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Protonation effects on the chemical shifts of Schiff bases derived from 3-hydroxypyridin-4-carboxaldehyde

AuthorsSanz, D.; Perona, Almudena ; Claramunt, Rosa M.; Pinilla, Elena; Torres, M. R.; Elguero, José
Issue Date2010
PublisherArkat USA
CitationARKIVOC 2010: 102- 113 (2010)
AbstractThe behavior of Schiff bases derived from 3-hydroxypyridin-4-carboxaldehyde and two N-aminoheterocycles in acid media is described. 1H, 13C, 15N NMR chemical shifts establish the different protonation sites and their influence on the hydroxyimino/oxoenamino tautomerism.
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