English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/132578
Share/Impact:
Statistics
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:

Title

A microwave-assisted domino rearrangement of propargyl vinyl ethers to multifunctionalized aromatic platforms

AuthorsTejedor, David ; Méndez-Abt, Gabriela ; Cotos, Leandro ; Ramírez, Miguel A.; García-Tellado, Fernando
Issue Date15-Feb-2011
PublisherJohn Wiley & Sons
CitationChemistry - A European Journal 17: 3318-3321 (2011)
AbstractH makes a difference! A novel reactivity profile of propargyl vinyl ethers has been developed, which is controlled by the presence of a hydrogen atom at the homopropargylic position (see scheme; EWG=electron-withdrawing group). This strategy was conveniently used to construct multifunctionalized phenolic platforms, including salicylaldehydes and the corresponding ketone derivatives. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publisher version (URL)http://dx.doi.org/10.1002/chem.201003532
URIhttp://hdl.handle.net/10261/132578
DOI10.1002/chem.201003532
Identifiersissn: 0947-6539
e-issn: 1521-3765
Appears in Collections:(IPNA) Artículos
Files in This Item:
File Description SizeFormat 
Microwave-Assisted_Domino_Rearrangement-Garcia_Tellado.pdf533,63 kBAdobe PDFThumbnail
View/Open
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.