1289376-75-5Relevant academic research and scientific papers
Chemoselective staudinger strategy in the practical, fit for purpose, gram-scale synthesis of an HCV RNA polymerase inhibitor
Campeau, Louis-Charles,O'Shea, Paul D.
scheme or table, p. 57 - 60 (2011/02/25)
The use of a late-stage selective Staudinger reaction in the preparation of the novel HCV RNA polymerase inhibitor is described. Georg Thieme Verlag Stuttgart - New York.
Synthesis and anti-HIV-1 activity of 4-substituted-7-(2′-deoxy- 2′-fluoro-4′-azido-β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidine analogues
Guo, Xiaohe,Li, Yujiang,Tao, Le,Wang, Qiang,Wang, Shuyang,Hu, Weidong,Pan, Zhenliang,Yang, Qinghua,Cui, Yanmei,Ge, Zhaopeng,Dong, Lihong,Yu, Xuejun,An, Haoyun,Song, Chuanjun,Chang, Junbiao
, p. 6770 - 6772 (2011/12/21)
Three novel 4-subsituted-7-(2′-deoxy-2′-fluoro-4′-azido- β-d-ribofuranosyl)pyrrolo[2,3-d]pyrimidine analogues were designed, synthesized, and tested for their anti-HIV-1 activity. Initial biological studies indicated that among these pyrrolo[2,3-d]pyrimid
