1-heteroaryl-pyrazoles : Stabilization of the 5-hydroxy tautomeric form by an α-nitrogen atom and effect on spectral properties
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference7 articles.
1. LXXIII.—Derivatives of 2-pyridylhydrazine and 2-quinolylhydrazine
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4. A study of pyrazolin-5-one tautomerism—I
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1. Synthesis, crystal structure, computational study of 1-(6-chloro-pyridin-2-yl)-5-hydroxy-1H-pyrazole-3-carboxylic acid methyl ester and its 5-acetoxy analogs;Journal of Molecular Structure;2012-08
2. N-arylation of 3-alkoxypyrazoles, the case of the pyridines;Tetrahedron;2010-04
3. Tautomeric forms study of 1H-(2′-pyridyl)-3-methyl-5-hydroxypyrazole and 1H-(2′-pyridyl)-3-phenyl-5-hydroxypyrazole. Synthesis, structure, and cytotoxic activity of their complexes with palladium(II) ions;Journal of Enzyme Inhibition and Medicinal Chemistry;2009-11-16
4. IR-spectral study of photoinduced tautomerization in 1,3-diphenyl-pyrazol-5-one;Open Chemistry;2003-12-01
5. NMR spectroscopic investigations with ethyl 1-(hetero)aryl-5-hydroxy-1H-pyrazole-4-carboxylates;Journal of Heterocyclic Chemistry;1995-07
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