Synthesis of nucleoside analogs and new Tat protein inhibitors
@article{Ane2001SynthesisON, title={Synthesis of nucleoside analogs and new Tat protein inhibitors}, author={A. Ane and G. Prestat and G. T. Manh and M. Thiam and S. Josse and M. Pipelier and J. Lebreton and J. Prad{\`e}re and D. Dubreuil}, journal={Pure and Applied Chemistry}, year={2001}, volume={73}, pages={1189 - 1196} }
Two studies, concerning the synthesis of original nucleoside analogs regarded as an application of heterochemistry on thiaazaheterocycle systems from thiaazabutadienes are discussed. The preparation of new N- and C-nucleosides is presented. In the second part, the discovery of aromatic polycyclic derivatives as inhibitors of Tat protein is exposed. The work presented takes into account the participation of African partners in further synthetic research programs carried out in collaboration with… CONTINUE READING
6 Citations
A convenient tandem one-pot synthesis of donor-acceptor-type triphenylene 2,3-dicarboxylic esters from diarylacetylene.
- Chemistry, Medicine
- Organic & biomolecular chemistry
- 2014
- 11
- PDF
References
SHOWING 1-3 OF 3 REFERENCES
IUPAC, Pure and Applied Chemistry
- Acta 82,
- 1999
Imbach. Nucleosides Nucleotides
- Chem. Rev. 92,
- 1992