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oai:docta.ucm.es:20.500.14352/1138152025-03-18T15:30:29Zcom_20.500.14352_14col_20.500.14352_15

Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones Luna Costales, Amparo Herrera García, Fernando Almendros Requena, Pedro Fernández López, Israel 547 quinone 1,4-naphthoquinones allenynols Química orgánica (Química) 2306 Química Orgánica 2306.10 Compuestos Heterocíclicos The controlled synthesis of 1,4-naphthoquinones and tetraphene7,12-diones, which bear the ABCD-ring of landomycins, has been accomplished directly through oxidative rearrangement of common stable precursors, namely, previously non-isolable cyclobuta[a]naphthalen4(2H)-ones. Ministerio de Ciencia e Innovación (España) European Commission Depto. de Química Orgánica Fac. de Ciencias Químicas TRUE pub 2025-01-10T18:57:47Z 2025-01-10T18:57:47Z 2019-12-19 journal article AM https://hdl.handle.net/20.500.14352/113815 1359-7345 10.1039/C9CC08628E 1364-548X eng PGC2018-095025-B-I00 CTQ2016-78205-P CTQ2016-81797-REDC Herrera Fernando, Luna Amparo, Fernández Israel, Almendros Pedro. Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: controlled access to functionalized quinones. Chem. Commun., 2020, 56 (8), 1290-1293 Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ open access application/pdf application/pdf Royal Society of Chemistry