![Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0009250921003110-ga1.jpg)
Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect
Facile synthesis of chain end functionalized polyethylenes via epoxide ring- opening and thiol–ene addition click chemistry - Polymer Chemistry (RSC Publishing)
![Epoxide ring opening with alcohol and amine in nitromethane at room... | Download Scientific Diagram Epoxide ring opening with alcohol and amine in nitromethane at room... | Download Scientific Diagram](https://www.researchgate.net/publication/263311953/figure/fig1/AS:613887812587537@1523373668154/Epoxide-ring-opening-with-alcohol-and-amine-in-nitromethane-at-room-temperature.png)
Epoxide ring opening with alcohol and amine in nitromethane at room... | Download Scientific Diagram
![Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis - ScienceDirect Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S245192942200208X-fx1.jpg)
Catalytic reductive ring opening of epoxides enabled by zirconocene and photoredox catalysis - ScienceDirect
![Synthetic and biosynthetic methods for selective cyclisations of 4,5-epoxy alcohols to tetrahydropyrans - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB01905H Synthetic and biosynthetic methods for selective cyclisations of 4,5-epoxy alcohols to tetrahydropyrans - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB01905H](https://pubs.rsc.org/image/article/2022/OB/d1ob01905h/d1ob01905h-f3_hi-res.gif)
Synthetic and biosynthetic methods for selective cyclisations of 4,5-epoxy alcohols to tetrahydropyrans - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB01905H
![Brønsted Acid‐Catalysed Epoxide Ring‐Opening Using Amine Nucleophiles: A Facile Access to β‐Amino Alcohols - Tyagi - 2022 - Chemistry – An Asian Journal - Wiley Online Library Brønsted Acid‐Catalysed Epoxide Ring‐Opening Using Amine Nucleophiles: A Facile Access to β‐Amino Alcohols - Tyagi - 2022 - Chemistry – An Asian Journal - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/b8faa5c2-141d-4608-a6c5-5193524c582a/asia202200379-toc-0001-m.jpg)
Brønsted Acid‐Catalysed Epoxide Ring‐Opening Using Amine Nucleophiles: A Facile Access to β‐Amino Alcohols - Tyagi - 2022 - Chemistry – An Asian Journal - Wiley Online Library
![Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0009250921003110-gr10.jpg)