English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/81524
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 convenient and efficient synthesis of the first (nitroimidazolyl)succinic esters and their diacids

AuthorsPacheco-Torres, Jesús; Pérez-Mayoral, Elena; Soriano, Elena ; López-Larrubia, Pilar ; Ouari, Olivier; Cerdán, Sebastián ; Ballesteros, Paloma
Issue Date2006
PublisherThieme
CitationSynthesis 22: 3859-3864 (2006)
AbstractWe report an easy and efficient synthetic approach to the first series of (nitroimidazolyl)succinic esters and diacids involving the Michael-type addition of the nitroimidazole to the α,β-unsaturated ester. Voltammetric measurements revealed similar redox potentials to those of previous nitroimidazoles used in hypoxia detection. Theoretical calculations were implemented to understand the mechanism of the addition. © Georg Thieme Verlag Stuttgart.
URIhttp://hdl.handle.net/10261/81524
DOI10.1055/s-2006-950320
Identifiersdoi: 10.1055/s-2006-950320
issn: 0039-7881
e-issn: 1437-210X
Appears in Collections:(IIBM) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 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.