TCI uses cookies to personalize and improve your user experience. By continuing on our website, you accept the use of cookies. You can change or update your cookiesettings at any time.
Maintenance Notice (5:30 AM - 12:00 PM December 21, 2024): This website is scheduled to be unavailable due to maintenance. We appreciate your patience and understanding.
An Epoxidation of Alkenes using H2O2 (aq.) and 2,2,2-Trifluoroacetophenone
Limnios and Kokotos have reported the environmentally friendly epoxidation of alkenes using 2,2,2-trifluoroacetophenone as an organocatalyst in combination with a green oxidant aqueous H2O2. Various olefins are epoxidized chemoselectively in high to quantitative yields utilizing 2-5 mol% of the organocatalyst loading in acetonitrile and tert-butyl alcohol.
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.