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13 C NMR spectra of wyosine, a hypermodified nucleoside of transfer RNAs, and related compounds
Ist Teil von
Magnetic resonance in chemistry, 1985-11, Vol.23 (11), p.920-924
Erscheinungsjahr
1985
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Abstract
Complete
13
C NMR spectral assignments were made for wyosine, 4,9‐dihydro‐4,6‐dimethyl‐9‐oxo‐3‐(β‐D‐ribofuranosyl)imidazo [1,2‐
a
]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
13
C chemical shifts of the tricyclic nucleoside is discussed. In relation to the parent
N
‐unsubstituted compound, the most pronounced changes of chemical shifts appear in wyosime. Chemical shift data for the sugar moiety suggest that the population of the
anti
conformer in wyosine is higher than in the other tricyclic nucleosides.