Annular Tautomerism of 3(5)-Disubstituted-1H-pyrazoles with Ester and Amide Groups

A series of disubstituted 1H-pyrazoles with methyl (1), amino (2), and nitro (3) groups, as well as ester (a) or amide (b) groups in positions 3 and 5 was synthesized, and annular tautomerism was investigated using X-ray, theoretical calculations, NMR, and FT-IR methods. The X-ray experiment in the...

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Detalles Bibliográficos
Autores principales: Kusakiewicz-Dawid, Anna, Porada, Monika, Dziuk, Błażej, Siodłak, Dawid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680591/
https://www.ncbi.nlm.nih.gov/pubmed/31330976
http://dx.doi.org/10.3390/molecules24142632

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6680591/
https://www.ncbi.nlm.nih.gov/pubmed/31330976
http://dx.doi.org/10.3390/molecules24142632

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