Grison Claude, Joliez Stéphane, De Clercq E, Coutrot Philippe
Laboratoire de Chimie Biomoléculaire, UMR CNRS 7565, Institut Nancéien de Chimie Moléculaire, Université Henri Poincaré, Nancy 1, BP 239, F-54506 Vandoeuvre-lès-Nancy, France.
Carbohydr Res. 2006 Jul 3;341(9):1117-29. doi: 10.1016/j.carres.2006.03.023. Epub 2006 Apr 18.
A direct and general access to D-glycosyl 3-, 5-, or 6-methylenediphosphonates, di-D-glycosyl 1,5-, 3,5-, 3,6-, 5,5-, or 6,6-methylenediphosphonates and dithymidine 3',5'-methylenediphosphonate is described. The method involves the one-pot alkylidenediphosphorylation of glycosyl or thymidine derivatives. No antiviral activity was detected against a panel of RNA and DNA viruses.
描述了一种直接且通用的方法来制备D-糖基3-、5-或6-亚甲基二膦酸酯、二-D-糖基1,5-、3,5-、3,6-、5,5-或6,6-亚甲基二膦酸酯以及二胸苷3',5'-亚甲基二膦酸酯。该方法涉及糖基或胸苷衍生物的一锅法亚烷基二磷酸化反应。针对一组RNA和DNA病毒未检测到抗病毒活性。