2026-06-17T15:56:08Zhttps://riubu.ubu.es/oai/request

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

Gómez Ayuso, Javier Lezcano, Mario Carreira Barral, Israel González Saiz, Beatriz Quesada Pato, Roberto García Valverde, María 2024-02-06T13:16:37Z 2024-02-06T13:16:37Z 2023-08 1615-4150 http://hdl.handle.net/10259/8607 10.1002/adsc.202300662 1615-4169 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. eng http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess Attribution-NonCommercial-NoDerivatives 4.0 Internacional 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 info:eu-repo/semantics/article