1-Aryl-4-carboxy-5-methyl-1,2,3-triazoles were prepared by the condensation of aryl azides with ethyl acetoacetate. The structures of these compounds were characterized by MS, IR and 1H and 13C NMR spectroscopy. The measured and calculated 13C chemical shifts of the aromatic carbons were compared.
1H and 13C NMR study of novel fused 1,2,4-triazole heterocycles
✍ Scribed by Zoltán Szabó; Ferenc Kóródi; Gyula Batta
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 449 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^1^H and ^13^C NMR spectra of some novel 1,2,4‐triazolo [1,3] thiazinoquinoline isomeric pairs are interpreted in terms of structural assignments. The structure of most compounds has been confirmed by NOE difference spectroscopy. Characteristic differences have been observed in both ^1^H and ^13^C NMR spectra of these isomeric Pairs: some of the ^1^H and ^13^C chemical shifts, and also the one bond ^13^C^1^H couplings of triazole protons, differ consistently in the NMR spectra of the isomers. The coupling constants have been determined using a combination of INEPT and chemical shift selective filtering.
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