论文信息 - Design and Synthesis of 2′,3′‐Dideoxy‐2′,3′‐didehydro‐β‐L‐ cytidine (β‐L‐d4C) and 2′,3′‐Dideoxy‐2′,3′‐didehydro‐β‐L‐5‐ fluorocytidine (β‐L‐Fd4C), Two Exceptionally Potent Inhibitors of Human Hepatitis B Virus (HBV) and Potent Inhibitors of Human Immunodeficiency Virus (HIV) in vitro. - 字舞流文

Design and Synthesis of 2′,3′‐Dideoxy‐2′,3′‐didehydro‐β‐L‐ cytidine (β‐L‐d4C) and 2′,3′‐Dideoxy‐2′,3′‐didehydro‐β‐L‐5‐ fluorocytidine (β‐L‐Fd4C), Two Exceptionally Potent Inhibitors of Human Hepatitis B Virus (HBV) and Potent Inhibitors of Human Immunodeficiency Virus (HIV) in vitro.

E. Gullen | G. Dutschman | M. Luo | Mao Liu | Yung‐chi Cheng | T. Lin | Yan Zhu

[1] E. Gullen,et al. Design and Synthesis of 2‘,3‘-Dideoxy- 2‘,3‘-didehydro-β-l-cytidine (β-l-d4C) and 2‘,3‘-Dideoxy-2‘,3‘-didehydro-β-l-5- fluorocytidine (β-l-Fd4C), Two Exceptionally Potent Inhibitors of Human Hepatitis B Virus (HBV) and Potent Inhibitors of Human Immunodeficiency Virus (HIV) in Vitro , 1996 .