Abstract
Six 1(2)H-3-aryl-4-p-chlorophenyl-dihydropyrazolo[3,4-b]pyridin-6-ones have been prepared from the corresponding arylaminopyrazoles. The NMR study of these compounds reveals that all of them exist as 2H-tautomers in solution (DMSO-d6) as well and in the solid state.
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APA
Quiroga, J., Insuasty, B., Hormaza, A., Cabildo, P., Claramunt, R. M., & Elguero, J. (1999). Synthesis, molecular structure and tautomerism of 1(2)H-dihydropyrazolo[3,4-b]pyridin-6-ones. Heterocyclic Communications, 5(2), 115–122. https://doi.org/10.1515/HC.1999.5.2.115
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