Synthesis of nucleoside analogs and new Tat protein inhibitors

被引:4
作者
Ané, A
Prestat, G
Manh, GT
Thiam, M
Josse, S
Pipelier, M
Lebreton, J
Pradère, JP
Dubreuil, D
机构
[1] Fac Sci & Tech, CNRS, UMR 6513, Synth Organ Lab, F-44322 Nantes 3, France
[2] Fac Sci & Tech, Chim Organ Struct Lab, Abidjan, Cote Ivoire
[3] Univ Cheikh Anta Diop, Fac Sci & Tech, Synth Organ Lab, Dakar, Senegal
关键词
D O I
10.1351/pac200173071189
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 the laboratory of Nantes.
引用
收藏
页码:1189 / 1196
页数:8
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