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
- DOI
- 10.1002/mrc.2278
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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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