I. Vrijens scite author profile

The total synthesis of 3-chloro-4-(D-ribofuranosyl)-pyridine and 3-(D-ribofuranosyl)-2-pyridone was elaborated using the appropriate lithiopyridines and 2,4:3,5-di-O-benzylidene-aldehydo-D-nbose. The conformation of these compounds was investigated by 360 h4Hz IH-NMR. The compounds were evaluated as a$-mixtures for their antiviral and cytostatic properties. However, no significant biological activity was found.

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I. Vrijens

Synthests and Biological Evaluation of a Series of Substituted-2-Pyridine-C-Nucleosides. Part II

Analysis of Substituted Pyridine-C-Nucleosides by Direct Liquid Introduction Liquid Chromatography/Mass Spectrometry

Synthesis and Biological Evaluation of 2-Carbamoyl-5-D-Ribofuranosylpyridine

Synthesis and Biological Evaluation of 3-Chloro-4-(D-Ribofuranosyl)-Pyridine and 3-(D-Ribofuranosyl)-2- Pyridone

Synthesis and Biological Evaluation of a Series of Substituted Pyridine-C-Nucleosides. Part V: 3-Chloro-4-(D-Ribofuranosyl)Pyridine and 3-(D-Ribofuranosyl)-2-Pyridone

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