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
Caro's Acid-Silica Gel Catalyzed Regioselective Ring Opening of Epoxides with Indoles and Imidazoles under Solvent-
Base-Catalyzed Epoxide Ring-Opening | Channels for Pearson+
Epoxide ring opening with alcohol and amine in nitromethane at room... | Download Scientific Diagram
Acid Catalyzed Epoxide Ring Opening - YouTube
Epoxides Ring-Opening Reactions - Chemistry Steps
organic chemistry - acid-catalyzed ring opening of epoxide - Chemistry Stack Exchange
Epoxide Ring Opening 2 - YouTube
Epoxide Ring Opening With Base – Master Organic Chemistry
Highly regioselective ring-opening of epoxides with amines: a metal- and solvent-free protocol for the synthesis of β-amino alcohols - Chemical Communications (RSC Publishing)
Epoxides Ring-Opening Reactions - Chemistry Steps
Regiodivergent Hydroborative Ring Opening of Epoxides via Selective C–O Bond Activation | Journal of the American Chemical Society
How to predict the regioselectivity of epoxide ring opening. | Henry Rzepa's Blog
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
Epoxides Ring-Opening Reactions - Chemistry Steps
Epoxide Ring Opening With Base – Master Organic Chemistry
Epoxide Reactions - An Overview of Epoxide Reactions - Ring-Opening Reactions along with FAQs
Regioselectivity of Epoxide Ring‐Openings via SN2 Reactions Under Basic and Acidic Conditions - Hansen - 2020 - European Journal of Organic Chemistry - Wiley Online Library
Opening of Epoxides With Acid – Master Organic Chemistry
Proposed model for epoxide ring-opening by organomagnesium reagents. | Download Scientific Diagram
Synthetic and biosynthetic methods for selective cyclisations of 4,5-epoxy alcohols to tetrahydropyrans - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB01905H
