Artículos de revistas sobre el tema "Chiral Enantiodiscrimination"
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Arnaboldi, Serena, Tiziana Benincori, Roberto Cirilli, Włodzimierz Kutner, Mirko Magni, Patrizia Romana Mussini, Krzysztof Noworyta y Francesco Sannicolò. "Inherently chiral electrodes: the tool for chiral voltammetry". Chemical Science 6, n.º 3 (2015): 1706–11. http://dx.doi.org/10.1039/c4sc03713h.
Texto completoArnaboldi, Serena, Silvia Cauteruccio, Sara Grecchi, Tiziana Benincori, Massimo Marcaccio, Alessio Orbelli Biroli, Giovanna Longhi, Emanuela Licandro y Patrizia Romana Mussini. "Thiahelicene-based inherently chiral films for enantioselective electroanalysis". Chemical Science 10, n.º 5 (2019): 1539–48. http://dx.doi.org/10.1039/c8sc03337d.
Texto completoPal, Indrani, Sachin Rama Chaudhari y Nagarajarao Suryaprakash. "A versatile ternary ionic complex for chiral discrimination of molecules with diverse functionalities using 1H NMR". New J. Chem. 38, n.º 10 (2014): 4908–12. http://dx.doi.org/10.1039/c4nj00417e.
Texto completoAi, Bin, Hoang M. Luong y Yiping Zhao. "Chiral nanohole arrays". Nanoscale 12, n.º 4 (2020): 2479–91. http://dx.doi.org/10.1039/c9nr09722h.
Texto completoZhang, Xuebo, Jing Xu, Zhaofeng Sun, Guangling Bian y Ling Song. "NMR analysis of the enantiomeric purity of chiral diols by a new chiral boron agent". RSC Advances 12, n.º 8 (2022): 4692–96. http://dx.doi.org/10.1039/d2ra00428c.
Texto completoBerdagué, Philippe, Boris Gouilleux, Markus Noll, Stefan Immel, Michael Reggelin y Philippe Lesot. "Study and quantification of the enantiodiscrimination power of four polymeric chiral LLCs using NAD 2D-NMR". Physical Chemistry Chemical Physics 24, n.º 12 (2022): 7338–48. http://dx.doi.org/10.1039/d1cp04915a.
Texto completoLi, Gaowei, Jiangming Cao, Wen Zong, Xinxiang Lei y Renxiang Tan. "Enantiodiscrimination of carboxylic acids using the diphenylprolinol NMR chiral solvating agents". Organic Chemistry Frontiers 3, n.º 1 (2016): 96–102. http://dx.doi.org/10.1039/c5qo00264h.
Texto completoLee, Wonjae, Eunjung Bang, Ji-Hye Yun, Man-Jeong Paik y Weontae Lee. "Enantiodiscrimination Using a Chiral Crown Ether as a Chiral Solvating Agent Using NMR Spectroscopy". Natural Product Communications 14, n.º 5 (1 de mayo de 2019): 1934578X1984919. http://dx.doi.org/10.1177/1934578x19849191.
Texto completoHuang, Huayin, Guangling Bian, Hua Zong, Yabai Wang, Shiwei Yang, Huifeng Yue, Ling Song y Hongjun Fan. "Chiral Sensor for Enantiodiscrimination of Varied Acids". Organic Letters 18, n.º 11 (18 de mayo de 2016): 2524–27. http://dx.doi.org/10.1021/acs.orglett.6b00088.
Texto completoOhmiya, Hirohisa, Masaya Sawamura y Yuto Yasuda. "Copper-Catalyzed Enantioselective Coupling between Allylboronates and Phosphates Using a Phenol–Carbene Chiral Ligand: Asymmetric Synthesis of Chiral Branched 1,5-Dienes". Synthesis 50, n.º 11 (20 de marzo de 2018): 2235–46. http://dx.doi.org/10.1055/s-0036-1591548.
Texto completoUccello-Barretta, Gloria, Federica Balzano, Jonathan Martinelli, Margherita-Giulia Berni, Claudio Villani y Francesco Gasparrini. "NMR enantiodiscrimination by cyclic tetraamidic chiral solvating agents". Tetrahedron: Asymmetry 16, n.º 22 (noviembre de 2005): 3746–51. http://dx.doi.org/10.1016/j.tetasy.2005.10.016.
Texto completoBalzano, Federica, Gloria Uccello-Barretta, Giuseppe Sicoli, Letizia Vanni, Alessandra Recchimurzo y Federica Aiello. "Chiral Discrimination Mechanisms by Silylated-Acetylated Cyclodextrins: Superficial Interactions vs. Inclusion". International Journal of Molecular Sciences 23, n.º 21 (29 de octubre de 2022): 13169. http://dx.doi.org/10.3390/ijms232113169.
Texto completoBonetti, Giorgia, Serena Arnaboldi, Sara Grecchi, Giulio Appoloni, Elisabetta Massolo, Sergio Rossi, Rocco Martinazzo, Francesco Orsini, Patrizia R. Mussini y Tiziana Benincori. "Effective Enantiodiscrimination in Electroanalysis Based on a New Inherently Chiral 1,1′-Binaphthyl Selector Directly Synthesizable in Enantiopure Form". Molecules 25, n.º 9 (6 de mayo de 2020): 2175. http://dx.doi.org/10.3390/molecules25092175.
Texto completoFontana, Francesca, Benedetta Bertolotti, Sara Grecchi, Patrizia Romana Mussini, Laura Micheli, Roberto Cirilli, Matteo Tommasini y Simona Rizzo. "2,12-Diaza[6]helicene: An Efficient Non-Conventional Stereogenic Scaffold for Enantioselective Electrochemical Interphases". Chemosensors 9, n.º 8 (10 de agosto de 2021): 216. http://dx.doi.org/10.3390/chemosensors9080216.
Texto completoGospodarowicz, Krzysztof, Małgorzata Hołyńska, Marta Paluch y Jerzy Lisowski. "Novel chiral hexaazamacrocycles for the enantiodiscrimination of carboxylic acids". Tetrahedron 68, n.º 48 (diciembre de 2012): 9930–35. http://dx.doi.org/10.1016/j.tet.2012.09.093.
Texto completoPaladini, A., C. Calcagni, T. Di Palma, M. Speranza, A. Laganà, G. Fago, A. Filippi, M. Satta y A. Giardini Guidoni. "Enantiodiscrimination of chiral α-aminophosphonic acids by mass spectrometry". Chirality 13, n.º 10 (2001): 707–11. http://dx.doi.org/10.1002/chir.10022.
Texto completoRecchimurzo, Alessandra, Federica Balzano, Gloria Uccello Barretta, Luca Gherardi, Milo Malanga y Federica Aiello. "Silylated-Acetylated Cyclodextrins as Chiral Sensors for the Enantiodiscrimination of Fluorinated Anesthetics". Molecules 28, n.º 6 (20 de marzo de 2023): 2804. http://dx.doi.org/10.3390/molecules28062804.
Texto completoPrata, José V., Alexandra I. Costa, Gennaro Pescitelli y Hugo D. Pinto. "Chiroptical and emissive properties of a calix[4]arene-containing chiral poly(p-phenylene ethynylene) with enantioselective recognition ability". Polym. Chem. 5, n.º 19 (2014): 5793–803. http://dx.doi.org/10.1039/c4py00729h.
Texto completoCen, Mengjia, Jiawei Wang, Jianxun Liu, Huilin He, Ke Li, Wenfeng Cai, Tun Cao y Yan Jun Liu. "Ultrathin Suspended Chiral Metasurfaces for Enantiodiscrimination (Adv. Mater. 37/2022)". Advanced Materials 34, n.º 37 (septiembre de 2022): 2270263. http://dx.doi.org/10.1002/adma.202270263.
Texto completoAndreani, Romana, Cecilia Bombelli, Stefano Borocci, Juri Lah, Giovanna Mancini, Paolo Mencarelli, Gorazd Vesnaver y Claudio Villani. "New biphenylic derivatives: synthesis, characterisation and enantiodiscrimination in chiral aggregates". Tetrahedron: Asymmetry 15, n.º 6 (marzo de 2004): 987–94. http://dx.doi.org/10.1016/j.tetasy.2004.01.038.
Texto completoLuo, Zengwei, Baohua Li, Xiantao Fang, Kai Hu, Xiaojun Wu y Enqin Fu. "Novel chiral solvating agents derived from natural amino acid: enantiodiscrimination for chiral α-arylalkylamines". Tetrahedron Letters 48, n.º 10 (marzo de 2007): 1753–56. http://dx.doi.org/10.1016/j.tetlet.2007.01.036.
Texto completoPuglisi, Roberta, Francesco P. Ballistreri, Chiara M. A. Gangemi, Rosa Maria Toscano, Gaetano A. Tomaselli, Andrea Pappalardo y Giuseppe Trusso Sfrazzetto. "Chiral Zn–salen complexes: a new class of fluorescent receptors for enantiodiscrimination of chiral amines". New Journal of Chemistry 41, n.º 3 (2017): 911–15. http://dx.doi.org/10.1039/c6nj03592b.
Texto completoNoreen, Samar, Ameer Fawad Zahoor, Sajjad Ahmad, Irum Shahzadi, Ali Irfan y Sadia Faiz. "Novel Chiral Ligands for Palladium-catalyzed Asymmetric Allylic Alkylation/ Asymmetric Tsuji-Trost Reaction: A Review". Current Organic Chemistry 23, n.º 11 (29 de agosto de 2019): 1168–213. http://dx.doi.org/10.2174/1385272823666190624145039.
Texto completoLankhorst, Peter, Jozef van Rijn y Alexander Duchateau. "One-Dimensional 13C NMR Is a Simple and Highly Quantitative Method for Enantiodiscrimination". Molecules 23, n.º 7 (20 de julio de 2018): 1785. http://dx.doi.org/10.3390/molecules23071785.
Texto completoReddy, U. Venkateswara y N. Suryaprakash. "Scalable weak aligning medium for enantiodiscrimination of water soluble chiral molecules". Chemical Communications 47, n.º 29 (2011): 8364. http://dx.doi.org/10.1039/c1cc12564h.
Texto completoSchefzick, Sabine, Wolfgang Lindner, Kenny B. Lipkowitz y Mehran Jalaie. "Enantiodiscrimination by a quinine-based chiral stationary phase: A computational study". Chirality 12, n.º 1 (2000): 7–15. http://dx.doi.org/10.1002/(sici)1520-636x(2000)12:1<7::aid-chir3>3.0.co;2-q.
Texto completoGrecchi, Sara, Serena Arnaboldi, Marcus Korb, Roberto Cirilli, Silvia Araneo, Vittoria Guglielmi, Giorgio Tomboni et al. "Widening the Scope of “Inherently Chiral” Electrodes: Enantiodiscrimination of Chiral Electroactive Probes with Planar Stereogenicity". ChemElectroChem 7, n.º 16 (13 de julio de 2020): 3429–38. http://dx.doi.org/10.1002/celc.202000657.
Texto completoGrecchi, Sara, Serena Arnaboldi, Marcus Korb, Roberto Cirilli, Silvia Araneo, Vittoria Guglielmi, Giorgio Tomboni et al. "Widening the Scope of “Inherently Chiral” Electrodes: Enantiodiscrimination of Chiral Electroactive Probes with Planar Stereogenicity". ChemElectroChem 7, n.º 16 (29 de julio de 2020): 3382. http://dx.doi.org/10.1002/celc.202000891.
Texto completoTalotta, Carmen, Gerardo Concilio, Paolo Della Sala, Carmine Gaeta, Christoph A. Schalley y Placido Neri. "Study on the Influence of Chirality in the Threading of Calix[6]arene Hosts with Dialkylammonium Axles". Molecules 25, n.º 22 (15 de noviembre de 2020): 5323. http://dx.doi.org/10.3390/molecules25225323.
Texto completoLi, Le, Xiaofei Ma, Yin Xiao y Yong Wang. "Construction and Application of Graphene Oxide-Bovine Serum Albumin Modified Extended Gate Field Effect Transistor Chiral Sensor". Sensors 21, n.º 11 (7 de junio de 2021): 3921. http://dx.doi.org/10.3390/s21113921.
Texto completoMartín-Rodríguez, María, Luis M. Castelló, Carmen Nájera, José M. Sansano, Olatz Larrañaga, Abel de Cózar y Fernando P. Cossío. "Synthetic scope and DFT analysis of the chiral binap–gold(I) complex-catalyzed 1,3-dipolar cycloaddition of azlactones with alkenes". Beilstein Journal of Organic Chemistry 9 (11 de noviembre de 2013): 2422–33. http://dx.doi.org/10.3762/bjoc.9.280.
Texto completoKotora, Martin. "Synthesis of axially chiral bipyridine N,N'-dioxides and enantioselective allylation of aldehydes". Pure and Applied Chemistry 82, n.º 9 (7 de junio de 2010): 1813–26. http://dx.doi.org/10.1351/pac-con-09-10-01.
Texto completoJávor, Bálint, Panna Vezse, Ádám Golcs, Péter Huszthy y Tünde Tóth. "Enantiodiscriminating Lipophilic Liquid Membrane-Based Assay for High-Throughput Nanomolar Enantioenrichment of Chiral Building Blocks". Membranes 13, n.º 1 (11 de enero de 2023): 94. http://dx.doi.org/10.3390/membranes13010094.
Texto completoErol Gunal, Sule, Senel Teke Tuncel y Ilknur Dogan. "Enantiodiscrimination of carboxylic acids using single enantiomer thioureas as chiral solvating agents". Tetrahedron 76, n.º 18 (mayo de 2020): 131141. http://dx.doi.org/10.1016/j.tet.2020.131141.
Texto completoDeger, Wolfgang, Martin Gessner, Claus Guenther, Gabriele Singer y Armin Mosandl. "Stereoisomeric flavor compounds. 18. Enantiodiscrimination of chiral flavor compounds by diastereomeric derivatization". Journal of Agricultural and Food Chemistry 36, n.º 6 (noviembre de 1988): 1260–64. http://dx.doi.org/10.1021/jf00084a033.
Texto completoBarry, Nicolas P. E., Martina Austeri, Jérôme Lacour y Bruno Therrien. "Highly Efficient NMR Enantiodiscrimination of Chiral Octanuclear Metalla-Boxes in Polar Solvent". Organometallics 28, n.º 16 (24 de agosto de 2009): 4894–97. http://dx.doi.org/10.1021/om900461s.
Texto completoYang, Xuemei, Guitao Wang, Cheng Zhong, Xiaojun Wu y Enqin Fu. "Novel NMR chiral solvating agents derived from (1R,2R)-diaminocyclohexane: synthesis and enantiodiscrimination for chiral carboxylic acids". Tetrahedron: Asymmetry 17, n.º 6 (marzo de 2006): 916–21. http://dx.doi.org/10.1016/j.tetasy.2006.03.011.
Texto completoAdhikari, Suraj, Kwang Joon Kim y Wonjae Lee. "Enantiodiscrimination of Chiral Amines as Naphthaldimine Derivatives on Polysaccharide-derived Chiral Stationary Phases by Normal Phase HPLC". Yakhak Hoeji 63, n.º 2 (30 de abril de 2019): 90–94. http://dx.doi.org/10.17480/psk.2019.63.2.90.
Texto completoSzabó, Zoltán-István, Francisc Boda, Béla Fiser, Máté Dobó, Levente Szőcs y Gergő Tóth. "Chiral Separation of Oxazolidinone Analogs by Capillary Electrophoresis Using Anionic Cyclodextrins as Chiral Selectors: Emphasis on Enantiomer Migration Order". Molecules 28, n.º 11 (2 de junio de 2023): 4530. http://dx.doi.org/10.3390/molecules28114530.
Texto completoPeluso, Paola, Alessandro Dessì, Roberto Dallocchio, Barbara Sechi, Carlo Gatti, Bezhan Chankvetadze, Victor Mamane et al. "Enantioseparation of 5,5′-Dibromo-2,2′-dichloro-3-selanyl-4,4′-bipyridines on Polysaccharide-Based Chiral Stationary Phases: Exploring Chalcogen Bonds in Liquid-Phase Chromatography". Molecules 26, n.º 1 (4 de enero de 2021): 221. http://dx.doi.org/10.3390/molecules26010221.
Texto completoAroulanda, Christie y Philippe Lesot. "Molecular enantiodiscrimination by NMR spectroscopy in chiral oriented systems: Concept, tools, and applications". Chirality 34, n.º 2 (22 de diciembre de 2021): 182–244. http://dx.doi.org/10.1002/chir.23386.
Texto completoTanaka, Koichi, Tomoharu Iwashita, Chihiro Sasaki y Hiroki Takahashi. "Ring-expanded chiral rhombamine macrocycles for efficient NMR enantiodiscrimination of carboxylic acid derivatives". Tetrahedron: Asymmetry 25, n.º 8 (abril de 2014): 602–9. http://dx.doi.org/10.1016/j.tetasy.2014.03.009.
Texto completoBerkecz, Róbert, Gábor Németi, Antal Péter y István Ilisz. "Liquid Chromatographic Enantioseparations Utilizing Chiral Stationary Phases Based on Crown Ethers and Cyclofructans". Molecules 26, n.º 15 (31 de julio de 2021): 4648. http://dx.doi.org/10.3390/molecules26154648.
Texto completoHernández-Rodríguez, Marcos y Eusebio Juaristi. "Structurally simple chiral thioureas as chiral solvating agents in the enantiodiscrimination of α-hydroxy and α-amino carboxylic acids". Tetrahedron 63, n.º 32 (agosto de 2007): 7673–78. http://dx.doi.org/10.1016/j.tet.2007.05.021.
Texto completoChaudhari, Sachin Rama y N. Suryaprakash. "Three-Component Chiral Derivatizing Protocols for NMR Spectroscopic Enantiodiscrimination of Hydroxy Acids and Primary Amines". Journal of Organic Chemistry 77, n.º 1 (21 de diciembre de 2011): 648–51. http://dx.doi.org/10.1021/jo202334d.
Texto completoPeña, Carmen, Javier González-Sabín, Ignacio Alfonso, Francisca Rebolledo y Vicente Gotor. "Cycloalkane-1,2-diamine derivatives as chiral solvating agents. Study of the structural variables controlling the NMR enantiodiscrimination of chiral carboxylic acids". Tetrahedron 64, n.º 33 (agosto de 2008): 7709–17. http://dx.doi.org/10.1016/j.tet.2008.06.031.
Texto completoRivard, Michaël, Frédéric Guillen, Jean-Claude Fiaud, Christie Aroulanda y Philippe Lesot. "Efficient enantiodiscrimination of chiral monophosphine oxides and boranes by phosphorus coupled 13C NMR spectroscopy in the presence of chiral ordering agents". Tetrahedron: Asymmetry 14, n.º 9 (mayo de 2003): 1141–52. http://dx.doi.org/10.1016/s0957-4166(03)00202-7.
Texto completoFejős, Ida, Eszter Kalydi, Edit Luca Kukk, Mimimorena Seggio, Milo Malanga y Szabolcs Béni. "Single Isomer N-Heterocyclic Cyclodextrin Derivatives as Chiral Selectors in Capillary Electrophoresis". Molecules 26, n.º 17 (30 de agosto de 2021): 5271. http://dx.doi.org/10.3390/molecules26175271.
Texto completoArnaboldi, Serena, Andrea Mezzetta, Sara Grecchi, Mariangela Longhi, Elisa Emanuele, Simona Rizzo, Fabiana Arduini, Laura Micheli, Lorenzo Guazzelli y Patrizia Romana Mussini. "Natural-based chiral task-specific deep eutectic solvents: A novel, effective tool for enantiodiscrimination in electroanalysis". Electrochimica Acta 380 (junio de 2021): 138189. http://dx.doi.org/10.1016/j.electacta.2021.138189.
Texto completoJain, Nilesh, Aditya N. Khanvilkar, Sibaprasad Sahoo y Ashutosh V. Bedekar. "Modification of Kagan's amide for improved activity as Chiral Solvating Agent in enantiodiscrimination during NMR analysis". Tetrahedron 74, n.º 1 (enero de 2018): 68–76. http://dx.doi.org/10.1016/j.tet.2017.11.036.
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