## Abstract The ^13^C n.m.r. spectrum of benzofuroxan at −15°C is assigned on the basis of selective decoupling experiments and by comparison with the ^13^C chemical shifts of model compounds. The ^13^C spectra were also measured in trifluoroacetic acid as a solvent. From the temperature dependence
13C NMR spectra of wyosine, a hypermodified nucleoside of transfer RNAs, and related compounds
✍ Scribed by Bożenna Golankiewicz; Wojciech Folkman
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 509 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Complete
I3C NMR spectral assignments were made for wyosine, 4,9-dihydro-4,6-dimethyl-9-0~0-3-(p-~ribofuranosyl)imidazo[l,2-~]purine, a hpermodified, fluorescent nucleoside of transfer RNAs, and its isomers methylated at N-5 and at N-1. The influence of the position of N-methylation on the -C chemical shifts of the tricyclic nucleoside is discussed. In relation to the parent N-unsubstituted compound, the most pronounced changes of chemical sbifts appear in wyosbe. Chemical sbfi data for tbe sugar moiety suggest that the population of the anti conformer in wyosine is higher than in the other tricyclic nucleosides.
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