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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1995-10-25
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pubmed:abstractText |
The kinetics of enolization and degradation of N-(5-methyl-4-isoxazolyl)-4-amino-1,2-naphthoquinone (1) was investigated in aqueous solutions over a pH range of 7.30 to 12.25, at 35 degrees C and at constant ionic strength (mu = 0.5) using reversed-phase HPLC. Pseudo-first-order kinetics was observed throughout the pH range studied. The rate of enolization (ke), the keto-enol equilibrium constant (Kt), and specific base catalysis rate constant (kCH) were determined. Good agreement between the theoretical pH-rate profile and the experimental data supports the proposed transformation process. The average recovery for 1 and its tautomerization product 2-hydroxy-N-(5-methyl-4-isoxazolyl)-1,4-naphthoquinone 4-imine (2) from mixtures of different composition was evaluated.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0022-3549
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
84
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
783-5
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7562423-Buffers,
pubmed-meshheading:7562423-Chromatography, High Pressure Liquid,
pubmed-meshheading:7562423-Hydrogen-Ion Concentration,
pubmed-meshheading:7562423-Isomerism,
pubmed-meshheading:7562423-Isoxazoles,
pubmed-meshheading:7562423-Kinetics,
pubmed-meshheading:7562423-Naphthoquinones,
pubmed-meshheading:7562423-Solutions,
pubmed-meshheading:7562423-Spectrophotometry, Ultraviolet
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pubmed:year |
1995
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pubmed:articleTitle |
Isoxazoles. 10. Degradation and enolization kinetics of 4-aminoisoxazolyl-1,2-naphthoquinone in basic aqueous solution.
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pubmed:affiliation |
Departamento de Farmacia, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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