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For: Vergaelen M, Verbraeken B, Monnery BD, Hoogenboom R. Sulfolane as Common Rate Accelerating Solvent for the Cationic Ring-Opening Polymerization of 2-Oxazolines. ACS Macro Lett 2015;4:825-8. [PMID: 35596503 DOI: 10.1021/acsmacrolett.5b00392] [Cited by in Crossref: 32] [Cited by in F6Publishing: 32] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Vergaelen M, Monnery BD, Jerca VV, Hoogenboom R. Detailed Understanding of Solvent Effects for the Cationic Ring-Opening Polymerization of 2-Ethyl-2-oxazoline. Macromolecules 2023. [DOI: 10.1021/acs.macromol.2c01930] [Reference Citation Analysis]
2 Yao X, Qi C, Sun C, Huo F, Jiang X. Poly(ethylene glycol) alternatives in biomedical applications. Nano Today 2023;48:101738. [DOI: 10.1016/j.nantod.2022.101738] [Reference Citation Analysis]
3 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]
4 Hoogenboom R. The future of poly(2-oxazoline)s. European Polymer Journal 2022;179:111521. [DOI: 10.1016/j.eurpolymj.2022.111521] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Kurlykin MP, Dudkina MM, Kirila TY, Filippov AP, Ten’kovtsev AV. New Approach to the Synthesis of Thermoresponsive Polyrotaxanes. Polym Sci Ser B 2022. [DOI: 10.1134/s156009042270021x] [Reference Citation Analysis]
6 Van Guyse JFR, Hoogenboom R. Poly(2‐Oxazoline)s. Macromolecular Engineering 2022. [DOI: 10.1002/9783527815562.mme0012] [Reference Citation Analysis]
7 Blokhin AN, Kirila TY, Kozina ND, Razina AB, Filippov AP, Tenkovtsev AV. Synthesis and hydrodynamic properties of star poly(2-alkyl-2-oxazolines) and poly(2-alkyl-2-oxazines) based on sulfochlorinated calix[4]arene initiator. Mendeleev Communications 2022;32:247-8. [DOI: 10.1016/j.mencom.2022.03.031] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Born M, Plank J, Klapötke TM. Energetic Polymers: A Chance for Lightweight Reactive Structure Materials? Propellants Explo Pyrotec 2022;47. [DOI: 10.1002/prep.202100368] [Reference Citation Analysis]
9 Blokhin AN, Razina AB, Tenkovtsev AV. Novel Amphiphilic Star-Shaped Poly(2-Oxazoline)s with Calix[4]Arene Branching Center. KEM 2021;899:300-308. [DOI: 10.4028/www.scientific.net/kem.899.300] [Reference Citation Analysis]
10 Lavikainen J, Dauletbekova M, Toleutay G, Kaliva M, Chatzinikolaidou M, Kudaibergenov SE, Tenkovtsev A, Khutoryanskiy VV, Vamvakaki M, Aseyev V. Poly(2‐ethyl‐2‐oxazoline) grafted gellan gum for potential application in transmucosal drug delivery. Polym Adv Technol 2021;32:2770-80. [DOI: 10.1002/pat.5298] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Zahoranová A, Luxenhofer R. Poly(2-oxazoline)- and Poly(2-oxazine)-Based Self-Assemblies, Polyplexes, and Drug Nanoformulations-An Update. Adv Healthc Mater 2021;10:e2001382. [PMID: 33448122 DOI: 10.1002/adhm.202001382] [Cited by in Crossref: 23] [Cited by in F6Publishing: 24] [Article Influence: 11.5] [Reference Citation Analysis]
12 Blokhin AN, Razina AB, Bursian AE, Ten’kovtsev AV. Synthesis of a New Type of Star-Shaped Poly(2-alkyl-2-oxazolines) on the Basis of Sulfochlorinated Calix[8]arene. Polym Sci Ser B 2021;63:52-62. [DOI: 10.1134/s1560090421010024] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
13 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]
14 Van Den Broeck E, Verbraeken B, Dedecker K, Cnudde P, Vanduyfhuys L, Verstraelen T, Van Hecke K, Jerca VV, Catak S, Hoogenboom R, Van Speybroeck V. Cation−π Interactions Accelerate the Living Cationic Ring-Opening Polymerization of Unsaturated 2-Alkyl-2-oxazolines. Macromolecules 2020;53:3832-46. [DOI: 10.1021/acs.macromol.0c00865] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
15 Zhou YN, Li JJ, Wu YY, Luo ZH. Role of External Field in Polymerization: Mechanism and Kinetics. Chem Rev 2020;120:2950-3048. [PMID: 32083844 DOI: 10.1021/acs.chemrev.9b00744] [Cited by in Crossref: 88] [Cited by in F6Publishing: 92] [Article Influence: 29.3] [Reference Citation Analysis]
16 Yan H, Huang G, Hu F, Zhou X, Li Z. Rhodium-Catalyzed Oxidative Olefination of N-(2-(4,5-Dihydrooxazol-2-yl)phenyl)amides with Arylethenes via Extraordinary N-Aryl C-H Bond Functionalization. HETEROCYCLES 2020;100:1979. [DOI: 10.3987/com-20-14346] [Reference Citation Analysis]
17 Hu F, Cui X, Lu G, Huang G. Base-promoted Lewis acid catalyzed synthesis of quinazoline derivatives. Org Biomol Chem 2020;18:4376-80. [DOI: 10.1039/d0ob00225a] [Cited by in Crossref: 3] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
18 Vergaelen M, Verbraeken B, Van Guyse JFR, Podevyn A, Tigrine A, de la Rosa VR, Monnery BD, Hoogenboom R. Ethyl acetate as solvent for the synthesis of poly(2-ethyl-2-oxazoline). Green Chem 2020;22:1747-53. [DOI: 10.1039/c9gc03872h] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
19 Daubian D, Gaitzsch J, Meier W. Synthesis and complex self-assembly of amphiphilic block copolymers with a branched hydrophobic poly(2-oxazoline) into multicompartment micelles, pseudo-vesicles and yolk/shell nanoparticles. Polym Chem 2020;11:1237-48. [DOI: 10.1039/c9py01559k] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 9.0] [Reference Citation Analysis]
20 Lübtow MM, Nelke LC, Seifert J, Kühnemundt J, Sahay G, Dandekar G, Nietzer SL, Luxenhofer R. Drug induced micellization into ultra-high capacity and stable curcumin nanoformulations: Physico-chemical characterization and evaluation in 2D and 3D in vitro models. Journal of Controlled Release 2019;303:162-80. [DOI: 10.1016/j.jconrel.2019.04.014] [Cited by in Crossref: 45] [Cited by in F6Publishing: 42] [Article Influence: 11.3] [Reference Citation Analysis]
21 Gao T, Wang C, Tang K, Xu Y, Sun L. Amide-Oxazoline Directed ortho -C-H Nitration Mediated by Cu II: Amide-Oxazoline Directed ortho -C-H Nitration Mediated by Cu II. Eur J Org Chem 2019;2019:3005-11. [DOI: 10.1002/ejoc.201900117] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 1.5] [Reference Citation Analysis]
22 Sedlacek O, Monnery BD, Hoogenboom R. Synthesis of defined high molar mass poly(2-methyl-2-oxazoline). Polym Chem 2019;10:1286-90. [DOI: 10.1039/c9py00013e] [Cited by in Crossref: 20] [Cited by in F6Publishing: 20] [Article Influence: 5.0] [Reference Citation Analysis]
23 Bera D, Sedlacek O, Jager E, Pavlova E, Vergaelen M, Hoogenboom R. Solvent-control over monomer distribution in the copolymerization of 2-oxazolines and the effect of a gradient structure on self-assembly. Polym Chem 2019;10:5116-23. [DOI: 10.1039/c9py00927b] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
24 Monnery BD, Hoogenboom R. Thermoresponsive hydrogels formed by poly(2-oxazoline) triblock copolymers. Polym Chem 2019;10:3480-7. [DOI: 10.1039/c9py00300b] [Cited by in Crossref: 27] [Cited by in F6Publishing: 27] [Article Influence: 6.8] [Reference Citation Analysis]
25 Tenkovtsev AV, Amirova AI, Filippov AP. Star-shaped Poly(2-alkyl-2-oxazolines): Synthesis and Properties. Temperature-Responsive Polymers 2018. [DOI: 10.1002/9781119157830.ch3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
26 Verbraeken B, Monnery BD, Lava K, Hoogenboom R. The Chemistry of Poly(2-oxazoline)s. Encyclopedia of Polymer Science and Technology 2018. [DOI: 10.1002/0471440264.pst626.pub2] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
27 Blokhin AN, Razina AB, Ten’kovtsev AV. Star Poly(2-alkyl-2-oxazolines) Based on Octa-(chlorosulfonyl)-calix[8]arene. Polym Sci Ser B 2018;60:307-316. [DOI: 10.1134/s1560090418030028] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
28 Amirova A, Tobolina A, Kirila T, Blokhin A, Razina A, Tenkovtsev A, Filippov A. Influence of core configuration and arm structure on solution properties of new thermosensitive star-shaped poly(2-alkyl-2-oxazolines). International Journal of Polymer Analysis and Characterization 2018;23:278-85. [DOI: 10.1080/1023666x.2018.1441483] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 2.6] [Reference Citation Analysis]
29 Glassner M, Vergaelen M, Hoogenboom R. Poly(2-oxazoline)s: A comprehensive overview of polymer structures and their physical properties: Poly(2-oxazoline)s. Polym Int 2018;67:32-45. [DOI: 10.1002/pi.5457] [Cited by in Crossref: 148] [Cited by in F6Publishing: 151] [Article Influence: 24.7] [Reference Citation Analysis]
30 Wan L, Qiao K, Yuan X, Zheng M, Fan B, Di ZC, Zhang D, Fang Z, Guo K. Nickel-Catalyzed Regioselective C-H Bond Mono- and Bis-Nitration of Aryloxazolines with tert- Butyl Nitrite as Nitro Source. Adv Synth Catal 2017;359:2596-604. [DOI: 10.1002/adsc.201700186] [Cited by in Crossref: 26] [Cited by in F6Publishing: 28] [Article Influence: 4.3] [Reference Citation Analysis]
31 Verbraeken B, Monnery BD, Lava K, Hoogenboom R. The chemistry of poly(2-oxazoline)s. European Polymer Journal 2017;88:451-69. [DOI: 10.1016/j.eurpolymj.2016.11.016] [Cited by in Crossref: 171] [Cited by in F6Publishing: 174] [Article Influence: 28.5] [Reference Citation Analysis]
32 Konishcheva EV, Zhumaev UE, Meier WP. PEO- b -PCL- b -PMOXA Triblock Copolymers: From Synthesis to Microscale Polymersomes with Asymmetric Membrane. Macromolecules 2017;50:1512-20. [DOI: 10.1021/acs.macromol.6b02743] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 5.5] [Reference Citation Analysis]
33 Sharma S, Kumar M, Sharma S, Nayal OS, Kumar N, Singh B, Sharma U. Microwave assisted synthesis of phenanthridinones and dihydrophenanthridines by vasicine/KOtBu promoted intramolecular C–H arylation. Org Biomol Chem 2016;14:8536-44. [DOI: 10.1039/c6ob01362g] [Cited by in Crossref: 17] [Cited by in F6Publishing: 18] [Article Influence: 2.4] [Reference Citation Analysis]