![Metal-Catalyzed Directed Regio- and Enantioselective Ring-Opening of Epoxides | Accounts of Chemical Research Metal-Catalyzed Directed Regio- and Enantioselective Ring-Opening of Epoxides | Accounts of Chemical Research](https://pubs.acs.org/cms/10.1021/acs.accounts.5b00428/asset/images/large/ar-2015-004286_0001.jpeg)
Metal-Catalyzed Directed Regio- and Enantioselective Ring-Opening of Epoxides | Accounts of Chemical Research
Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C–O Bond Activation | Journal of the American Chemical Society
![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
![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
![The alcohol A may be prepared by acid-catalyzed epoxide ring opening as shown below. Find a suitable starting material and the necessary reagents to prepare the other regioisomer B from the choices The alcohol A may be prepared by acid-catalyzed epoxide ring opening as shown below. Find a suitable starting material and the necessary reagents to prepare the other regioisomer B from the choices](https://homework.study.com/cimages/multimages/16/55766374734917687956989631.png)
The alcohol A may be prepared by acid-catalyzed epoxide ring opening as shown below. Find a suitable starting material and the necessary reagents to prepare the other regioisomer B from the choices
![Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C–O Bond Activation | Journal of the American Chemical Society Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C–O Bond Activation | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/jacs.0c05917/asset/images/medium/ja0c05917_0005.gif)
Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C–O Bond Activation | Journal of the American Chemical Society
![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
![Scheme 2. Computationally analyzed ring-opening reactions of epoxide 1... | Download Scientific Diagram Scheme 2. Computationally analyzed ring-opening reactions of epoxide 1... | Download Scientific Diagram](https://www.researchgate.net/publication/341718003/figure/fig2/AS:897516337913857@1590995978627/Scheme-2-Computationally-analyzed-ring-opening-reactions-of-epoxide-1-under-basic-1-a.png)