Synthesis and stereochemical characterization of diastereomeric nucleoside-phosphorothioselenoates by NMR methods.

Abstract

Synthesis and stereochemical characterization of enantiomerically pure nucleoside-phosphorothioselenoates are reported. The effects of solvent and temperature on the vicinal carbon-phosphorus couplings are described and the results are interpreted in terms of conformational changes influenced by stacking interactions between the bases and the phenyl rings. 

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Cite this paper

@article{KajtrPeredy2001SynthesisAS, title={Synthesis and stereochemical characterization of diastereomeric nucleoside-phosphorothioselenoates by NMR methods.}, author={M{\'a}ria Kajt{\'a}r-Peredy and I T{\"{o}m{\"{o}sk{\"{o}zi and Eszter G{\'a}cs-Baitz}, journal={Nucleosides, nucleotides & nucleic acids}, year={2001}, volume={20 9}, pages={1615-23} }