522607-76-7Relevant academic research and scientific papers
Mild, fast, and stereoselective epoxide opening by ketone enolate anions. Application to synthesis of the norlignan curculigine
Posner, Gary H.,Maxwell, John P.,Kahraman, Mehmet
, p. 3049 - 3054 (2007/10/03)
We report here that (1) enolate anions of five- to seven-membered cycloalkanones nucleophilically open cyclopentene and cyclohexene oxides in 57-76% yields and with 4-8:1 diastereoselectivity; (2) enolate anions formed regiospecifically via kinetic deprot
