Lewis Acids Promoted 3 + 2 Cycloaddition of Oxaziridines and Cyclic Allylic Alcohols through Carbonyl Imine Intermediates Erbao Zhao Feilong Zhou Yujun Zhao 10.1021/acs.joc.9b00246.s002 https://acs.figshare.com/articles/dataset/Lewis_Acids_Promoted_3_2_Cycloaddition_of_Oxaziridines_and_Cyclic_Allylic_Alcohols_through_Carbonyl_Imine_Intermediates/7887467 Syntheses of isoxazolidines through the carbonyl imine intermediates are currently limited to monosubstituted olefin substrates. Herein, we reported syntheses of novel bicyclic isoxazolidine-containing compounds through 1,3-dipolar cycloaddition reactions using cyclic allylic alcohols as substrates, which proved challenging in previous reports. Generally, the reaction yields range from good to high, and the reaction substrates tolerate various functional groups, including the cyclopropyl and amine groups. Mechanistic studies suggest that an allylic cation and a carbonyl imine intermediate are involved and responsible for the observed stereochemistry and diastereoselectivity. 2019-03-14 00:00:00 carbonyl imine intermediates Carbonyl Imine Intermediates Syntheses reaction substrates 2 Cycloaddition Cyclic Allylic Alcohols monosubstituted olefin substrates Mechanistic studies cyclic allylic alcohols allylic cation carbonyl imine reaction yields range novel bicyclic isoxazolidine-containing compounds Lewis Acids Promoted 3 amine groups