Relevant bibliographies by topics / Chiral analysis

Academic literature on the topic 'Chiral analysis'

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Published: 4 June 2021
Last updated: 6 September 2023

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Journal articles on the topic "Chiral analysis"

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Partini, Juliasih, Kamsul Abraha, and Arief Hermanto. "Chirality Analysis on a Square Chiral Metamaterial." Materials Science Forum 901 (July 2017): 65–68. http://dx.doi.org/10.4028/www.scientific.net/msf.901.65.

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We have analyzed the chirality of terahertz (THz) wave emission from a square chiral metamaterial. The sample was manufactured with a periodic structure formed by a square pattern of chiral with different depth on a silver film. We have yield the specific polarization rotation in the THz region when the THz wave is emitted from a square chiral metamaterial. The THz emissions from these chiral metamaterials were elliptic polarization. A square chiral metamaterial was shown circular dichroism and optical activity properties at different frequencies. The ellipticity and rotation angle will reach a maximum value at a frequency of 1.2 THz and 0.6 THz, respectively. The results were indicated the possibility to controlled the polarization with chiral metamaterial structures.
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Oromí-Farrús, Mireia, Mercè Torres, and Ramon Canela. "Acylation of Chiral Alcohols: A Simple Procedure for Chiral GC Analysis." Journal of Analytical Methods in Chemistry 2012 (2012): 1–10. http://dx.doi.org/10.1155/2012/452949.

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The use of iodine as a catalyst and either acetic or trifluoroacetic acid as a derivatizing reagent for determining the enantiomeric composition of acyclic and cyclic aliphatic chiral alcohols was investigated. Optimal conditions were selected according to the molar ratio of alcohol to acid, the reaction time, and the reaction temperature. Afterwards, chiral stability of chiral carbons was studied. Although no isomerization was observed when acetic acid was used, partial isomerization was detected with the trifluoroacetic acid. A series of chiral alcohols of a widely varying structural type were then derivatized with acetic acid using the optimal conditions. The resolution of the enantiomeric esters and the free chiral alcohols was measured using a capillary gas chromatograph equipped with a CP Chirasil-DEX CB column. The best resolutions were obtained with 2-pentyl acetates (α=3.00) and 2-hexyl acetates (α=1.95). This method provides a very simple and efficient experimental workup procedure for analyzing chiral alcohols by chiral-phase GC.
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ITABASHI, Yutaka. "Analysis of Chiral Glycerolipids by Chiral Phase HPLC." Journal of Japan Oil Chemists' Society 47, no. 10 (1998): 971–81. http://dx.doi.org/10.5650/jos1996.47.971.

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Deng, Xiaoqiao, Zucun Zhang, Jiang Cao, Zhenkai Zhang, and Yubo Tian. "Electromagnetic scattering analysis of normal chiral, metamaterials chiral and chiral nihility materials." Electromagnetics 39, no. 4 (May 3, 2019): 227–40. http://dx.doi.org/10.1080/02726343.2019.1595385.

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Ali, Imran, Mohd Suhail, and Hassan Y. Aboul-Enein. "Chiral analysis of macromolecules." Journal of Liquid Chromatography & Related Technologies 41, no. 11 (July 3, 2018): 749–60. http://dx.doi.org/10.1080/10826076.2018.1514509.

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Boesl, Ulrich, and Aras Kartouzian. "Mass-Selective Chiral Analysis." Annual Review of Analytical Chemistry 9, no. 1 (June 12, 2016): 343–64. http://dx.doi.org/10.1146/annurev-anchem-071015-041658.

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Sihvola, A. H., and I. V. Lindell. "Analysis on Chiral Mixtures." Journal of Electromagnetic Waves and Applications 6, no. 5 (January 1, 1992): 553–72. http://dx.doi.org/10.1163/156939392x00841.

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Sihvola, A. H., and I. V. Lindell. "Analysis on Chiral Mixtures." Journal of Electromagnetic Waves and Applications 6, no. 5-6 (January 1, 1992): 553–72. http://dx.doi.org/10.1163/156939392x01318.

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Cifuentes, Alejandro, and Salvatore Fanali. "21st century chiral analysis." TrAC Trends in Analytical Chemistry 127 (June 2020): 115911. http://dx.doi.org/10.1016/j.trac.2020.115911.

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Lee, Seon Hwa, Michelle V. Williams, and Ian A. Blair. "Targeted chiral lipidomics analysis." Prostaglandins & Other Lipid Mediators 77, no. 1-4 (September 2005): 141–57. http://dx.doi.org/10.1016/j.prostaglandins.2004.01.009.

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Dissertations / Theses on the topic "Chiral analysis"

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Layton, Sherry E. "Comparison of various chiral stationary phases for the chromatographic separation of chiral pharmaceuticals /." Electronic version (PDF), 2005. http://dl.uncw.edu/etd/2005/laytons/sherrylayton.pdf.

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Fulwood, Russell. "Chiral analysis by NMR spectroscopy." Thesis, Durham University, 1992. http://etheses.dur.ac.uk/5979/.

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The analysis of the enantiomeric purity of chiral carboxylic acids requires a reagent to give acceptable NMR chemical shift non-equivalence with a wide range of substrate acids. Extensive studies of the behaviour of N-mono- methyl, N,N-dimethyl and cyclic amines as chiral solvating agents led to the finding that 1,2 diphenyl-1,2-diaminoethane can induce substantial non- equivalence in the diastereomeric salts of chiral a-phenyl and a-halo carboxylic acids. The diastereoisomeric complexes of the diamine with primary carboxylic acids (RCH(_2)CO(_2)H) presents an unusual case in which the internally enantiotopic methylene protons are rendered internally diasteretopic by an external non-covalently bonded reagent. Investigations of the physical parameters determining non-equivalence (stoichiometry, concentration, temperature and substrate enantiomeric purity), combined with NOE observations of the diastereomeric pairs and the crystal structure of the mono- hydrobromide salt were used to suggest the structure for the conformation responsible for shift non-equivalence. The zero valent platinum complex, 3-0-isopropylidene-2,3-dihydroxy-1,4- bis(diphenyl-phosphino)butane-platinum(0)-ethene (DlOP-Pt-ethene) was shown to be a versatile chiral derivatising agent for electron poor and strained η(^2)-donors. This was demonstrated by the enantiomeric purity determinations for alkynes, enones and norbornene derivatives. The crystal structure of DIOP-Pt-ethene was determined and found to be similar to the palladium analogue. If the achiral rhodium complex rhodium(I)-acetylacetone-diethene undergoes a reaction with 2 equivalents of a suitable chiral η(^2)-donor, it will result in the formation of 4 stereoisomers, two meso forms and a pair of enantiomers. The diasteroisomers should display chemical shift non-equivalence in the NMR spectrum of the product, reflecting the enantiomeric purity of the η(^2)-donor (self recognition). The derivatisation of rhodium(l)-acetylacetone-diethene with chiral η(^2)-donors was attempted.
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Penn, Sharron Gaynor. "Chiral analysis by capillary electrophoresis." Thesis, University of York, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241074.

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Mertzman, Melissa Danielle Foley Joe Preston. "Chiral microemulsion electrokinetic chromatography /." Philadelphia, Pa. : Drexel University, 2004. http://dspace.library.drexel.edu/handle/1860/340.

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Modzabi, Selorm Kwame Busch Kenneth W. Busch Marianna A. "Studies on new approaches of chiral discrimination for chiral analysis by regression modeling of spectral data." Waco, Tex. : Baylor University, 2009. http://hdl.handle.net/2104/5349.

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Kahle, Kimberly Ann Foley Joe Preston. "Effect of identity and number of chiral microemulsion components in chiral microemulsion electrokinetic chromatography /." Philadelphia, Pa. : Drexel University, 2007. http://hdl.handle.net/1860/1293.

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Carlsson, Björn. "From achiral to chiral analysis of citalopram." Doctoral thesis, Linköpings universitet, Klinisk farmakologi, 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-5217.

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Within the field of depression the “monoamine hypothesis” has been the leading theory to explain the biological basis of depression. This theory proposes that the biological basis of depression is due to a deficiency in one or more of three key neurotransmitter systems, namely noradrenaline, dopamine and serotonin which are thought to mediate the therapeutic actions of virtually every known antidepressant agent. Citalopram is a selective serotonin-reuptake inhibitor (SSRI) used for the treatment of depression and anxiety disorders. Citalopram is a racemic compound, in other words composed of a 50:50 mixture of two enantiomers (S-(+)-citalopram and R-(-)-citalopram) and with one of the enantiomers (S-(+)-citalopram) accounting for the inhibitory effect. At the time of introduction of citalopram the physician needed a therapeutic drug monitoring service to identify patients with interactions, compliance problems and for handling questions concerning polymorphic enzymes and drug metabolism. An achiral analytical separation method based on solid-phase extraction followed by high-performance liquid chromatography (HPLC) was developed for routine therapeutic drug monitoring (TDM) of citalopram and its two main demethylated metabolites. As the data available on citalopram were from achiral concentration determinations and to be able to further investigate citalopram enantiomers effects and distribution, a chiral method for separation of the enantiomers of citalopram and its demethylated metabolites was established. The advances within chiral separation techniques have made measurement of the concentrations of the individual enantiomers in biological fluids possible. The process behind enantioselective separation is however not fully understood and the mechanism behind the separation can be further scrutinized by the use of multivariate methods. A study of the optimization and characterization of the separation of the enantiomers of citalopram, desmethylcitalopram and didesmethylcitalopram on an acetylated ß-cyclodextrin column, by use of two different chemometric programs - response surface modelling and sequential optimization was performed. Sequential optimization can be a quicker mean of optimizing a chromatographic separation; response surface modelling, in addition to enabling optimization of the chromatographic process, also serves as a tool for learning more about the separation mechanism. Studies of the antidepressant effect and pharmacokinetics of citalopram have been performed in adults, but the effects on children and adolescents have only been studied to a minor extent, despite the increasing use of citalopram in these age groups. A study was initiated to investigate adolescents treated for depression, with respect to the steady-state plasma concentrations of the enantiomers of citalopram and its demethylated metabolites. The ratios between the S- and R-enantiomers of citalopram and didesmethylcitalopram were in agreement with studies involving older patients. The concentrations of the S-(+)- and R-(-) enantiomers of citalopram and desmethylcitalopram were also in agreement with values from earlier studies. The results indicate that the use of oral contraceptives may have some influence on the metabolism of citalopram. This might be because of an interaction of the contraceptive hormones with the polymorphic CYP2C19 enzyme. Even though the SSRIs are considered less toxic compared with older monoamine-active drugs like the tricyclic/tetracyclic antidepressants, the risk of developing serious side effects such as ECG abnormalities and convulsions has been seen for citalopram, when larger doses have been ingested. Furthermore, fatal overdoses have been reported where citalopram alone was the cause of death. Data on the toxicity of each of the enantiomers in humans have not been reported and no data on blood levels of the enantiomers in cases of intoxication have been presented. An investigation was initiated on forensic autopsy cases where citalopram had been found at the routine screening and these cases were further analysed with enantioselective analysis to determine the blood concentrations of the enantiomers of citalopram and metabolites. Furthermore the genotyping regarding the polymorphic enzymes CYP2D6 and CYP2C19 were performed. In 53 autopsy cases, we found increasing S/R ratios with increasing concentrations of citalopram. We found also that high citalopram S/R ratio were associated with high parent drug to metabolite ratio and may be an indicator of recent intake. Only 3.8 % were found to be poor metabolizers regarding CYP2D6 and for CYP2C19 no poor metabolizer was found. Enantioselective analysis of citalopram and its metabolites can provide valuable information about the time that has elapsed between intake and death. Genotyping can be of help in specific cases but the possibility of pharmacokinetic interactions is apparently a far greater problem than genetic enzyme deficiency.
On the day of the public defence the status of article IV was: Submitted.
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Carlsson, Björn. "From achiral to chiral analysis of citalopram /." Linköping : Univ, 2003. http://www.ep.liu.se/diss/med/07/93/index.html.

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Lundgren, Stina. "Efficient Synthesis and Analysis of Chiral Cyanohydrins." Doctoral thesis, Stockholm : Kungliga Tekniska högskolan (KTH), 2007. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4315.

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Kröner, Dominik (Dr rer nat ). "Analysis and control of light-induced processes in molecules: Electron and nuclear quantum dynamics for aspects of stereoisomerism and spectroscopy." Thesis, Universität Potsdam, 2013. http://opus.kobv.de/ubp/volltexte/2014/7047/.

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The habilitation thesis covers theoretical investigations on light-induced processes in molecules. The study is focussed on changes of the molecular electronic structure and geometry, caused either by photoexcitation in the event of a spectroscopic analysis, or by a selective control with shaped laser pulses. The applied and developed methods are predominantly based on quantum chemistry as well as on electron and nuclear quantum dynamics, and in parts on molecular dynamics. The studied scientific problems deal with stereoisomerism and the question of how to either switch or distinguish chiral molecules using laser pulses, and with the essentials for the simulation of the spectroscopic response of biochromophores, in order to unravel their photophysics. The accomplished findings not only explain experimental results and extend existing approaches, but also contribute significantly to the basic understanding of the investigated light-driven molecular processes. The main achievements can be divided in three parts: First, a quantum theory for an enantio- and diastereoselective or, in general, stereoselective laser pulse control was developed and successfully applied to influence the chirality of molecular switches. The proposed axially chiral molecules possess different numbers of "switchable" stable chiral conformations, with one particular switch featuring even a true achiral "off"-state which allows to enantioselectively "turn on" its chirality. Furthermore, surface mounted chiral molecular switches with several well-defined orientations were treated, where a newly devised highly flexible stochastic pulse optimization technique provides high stereoselectivity and efficiency at the same time, even for coupled chirality-changing degrees of freedom. Despite the model character of these studies, the proposed types of chiral molecular switches and, all the more, the developed basic concepts are generally applicable to design laser pulse controlled catalysts for asymmetric synthesis, or to achieve selective changes in the chirality of liquid crystals or in chiroptical nanodevices, implementable in information processing or as data storage. Second, laser-driven electron wavepacket dynamics based on ab initio calculations, namely time-dependent configuration interaction, was extended by the explicit inclusion of magnetic field-magnetic dipole interactions for the simulation of the qualitative and quantitative distinction of enantiomers in mass spectrometry by means of circularly polarized ultrashort laser pulses. The developed approach not only allows to explain the origin of the experimentally observed influence of the pulse duration on the detected circular dichroism in the ion yield, but also to predict laser pulse parameters for an optimal distinction of enantiomers by ultrashort shaped laser pulses. Moreover, these investigations in combination with the previous ones provide a fundamental understanding of the relevance of electric and magnetic interactions between linearly or non-linearly polarized laser pulses and (pro-)chiral molecules for either control by enantioselective excitation or distinction by enantiospecific excitation. Third, for selected light-sensitive biological systems of central importance, like e.g. antenna complexes of photosynthesis, simulations of processes which take place during and after photoexcitation of their chromophores were performed, in order to explain experimental (spectroscopic) findings as well as to understand the underlying photophysical and photochemical principles. In particular, aspects of normal mode mixing due to geometrical changes upon photoexcitation and their impact on (time-dependent) vibronic and resonance Raman spectra, as well as on intramolecular energy redistribution were addressed. In order to explain unresolved experimental findings, a simulation program for the calculation of vibronic and resonance Raman spectra, accounting for changes in both vibrational frequencies and normal modes, was created based on a time-dependent formalism. In addition, the influence of the biochemical environment on the electronic structure of the chromophores was studied by electrostatic interactions and mechanical embedding using hybrid quantum-classical methods. Environmental effects were found to be of importance, in particular, for the excitonic coupling of chromophores in light-harvesting complex II. Although the simulations for such highly complex systems are still restricted by various approximations, the improved approaches and obtained results have proven to be important contributions for a better understanding of light-induced processes in biosystems which also adds to efforts of their artificial reproduction.
Die Habilitationsschrift behandelt theoretische Untersuchungen von durch Licht ausgelösten Prozessen in Molekülen. Der Schwerpunkt liegt dabei auf Veränderungen in der Elektronenstruktur und der Geometrie der Moleküle, die durch Bestrahlung mit Licht entweder bei einer spektroskopischen Untersuchung oder bei gezielter Kontrolle durch geformte Laserpulse herbeigeführt werden. Um die dabei auftretende Elektronen- und Kerndynamik zu simulieren, wurden vornehmlich quantentheoretische Methoden eingesetzt und weiterentwickelt. Die wissenschaftlichen Fragestellungen beschäftigen sich mit dem gezielten Verändern und dem Erkennen der räumlichen Struktur von Molekülen ohne Drehspiegelachse, der sog. molekularen Chiralität, sowie mit durch Licht eingeleiteten Prozessen in biologisch relevanten Pigmenten auf sehr kurzen Zeitskalen. Die entwickelten Ansätze und gewonnenen Erkenntnisse lassen sich drei Haupterfolge unterteilen: Erstens gelang die Entwicklung einer generellen Kontrolltheorie für das Ein- und Umschalten von molekularer Chiralität mit geformten Laserpulsen. Dabei wird die räumliche Struktur der vorgeschlagenen molekularen Schalter zwischen ihren stabilen sog. stereoisomeren Formen selektiv geändert, was sich auf ihre optischen und chemischen Eigenschaften auswirkt. Für komplexere Bedingungen, wie z.B. auf einer Oberfläche verankerten molekularen Schaltern verschiedener Orientierung, wurde eine neue Pulsoptimierungsmethode basierend auf Wahrscheinlichkeiten und Statistik entwickelt. Solche laserpulskontrollierten chiralen molekularen Schalter hofft man u.a. in der Nanotechnologie zum Einsatz zu bringen, wo sie z.B. als Informationsspeicher dienen könnten. Zweitens konnte geklärt werden, welche die wesentlichen Einflüsse sind, die das Erkennen von sog. Enantiomeren, das sind spiegelbildliche Moleküle von entgegengesetzter Chiralität, nach Ionisierung durch ultrakurze zirkular polarisierte Laserpulse ermöglichen. Diese Form des sog. Zirkulardichroismus in der Ionenausbeute erlaubt die quantitative und qualitative Unterscheidung von Enantiomeren in der Massenspektrometrie. Durch Simulation der Elektronendynamik während der Laseranregung konnte u.a. erstmals gezeigt werden, dass neben der Zirkularpolarisation der Laserpulse vor allem die schwachen magnetischen Wechselwirkungen für die Unterscheidung entscheidend sind. Drittens wurden die Spektren von in der Natur vorkommenden Pigmenten simuliert, welche u.a. an wichtigen biologischen Funktionen, wie dem Sammeln von Sonnenenergie für die Photosynthese, beteiligt sind. Die Lichtanregung führt dabei zu einer Veränderung der Elektronenstruktur und Geometrie der Pigmente, wobei letzteres wichtige Konsequenzen für die Verteilung der Energie auf die spektroskopisch beobachteten Molekülschwingungen mit sich bringen. Auch der wichtige Einfluss der biochemischen Umgebung auf die Elektronenstruktur der Pigmente bzw. den Energietransfer zwischen solchen wurde untersucht. Neben der Klärung experimenteller Ergebnisse ermöglichen die Untersuchungen neue Einblicke in die fundamentalen Prozesse kurz nach der Lichtanregung -- Erkenntnisse, die auch für die technische Nachahmung der biologischen Funktionen von Bedeutung sein können.
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Books on the topic "Chiral analysis"

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Chiral separations by chromatography. Oxford [England]: Oxford University Press, 2000.

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Scott, Raymond P. W. 1924-, ed. Chiral chromatography. Chichester, England: J. Wiley, 1998.

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Beesley, Thomas E. Chiral chromatography. Chichester, England: J. Wiley, 1998.

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Chankvetadze, Bezhan. Capillary electrophoresis in chiral analysis. Chichester: John Wiley, 1997.

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Morris, Zief, and Crane Laura J. 1941-, eds. Chromatographic chiral separations. New York: M. Dekker, 1988.

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1944-, Hühnerfuss H., ed. Chiral environmental pollutants: Trace analysis and ecotoxicology. Berlin: Springer, 2001.

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Kallenborn, Roland. Chiral Environmental Pollutants: Trace Analysis and Ecotoxicology. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001.

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Alexander, Bernreuther, and Huffer Manfred, eds. Analysis of chiral organic molecules: Methodologyand applications. New York: Walter de Gruyter, 1995.

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Zehnacker, Anne. Chiral recognition in the gas phase. Boca Raton: Taylor & Francis, 2010.

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Schreier, Peter. Analysis of chiral organic molecules: Methodology and applications. New York: Walter de Gruyter, 1995.

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Book chapters on the topic "Chiral analysis"

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Yáñez, Jaime A., Casey L. Sayre, Stephanie E. Martinez, and Neal M. Davies. "Chiral Methods of Flavonoid Analysis." In FLAVONOID PHARMACOKINETICS, 117–59. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118468524.ch3.

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Fell, Anthony F., and Terence A. G. Noctor. "Strategies for Optimising Chiral Separations in Drug Analysis." In Chiral Separations, 121–25. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-6634-2_13.

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He, Brian Lingfeng. "Chiral Recognition Mechanism: Practical Considerations for Pharmaceutical Analysis of Chiral Compounds." In Chiral Recognition in Separation Methods, 153–201. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-12445-7_6.

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Cho, Seung Il, Jiyeon Shim, Min-Su Kim, Doo Soo Chung, and Yong-Kweon Kim. "Removal of Sodium Ion and Chiral Analysis Using Crown Ether as a Chiral Selector in Microchip Electrophoresis." In Micro Total Analysis Systems 2002, 575–77. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-010-0295-0_192.

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Sensharma, Nirupama. "Analysis." In Wobbling Motion in Nuclei: Transverse, Longitudinal, and Chiral, 63–95. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-17150-5_4.

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Schwarz, Maria A., and Peter C. Hauser. "Fast Chiral On-Chip Separations with Amperometric Detection." In Micro Total Analysis Systems 2001, 547–48. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-010-1015-3_236.

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Jin, Lixia, Weiping Liu, Chunmian Lin, and Jay Gan. "Enantioselective Separation and Analysis of Chiral Herbicides." In ACS Symposium Series, 67–79. Washington, DC: American Chemical Society, 2011. http://dx.doi.org/10.1021/bk-2011-1085.ch004.

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Kallenborn, Roland, and Heinrich Hühnerfuss. "Enantioselective Chromatographic Methods for the Analysis of Chiral Environmental Pollutants." In Chiral Environmental Pollutants, 15–52. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-662-06243-2_2.

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Wainer, Irving W., Rose M. Stiffin, and Ya-Qin Chu. "Drug Analysis using High-Performance Liquid Chromatographic (HPLC) Chiral Stationary Phases: Where to Begin and Which to Use." In Chiral Separations, 11–21. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-6634-2_2.

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Balzano, Federica, Gloria Uccello-Barretta, and Federica Aiello. "Chiral Analysis by NMR Spectroscopy: Chiral Solvating Agents." In Chiral Analysis, 367–427. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-444-64027-7.00009-4.

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Conference papers on the topic "Chiral analysis"

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Pate, Brooks, Luca Evangelisti, Channing West, Kevin Mayer, and Reilly Sonstrom. "CHIRAL ANALYSIS OF MOLECULES WITH MULTIPLE CHIRAL CENTERS USING CHIRAL TAG ROTATIONAL SPECTROSCOPY." In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.mh10.

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Scolati, Haley, Brooks Pate, and Kevin Mayer. "CHIRAL TAG ROTATIONAL SPECTROSCOPY FOR CHIRAL ANALYSIS OF CARBOXYLIC ACIDS." In 2020 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2020. http://dx.doi.org/10.15278/isms.2020.wk05.

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Scolati, Haley, Brooks Pate, and Kevin Mayer. "CHIRAL TAG ROTATIONAL SPECTROSCOPY FOR CHIRAL ANALYSIS OF CARBOXYLIC ACIDS." In 2021 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.fm03.

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Scolati, Haley, Brooks Pate, Martin Holdren, and Kevin Mayer. "CHIRAL TAG ROTATIONAL SPECTROSCOPY FOR STRUCUTRE ANALYSIS OF CHIRAL METHYLPHENYL OXIRANE." In 2021 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2021. http://dx.doi.org/10.15278/isms.2021.fm07.

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Twu, Ruey-Ching, and Jhao-Sheng Wang. "A Study of Homodyen Chiral Polarimetry for Refractive Index Variation Measurements." In Adaptive Optics: Analysis, Methods & Systems. Washington, D.C.: OSA, 2015. http://dx.doi.org/10.1364/aoms.2015.jt5a.8.

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Sonstrom, Reilly, Brooks Pate, Channing West, and Kevin Mayer. "CHIRAL ANALYSIS OF THUJONE IN ESSENTIAL OIL SAMPLES." In 74th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2019. http://dx.doi.org/10.15278/isms.2019.wl05.

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Horváth, Miklós, Defu Hou, and Hai-cang Ren. "Non-static Analysis of the Anomalous Chiral Conductivities." In Proceedings of the 8th International Conference on Quarks and Nuclear Physics (QNP2018). Journal of the Physical Society of Japan, 2019. http://dx.doi.org/10.7566/jpscp.26.024026.

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Guler, Sadri, Birol Solak, Ugur Meric Gur, and Ozgur Ergul. "Full-wave computational analysis of optical chiral metamaterials." In 2017 IV International Electromagnetic Compatibility Conference (EMC Turkiye). IEEE, 2017. http://dx.doi.org/10.1109/emct.2017.8090376.

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Sabah, C. "Characterization and analysis of left-handed chiral materials." In 2008 International Conference on Mathematical Methods in Electromagnetic Theory (MEET). IEEE, 2008. http://dx.doi.org/10.1109/mmet.2008.4581047.

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Torres‐Silva, H. "SAR Simulation with Magneto Chiral Effects for Human Head Radiated from Cellular Phones." In NUMERICAL ANALYSIS AND APPLIED MATHEMATICS: International Conference on Numerical Analysis and Applied Mathematics 2008. American Institute of Physics, 2008. http://dx.doi.org/10.1063/1.2990985.

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Reports on the topic "Chiral analysis"

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Zhong, Wenwan. High-Throughput Genetic Analysis and Combinatorial Chiral Separations Based on Capillary Electrophoresis. Office of Scientific and Technical Information (OSTI), January 2003. http://dx.doi.org/10.2172/816440.

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Desai, Meera Jay. Development of Chiral LC-MS Methods for small Molecules and Their Applications in the Analysis of Enantiomeric Composition and Pharmacokinetic Studies. Office of Scientific and Technical Information (OSTI), January 2004. http://dx.doi.org/10.2172/837266.

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Nawawi, Ahmad H. M. China-Asean Future Relations-An Analysis. Fort Belvoir, VA: Defense Technical Information Center, March 2005. http://dx.doi.org/10.21236/ada432723.

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Urias, Vincent. CHIRP Technology - Initial Business Case Analysis Questions. Office of Scientific and Technical Information (OSTI), July 2020. http://dx.doi.org/10.2172/1638781.

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Duda, Timothy F. Scientific Analysis of ASIAEX South China Sea Data. Fort Belvoir, VA: Defense Technical Information Center, August 2005. http://dx.doi.org/10.21236/ada437817.

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Whiting, Michael D. The Great Firewall of China: A Critical Analysis. Fort Belvoir, VA: Defense Technical Information Center, June 2008. http://dx.doi.org/10.21236/ada488175.

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Wilborn, Thomas L. Security Cooperation With China: Analysis and a Proposal. Fort Belvoir, VA: Defense Technical Information Center, November 1994. http://dx.doi.org/10.21236/ada288850.

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Xu, Peng, Han-Bo Xu, Gao-Hong Chen, and Lu-Lu Lv. Accessory hepatic vein recanalization for Budd-Chiari syndrome: a meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, November 2022. http://dx.doi.org/10.37766/inplasy2022.11.0071.

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Kaiser, D. P. Analysis of monthly mean cloud amount for China: 1951--1994. Office of Scientific and Technical Information (OSTI), December 1998. http://dx.doi.org/10.2172/563241.

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Hammond, James, Dr Zhuangfang Yi, Timothy McLellan, and Jiawen Zhao. Situational Analysis Report: Xishuangbanna Autonomous Dai Prefecture, Yunnan Province, China. World Agroforestry Centre, 2015. http://dx.doi.org/10.5716/wp14255.pdf.

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