10.1021/ol402305b.s002 Ganesan Bharathiraja Ganesan Bharathiraja Sekarpandi Sakthivel Sekarpandi Sakthivel Mani Sengoden Mani Sengoden Tharmalingam Punniyamurthy Tharmalingam Punniyamurthy A Novel Tandem Sequence to Pyrrole Syntheses by 5-<i>endo</i>-<i>dig</i> Cyclization of 1,3-Enynes with Amines American Chemical Society 2016 Enyne pentasubstituted pyrroles iodine Cyclization oxidative aromatization AminesThe synthesis enyne sequential Novel Tandem Sequence amines iodocyclization tandem ambient conditions Pyrrole Syntheses target products 2016-02-18 18:12:44 Dataset 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.