2026-07-18T21:25:27Zhttps://docta.ucm.es/rest/oai/requestoai:docta.ucm.es:20.500.14352/919332025-03-18T15:48:08Zcom_20.500.14352_14col_20.500.14352_15
2,3‐Diodocarbazoles by a domino iodocyclization/iodo‐translocation of (3‐iodoindolyl)butynols
Martín‐Mejías, Irene
Petcu, Sonia
Alonso Gómez, José Miguel
Aragoncillo Abanades, Cristina
Almendros Requena, Pedro
547
Carbazole
Cascade reactions
Cyclization
Iodine translocation
Metal-free
Química orgánica (Química)
2306 Química Orgánica
2306.10 Compuestos Heterocíclicos
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.
Ministerio de Ciencia e Innovación (España)
European Commission
Depto. de Química Orgánica
Fac. de Ciencias Químicas
TRUE
pub
2024-01-09T09:16:42Z
2024-01-09T09:16:42Z
2022
journal article
VoR
https://hdl.handle.net/20.500.14352/91933
1615-4150
10.1002/adsc.202200564
1615-4169
eng
(Project PGC2018-095025-B-I00)
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
open access
application/pdf
application/pdf
Wiley-VCH GmbH