10.1021/ol101607z.s002 Luo Yang Luo Yang Chuan-Hu Lei Chuan-Hu Lei De-Xian Wang De-Xian Wang Zhi-Tang Huang Zhi-Tang Huang Mei-Xiang Wang Mei-Xiang Wang Highly Efficient and Expedient Synthesis of 5-Hydroxy-1<i>H</i>-pyrrol-2-(5<i>H</i>)-ones from FeCl<sub>3</sub>-Catalyzed Tandem Intramolecular Enaminic Addition of Tertiary Enamides to Ketones and 1,3-Hydroxy Rearrangement American Chemical Society 2010 Efficient enamide Expedient Synthesis Tandem ketonic carbonyls intramolecular enaminic addition reaction Ketone Rearrangement FeCl 3 Catalyzed Hydroxy Enaminic yield Tertiary Enamides Intramolecular rearrangement hydroxy 2010-09-03 00:00:00 Dataset https://acs.figshare.com/articles/dataset/Highly_Efficient_and_Expedient_Synthesis_of_5_Hydroxy_1_i_H_i_pyrrol_2_5_i_H_i_ones_from_FeCl_sub_3_sub_Catalyzed_Tandem_Intramolecular_Enaminic_Addition_of_Tertiary_Enamides_to_Ketones_and_1_3_Hydroxy_Rearrangement/2735926 Catalyzed by FeCl<sub>3</sub> under very mild conditions, tertiary enamides underwent a highly efficient intramolecular enaminic addition reaction to the ketonic carbonyls followed by 1,3-hydroxy rearrangement to produce 5-hydroxy-1<i>H</i>-pyrrol-2(5<i>H</i>)-ones in excellent yields.