Novel (E)- and (Z)-3(5)-(2-hydroxyphenyl)-4-styrylpyrazoles from (E)- and (Z)-3-styrylchromones: the unexpected case of (E)-3(5)-(2-hydroxyphenyl)-4-(4-nitrostyryl)pyrazoles |
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Authors: | Vera L.M. Silva,Diana C.G.A. Pinto,José Elguero |
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Affiliation: | a Department of Chemistry, University of Aveiro, 3810-193 Aveiro, Portugal b Instituto de Química Médica, Juan de la Cierva, 3, E-28006 Madrid, Spain |
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Abstract: | An efficient synthetic method for the preparation of (E)- and (Z)-3(5)-(2-hydroxyphenyl)-4-styrylpyrazoles has been developed. The reaction of (E)- and (Z)-3-styrylchromones with hydrazine hydrate afforded the corresponding (E)- and (Z)-4-styrylpyrazoles, respectively, saved 4′-nitro-derivatives where both (E)- and (Z)-4′-nitro-3-styrylchromones afforded (E)-3(5)-(2-hydroxyphenyl)-4-(4-nitrostyryl)pyrazoles. The reaction mechanism for these transformations was discussed and the stereochemistry of all products was assigned by NMR experiments. |
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Keywords: | 3-Styrylchromones 3(5)-(2-Hydroxyphenyl)-4-styrylpyrazoles NMR Nitrogen heterocycles Reaction mechanism |
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