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http://hdl.handle.net/10261/209781
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Title: | Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: Controlled access to functionalized quinones |
Authors: | Herrera, Fernando; Luna, Amparo; Fernández, I.; Almendros, Pedro ![]() |
Issue Date: | 2020 |
Publisher: | Royal Society of Chemistry (UK) |
Citation: | Chemical Communications 56(8): 1290-1293 (2020) |
Abstract: | The controlled synthesis of 1,4-naphthoquinones and tetraphene-7,12-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]naphthalen-4(2H)-ones. |
Publisher version (URL): | http://dx.doi.org/10.1039/c9cc08628e |
URI: | http://hdl.handle.net/10261/209781 |
DOI: | 10.1039/c9cc08628e |
ISSN: | 1359-7345 |
E-ISSN: | 1364-548X |
Appears in Collections: | (IQOG) Artículos |
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