A Novel Tandem Sequence to Pyrrole Syntheses by 5-<i>endo</i>-<i>dig</i> Cyclization of 1,3-Enynes with Amines Ganesan Bharathiraja Sekarpandi Sakthivel Mani Sengoden Tharmalingam Punniyamurthy 10.1021/ol402305b.s002 https://acs.figshare.com/articles/dataset/A_Novel_Tandem_Sequence_to_Pyrrole_Syntheses_by_5_i_endo_i_i_dig_i_Cyclization_of_1_3_Enynes_with_Amines/2370325 The synthesis of pentasubstituted pyrroles has been described using molecular iodine from 1,3-enynes and amines via a sequential tandem aza-Michael addition, iodocyclization, and oxidative aromatization. The protocol is simple and efficient to afford the target products at ambient conditions. 2016-02-18 18:12:44 Enyne pentasubstituted pyrroles iodine Cyclization oxidative aromatization AminesThe synthesis enyne sequential Novel Tandem Sequence amines iodocyclization tandem ambient conditions Pyrrole Syntheses target products