![Cationic ring-opening copolymerization of propylene oxide with tetrahydrofuran by acid exchanged montmorillonite clay | Semantic Scholar Cationic ring-opening copolymerization of propylene oxide with tetrahydrofuran by acid exchanged montmorillonite clay | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/5b4a9e296af151a9b04cc7f25ff62a3ecdc6d79b/3-Table1-1.png)
Cationic ring-opening copolymerization of propylene oxide with tetrahydrofuran by acid exchanged montmorillonite clay | Semantic Scholar
Cationic ring-opening polymerization of a five membered cyclic dithiocarbonate having a tertiary amine moiety - Polymer Chemistry (RSC Publishing)
![Anionic Ring-Opening Polymerization of a Functional Epoxide Monomer with an Oxazoline Protecting Group for the Synthesis of Polyethers with Carboxylic Acid Pendants | Macromolecules Anionic Ring-Opening Polymerization of a Functional Epoxide Monomer with an Oxazoline Protecting Group for the Synthesis of Polyethers with Carboxylic Acid Pendants | Macromolecules](https://pubs.acs.org/cms/10.1021/acs.macromol.2c00761/asset/images/large/ma2c00761_0008.jpeg)
Anionic Ring-Opening Polymerization of a Functional Epoxide Monomer with an Oxazoline Protecting Group for the Synthesis of Polyethers with Carboxylic Acid Pendants | Macromolecules
![Completely recyclable biopolymers with linear and cyclic topologies via ring -opening polymerization of γ-butyrolactone | Nature Chemistry Completely recyclable biopolymers with linear and cyclic topologies via ring -opening polymerization of γ-butyrolactone | Nature Chemistry](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fnchem.2391/MediaObjects/41557_2016_Article_BFnchem2391_Fig1_HTML.jpg)
Completely recyclable biopolymers with linear and cyclic topologies via ring -opening polymerization of γ-butyrolactone | Nature Chemistry
Organocatalytic Cationic Ring-Opening Polymerization of a Cyclic Hemiacetal Ester | Industrial & Engineering Chemistry Research
![Living Cationic Ring‐Opening Polymerization of Hetero Diels–Alder Adducts to Give Multifactor‐Controlled and Fast‐Photodegradable Vinyl Polymers - Chae - 2023 - Angewandte Chemie International Edition - Wiley Online Library Living Cationic Ring‐Opening Polymerization of Hetero Diels–Alder Adducts to Give Multifactor‐Controlled and Fast‐Photodegradable Vinyl Polymers - Chae - 2023 - Angewandte Chemie International Edition - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/afdc18cf-033e-4a3d-b070-a721206d52be/anie202305414-fig-0001-m.jpg)
Living Cationic Ring‐Opening Polymerization of Hetero Diels–Alder Adducts to Give Multifactor‐Controlled and Fast‐Photodegradable Vinyl Polymers - Chae - 2023 - Angewandte Chemie International Edition - Wiley Online Library
![Chemistry of 2‐oxazolines: A crossing of cationic ring‐opening polymerization and enzymatic ring‐opening polyaddition - Makino - 2010 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library Chemistry of 2‐oxazolines: A crossing of cationic ring‐opening polymerization and enzymatic ring‐opening polyaddition - Makino - 2010 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f8a4d291-ae39-4f32-b158-cc111da2b9ca/msch004.jpg)
Chemistry of 2‐oxazolines: A crossing of cationic ring‐opening polymerization and enzymatic ring‐opening polyaddition - Makino - 2010 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library
![Cationic ring‐opening polymerization (CROP) major mechanistic phenomena - Penczek - 2000 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library Cationic ring‐opening polymerization (CROP) major mechanistic phenomena - Penczek - 2000 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/3f6f9cc2-4429-4abe-a827-ce0aa9f309f7/msch010.jpg)
Cationic ring‐opening polymerization (CROP) major mechanistic phenomena - Penczek - 2000 - Journal of Polymer Science Part A: Polymer Chemistry - Wiley Online Library
![Quasiliving cationic ring-opening polymerization of 2-ethyl-2-oxazoline in benzotrifluoride, as an alternative reaction medium - ScienceDirect Quasiliving cationic ring-opening polymerization of 2-ethyl-2-oxazoline in benzotrifluoride, as an alternative reaction medium - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0032386120309903-fx1.jpg)
Quasiliving cationic ring-opening polymerization of 2-ethyl-2-oxazoline in benzotrifluoride, as an alternative reaction medium - ScienceDirect
![Scheme 13. Mechanism of the cationic ring-opening polymerization of... | Download Scientific Diagram Scheme 13. Mechanism of the cationic ring-opening polymerization of... | Download Scientific Diagram](https://www.researchgate.net/publication/235675683/figure/fig2/AS:669026795663379@1536519826721/Scheme-13-Mechanism-of-the-cationic-ring-opening-polymerization-of-2-oxazolines-to-yield.png)
Scheme 13. Mechanism of the cationic ring-opening polymerization of... | Download Scientific Diagram
![Reaction mechanism for ring-opening polymerization of caprolactones:... | Download Scientific Diagram Reaction mechanism for ring-opening polymerization of caprolactones:... | Download Scientific Diagram](https://www.researchgate.net/publication/368377147/figure/fig5/AS:11431281119015284@1675953276681/Reaction-mechanism-for-ring-opening-polymerization-of-caprolactones-a-anionic.png)