English
español
Please use this identifier to cite or link to this item:
http://hdl.handle.net/10261/209781Share/Impact:
| Statistics |
 SHARE
 CORE
 MendeleyBASE
|
|
|
| Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |||
|
|
| 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 |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| ChemComm.pdf | 1,78 MB | Adobe PDF |  View/Open |
Show full item record
Review this work
Review this work
Related articles:
WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.