Gotowa bibliografia na temat „Chiral ligand-exchange chromatography”
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Artykuły w czasopismach na temat "Chiral ligand-exchange chromatography"
Schmid, Martin G., i Gerald Gübitz. "Chiral separation by ligand-exchange". Macedonian Journal of Chemistry and Chemical Engineering 30, nr 2 (25.12.2011): 127. http://dx.doi.org/10.20450/mjcce.2011.4.
Pełny tekst źródłaMathur, R., S. Bohra, V. Mathur, C. K. Narang i N. K. Mathur. "Chiral ligand exchange chromatography on polygalactomannan (Guaran)". Chromatographia 33, nr 7-8 (kwiecień 1992): 336–38. http://dx.doi.org/10.1007/bf02275913.
Pełny tekst źródłaRizzi, Andreas M. "Efficiency in chiral high-performance ligand-exchange chromatography". Journal of Chromatography A 542 (styczeń 1991): 221–37. http://dx.doi.org/10.1016/s0021-9673(01)88763-x.
Pełny tekst źródłaZhou, Jie, Suzhen Zhao, Guangjun Fu i Zhenzhong Zhang. "Isoleucine ionic liquids as additives to separate mandelic acid and their derivative enantiomers by HPLC". Anal. Methods 6, nr 15 (2014): 5627–31. http://dx.doi.org/10.1039/c3ay41669k.
Pełny tekst źródłaTian, Minglei, Hyung Sang Row i Kyung Ho Row. "Chiral separation of ofloxacin enantiomers by ligand exchange chromatography". Monatshefte für Chemie - Chemical Monthly 141, nr 3 (18.02.2010): 285–90. http://dx.doi.org/10.1007/s00706-010-0264-x.
Pełny tekst źródłaRemelli, M., P. Fornasari, F. Dondi i F. Pulidori. "Dynamic column-coating procedure for chiral ligand-exchange chromatography". Chromatographia 37, nr 1-2 (lipiec 1993): 23–30. http://dx.doi.org/10.1007/bf02272183.
Pełny tekst źródłaSanaie, Nooshafarin, i Charles A. Haynes. "Modeling l-dopa purification by chiral ligand-exchange chromatography". AIChE Journal 53, nr 3 (2007): 617–26. http://dx.doi.org/10.1002/aic.11111.
Pełny tekst źródłaXiong, Qing, Jing Jin, Liqiong Lv, Zhisi Bu i Shengqiang Tong. "Chiral ligand exchange countercurrent chromatography: Enantioseparation of amino acids". Journal of Separation Science 41, nr 6 (6.02.2018): 1479–88. http://dx.doi.org/10.1002/jssc.201701117.
Pełny tekst źródłaNikolić, N., D. Veselinović, J. Vučina, H. Lingeman i K. Karljiković-Rajić. "Chiral ligand-exchange chromatography for diastereo-enantio separation of exametazime". Journal of Pharmaceutical and Biomedical Analysis 32, nr 6 (sierpień 2003): 1159–66. http://dx.doi.org/10.1016/s0731-7085(03)00230-9.
Pełny tekst źródłaNatalini, Benedetto, Antonio Macchiarulo, Roccaldo Sardella, Alberto Massarotti i Roberto Pellicciari. "Descriptive structure-separation relationship studies in chiral ligand-exchange chromatography". Journal of Separation Science 31, nr 13 (lipiec 2008): 2395–403. http://dx.doi.org/10.1002/jssc.200800102.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaThe 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.
Pełny tekst źródłaApplied Science, Faculty of
Chemical and Biological Engineering, Department of
Graduate
Części książek na temat "Chiral ligand-exchange chromatography"
Lam, S. "Chiral ligand exchange chromatography". W Chiral Liquid Chromatography, 83–101. Dordrecht: Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-009-0861-1_5.
Pełny tekst źródłaLam, S. "Chiral ligand exchange chromatography". W Chiral Liquid Chromatography, 83–101. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4613-0699-3_5.
Pełny tekst źródłaBrückner, Hans, Barbara Sorsche, Ali Esna-Ashari i Rolf Jöster. "Chiral ligand-exchange chromatography of amino acid derivatives". W Amino Acids, 152–58. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-2262-7_18.
Pełny tekst źródłaIanni, Federica, Lucia Pucciarini, Andrea Carotti, Roccaldo Sardella i Benedetto Natalini. "Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand Exchange". W 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.
Pełny tekst źródłaNatalini, Benedetto, Roccaldo Sardella i Federica Ianni. "Enantioseparations by High-Performance Liquid Chromatography Based on Chiral Ligand-Exchange". W Methods in Molecular Biology, 191–208. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-263-6_11.
Pełny tekst źródłaUdvarhelyi, P. M., D. C. Sunter i J. C. Watkins. "Separation and Assignment of the Stereoisomers of β-(p-Chlorophenyl) Glutamic Acid by Ligand Exchange Chromatography". W 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.
Pełny tekst źródłaDavankov, V. A. "Ligand-Exchange Chromatography of Chiral Compounds". W Complexation Chromatography, 197–246. CRC Press, 2020. http://dx.doi.org/10.1201/9781003066781-5.
Pełny tekst źródłaDavankov, V. A. "CHIRAL SEPARATIONS | Ligand Exchange Chromatography". W Encyclopedia of Separation Science, 2369–80. Elsevier, 2000. http://dx.doi.org/10.1016/b0-12-226770-2/03111-2.
Pełny tekst źródła"Ligand Exchange-Based Chiral Stationary Phases". W Chiral Separations By Liquid Chromatography And Related Technologies, 247–80. CRC Press, 2003. http://dx.doi.org/10.1201/9780203911112.ch7.
Pełny tekst źródła"Mechanistic Aspects and Applications of Chiral Ligand- Exchange Chromatography". W Advances in Chromatography, Volume 49, 80–143. CRC Press, 2016. http://dx.doi.org/10.1201/b10721-5.
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