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For: Zhang C, Yan K, Fu C, Peng H, Hawker CJ, Whittaker AK. Biological Utility of Fluorinated Compounds: from Materials Design to Molecular Imaging, Therapeutics and Environmental Remediation. Chem Rev 2021. [PMID: 34609131 DOI: 10.1021/acs.chemrev.1c00632] [Cited by in Crossref: 33] [Cited by in F6Publishing: 38] [Article Influence: 33.0] [Reference Citation Analysis]
Number Citing Articles
1 Li D, Tu S, Le Y, Zhou Y, Yang L, Ding Y, Huang L, Liu L. Development of carbazole-based fluorescent probe for highly sensitive application in fluoride ion detection. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 2023;285:121816. [DOI: 10.1016/j.saa.2022.121816] [Reference Citation Analysis]
2 Qiao B, Song X, Zhang W, Xu M, Zhuang B, Li W, Guo H, Wu W, Huang G, Zhang M, Xie X, Zhang N, Luan Y, Zhang C. Intensity-adjustable pain management with prolonged duration based on phase-transitional nanoparticles-assisted ultrasound imaging-guided nerve blockade. J Nanobiotechnology 2022;20:498. [PMID: 36424657 DOI: 10.1186/s12951-022-01707-z] [Reference Citation Analysis]
3 Ma Z, Wu X, Zhu C. Merging Fluorine Incorporation and Functional Group Migration. The Chemical Record 2022. [DOI: 10.1002/tcr.202200221] [Reference Citation Analysis]
4 Xie R, Zhang P, Cai L, Guo R, Wang L, Qiu X, Tian Y. Tumor-specific cyclic amplification of oxidative stress by disulfide-loaded fluoropolymer nanogels. European Journal of Pharmaceutics and Biopharmaceutics 2022;180:212-223. [DOI: 10.1016/j.ejpb.2022.10.010] [Reference Citation Analysis]
5 Li D, Tu S, Le Y, Zhou Y, Yang L, Ding Y, Huang L, Liu L. Development of a carbazole-based fluorescent probe for quantitative detection of fluoride ions in aqueous systems. Chem Pap 2022. [DOI: 10.1007/s11696-022-02557-7] [Reference Citation Analysis]
6 Panakkal VM, Havlicek D, Pavlova E, Filipová M, Bener S, Jirak D, Sedlacek O. Synthesis of 19F MRI Nanotracers by Dispersion Polymerization-Induced Self-Assembly of N-(2,2,2-Trifluoroethyl)acrylamide in Water. Biomacromolecules 2022. [PMID: 36251480 DOI: 10.1021/acs.biomac.2c00981] [Reference Citation Analysis]
7 Pawar AP, Yadav J, Dolas AJ, Nagare YK, Iype E, Rangan K, Kumar I. Enantioselective Direct Synthesis of C3-Hydroxyalkylated Pyrrole via an Amine-Catalyzed Aldol/Paal-Knorr Reaction Sequence. Org Lett 2022. [PMID: 36219141 DOI: 10.1021/acs.orglett.2c02922] [Reference Citation Analysis]
8 Zhang H, Song Y, Gong Z, Zheng L, Tang G, Wang Y. Drug Ambroxol-based luminescent materials with sulfonate group: Synthesis, crystal structure and Hirshfeld surface analysis. Journal of Solid State Chemistry 2022;314:123387. [DOI: 10.1016/j.jssc.2022.123387] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
9 Brondi C, Mosciatti T, Di Maio E. Ostwald Ripening Modulation by Organofluorine Additives in Rigid Polyurethane Foams. Ind Eng Chem Res 2022. [DOI: 10.1021/acs.iecr.2c01829] [Reference Citation Analysis]
10 Rosa M, Jędryka N, Skorupska S, Grabowska-jadach I, Malinowski M. New Route to Glycosylated Porphyrins via Aromatic Nucleophilic Substitution (SNAr)—Synthesis and Cellular Uptake Studies. IJMS 2022;23:11321. [DOI: 10.3390/ijms231911321] [Reference Citation Analysis]
11 Zhou L, Emenuga M, Kumar S, Lamantia Z, Figueiredo M, Emrick T. Designing Synthetic Polymers for Nucleic Acid Complexation and Delivery: From Polyplexes to Micelleplexes to Triggered Degradation. Biomacromolecules 2022. [PMID: 36125365 DOI: 10.1021/acs.biomac.2c00767] [Reference Citation Analysis]
12 Xu P, Daniliuc CG, Bergander K, Stein C, Studer A. Synthesis of Five-Membered Ring Systems Bearing gem -Difluoroalkenyl and Monofluoroalkenyl Substituents via Radical β-Bromo Fragmentation. ACS Catal . [DOI: 10.1021/acscatal.2c03775] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Wang Y, Tan X, Usman A, Zhang Y, Sawczyk M, Král P, Zhang C, Whittaker AK. Elucidating the Impact of Hydrophilic Segments on 19 F MRI Sensitivity of Fluorinated Block Copolymers. ACS Macro Lett . [DOI: 10.1021/acsmacrolett.2c00414] [Reference Citation Analysis]
14 Pietsch M, Casado N, Mecerreyes D, Hernandez-sosa G. Inkjet-Printed Dual-Mode Electrochromic and Electroluminescent Displays Incorporating Ecofriendly Materials. ACS Appl Mater Interfaces. [DOI: 10.1021/acsami.2c12799] [Reference Citation Analysis]
15 de Zordo‐banliat A, Grollier K, Vigier J, Jeanneau E, Dagousset G, Pegot B, Magnier E, Billard T. Vinylic Trifluoromethylselenolation via Pd‐Catalyzed C−H Activation. Chemistry A European J 2022. [DOI: 10.1002/chem.202202299] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
16 Nakano T, Fujikawa S. Aryl/Heteroaryl Substituted Boron-Difluoride Complexes Bearing 2-(Isoquinol-1-yl)pyrrole Ligands Exhibiting High Luminescence Efficiency with a Large Stokes Shift. J Org Chem 2022. [PMID: 35969831 DOI: 10.1021/acs.joc.2c01343] [Reference Citation Analysis]
17 Hu M, Tan BB, Ge S. Enantioselective Cobalt-Catalyzed Hydroboration of Fluoroalkyl-Substituted Alkenes to Access Chiral Fluoroalkylboronates. J Am Chem Soc 2022. [PMID: 35953077 DOI: 10.1021/jacs.2c06488] [Reference Citation Analysis]
18 Zhou XY, Zhang M, Liu Z, He JH, Wang XC. C3-Selective Trifluoromethylthiolation and Difluoromethylthiolation of Pyridines and Pyridine Drugs via Dihydropyridine Intermediates. J Am Chem Soc 2022. [PMID: 35913823 DOI: 10.1021/jacs.2c06776] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
19 Bonnefoy C, Chefdeville E, Tourvieille C, Panossian A, Hanquet G, Leroux F, Toulgoat F, Billard T. Study of Carbamoyl Fluoride: Synthesis, Properties and Applications. Chemistry 2022;28:e202201589. [PMID: 35639343 DOI: 10.1002/chem.202201589] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Yu ZL, Chen JW, Chen YL, Zheng RJ, Ma M, Chen JP, Shen ZL, Chu XQ. DMSO-Promoted Difluoroalkylation of Organophosphonium Salts with Difluoroenol Silyl Ethers. Org Lett 2022. [PMID: 35867631 DOI: 10.1021/acs.orglett.2c02088] [Reference Citation Analysis]
21 Wang X, Zhang C, Sawczyk M, Sun J, Yuan Q, Chen F, Mendes TC, Howlett PC, Fu C, Wang Y, Tan X, Searles DJ, Král P, Hawker CJ, Whittaker AK, Forsyth M. Ultra-stable all-solid-state sodium metal batteries enabled by perfluoropolyether-based electrolytes. Nat Mater 2022. [PMID: 35788569 DOI: 10.1038/s41563-022-01296-0] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
22 Zhang Y, Zhu J, Shen Q. Bromodifluoromethyl Sulfonium Ylide: An Easily Available Electrophilic Bromodifluoromethylating Reagent for Bromodifluoromethylation of Styrenes and Heteroarenes by Visible-Light-Promoted Photoredox. Journal of Fluorine Chemistry 2022. [DOI: 10.1016/j.jfluchem.2022.110021] [Reference Citation Analysis]
23 Wang T, Zhang X, Xu Y, Xu Y, Zhang Y, Zhang K. Emerging nanobiotechnology-encoded relaxation tuning establishes new MRI modes to localize, monitor and predict diseases. J Mater Chem B 2022. [PMID: 35770674 DOI: 10.1039/d2tb00600f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Li L, Li A, Lin Y, Chen D, Kang B, Lin H, Gao J. An Activatable 19 F MRI Molecular Probe for Sensing and Imaging of Norepinephrine. ChemistryOpen 2022;:e202200110. [PMID: 35762743 DOI: 10.1002/open.202200110] [Reference Citation Analysis]
25 Zhang C. Fluorine in Medicinal Chemistry: In Perspective to COVID-19. ACS Omega 2022;7:18206-12. [PMID: 35663284 DOI: 10.1021/acsomega.2c01121] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
26 Yan K, Mu C, Zhang C, Xu Q, Xu Z, Wang D, Jing X, Meng L. Pt nanoenzyme decorated yolk-shell nanoplatform as an oxygen generator for enhanced multi-modality imaging-guided phototherapy. Journal of Colloid and Interface Science 2022;616:759-68. [DOI: 10.1016/j.jcis.2022.02.042] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
27 Gaines LGT. Historical and current usage of per- and polyfluoroalkyl substances (PFAS): A literature review. Am J Ind Med 2022. [PMID: 35614869 DOI: 10.1002/ajim.23362] [Reference Citation Analysis]
28 Xu C, Wang S, Shen Q. Recent Progress on Trifluoromethylthiolation of (Hetero)Aryl C–H Bonds with Electrophilic Trifluoromethylthiolating Reagents. ACS Sustainable Chem Eng 2022;10:6889-99. [DOI: 10.1021/acssuschemeng.2c01006] [Reference Citation Analysis]
29 Zhang Q, Yuan W, Shi Y, Pan F. Organophotocatalytic ring opening/remote trifluoromethylselenolation of cycloalkanols. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153787] [Reference Citation Analysis]
30 Lv J, Wang H, Rong G, Cheng Y. Fluorination Promotes the Cytosolic Delivery of Genes, Proteins, and Peptides. Acc Chem Res 2022;55:722-33. [PMID: 35175741 DOI: 10.1021/acs.accounts.1c00766] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 12.0] [Reference Citation Analysis]
31 Tan X, Sawczyk M, Chang Y, Wang Y, Usman A, Fu C, Král P, Peng H, Zhang C, Whittaker AK. Revealing the Molecular-Level Interactions between Cationic Fluorinated Polymer Sorbents and the Major PFAS Pollutant PFOA. Macromolecules. [DOI: 10.1021/acs.macromol.1c02435] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Fang Z, Zhang Y, Wang H, Zanoni G, Li J, Li X, Liu Z, Ning Y. Straightforward access to fluoroalkyl tetrazoles from fluoroalkyl N -sulfonylhydrazones. Org Chem Front . [DOI: 10.1039/d2qo00962e] [Reference Citation Analysis]
33 Feng J, Jia X, Zhang S, Lu K, Cahard D. State of knowledge in photoredox-catalysed direct difluoromethylation. Org Chem Front 2022;9:3598-623. [DOI: 10.1039/d2qo00551d] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
34 Lin C, Chen L, Lin H, Li Y, Shen C, Zhang M. Direct access to α,α-chlorofluoro arylketones via mild electrophilic heterohalogenation of arylalkynes. Org Chem Front 2022;9:2944-8. [DOI: 10.1039/d2qo00074a] [Cited by in F6Publishing: 3] [Reference Citation Analysis]