English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/209781
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:


Transition metal-free cyclobutene rearrangement in fused naphthalen-1-ones: Controlled access to functionalized quinones

AuthorsHerrera, F.; Luna, A.; Fernández, I.; Almendros, Pedro
Issue Date2020
PublisherRoyal Society of Chemistry (UK)
CitationChemical Communications 56: 1290-1293 (2020)
AbstractThe 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
Identifiersdoi: 10.1039/c9cc08628e
issn: 1359-7345
issn: 1364-548X
Appears in Collections:(IQOG) Artículos
Files in This Item:
File Description SizeFormat 
ChemComm.pdf1,78 MBAdobe PDFThumbnail
Show full item record
Review this work

WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.