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For: Calcaterra A, D’acquarica I. The market of chiral drugs: Chiral switches versus de novo enantiomerically pure compounds. Journal of Pharmaceutical and Biomedical Analysis 2018;147:323-40. [DOI: 10.1016/j.jpba.2017.07.008] [Cited by in Crossref: 148] [Cited by in F6Publishing: 103] [Article Influence: 37.0] [Reference Citation Analysis]
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7 Agarkov AS, Litvinov IA, Gabitova ER, Ovsyannikov AS, Dorovatovskii PV, Shiryaev AK, Solovieva SE, Antipin IS. Crystalline State Hydrogen Bonding of 2-(2-Hydroxybenzylidene)Thiazolo[3,2-a]Pyrimidines: A Way to Non-Centrosymmetric Crystals. Crystals 2022;12:494. [DOI: 10.3390/cryst12040494] [Reference Citation Analysis]
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9 Zeng L, Liu Q, Yi Q, Tang K, Van der Bruggen B. Novel Chiral Drug Recovery and Enantioseparation Method: Hollow Fiber Membrane Extraction and In Situ Coupling of Back-Extraction with Crystallization. Ind Eng Chem Res 2020;59:13735-43. [DOI: 10.1021/acs.iecr.0c02123] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
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11 Casciaro B, Calcaterra A, Cappiello F, Mori M, Loffredo MR, Ghirga F, Mangoni ML, Botta B, Quaglio D. Nigritanine as a New Potential Antimicrobial Alkaloid for the Treatment of Staphylococcus aureus-Induced Infections. Toxins (Basel) 2019;11:E511. [PMID: 31480508 DOI: 10.3390/toxins11090511] [Cited by in Crossref: 20] [Cited by in F6Publishing: 18] [Article Influence: 6.7] [Reference Citation Analysis]
12 Vaňkátová P, Kubíčková A, Kalíková K. Enantioseparation of liquid crystals and their utilization as enantiodiscrimination materials. Journal of Chromatography A 2022. [DOI: 10.1016/j.chroma.2022.463074] [Reference Citation Analysis]
13 Nie L, Yohannes A, Yao S. Recent advances in the enantioseparation promoted by ionic liquids and their resolution mechanisms. J Chromatogr A 2020;1626:461384. [PMID: 32797857 DOI: 10.1016/j.chroma.2020.461384] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 3.5] [Reference Citation Analysis]
14 Coelho MM, Fernandes C, Remião F, Tiritan ME. Enantioselectivity in Drug Pharmacokinetics and Toxicity: Pharmacological Relevance and Analytical Methods. Molecules 2021;26:3113. [PMID: 34070985 DOI: 10.3390/molecules26113113] [Reference Citation Analysis]
15 Alkhayer G, Khudr H, Koudsi Y. Spectroscopic and chromatographic investigation of chiral interactions between tiaprofenic acid and alginate–metal-complexes. RSC Adv 2020;10:35121-30. [DOI: 10.1039/d0ra07665a] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
16 Otmar M, Gaálová J, Žitka J, Brožová L, Cuřínová P, Kohout M, Hovorka Š, Bara JE, Van der Bruggen B, Jirsák J, Izák P. Preparation of PSEBS membranes bearing (S)-(−)-methylbenzylamine as chiral selector. European Polymer Journal 2020;122:109381. [DOI: 10.1016/j.eurpolymj.2019.109381] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 4.5] [Reference Citation Analysis]
17 Guo Y, Wu L, Gou K, Wang Y, Hu B, Pang Y, Li S, Li H. Functional mesoporous silica nanoparticles for delivering nimesulide with chiral recognition performance. Microporous and Mesoporous Materials 2020;294:109862. [DOI: 10.1016/j.micromeso.2019.109862] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
18 Li M, Liu M, Sha Y. Induced and Inversed Circularly Polarized Luminescence of Achiral Thioflavin T Assembled on Peptide Fibril. Small 2021;:e2106130. [PMID: 34881501 DOI: 10.1002/smll.202106130] [Reference Citation Analysis]
19 Pinto MMM, Fernandes C, Tiritan ME. Chiral Separations in Preparative Scale: A Medicinal Chemistry Point of View. Molecules 2020;25:E1931. [PMID: 32326326 DOI: 10.3390/molecules25081931] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
20 Alothman ZA, Alanazi AG, Suhail M, Ali I. HPLC enantio-separation and chiral recognition mechanism of quinolones on vancomycin CSP. Journal of Chromatography B 2020;1157:122335. [DOI: 10.1016/j.jchromb.2020.122335] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
21 Abram M, Jakubiec M, Kamiński K. Chirality as an Important Factor for the Development of New Antiepileptic Drugs. ChemMedChem 2019;14:1744-61. [PMID: 31476107 DOI: 10.1002/cmdc.201900367] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 3.0] [Reference Citation Analysis]
22 Hellinghausen G, Readel ER, Wahab MF, Lee JT, Lopez DA, Weatherly CA, Armstrong DW. Mass Spectrometry-Compatible Enantiomeric Separations of 100 Pesticides Using Core–Shell Chiral Stationary Phases and Evaluation of Iterative Curve Fitting Models for Overlapping Peaks. Chromatographia 2019;82:221-33. [DOI: 10.1007/s10337-018-3604-3] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
23 Yao W, Bazan‐bergamino EA, Ngai M. Asymmetric Photocatalysis Enabled by Chiral Organocatalysts. ChemCatChem 2022;14. [DOI: 10.1002/cctc.202101292] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
24 Carreira AR, Ferreira AM, Almeida MR, Coutinho JA, Sintra TE. Propranolol resolution using enantioselective biphasic systems. Separation and Purification Technology 2021;254:117682. [DOI: 10.1016/j.seppur.2020.117682] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
25 Carneiro T, Bhandari S, Temmel E, Lorenz H, Seidel-Morgenstern A. Shortcut Model for Describing Isothermal Batch Preferential Crystallization of Conglomerates and Estimating the Productivity. Cryst Growth Des 2019;19:5189-203. [PMID: 32952449 DOI: 10.1021/acs.cgd.9b00592] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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27 Hu M, Yuan YX, Wang W, Li DM, Zhang HC, Wu BX, Liu M, Zheng YS. Chiral recognition and enantiomer excess determination based on emission wavelength change of AIEgen rotor. Nat Commun 2020;11:161. [PMID: 31919426 DOI: 10.1038/s41467-019-13955-z] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 5.5] [Reference Citation Analysis]
28 Mo X, Cheng Q, Zhang P, Tang K, Huang Y, Xu W. Preparative enantioseparation of 2-(4-hydroxyphenyl)propionic acid by high speed counter-current chromatography with hydroxyethyl-β-cyclodextrin as chiral selector. Separation Science and Technology 2018;53:2981-9. [DOI: 10.1080/01496395.2018.1488868] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
29 Estrada-Valenzuela D, Ramos-Sánchez VH, Zaragoza-Galán G, Espinoza-Hicks JC, Bugarin A, Chávez-Flores D. Lipase Assisted (S)-Ketoprofen Resolution from Commercially Available Racemic Mixture. Pharmaceuticals (Basel) 2021;14:996. [PMID: 34681221 DOI: 10.3390/ph14100996] [Reference Citation Analysis]
30 Xu W, Li X, Wang L, Li S, Chu S, Wang J, Li Y, Hou J, Luo Q, Liu J. Design of Cyclodextrin-Based Functional Systems for Biomedical Applications. Front Chem 2021;9:635507. [PMID: 33681149 DOI: 10.3389/fchem.2021.635507] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
31 Sargolzaei M. Effect of nelfinavir stereoisomers on coronavirus main protease: Molecular docking, molecular dynamics simulation and MM/GBSA study. J Mol Graph Model 2021;103:107803. [PMID: 33333424 DOI: 10.1016/j.jmgm.2020.107803] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
32 Dehghani Z, Akhond M, Absalan G. Carbon quantum dots embedded silica molecular imprinted polymer as a novel and sensitive fluorescent nanoprobe for reproducible enantioselective quantification of naproxen enantiomers. Microchemical Journal 2021;160:105723. [DOI: 10.1016/j.microc.2020.105723] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
33 Newgas SA, Jeffries JWE, Moody TS, Ward JM, Hailes HC. Discovery of New Carbonyl Reductases Using Functional Metagenomics and Applications in Biocatalysis. Adv Synth Catal 2021;363:3044-52. [PMID: 34413714 DOI: 10.1002/adsc.202100199] [Reference Citation Analysis]
34 Xu P, Liu Y, Wang L, Wu Y, Zhou X, Xiao J, Zheng J, Xue M. Phencynonate S-isomer as a eutomer is a novel central anticholinergic drug for anti-motion sickness. Sci Rep 2019;9:2000. [PMID: 30760797 DOI: 10.1038/s41598-018-38305-9] [Reference Citation Analysis]
35 Verma NK, Kumar S, Prasad G, Bhattacharyya MS. Biocatalytic deracemization of racemic naphthyl alcohols by using a novel yeast isolate Rhodotorula kratochvilovae (MTCC 13029). Sustainable Chemistry and Pharmacy 2022;26:100609. [DOI: 10.1016/j.scp.2022.100609] [Reference Citation Analysis]
36 N L Batista A, M Dos Santos F, Batista JM, Cass QB. Enantiomeric Mixtures in Natural Product Chemistry: Separation and Absolute Configuration Assignment. Molecules 2018;23:E492. [PMID: 29473869 DOI: 10.3390/molecules23020492] [Cited by in Crossref: 24] [Cited by in F6Publishing: 15] [Article Influence: 6.0] [Reference Citation Analysis]
37 Khatiashvili T, Kakava R, Matarashvili I, Tabani H, Fanali C, Volonterio A, Farkas T, Chankvetadze B. Separation of enantiomers of selected chiral sulfoxides with cellulose tris(4-chloro-3-methylphenylcarbamate)-based chiral columns in high-performance liquid chromatography with very high separation factor. Journal of Chromatography A 2018;1545:59-66. [DOI: 10.1016/j.chroma.2018.02.054] [Cited by in Crossref: 22] [Cited by in F6Publishing: 19] [Article Influence: 5.5] [Reference Citation Analysis]
38 Zhai L, Yang S, Lai Y, Meng D, Tian Q, Guan Z, Cai Y, Liao X. Mining of aminotransferase gene ota3 from Bacillus pumilus W3 via genome analysis, gene cloning and expressing for compound bioamination. Gene 2019;686:21-8. [PMID: 30408548 DOI: 10.1016/j.gene.2018.10.082] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.3] [Reference Citation Analysis]
39 Suzuki N, Kinoshita M, Miyabe K. Kinetic Study of Chiral Intermolecular Interactions by Moment Analysis Based on Affinity Capillary Electrophoresis. Anal Chem 2018;90:11048-53. [DOI: 10.1021/acs.analchem.8b02823] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
40 Facchetti G, Christodoulou MS, Mendoza LB, Cusinato F, Dalla Via L, Rimoldi I. Biological Properties of New Chiral 2-Methyl-5,6,7,8-tetrahydroquinolin-8-amine-based Compounds. Molecules 2020;25:E5561. [PMID: 33260896 DOI: 10.3390/molecules25235561] [Reference Citation Analysis]
41 Dybtsev DN, Bryliakov KP. Asymmetric catalysis using metal-organic frameworks. Coordination Chemistry Reviews 2021;437:213845. [DOI: 10.1016/j.ccr.2021.213845] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
42 Zhao B, Yang S, Deng J, Pan K. Chiral Graphene Hybrid Materials: Structures, Properties, and Chiral Applications. Adv Sci (Weinh) 2021;8:2003681. [PMID: 33854894 DOI: 10.1002/advs.202003681] [Cited by in Crossref: 19] [Cited by in F6Publishing: 13] [Article Influence: 19.0] [Reference Citation Analysis]
43 Großkopf J, Plaza M, Seitz A, Breitenlechner S, Storch G, Bach T. Photochemical Deracemization at sp3-Hybridized Carbon Centers via a Reversible Hydrogen Atom Transfer. J Am Chem Soc 2021;143:21241-5. [PMID: 34902253 DOI: 10.1021/jacs.1c11266] [Reference Citation Analysis]
44 Scriba GK. Chiral recognition in separation sciences. Part II: Macrocyclic glycopeptide, donor-acceptor, ion-exchange, ligand-exchange and micellar selectors. TrAC Trends in Analytical Chemistry 2019;119:115628. [DOI: 10.1016/j.trac.2019.115628] [Cited by in Crossref: 27] [Cited by in F6Publishing: 19] [Article Influence: 9.0] [Reference Citation Analysis]
45 Corso CR, Acco A, Bach C, Bonatto SJR, de Figueiredo BC, de Souza LM. Pharmacological profile and effects of mitotane in adrenocortical carcinoma. Br J Clin Pharmacol 2021;87:2698-710. [PMID: 33382119 DOI: 10.1111/bcp.14721] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
46 Tok KC, Gumustas M, Jibuti G, Suzen HS, Ozkan SA, Chankvetadze B. The Effect of Enantiomer Elution Order on the Determination of Minor Enantiomeric Impurity in Ketoprofen and Enantiomeric Purity Evaluation of Commercially Available Dexketoprofen Formulations. Molecules 2020;25:E5865. [PMID: 33322449 DOI: 10.3390/molecules25245865] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
47 Lopes DT, Hoye TR, Alvarenga ES. Characterization of stereoisomeric 5-(2-nitro-1-phenylethyl)furan-2(5H)-ones by computation of 1 H and 13 C NMR chemical shifts and electronic circular dichroism spectra. Magn Reson Chem 2021;59:43-51. [PMID: 32621355 DOI: 10.1002/mrc.5073] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
48 Zhao Y, Zhu X, Jiang W, Liu H, Sun B. Chiral Recognition for Chromatography and Membrane-Based Separations: Recent Developments and Future Prospects. Molecules 2021;26:1145. [PMID: 33669919 DOI: 10.3390/molecules26041145] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
49 Rehman GU, Vetter T, Martin PA. Design, Development, and Analysis of an Automated Sampling Loop for Online Monitoring of Chiral Crystallization. Org Process Res Dev . [DOI: 10.1021/acs.oprd.1c00320] [Reference Citation Analysis]
50 Bolognino I, Carrieri A, Purgatorio R, Catto M, Caliandro R, Carrozzini B, Belviso BD, Majellaro M, Sotelo E, Cellamare S, Altomare CD. Enantiomeric Separation and Molecular Modelling of Bioactive 4-Aryl-3,4-dihydropyrimidin-2(1H)-one Ester Derivatives on Teicoplanin-Based Chiral Stationary Phase. Separations 2022;9:7. [DOI: 10.3390/separations9010007] [Reference Citation Analysis]
51 Zhang H, Zhao H, Wen J, Zhang Z, Stavropoulos P, Li Y, Ai L, Zhang J. Discrimination of enantiomers of amides with two stereogenic centers enabled by chiral bisthiourea derivatives using 1H NMR spectroscopy. Org Biomol Chem 2021;19:6697-706. [PMID: 34296731 DOI: 10.1039/d1ob00742d] [Reference Citation Analysis]
52 Papp LA, Hancu G, Kelemen H, Tóth G. Chiral separation in the class of proton pump inhibitors by chromatographic and electromigration techniques: An overview. Electrophoresis 2021. [PMID: 34004039 DOI: 10.1002/elps.202100032] [Reference Citation Analysis]
53 Saleh B, Ding T, Wang Y, Zheng X, Liu R, He L. Analytical Separation of Closantel Enantiomers by HPLC. Molecules 2021;26:7288. [PMID: 34885866 DOI: 10.3390/molecules26237288] [Reference Citation Analysis]
54 Knežević A, Novak J, Vinković V. New Brush-Type Chiral Stationary Phases for Enantioseparation of Pharmaceutical Drugs. Molecules 2019;24:E823. [PMID: 30823585 DOI: 10.3390/molecules24040823] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
55 Dobó M, Foroughbakhshfasaei M, Horváth P, Szabó ZI, Tóth G. Chiral separation of oxazolidinone analogues by liquid chromatography on polysaccharide stationary phases using polar organic mode. J Chromatogr A 2021;1662:462741. [PMID: 34929572 DOI: 10.1016/j.chroma.2021.462741] [Reference Citation Analysis]
56 Ariga K, Mori T, Kitao T, Uemura T. Supramolecular Chiral Nanoarchitectonics. Adv Mater 2020;32:e1905657. [PMID: 32191374 DOI: 10.1002/adma.201905657] [Cited by in Crossref: 76] [Cited by in F6Publishing: 62] [Article Influence: 38.0] [Reference Citation Analysis]
57 Wang L, Lv W, Han S, Yu Q, Pei D, Xu J, Wang M, Gao G, Lv M. Preparation and chiral resolution properties of bridged bis(cyclodextrin)s hybrid spheres for high performance liquid chromatography. J Sep Sci 2021. [PMID: 34931462 DOI: 10.1002/jssc.202100629] [Reference Citation Analysis]
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59 Shi Y, Zheng C, Li J, Yang L, Wang Z, Wang R. Separation and Quantification of Four Main Chiral Glucosinolates in Radix Isatidis and Its Granules Using High-Performance Liquid Chromatography/Diode Array Detector Coupled with Circular Dichroism Detection. Molecules 2018;23:E1305. [PMID: 29844266 DOI: 10.3390/molecules23061305] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
60 Tuwahatu CA, Yeung CC, Lam YW, Roy VAL. The molecularly imprinted polymer essentials: curation of anticancer, ophthalmic, and projected gene therapy drug delivery systems. J Control Release 2018;287:24-34. [PMID: 30110614 DOI: 10.1016/j.jconrel.2018.08.023] [Cited by in Crossref: 34] [Cited by in F6Publishing: 21] [Article Influence: 8.5] [Reference Citation Analysis]
61 Silvestri IP, Colbon PJJ. The Growing Importance of Chirality in 3D Chemical Space Exploration and Modern Drug Discovery Approaches for Hit-ID: Topical Innovations. ACS Med Chem Lett 2021;12:1220-9. [PMID: 34413951 DOI: 10.1021/acsmedchemlett.1c00251] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
62 Declerck S, Vander Heyden Y, Mangelings D. Rendering A Chiral Screening Step In Supercritical Fluid Chromatography Mass-Spectrometry Compatible. Journal of Chromatography A 2020;1624:461201. [DOI: 10.1016/j.chroma.2020.461201] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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65 Liu C, Huang Y, Hu F, E Y, Dong X, Yang Y, Jin Y, Xu X. Giant Asymmetric Transmission and Circular Dichroism with Angular Tunability in Chiral Terahertz Metamaterials. ANNALEN DER PHYSIK 2020;532:1900398. [DOI: 10.1002/andp.201900398] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
66 Krasowska D, Karpowicz R, Drabowicz J. Chiral Polythiophenes: Part I: Syntheses of Monomeric Precursors. Molecules 2021;26:4205. [PMID: 34299480 DOI: 10.3390/molecules26144205] [Reference Citation Analysis]
67 Rosetti A, Ferretti R, Zanitti L, Casulli A, Villani C, Cirilli R. Single-run reversed-phase HPLC method for determining sertraline content, enantiomeric purity, and related substances in drug substance and finished product. J Pharm Anal 2020;10:610-6. [PMID: 33425455 DOI: 10.1016/j.jpha.2020.11.002] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
68 Yamashika K, Morishitabara S, Yamada S, Kubota T, Konno T. An asymmetric tertiary carbon center with a tetrafluoroethylene (–CF 2 CF 2 –) fragment: Novel construction method and application in a chiral liquid crystalline molecule. Journal of Fluorine Chemistry 2018;207:24-37. [DOI: 10.1016/j.jfluchem.2017.12.013] [Cited by in Crossref: 8] [Article Influence: 2.0] [Reference Citation Analysis]
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