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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

00925njm 22002777a 4500 dc Gómez Ayuso, Javier author Lezcano, Mario author Carreira Barral, Israel author González Saiz, Beatriz author Quesada Pato, Roberto author García Valverde, María author 2023-08 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. 1615-4150 http://hdl.handle.net/10259/8607 10.1002/adsc.202300662 1615-4169 Multicomponent reactions Radical reactions Copper Lactams Post-Ugi reactions Synthesis of Tetrahydronaphthoazetidinones, 2,5‐Dioxo‐1,4‐methanobenzoazepines and 3‐Hydroxypyrrolidinones Through Copper‐Assisted Post‐Ugi Reactions