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| Title: | Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: Controlled access to functionalized quinones |
| Authors: | Herrera, F.; Luna, A.; Fernández, I.; Almendros, Pedro  |
| Issue Date: | 2020 |
| Publisher: | Royal Society of Chemistry (UK) |
| Citation: | Chemical Communications 56: 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 |
| Identifiers: | doi: 10.1039/c9cc08628e issn: 1359-7345 issn: 1364-548X |
| Appears in Collections: | (IQOG) Artículos |
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| ChemComm.pdf | 1,78 MB | Adobe PDF |  View/Open |
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