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For: Sahn M, Weber C, Schubert US. Poly(2-oxazoline)-Containing Triblock Copolymers: Synthesis and Applications. Polymer Reviews 2019;59:240-79. [DOI: 10.1080/15583724.2018.1496930] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
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2 Shin C, Hong K, Lee J, Jang W. Multimodal stimuli-responsive behaviors of photochromic spiropyran-bearing telechelic poly(2-isopropyl-2-oxazoline). Materials Today Chemistry 2022;24:100884. [DOI: 10.1016/j.mtchem.2022.100884] [Reference Citation Analysis]
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5 Soleymani Movahed F, Foo SW, Mori S, Ogawa S, Saito S. Phosphorus-Based Organocatalysis for the Dehydrative Cyclization of N-(2-Hydroxyethyl)amides into 2-Oxazolines. J Org Chem 2021. [PMID: 34882422 DOI: 10.1021/acs.joc.1c02318] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Vrbata D, Kereiche S, Kalíková K, Uchman M. Stimuli-responsive multifunctional micelles of ABC vs. ACB triblock terpolymers using reversible covalent bonding of phenylboronic acid: controlled synthesis, self-assembly and model drug release. Journal of Molecular Liquids 2021;335:116528. [DOI: 10.1016/j.molliq.2021.116528] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Dirauf M, Fritz N, Gottschaldt M, Weber C, Schubert US. Poly(2-ethyl-2-oxazoline) Featuring a Central Amino Moiety. Macromol Rapid Commun 2021;42:e2100132. [PMID: 33960561 DOI: 10.1002/marc.202100132] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
8 Pásztói B, Trötschler TM, Szabó Á, Kerscher B, Tenhu H, Mülhaupt R, Iván B. Quasiliving cationic ring-opening polymerization of 2-ethyl-2-oxazoline in benzotrifluoride, as an alternative reaction medium. Polymer 2021;212:123165. [DOI: 10.1016/j.polymer.2020.123165] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
9 Farnaz Fazlalizadeh, Massoumi B, Banaei A, Jaymand M. A Thermal-Responsive Y-Shaped Miktoarm Amphiphilic Block Copolymer Composed of Poly(ε-caprolactone) and Poly(N-isopropylacrylamide) as a Nano-micellar Carrier for Anti-cancer Drugs. Polym Sci Ser B 2020;62:540-9. [DOI: 10.1134/s1560090420050061] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
10 Park JM, Kim YJ, Jang W. Multimodal Stimuli-Responsive Fluorophore-Functionalized Heterotelechelic Poly(2-isopropyl-2-oxazoline). ACS Appl Polym Mater 2020;2:3535-42. [DOI: 10.1021/acsapm.0c00543] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
11 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]
12 Pizzi D, Humphries J, Morrow JP, Fletcher NL, Bell CA, Thurecht KJ, Kempe K. Poly(2-oxazoline) macromonomers as building blocks for functional and biocompatible polymer architectures. European Polymer Journal 2019;121:109258. [DOI: 10.1016/j.eurpolymj.2019.109258] [Cited by in Crossref: 30] [Cited by in F6Publishing: 29] [Article Influence: 7.5] [Reference Citation Analysis]
13 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]