2026-07-19T20:42:52Zhttps://docta.ucm.es/rest/oai/request

oai:docta.ucm.es:20.500.14352/919332025-03-18T15:48:08Zcom_20.500.14352_14col_20.500.14352_15

Martín‐Mejías, Irene Petcu, Sonia Alonso Gómez, José Miguel Aragoncillo Abanades, Cristina Almendros Requena, Pedro 2024-01-09T09:16:42Z 2024-01-09T09:16:42Z 2022 Martín-Mejías I, Petcu AS, Alonso JM, Aragoncillo C, Almendros P. 2,3-Diodocarbazoles by a Domino Iodocyclization/Iodo-Translocation of (3-Iodoindolyl)butynols. Adv. Synth. Catal. 2022 , 364, 3954-3959 1615-4150 10.1002/adsc.202200564 https://hdl.handle.net/20.500.14352/91933 1615-4169 https://doi.org/10.1002/adsc.202200564 A controlled access to 1‐aryl 2,3‐diiodo‐carbazoles involving iodine transposition has been accomplished directly from acyclic precursors. The 2,3‐diiodo‐carbazole core was prone to further chemoselective decoration at C3−I or double difunctionalization. eng open access 2,3‐Diodocarbazoles by a domino iodocyclization/iodo‐translocation of (3‐iodoindolyl)butynols journal article