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

✍ Scribed by Almudena Perona; Dionisia Sanz; Rosa M. Claramunt; José Elguero


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
237 KB
Volume
46
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

Schiff 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‐1__H__‐imidazo[4,5‐c]pyridine was formed as a by‐product. ^1^H, ^13^C, ^15^N‐NMR spectral data and density functional theory (DFT) calculations established the structure of all compounds. Copyright © 2008 John Wiley & Sons, Ltd.


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