Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect
Synthetic and biosynthetic methods for selective cyclisations of 4,5-epoxy alcohols to tetrahydropyrans - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/D1OB01905H
Epoxide Reactions: Definition, Examples, and Mechanism
Opening of Epoxides With Acid – Master Organic Chemistry
Mechanism and kinetics of epoxide ring-opening with carboxylic acids catalyzed by the corresponding carboxylates - ScienceDirect
organic chemistry - acid-catalyzed ring opening of epoxide - Chemistry Stack Exchange
Reactions of Epoxides - Course Hero
Caro's Acid-Silica Gel Catalyzed Regioselective Ring Opening of Epoxides with Indoles and Imidazoles under Solvent-
Opening of Epoxides With Acid – Master Organic Chemistry
Acid Catalyze ring opening of Epoxides - HBr, HCl, HI, H2SO4/H20 - Organic Chemistry - YouTube
Flavin-enabled reductive and oxidative epoxide ring opening reactions | Nature Communications
Epoxide Reactions: Definition, Examples, and Mechanism
a) Computationally analyzed epoxide ring-opening reactions under basic... | Download Scientific Diagram
Opening of Epoxides With Acid – Master Organic Chemistry
9.14: Opening of Epoxides - Acidic versus Basic Conditions - Chemistry LibreTexts
Opening of Epoxides With Acid – Master Organic Chemistry
Epoxides: Small Rings to Play with under Asymmetric Organocatalysis | ACS Organic & Inorganic Au
SOLVED: In acidic conditions epoxides can be protonated. Protonated epoxides can undergo ring opening in the presence of poor nucleophiles: In these reactions the nucleophile preferentially attacks the more substituted carbon atom
Ch16: SN1 type reactions of epoxides
9.6. Epoxide reactions | Organic Chemistry 1: An open textbook