%0 Generic
%A Yang, Luo
%A Lei, Chuan-Hu
%A Wang, De-Xian
%A Huang, Zhi-Tang
%A Wang, Mei-Xiang
%D 2010
%T Highly Efficient and Expedient Synthesis of 5-Hydroxy-1H-pyrrol-2-(5H)-ones from FeCl3-Catalyzed Tandem Intramolecular Enaminic Addition of Tertiary Enamides to Ketones and 1,3-Hydroxy Rearrangement
%U 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
%R 10.1021/ol101607z.s002
%2 https://ndownloader.figshare.com/files/4412665
%K Efficient
%K enamide
%K Expedient Synthesis
%K Tandem
%K ketonic carbonyls
%K intramolecular enaminic addition reaction
%K Ketone
%K Rearrangement
%K FeCl 3
%K Catalyzed
%K Hydroxy
%K Enaminic
%K yield
%K Tertiary Enamides
%K Intramolecular
%K rearrangement
%K hydroxy
%X Catalyzed by FeCl3 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-1H-pyrrol-2(5H)-ones in excellent yields.
%I ACS Publications