G. Luoni

Application of the phosphoramidate ProTide approach to 4'-azidouridine confers sub-micromolar potency versus hepatitis C virus on an inactive nucleoside.

C. Mcguigan, S. Le Pogam, K. Klumpp, 2007, Journal of medicinal chemistry.

The application of phosphoramidate ProTide technology to the potent anti-HCV compound 4'-azidocytidine (R1479).

C. Mcguigan, S. Le Pogam, K. Klumpp, 2009, Bioorganic & medicinal chemistry letters.

Furano Pyrimidines as Novel Potent and Selective Anti-VZV Agents

E. De Clercq, A. Brancale, O. Bidet, 2001, Antiviral chemistry & chemotherapy.

Bicyclic Nucleoside Inhibitors of Varicella-Zoster Virus Modified on the Sugar Moiety: 3′ and 5′ Derivatives

E. De Clercq, J. Balzarini, C. Mcguigan, 2004, Antiviral chemistry & chemotherapy.

Preclinical development of bicyclic nucleoside analogues as potent and selective inhibitors of varicella zoster virus.

L. Naesens, A. Jones, E. Verbeken, 2007, The Journal of antimicrobial chemotherapy.

Bicyclic nucleoside inhibitors of Varicella-Zoster virus: the effect of branching in the p-alkylphenyl side chain.

E. De Clercq, J. Balzarini, C. Mcguigan, 2002, Bioorganic & medicinal chemistry letters.