TY  - JOUR
AU  - Martín‐Mejías, Irene
AU  - Petcu, Sonia
AU  - Alonso Gómez, José Miguel
AU  - Aragoncillo Abanades, Cristina
AU  - Almendros Requena, Pedro
PY  - 2022
DO  - 10.1002/adsc.202200564
SN  - 1615-4150
UR  - https://hdl.handle.net/20.500.14352/91933
T2  - Advance Synthesis & Catalysis
AB  - 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.
LA  - eng
M2  - 3954
PB  - Wiley-VCH GmbH
KW  - Carbazole
KW  - Cascade reactions
KW  - Cyclization
KW  - Iodine translocation
KW  - Metal-free
TI  - 2,3‐Diodocarbazoles by a domino iodocyclization/iodo‐translocation of (3‐iodoindolyl)butynols
TY  - journal article
VL  - 364
ER  -