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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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