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</script>doi: 10.1039/j39710002440
pmid: 5166603
A new route for the preparation of 4-amino-1-(β-D-ribofuranosyl)pyrazolo[3,4-d]pyrimidine (5)(6-azatubercidin) is described. The anomeric configuration of the product has been established unequivocally for the first time by cyclonucleoside formation, and agrees with previously reported anomeric assignments.
Magnetic Resonance Spectroscopy, Pyrimidines, Ultraviolet Rays, Spectrum Analysis, Nucleosides, Pyrroles, Anti-Bacterial Agents
Magnetic Resonance Spectroscopy, Pyrimidines, Ultraviolet Rays, Spectrum Analysis, Nucleosides, Pyrroles, Anti-Bacterial Agents
| citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 8 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
