A set of 3-alkylaminoacroleins (R1NHCHxCHCHxO, R1 \ alkyl) were studied by 13C and 1H NMR spectroscopy in solutions of di †erent solvents and, for the simplest representative of the series, 3methylaminoacrolein, at di †erent temperatures. The equilibrium solutions of these compounds consists of mixt
IR, 1H NMR and 13C NMR spectra of isomeric 1-aryl-4-methyl-3- and-5-pyrazolecarboxylic esters
✍ Scribed by Pál Sohár; Ödön Fehér; Endre Tihanyi
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 371 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The IR, ^1^H and ^13^C NMR spectra of six esters of 1‐aryl‐4‐methyl‐3‐ and 5‐pyrazolecarboxylic acids are reported. On the basis of their spectra the 3‐ or 5‐position of the substituent in such structural isomeric pairs can be established without recourse to the spectrum of the other member of the pair. The spectral data also give information on the conformation, which depends on the relative position and size of the hetero ring substituents.
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A series of 14 3-substituted 4-oxoquinolones with or without a substituent (methyl, ethyl) in position 1 were prepared. Literature and measured data were used to study the inÑuence of the substituent on the shifts of carbon atoms of these compounds, which are model compounds for antibacterial drugs
a See footnote d in Table 1. 'H and "C NMR Spectra of 4 4 - ## Substituted Chalcones KIKUKO HAYAMIZU (to whom correspondence should be addressed), MASARU YANAGISAWA, TETSUKO ISHII,
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