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.