English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/63731
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:


Prototropic tautomerism of 5-aryloxy-1(2)H-tetrazoles

AuthorsAlkorta, Ibon ; Elguero, José
Issue Date2012
PublisherJohn Wiley & Sons
CitationMagnetic Resonance in Chemistry 50: 193- 195 (2012)
AbstractThe structure of 5-(2,6-dimethylphenoxy)-1H- and 2H-tetrazoles together with those of 5-(2,6-diisopropyl-phenoxy)-1H and 2H-tetrazoles have been theoretically studied including absolute shieldings and energies. The conclusion of these studies is that a slow tautomerism between 1H- and 2H-tetrazoles cannot explain the experimental observations reported recently in the literature. Copyright © 2012 John Wiley & Sons, Ltd.
Publisher version (URL)http://dx.doi.org/10.1002/mrc.2866
Identifiersdoi: 10.1002/mrc.2866
issn: 0749-1581
e-issn: 1097-458X
Appears in Collections:(IQM) 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.