Publication | Closed Access
Determination of the Anomeric Configuration of C-Nucleosides by<sup>1</sup>H and<sup>13</sup>C NMR Spectroscopy
53
Citations
64
References
1984
Year
Bioorganic ChemistryMagnetic ResonanceAnomeric ConfigurationChemistryChemical BiologySpectra-structure CorrelationDrug ResistanceNucleic Acid ChemistrySeveral DerivativesBiophysicsSolid-state Nmr SpectroscopyBiochemistryOligonucleotideFirst C-nucleoside PseudouridineFormycin B. OxoformycinNatural SciencesProtein NmrMicrobiologyMedicineNuclear Magnetic Resonance Spectroscopy
Abstract Since the discovery by Cohn in 1959 of the first C-nucleoside pseudouridine, an isolate from t-RNA hydrolysates, a number of biologically interesting C-nucleosides [formycin. formycin B. oxoformycin, oxazinomycin (minimycin), showdomycin, pyrazofurin, and several derivatives of pseudouridine] have been isolated from the culture filtrates of various micro-organisms, and their structures have been elucidated. Several review articles dealing with the chemistry and/or biology of C-nucleosides have appeared.
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