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A<sup>1</sup>H and<sup>13</sup>C nuclear magnetic resonance and X-ray diffraction study of the tautomerism of 2-hydroxy- and 2,3-dihydroxy-pyridine N-oxides. X-Ray molecular structure of 2-hydroxypyridine N-oxide
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1990
Year
Inorganic Chemistry2-Oxo TautomersEngineeringBiochemistryAldehyde DehydrogenaseNatural SciencesDimethyl SulphoxideMolecular BiologyX-ray Diffraction MethodsStructure ElucidationOrganic ChemistryX-ray Diffraction StudyChemistryX-ray Molecular StructureCrystallographyStructural Biology2,3-Dihydroxy-pyridine N-oxides
From a 1H and 13C NMR study, in dimethyl sulphoxide, of twelve 2-hydroxy-, 2,3-dihydroxy-pyridines, 2,3-dihydroxypyridine N-oxides, and their methoxy derivatives it is possible to conclude that both pyridin-2-ones and 1-hydroxypyridine-2-ones exist in solution as 2-oxo tautomers. The molecular structure of 2-hydroxypyridine N-oxide has been determined by X-ray diffraction methods; as in solution, this compound exists in the crystal state as the 1-hydroxypyridin-2-one tautomer.
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