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For: Drain BA, Becer CR. Synthetic approaches on conjugation of poly(2-oxazoline)s with vinyl based polymers. European Polymer Journal 2019;119:344-51. [DOI: 10.1016/j.eurpolymj.2019.07.047] [Cited by in Crossref: 22] [Cited by in F6Publishing: 22] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Borova S, Luxenhofer R. Investigation of cationic ring-opening polymerization of 2-oxazolines in the "green" solvent dihydrolevoglucosenone. Beilstein J Org Chem 2023;19:217-30. [PMID: 36895428 DOI: 10.3762/bjoc.19.21] [Reference Citation Analysis]
2 Hayes G, Drain B, Lefley J, Becer CR. Hybrid Multiblock Copolymers of 2-Oxazoline and Acrylates via Cu-Catalyzed Azide–Alkyne Cycloaddition Step-Growth Mechanism. Macromolecules 2022. [DOI: 10.1021/acs.macromol.2c01865] [Reference Citation Analysis]
3 Kim J, Beyer V, Becer CR. Poly(2-oxazoline) with Pendant Hydroxyl Groups via a Silyl Ether-Based Protecting Group. Macromolecules 2022. [DOI: 10.1021/acs.macromol.2c02050] [Reference Citation Analysis]
4 Kim J, Cattoz B, Leung AHM, Parish JD, Becer CR. Enabling Reversible Addition-Fragmentation Chain-Transfer Polymerization for Brush Copolymers with a Poly(2-oxazoline) Backbone. Macromolecules. [DOI: 10.1021/acs.macromol.2c00497] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Aitken RA, Inwood RA. Oxazoles. Comprehensive Heterocyclic Chemistry IV 2022. [DOI: 10.1016/b978-0-12-818655-8.00157-8] [Reference Citation Analysis]
6 Goto T, Nitta R, Nukui T, Takemoto M, Takahashi T. Preparation of oxazoline-group-functionalized diamond using poly(2-vinyl-2-oxazoline) based on a model reaction between oxazoline and carboxylic acid. Diamond and Related Materials 2021;120:108693. [DOI: 10.1016/j.diamond.2021.108693] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Pan X, Ishaq MW, Ali MW, Yang J, Li L, Chen Y. Unraveling the conformational properties of comb-like Poly(propargyl acrylate)-graft-poly(2-ethyl-2-oxazoline) chains in dilute solutions. Polymer 2021;233:124224. [DOI: 10.1016/j.polymer.2021.124224] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
8 Warne NM, Finnegan JR, Feeney OM, Kempe K. Using 2‐isopropyl ‐2‐oxazine to explore the effect of monomer distribution and polymer architecture on the thermoresponsive behavior of copolymers. Journal of Polymer Science 2021;59:2783-96. [DOI: 10.1002/pol.20210551] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
9 Drain BA, Beyer VP, Cattoz B, Becer CR. Solvent Dependency in the Synthesis of Multiblock and Cyclic Poly(2-oxazoline)s. Macromolecules 2021;54:5549-56. [DOI: 10.1021/acs.macromol.1c00529] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
10 Leiske MN, Lai M, Amarasena T, Davis TP, Thurecht KJ, Kent SJ, Kempe K. Interactions of core cross-linked poly(2-oxazoline) and poly(2-oxazine) micelles with immune cells in human blood. Biomaterials 2021;274:120843. [PMID: 33984635 DOI: 10.1016/j.biomaterials.2021.120843] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 6.0] [Reference Citation Analysis]
11 Pizzi D, Mahmoud AM, Klein T, Morrow JP, Humphries J, Houston ZH, Fletcher NL, Bell CA, Thurecht KJ, Kempe K. Poly(2-ethyl-2-oxazoline) bottlebrushes: How nanomaterial dimensions can influence biological interactions. European Polymer Journal 2021;151:110447. [DOI: 10.1016/j.eurpolymj.2021.110447] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
12 Bouktab S, Saidat B, Belhocine M, Ammari A, Dergal F. Structural and dielectric properties of poly(2-ethyl-2-oxazoline)/montmorillonite nanocomposite. J Mater Sci: Mater Electron 2021;32:13871-81. [DOI: 10.1007/s10854-021-05963-x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
13 Menezes RNLD, Felisberti MI. Combining CROP and ATRP to synthesize pH-responsive poly(2-ethyl-2-oxazoline- b -4-vinylpyridine) block copolymers. Polym Chem 2021;12:4680-95. [DOI: 10.1039/d1py00730k] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
14 Cordero FM, Lascialfari L, Machetti F. Five-membered ring systems with O and N atoms. Progress in Heterocyclic Chemistry 2021. [DOI: 10.1016/b978-0-323-89812-6.00011-0] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
15 Černoch P, Jager A, Černochová Z, Sincari V, Albuquerque LJC, Konefal R, Pavlova E, Giacomelli FC, Jager E. Engineering of pH-triggered nanoplatforms based on novel poly(2-methyl-2-oxazoline)- b -poly[2-(diisopropylamino)ethyl methacrylate] diblock copolymers with tunable morphologies for biomedical applications. Polym Chem 2021;12:2868-80. [DOI: 10.1039/d1py00141h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
16 Zhao T, Drain B, Yilmaz G, Becer CR. One-pot synthesis of amphiphilic multiblock poly(2-oxazoline)s via para-fluoro-thiol click reactions. Polym Chem 2021;12:6392-6403. [DOI: 10.1039/d1py00944c] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Schoolaert E, Merckx R, Becelaere J, Everaerts M, Van Guyse JFR, Sedlacek O, De Geest BG, Van den Mooter G, D’hooge DR, De Clerck K, Hoogenboom R. Immiscibility of Chemically Alike Amorphous Polymers: Phase Separation of Poly(2-ethyl-2-oxazoline) and Poly(2- n -propyl-2-oxazoline). Macromolecules 2020;53:7590-600. [DOI: 10.1021/acs.macromol.0c00970] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
18 Bernhard Y, Sedlacek O, Van Guyse JFR, Bender J, Zhong Z, De Geest BG, Hoogenboom R. Poly(2-ethyl-2-oxazoline) Conjugates with Salicylic Acid via Degradable Modular Ester Linkages. Biomacromolecules 2020;21:3207-15. [PMID: 32639725 DOI: 10.1021/acs.biomac.0c00659] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.7] [Reference Citation Analysis]
19 Schoolaert E, Cossu L, Becelaere J, Van Guyse JF, Tigrine A, Vergaelen M, Hoogenboom R, De Clerck K. Nanofibers with a tunable wettability by electrospinning and physical crosslinking of poly(2-n-propyl-2-oxazoline). Materials & Design 2020;192:108747. [DOI: 10.1016/j.matdes.2020.108747] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 6.3] [Reference Citation Analysis]
20 Jana S, Uchman M. Poly(2-oxazoline)-based stimulus-responsive (Co)polymers: An overview of their design, solution properties, surface-chemistries and applications. Progress in Polymer Science 2020;106:101252. [DOI: 10.1016/j.progpolymsci.2020.101252] [Cited by in Crossref: 28] [Cited by in F6Publishing: 17] [Article Influence: 9.3] [Reference Citation Analysis]
21 Hoogenboom R. Poly(2-oxazoline)s and polypeptoids. European Polymer Journal 2020;131:109696. [DOI: 10.1016/j.eurpolymj.2020.109696] [Reference Citation Analysis]
22 Kim J, Waldron C, Cattoz B, Becer CR. An ε-caprolactone-derived 2-oxazoline inimer for the synthesis of graft copolymers. Polym Chem 2020;11:6847-52. [DOI: 10.1039/d0py01092h] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
23 Merckx R, Swift T, Rees R, Van Guyse JFR, Schoolaert E, De Clerck K, Ottevaere H, Thienpont H, Jerca VV, Hoogenboom R. Förster resonance energy transfer in fluorophore labeled poly(2-ethyl-2-oxazoline)s. J Mater Chem C 2020;8:14125-37. [DOI: 10.1039/d0tc02830d] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
24 Neumann S, Biewend M, Rana S, Binder WH. The CuAAC: Principles, Homogeneous and Heterogeneous Catalysts, and Novel Developments and Applications. Macromol Rapid Commun 2020;41:e1900359. [PMID: 31631449 DOI: 10.1002/marc.201900359] [Cited by in Crossref: 98] [Cited by in F6Publishing: 102] [Article Influence: 24.5] [Reference Citation Analysis]