2026-06-18T00:35:36Zhttps://riubu.ubu.es/oai/requestoai:riubu.ubu.es:10259/86072024-02-07T07:26:32Zcom_10259_3592com_10259_3591com_10259.4_106com_10259_2604com_10259_3924com_10259_5086col_10259_3930col_10259_3925
Synthesis of Tetrahydronaphthoazetidinones, 2,5‐Dioxo‐1,4‐methanobenzoazepines and 3‐Hydroxypyrrolidinones Through Copper‐Assisted Post‐Ugi Reactions
Gómez Ayuso, Javier
Lezcano, Mario
Carreira Barral, Israel
González Saiz, Beatriz
Quesada Pato, Roberto
García Valverde, María
Multicomponent reactions
Radical reactions
Copper
Lactams
Post-Ugi reactions
Copper-assisted post-Ugi reactions enable access to different heterocyclic systems, tetrahydronaphthoazetidinone, 2,5-dioxo-1,4-methanobenzoazepine and 3-hydroxypyrrolidinone derivatives. The described process affords complex scaffolds from readily available acyclic precursors using simple protocols.
2024-02-06
2024-02-06
2023-08
info:eu-repo/semantics/article
1615-4150
http://hdl.handle.net/10259/8607
10.1002/adsc.202300662
1615-4169
eng
Advanced Synthesis & Catalysis. 2023, V. 365, n. 21, p. 3658-3665
https://doi.org/10.1002/adsc.202300662
http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Wiley