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

Perona Almudena | Zendy; Sanz Dionisia | Zendy; Claramunt Rosa M. | Zendy; Elguero José | Zendy

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

Author(s) -

Perona Almudena,

Sanz Dionisia,

Claramunt Rosa M.,

Elguero José

Publication year - 2008

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.2278

Subject(s) - chemistry , pyridine , proton nmr , stereochemistry , schiff base , density functional theory , nuclear magnetic resonance spectroscopy , medicinal chemistry , computational chemistry

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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