English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/183874
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:


Synthesis of α-Quaternized 2,4-Cyclohexadienones from Propargyl Vinyl Ethers

AuthorsTejedor, David ; Delgado-Hernández, Samuel; Ingold, Mariana; García-Tellado, Fernando
Issue Date6-Oct-2016
PublisherAmerican Chemical Society
CitationJournal of Organic Chemistry 81(20): 10099-10105 (2016)
AbstractA microwave-assisted and base-catalyzed domino manifold to construct 2,4-cyclohexadienone derivatives has been implemented. The domino manifold uses easily accessible tertiary propargyl vinyl ethers bearing a methine group at the homopropargylic position and imidazole as the catalyst to deliver 2,4-cyclohexadienones featuring a key formyl group and a quaternized carbon atom in good yields.
Publisher version (URL)https://doi.org/10.1021/acs.joc.6b02137
Appears in Collections:(IPNA) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
Show full item record
Review this work

Related articles:

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