The complete assignments of the 13C NMR resonances of N-(alkanoyl)-and N-(3-oxoalkanoyl)-S-homoserine lactone are reported. These assignments were made by comparison with values for N-butanoyl-S-homoserine lactone, a model compound whose structure was comprehensively established by a combination of
NMR study of C- and N-trimethylsilylazole derivatives
✍ Scribed by Lyudmila I. Larina; Mikhail S. Sorokin; Aleksandr I. Albanov; Valentina N. Elokhina; Nadezhda I. Protsuk; Valentin A. Lopyrev
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 223 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
C-and N-trimethylsilylazole derivatives were studied by 1H, 13C and 29Si NMR spectroscopy. Degenerated prototropic tautomerism of 4-trimethylsilylpyrazole in methanol and the silylotropy of 1trimethylsilyl-4-methylpyrazole in a neat liquid were investigated for the Ðrst time. 3-and 5-tautomers of 3(5)methylpyrazole in a ratio of 54 : 46 were found in methanol by use 13C NMR spectroscopy K, (T c \
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