Pure and Applied Chemistry

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• Gegenava Maia, Chankvetadze Lali, Farkas Tivadar, Chankvetadze Bezhan: Enantioseparation of selected chiral sulfoxides in high-performance liquid chromatography with polysaccharide-based chiral selectors in polar organic mobile phases with emphasis on enantiomer elution order. J. Sep. Science 2014, n/a. <http://dx.doi.org/10.1002/jssc.201301318>
• Shen Guopeng, Jia Xin, Ma Sijia, Wang Tiantian, Du Bin, Zhang Zhenzhong: RESOLUTION OF RACEMIC γ-SUBSTITUTED BUTENOLIDE DERIVATIVES USING A POLYSACCHARIDE TYPE STATIONARY PHASE BY HIGH PERFORMANCE LIQUID CHROMATOGRAPHY. Journal of Liquid Chromatography & Related Technologies 2014, 37, 841. <http://dx.doi.org/10.1080/10826076.2012.758147>
• Kodali P., Stalcup A. M.: NORMAL PHASE CHIRAL SEPARATION OF HEXAHELICENE ISOMERS USING A CHIRAL SURFACE CONFINED IONIC LIQUID STATIONARY PHASE. Journal of Liquid Chromatography & Related Technologies 2014, 37, 893. <http://dx.doi.org/10.1080/10826076.2012.758151>
• Au-Yeung Patrick H., Resnick Sol M., Witt Paul M., Frank Timothy C., Donate Felipe A., Robbins Lanny A.: Horizontal reactive distillation for multicomponent chiral resolution. AIChE J. 2013, 59, 2603. <http://dx.doi.org/10.1002/aic.14138>
• Stavrou Ioannis J., Moore Leonard, Fernand Vivian E., Kapnissi-Christodoulou Constantina P., Warner Isiah M.: Facile preparation of polysaccharide-coated capillaries using a room temperature ionic liquid for chiral separations. ELECTROPHORESIS 2013, 34, 1334. <http://dx.doi.org/10.1002/elps.201200563>
• Matarashvili Iza, Chankvetadze Lali, Fanali Salvatore, Farkas Tivadar, Chankvetadze Bezhan: HPLC separation of enantiomers of chiral arylpropionic acid derivatives using polysaccharide-based chiral columns and normal-phase eluents with emphasis on elution order. J. Sep. Science 2013, 36, 140. <http://dx.doi.org/10.1002/jssc.201200885>
• Layton Catharine, Ma Shengli, Wu Ling, Lee Heewon, Fandrick Keith, Fandrick Daniel, Senanyake Chris, Yee Nathan, Grinberg Nelu, Clark Jody: Study of enantioselectivity on an immobilized amylose carbamate stationary phase under subcritical fluid chromatography. J. Sep. Science 2013, 36, 3941. <http://dx.doi.org/10.1002/jssc.201300800>
• Shi Jie-hua, Xu Shui-xing, Jia Qian-qian, Yan Xiao-qing: Characterization of a Cellulose Trisphenylcarbamate/1-Octyl-3-methylimidazolium Tetrafluoroborate Mixture as GC Stationary Phase: Thermodynamic Parameters and LSER Methodology. Chromatographia 2013, 76, 1021. <http://dx.doi.org/10.1007/s10337-013-2495-6>
• Chen Kai, Lynen Frédéric, Hitzel Laure, Hanna-Brown Melissa, Szucs Roman, Sandra Pat: A New Strategy for Fast Chiral Screening by Combining HPLC-DAD with a Multivariate Curve Resolution–Alternating Least Squares Algorithm. Chromatographia 2013, 76, 1055. <http://dx.doi.org/10.1007/s10337-013-2520-9>
• Ates Hasret, Younes Ahmed A., Mangelings Debby, Heyden Yvan Vander: Enantioselectivity of polysaccharide-based chiral selectors in polar organic solvents chromatography: Implementation of chlorinated selectors in a separation strategy. Journal of Pharmaceutical and Biomedical Analysis 2013, 74, 1. <http://dx.doi.org/10.1016/j.jpba.2012.09.025>
• Scriba Gerhard K. E.: Chiral Recognition Mechanisms in Analytical Separation Sciences. Chromatographia 2012, 75, 815. <http://dx.doi.org/10.1007/s10337-012-2261-1>
• Shen Jun, Liu Shuangyan, Li Pengfei, Shen Xiande, Okamoto Yoshio: Controlled synthesis and chiral recognition of immobilized cellulose and amylose tris(cyclohexylcarbamate)s/3-(triethoxysilyl)propylcarbamates as chiral packing materials for high-performance liquid chromatography. Journal of Chromatography A 2012, 1246, 137. <http://dx.doi.org/10.1016/j.chroma.2012.05.002>
• Fernandes Carla, Brandão Pedro, Santos Alexandre, Tiritan Maria Elizabeth, Afonso Carlos, Cass Quezia B., Pinto Madalena M.: Resolution and determination of enantiomeric purity of new chiral derivatives of xanthones using polysaccharide-based stationary phases. Journal of Chromatography A 2012, 1269, 143. <http://dx.doi.org/10.1016/j.chroma.2012.07.058>
• Younes Ahmed A., Mangelings Debby, Vander Heyden Yvan: Chiral separations in reversed-phase liquid chromatography: Evaluation of several polysaccharide-based chiral stationary phases for a separation strategy update. Journal of Chromatography A 2012, 1269, 154. <http://dx.doi.org/10.1016/j.chroma.2012.07.070>
• Chankvetadze Bezhan: Recent developments on polysaccharide-based chiral stationary phases for liquid-phase separation of enantiomers. Journal of Chromatography A 2012, 1269, 26. <http://dx.doi.org/10.1016/j.chroma.2012.10.033>
• Tang Mengling, Zhang Jing, Zhuang Shulin, Liu Weiping: Development of chiral stationary phases for high-performance liquid chromatographic separation. TrAC Trends in Analytical Chemistry 2012, 39, 180. <http://dx.doi.org/10.1016/j.trac.2012.07.006>
• Haleema Simimole, Sasi Paleapadam Vavan, Ibnusaud Ibrahim, Polavarapu Prasad L., Kagan Henri B.: Enantiomerically pure compounds related to chiral hydroxy acids derived from renewable resources. RSC Adv. 2012, 2, 9257. <http://dx.doi.org/10.1039/c2ra21205f>
• Bubba Massimo, Checchini Leonardo, Cincinelli Alessandra, Lepri Luciano: Enantiomeric resolution of chiral aromatic sulfoxides on non-commercial cellulose tribenzoate plates. JPC - Journal of Planar Chromatography - Modern TLC 2012, 25, 214. <http://dx.doi.org/10.1556/JPC.25.2012.3.5>
• Lee Jeong-Mi, Jang Myung-Duk, Park Jung-Hag: Chiral Separation on Sulfonated Cellulose Tris(3,5-dimethylphenylcarbamate)-coated Zirconia Monolith by Capillary Electrochromatography. Bulletin of the Korean Chemical Society 2012, 33, 2651. <http://dx.doi.org/10.5012/bkcs.2012.33.8.2651>
• Lu Wenjie Jessie, Ferlito Valentina, Xu Cong, Flockhart David Alastair, Caccamese Salvatore: Enantiomers of naringenin as pleiotropic, stereoselective inhibitors of cytochrome P450 isoforms. Chirality 2011, 23, 891. <http://dx.doi.org/10.1002/chir.21005>
• Okamoto Yoshio, Ikai Tomoyuki, Shen Jun: Controlled Immobilization of Polysaccharide Derivatives for Efficient Chiral Separation. Isr. J. Chem. 2011, 51, 1096. <http://dx.doi.org/10.1002/ijch.201100025>
• Dossou Katina S. S., Chiap Patrice, Servais Anne C., Fillet Marianne, Crommen Jacques: Evaluation of chlorine containing cellulose-based chiral stationary phases for the LC enantioseparation of basic pharmaceuticals using polar non-aqueous mobile phases. J Sep Science 2011, 34, 617. <http://dx.doi.org/10.1002/jssc.201000774>
• West Caroline, Zhang Yingru, Morin-Allory Luc: Insights into chiral recognition mechanisms in supercritical fluid chromatography. I. Non-enantiospecific interactions contributing to the retention on tris-(3,5-dimethylphenylcarbamate) amylose and cellulose stationary phases. J Chromatogr A 2011, 1218, 2019. <http://dx.doi.org/10.1016/j.chroma.2010.11.084>
• West Caroline, Guenegou Guillaume, Zhang Yingru, Morin-Allory Luc: Insights into chiral recognition mechanisms in supercritical fluid chromatography. II. Factors contributing to enantiomer separation on tris-(3,5-dimethylphenylcarbamate) of amylose and cellulose stationary phases. J Chromatogr A 2011, 1218, 2033. <http://dx.doi.org/10.1016/j.chroma.2010.11.085>
• Del Bubba M., Cincinelli A., Checchini L., Lepri L.: Chiral separations and quantitative analysis of optical isomers on cellulose tribenzoate plates. J Chromatogr A 2011, 1218, 2737. <http://dx.doi.org/10.1016/j.chroma.2011.01.012>
• Cirilli Roberto, Alcaro Stefano, Fioravanti Rossella, Ferretti Rosella, Bolasco Adriana, Gallinella Bruno, Faggi Cristina: A chromatographic study on the exceptional enantioselectivity of cellulose tris(4-methylbenzoate) towards C5-chiral 4,5-dihydro-(1H)-pyrazole derivatives. J Chromatogr A 2011, 1218, 5653. <http://dx.doi.org/10.1016/j.chroma.2011.06.081>
• Kumar Avvaru Praveen, Park Jung Hag: Chiral separation of basic compounds on a cellulose 3,5-dimethylphenylcarbamate-coated zirconia monolithin basic eluents by capillary electrochromatography. Journal of Chromatography A 2011, 1218, 6548. <http://dx.doi.org/10.1016/j.chroma.2011.06.101>
• Ferretti Rosella, Mai Antonello, Gallinella Bruno, Zanitti Leo, Valente Sergio, Cirilli Roberto: Application of 3μm particle-based amylose-derived chiral stationary phases for the enantioseparation of potential histone deacetylase inhibitors. Journal of Chromatography A 2011, 1218, 8394. <http://dx.doi.org/10.1016/j.chroma.2011.09.052>
• Younes Ahmed A., Mangelings Debby, Vander Heyden Yvan: Chiral separations in normal phase liquid chromatography: Enantioselectivity of recently commercialized polysaccharide-based selectors. Part I: Enantioselectivity under generic screening conditions. J  Pharm Biomed Anal 2011, 55, 414. <http://dx.doi.org/10.1016/j.jpba.2011.02.015>
• Ciogli Alessia, Bicker Wolfgang, Lindner Wolfgang: Determination of enantiomerization barriers of hypericin and pseudohypericin by dynamic high-performance liquid chromatography on immobilized polysaccharide-type chiral stationary phases and off-column racemization experiments. Chirality 2009, NA. <http://dx.doi.org/10.1002/chir.20764>
• Okamoto Yoshio: Chiral polymers for resolution of enantiomers. J Polym Sci A Polym Chem 2009, 47, 1731. <http://dx.doi.org/10.1002/pola.23215>
• Morin P.: Séparation de molécules pharmaceutiques chirales par les techniques chromatographiques et électrophorétiques. Annales Pharmaceutiques Françaises 2009, 67, 241. <http://dx.doi.org/10.1016/j.pharma.2009.03.008>
• Okamoto Yoshio, Ikai Tomoyuki: Chiral HPLC for efficient resolution of enantiomers. Chem Soc Rev 2008, 37, 2593. <http://dx.doi.org/10.1039/b808881k>