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For: Miller MA, Sletten EM. A General Approach to Biocompatible Branched Fluorous Tags for Increased Solubility in Perfluorocarbon Solvents. Org Lett 2018;20:6850-4. [PMID: 30354161 DOI: 10.1021/acs.orglett.8b02976] [Cited by in Crossref: 11] [Cited by in F6Publishing: 15] [Article Influence: 2.8] [Reference Citation Analysis]
Number Citing Articles
1 Fallot LB, Suresh RR, Fisher CL, Salmaso V, O’connor RD, Kaufman N, Gao Z, Auchampach JA, Jacobson KA. Structure–Activity Studies of 1H-Imidazo[4,5-c]quinolin-4-amine Derivatives as A3 Adenosine Receptor Positive Allosteric Modulators. J Med Chem 2022. [DOI: 10.1021/acs.jmedchem.2c01170] [Reference Citation Analysis]
2 Alemayehu AB, Ghosh A. Phenol- and resorcinol-appended metallocorroles and their derivatization with fluorous tags. Sci Rep 2022;12:19256. [DOI: 10.1038/s41598-022-23889-0] [Reference Citation Analysis]
3 Williams BA, Siedle AR, Jarrold CC. Identification of Stable Perfluorocarbons Formed by Hyperthermal Decomposition of Graphite Fluoride Using Anion Photoelectron Spectroscopy. J Phys Chem C. [DOI: 10.1021/acs.jpcc.2c02180] [Reference Citation Analysis]
4 Yoshinaga K, Swager TM. Revisiting the Heck Reaction for Fluorous Materials Applications. Synlett 2021;32:1725-9. [DOI: 10.1055/s-0040-1719827] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Day RA, Sletten EM. Perfluorocarbon nanomaterials for photodynamic therapy. Curr Opin Colloid Interface Sci 2021;54:101454. [PMID: 34504391 DOI: 10.1016/j.cocis.2021.101454] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 7.0] [Reference Citation Analysis]
6 Aggarwal A, Bhupathiraju NVSDK, Farley C, Singh S. Applications of Fluorous Porphyrinoids: An Update. Photochem Photobiol 2021. [PMID: 34343350 DOI: 10.1111/php.13499] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Estabrook DA, Day RA, Sletten EM. Redox-Responsive Gene Delivery from Perfluorocarbon Nanoemulsions through Cleavable Poly(2-oxazoline) Surfactants. Angew Chem Int Ed Engl 2021;60:17362-7. [PMID: 33930255 DOI: 10.1002/anie.202102413] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Estabrook DA, Day RA, Sletten EM. Redox‐Responsive Gene Delivery from Perfluorocarbon Nanoemulsions through Cleavable Poly(2‐oxazoline) Surfactants. Angew Chem 2021;133:17502-7. [DOI: 10.1002/ange.202102413] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Lim I, Vian A, van de Wouw HL, Day RA, Gomez C, Liu Y, Rheingold AL, Campàs O, Sletten EM. Fluorous Soluble Cyanine Dyes for Visualizing Perfluorocarbons in Living Systems. J Am Chem Soc 2020;142:16072-81. [PMID: 32808518 DOI: 10.1021/jacs.0c07761] [Cited by in Crossref: 22] [Cited by in F6Publishing: 23] [Article Influence: 11.0] [Reference Citation Analysis]
10 Day RA, Estabrook DA, Wu C, Chapman JO, Togle AJ, Sletten EM. Systematic Study of Perfluorocarbon Nanoemulsions Stabilized by Polymer Amphiphiles. ACS Appl Mater Interfaces 2020;12:38887-98. [PMID: 32706233 DOI: 10.1021/acsami.0c07206] [Cited by in Crossref: 15] [Cited by in F6Publishing: 15] [Article Influence: 7.5] [Reference Citation Analysis]
11 Yoshinaga K, Delage-laurin L, Swager TM. Fluorous phthalocyanines and subphthalocyanines. J Porphyrins Phthalocyanines 2020;24:1074-82. [DOI: 10.1142/s1088424620500182] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
12 Metelev VG, Bogdanov AA Jr. Synthesis and applications of theranostic oligonucleotides carrying multiple fluorine atoms. Theranostics 2020;10:1391-414. [PMID: 31938071 DOI: 10.7150/thno.37936] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
13 Miller MA, Day RA, Estabrook DA, Sletten EM. A Reduction-Sensitive Fluorous Fluorogenic Coumarin. Synlett 2020;31:450-4. [PMID: 34349356 DOI: 10.1055/s-0039-1690770] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Estabrook DA, Ennis AF, Day RA, Sletten EM. Controlling nanoemulsion surface chemistry with poly(2-oxazoline) amphiphiles. Chem Sci 2019;10:3994-4003. [PMID: 31015940 DOI: 10.1039/c8sc05735d] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 8.0] [Reference Citation Analysis]
15 Zhan X, Yadav P, Diskin-posner Y, Fridman N, Sundararajan M, Ullah Z, Chen Q, Shimon LJW, Mahammed A, Churchill DG, Baik M, Gross Z. Positive shift in corrole redox potentials leveraged by modest β-CF 3 -substitution helps achieve efficient photocatalytic C–H bond functionalization by group 13 complexes. Dalton Trans 2019;48:12279-86. [DOI: 10.1039/c9dt02150g] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 4.7] [Reference Citation Analysis]