![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/profile/Mehdi-Bakavoli/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
![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/profile/Thomas-Hansen-25/publication/341718003/figure/fig2/AS:897516337913857@1590995978627/Scheme-2-Computationally-analyzed-ring-opening-reactions-of-epoxide-1-under-basic-1-a.png)
Scheme 2. Computationally analyzed ring-opening reactions of epoxide 1... | Download Scientific Diagram
![Asymmetric Ring‐Opening of Epoxides and Aziridines with Carbon Nucleophiles - Pineschi - 2006 - European Journal of Organic Chemistry - Wiley Online Library Asymmetric Ring‐Opening of Epoxides and Aziridines with Carbon Nucleophiles - Pineschi - 2006 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/acdf8f72-fac2-4661-9f36-ccc748c2f253/mfig000.gif)
Asymmetric Ring‐Opening of Epoxides and Aziridines with Carbon Nucleophiles - Pineschi - 2006 - European Journal of Organic Chemistry - Wiley Online Library
![Molecules | Free Full-Text | Optimisation of Epoxide Ring-Opening Reaction for the Synthesis of Bio-Polyol from Palm Oil Derivative Using Response Surface Methodology Molecules | Free Full-Text | Optimisation of Epoxide Ring-Opening Reaction for the Synthesis of Bio-Polyol from Palm Oil Derivative Using Response Surface Methodology](https://www.mdpi.com/molecules/molecules-26-00648/article_deploy/html/images/molecules-26-00648-sch002.png)
Molecules | Free Full-Text | Optimisation of Epoxide Ring-Opening Reaction for the Synthesis of Bio-Polyol from Palm Oil Derivative Using Response Surface Methodology
![Regioselectivity of Epoxide Ring‐Openings via SN2 Reactions Under Basic and Acidic Conditions - Hansen - 2020 - European Journal of Organic Chemistry - Wiley Online Library Regioselectivity of Epoxide Ring‐Openings via SN2 Reactions Under Basic and Acidic Conditions - Hansen - 2020 - European Journal of Organic Chemistry - Wiley Online Library](https://chemistry-europe.onlinelibrary.wiley.com/cms/asset/f29894b4-e062-4f63-8fcc-2508db53680f/ejoc202000590-toc-0001-m.jpg)
Regioselectivity of Epoxide Ring‐Openings via SN2 Reactions Under Basic and Acidic Conditions - Hansen - 2020 - European Journal of Organic Chemistry - Wiley Online Library
![SOLVED:Question 7 0.5 pts Predict the major product of the epoxide ring-opening reaction: OH OH OH CHaOH 99 % ee A B SOLVED:Question 7 0.5 pts Predict the major product of the epoxide ring-opening reaction: OH OH OH CHaOH 99 % ee A B](https://cdn.numerade.com/ask_images/d6dcd8aeead1476aae881c26e8529d8e.jpg)
SOLVED:Question 7 0.5 pts Predict the major product of the epoxide ring-opening reaction: OH OH OH CHaOH 99 % ee A B
![A New and Efficient Epoxide Ring Opening via Poor Nucleophiles: Indole, p-Nitroaniline, Borane and O-Trimethylsilylhydroxylamine in Lithium Perchlorate A New and Efficient Epoxide Ring Opening via Poor Nucleophiles: Indole, p-Nitroaniline, Borane and O-Trimethylsilylhydroxylamine in Lithium Perchlorate](https://www.organic-chemistry.org/abstracts/literature/340m.gif)
A New and Efficient Epoxide Ring Opening via Poor Nucleophiles: Indole, p-Nitroaniline, Borane and O-Trimethylsilylhydroxylamine in Lithium Perchlorate
![Efficient method for ring opening of epoxides with amines by NaY zeolite under solvent-free conditions - ScienceDirect Efficient method for ring opening of epoxides with amines by NaY zeolite under solvent-free conditions - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381116906012040-fx1.gif)