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