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Cited by in F6Publishing
For: Park NH, Fevre M, Voo ZX, Ono RJ, Yang YY, Hedrick JL. Expanding the Cationic Polycarbonate Platform: Attachment of Sulfonium Moieties by Postpolymerization Ring Opening of Epoxides. ACS Macro Lett 2016;5:1247-52. [PMID: 35614734 DOI: 10.1021/acsmacrolett.6b00705] [Cited by in Crossref: 23] [Cited by in F6Publishing: 23] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Zong Q, Zhou S, Ye J, Peng X, Wu H, Li M, Ye X, Tian N, Sun W, Zhai Y. Aliphatic polycarbonate-based hydrogel dressing for wound healing. Journal of Drug Delivery Science and Technology 2023;79:104083. [DOI: 10.1016/j.jddst.2022.104083] [Reference Citation Analysis]
2 Oh J, Khan A. Main-Chain Polysulfonium Salts: Development of Non-Ammonium Antibacterial Polymers Similar in Their Activity to Antibiotic Drugs Vancomycin and Kanamycin. Biomacromolecules 2021;22:3534-42. [PMID: 34251178 DOI: 10.1021/acs.biomac.1c00627] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 2.5] [Reference Citation Analysis]
3 Xu F, Xue R, Yang F, Liu H, Zhang X, Luan S, Tang H. Preparation and solution properties of helical sulfonium-based polypeptides and their polyelectrolyte complexes. European Polymer Journal 2021;149:110390. [DOI: 10.1016/j.eurpolymj.2021.110390] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Zhu S, Xue R, Yu Z, Zhang X, Luan S, Tang H. Transition of Conformation and Solubility in β-Sheet-Structured Poly(l-cysteine)s with Methylthio or Sulfonium Pendants. Biomacromolecules 2021;22:1211-9. [PMID: 33533606 DOI: 10.1021/acs.biomac.0c01715] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
5 Jimaja S, Xie Y, Foster JC, Taton D, Dove AP, O'reilly RK. Functional nanostructures by NiCCo-PISA of helical poly(aryl isocyanide) copolymers. Polym Chem 2021;12:105-12. [DOI: 10.1039/d0py00791a] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
6 Jiang Y, Dong S, Qin G, Liu L, Zhao H. Oxidation and ATP dual-responsive block copolymer containing tertiary sulfoniums: self-assembly, protein complexation and triggered release. Polym Chem 2021;12:1125-35. [DOI: 10.1039/d0py01622e] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Dong Y, Zhou J, Wang C, Wang Y, Deng L, Zhang J, Dong A. Comb‐Like Amphiphilic Polycarbonates with Different Lengths of Cationic Branches for Enhanced siRNA Delivery. Macromol Biosci 2020;20:2000143. [DOI: 10.1002/mabi.202000143] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
8 Yeo H, Khan A. Photoinduced Proton-Transfer Polymerization: A Practical Synthetic Tool for Soft Lithography Applications. J Am Chem Soc 2020;142:3479-88. [PMID: 32040308 DOI: 10.1021/jacs.9b11958] [Cited by in Crossref: 26] [Cited by in F6Publishing: 26] [Article Influence: 8.7] [Reference Citation Analysis]
9 Gao L, Dong B, Zhang J, Chen Y, Qiao H, Liu Z, Chen E, Dong Y, Cao C, Huang D, Chen W. Functional Biodegradable Nitric Oxide Donor-Containing Polycarbonate-Based Micelles for Reduction-Triggered Drug Release and Overcoming Multidrug Resistance. ACS Macro Lett 2019;8:1552-8. [PMID: 35619381 DOI: 10.1021/acsmacrolett.9b00758] [Cited by in Crossref: 24] [Cited by in F6Publishing: 24] [Article Influence: 6.0] [Reference Citation Analysis]
10 Dai Y, Zhang X. Cationic polycarbonates via ring-opening polymerization: design, synthesis, and applications. Polym Chem 2019;10:296-305. [DOI: 10.1039/c8py01365a] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 4.0] [Reference Citation Analysis]
11 Yan B, Hou J, Wei C, Xiao Y, Lang M, Huang F. Synthesis of main chain sulfur-containing aliphatic polycarbonates by organocatalytic ring-opening polymerization of macrocyclic carbonates. Polym Chem 2019;10:5191-9. [DOI: 10.1039/c9py01205b] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
12 Kamphuis AJ, Picchioni F, Pescarmona PP. CO 2 -fixation into cyclic and polymeric carbonates: principles and applications. Green Chem 2019;21:406-48. [DOI: 10.1039/c8gc03086c] [Cited by in Crossref: 386] [Cited by in F6Publishing: 402] [Article Influence: 96.5] [Reference Citation Analysis]
13 Becker G, Wurm FR. Functional biodegradable polymers via ring-opening polymerization of monomers without protective groups. Chem Soc Rev 2018;47:7739-82. [PMID: 30221267 DOI: 10.1039/c8cs00531a] [Cited by in Crossref: 103] [Cited by in F6Publishing: 105] [Article Influence: 20.6] [Reference Citation Analysis]
14 Hwang J, Lee DG, Yeo H, Rao J, Zhu Z, Shin J, Jeong K, Kim S, Jung HW, Khan A. Proton Transfer Hydrogels: Versatility and Applications. J Am Chem Soc 2018;140:6700-9. [DOI: 10.1021/jacs.8b03514] [Cited by in Crossref: 30] [Cited by in F6Publishing: 31] [Article Influence: 6.0] [Reference Citation Analysis]
15 Wei C, Xu Y, Yan B, Hou J, Du Z, Lang M. Well-Defined Selenium-Containing Aliphatic Polycarbonates via Lipase-Catalyzed Ring-Opening Polymerization of Selenic Macrocyclic Carbonate Monomer. ACS Macro Lett 2018;7:336-40. [PMID: 35632908 DOI: 10.1021/acsmacrolett.8b00039] [Cited by in Crossref: 34] [Cited by in F6Publishing: 34] [Article Influence: 6.8] [Reference Citation Analysis]
16 Zhang J, Li M, Cheng L, Li T. Self-Healable and Tough Thermoplastic Materials from Metal-Thioether Block Polymers. Macromol Chem Phys 2018;219:1700430. [DOI: 10.1002/macp.201700430] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.2] [Reference Citation Analysis]
17 Hu S, Zhao J, Zhang G, Schlaad H. Macromolecular architectures through organocatalysis. Progress in Polymer Science 2017;74:34-77. [DOI: 10.1016/j.progpolymsci.2017.07.002] [Cited by in Crossref: 91] [Cited by in F6Publishing: 79] [Article Influence: 15.2] [Reference Citation Analysis]
18 Dai Y, Zhang X, Xia F. Click Chemistry in Functional Aliphatic Polycarbonates. Macromol Rapid Commun 2017;38:1700357. [DOI: 10.1002/marc.201700357] [Cited by in Crossref: 28] [Cited by in F6Publishing: 28] [Article Influence: 4.7] [Reference Citation Analysis]
19 Blasco E, Sims MB, Goldmann AS, Sumerlin BS, Barner-kowollik C. 50th Anniversary Perspective : Polymer Functionalization. Macromolecules 2017;50:5215-52. [DOI: 10.1021/acs.macromol.7b00465] [Cited by in Crossref: 240] [Cited by in F6Publishing: 248] [Article Influence: 40.0] [Reference Citation Analysis]
20 Deming TJ. Functional Modification of Thioether Groups in Peptides, Polypeptides, and Proteins. Bioconjugate Chem 2017;28:691-700. [DOI: 10.1021/acs.bioconjchem.6b00696] [Cited by in Crossref: 64] [Cited by in F6Publishing: 65] [Article Influence: 10.7] [Reference Citation Analysis]
21 Gregory GL, López-vidal EM, Buchard A. Polymers from sugars: cyclic monomer synthesis, ring-opening polymerisation, material properties and applications. Chem Commun 2017;53:2198-217. [DOI: 10.1039/c6cc09578j] [Cited by in Crossref: 86] [Cited by in F6Publishing: 89] [Article Influence: 14.3] [Reference Citation Analysis]
22 Ge C, Zhao L, Ling Y, Tang H. Thermo and pH dual responsive polypeptides derived from “clickable” poly(γ-3-methylthiopropyl- l -glutamate). Polym Chem 2017;8:1895-905. [DOI: 10.1039/c7py00170c] [Cited by in Crossref: 17] [Cited by in F6Publishing: 17] [Article Influence: 2.8] [Reference Citation Analysis]
23 Zhang J, Li M, Cheng L, Li T. Multifunctional polymers built on copper–thioether coordination. Polym Chem 2017;8:6527-33. [DOI: 10.1039/c7py01359k] [Cited by in Crossref: 16] [Cited by in F6Publishing: 16] [Article Influence: 2.7] [Reference Citation Analysis]