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NMR studies of novel Schiff bases derived from L-α-amino methyl esters and 3-hydroxypyridin-4-carboxaldehyde

AuthorsPerona, Almudena ; Sanz, D.; Claramunt, Rosa M.; Elguero, José
Issue Date2008
PublisherJohn Wiley & Sons
CitationMagnetic Resonance in Chemistry 46: 930- 938 (2008)
AbstractSchiff bases of 3-hydroxypyridin-4-carboxaldehyde and L-α-amino esters as well as those derived from the structurally related amines lacking the ester function have been synthesised. In two cases a tetrahydro-1H-imidazo[4,5- c]pyridine was formed as a by-product. 1H, 13C, 15N-NMR spectral data and density functional theory (DFT) calculations established the structure of all compounds. Copyright © 2008 John Wiley & Sons, Ltd.
Publisher version (URL)http://dx.doi.org/10.1002/mrc.2278
Identifiersdoi: 10.1002/mrc.2278
issn: 0749-1581
e-issn: 1097-458X
Appears in Collections:(IQM) Artículos
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