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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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| Pubblicato in: | Molecules |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6680591/ https://ncbi.nlm.nih.gov/pubmed/31330976 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/molecules24142632 |
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