsche, Ali Esna-Ashari, and Rolf Jöster. "Chiral ligand-exchange chromatography of amino acid derivatives." In Amino Acids, 152–58. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_18.
Повний текст джерелаIanni, Federica, Lucia Pucciarini, Andrea Carotti, Roccaldo Sardella, and Benedetto Natalini. "Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand Exchange." In 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.
Повний текст джерелаNatalini, Benedetto, Roccaldo Sardella, and Federica Ianni. "Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand-Exchange." In Methods in Molecular Biology, 191–208. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-263-6_11.
Повний текст джерелаUdvarhelyi, P. M., D. C. Sunter, and J. C. Watkins. "Separation and Assignment of the Stereoisomers of β-(p-Chlorophenyl) Glutamic Acid by Ligand Exchange Chromatography." In 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.
Повний текст джерелаDavankov, V. A. "Ligand-Exchange Chromatography of Chiral Compounds." In Complexation Chromatography, 197–246. CRC Press, 2020. http://dx.doi.org/10.1201/9781003066781-5.
Повний текст джерелаDavankov, V. A. "CHIRAL SEPARATIONS | Ligand Exchange Chromatography." In Encyclopedia of Separation Science, 2369–80. Elsevier, 2000. http://dx.doi.org/10.1016/b0-12-226770-2/03111-2.
Повний текст джерела"Ligand Exchange-Based Chiral Stationary Phases." In Chiral Separations By Liquid Chromatography And Related Technologies, 247–80. CRC Press, 2003. http://dx.doi.org/10.1201/9780203911112.ch7.
Повний текст джерела"Mechanistic Aspects and Applications of Chiral Ligand- Exchange Chromatography." In Advances in Chromatography, Volume 49, 80–143. CRC Press, 2016. http://dx.doi.org/10.1201/b10721-5.
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