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oai: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

2024-02-06T13:16:37Z urn:hdl:10259/8607 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. 2024-02-06T13:16:37Z 2024-02-06T13:16:37Z 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