Norbornane-based nucleoside and nucleotide analogues locked in North conformation.

[1]  B. Różycki,et al.  The crystal structure of the phosphatidylinositol 4‐kinase IIα , 2014, EMBO reports.

[2]  J. Neyts,et al.  Synthesis of Novel Purine‐Based Coxsackievirus Inhibitors Bearing Polycylic Substituents at the N‐9 Position , 2014, Archiv der Pharmazie.

[3]  J. Neyts,et al.  From norbornane-based nucleotide analogs locked in South conformation to novel inhibitors of feline herpes virus. , 2014, Bioorganic & medicinal chemistry.

[4]  S. Schneller,et al.  3-Bromo-3-deazaneplanocin and 3-bromo-3-deazaaristeromycin: synthesis and antiviral activity. , 2012, Bioorganic & medicinal chemistry letters.

[5]  M. Dračínský,et al.  One-pot build-up procedure for the synthesis of variously substituted purine derivatives , 2012 .

[6]  J. Neyts,et al.  Synthesis of novel thienonorbornylpurine derivatives , 2012 .

[7]  J. Neyts,et al.  Novel substituted 9-norbornylpurines and their activities against RNA viruses. , 2012, Bioorganic & medicinal chemistry letters.

[8]  L. Legnani,et al.  Synthesis of novel anthracene derivatives of isoxazolino-carbocyclic nucleoside analogues , 2012 .

[9]  Wonsuk Chang,et al.  Nucleoside, nucleotide, and non-nucleoside inhibitors of hepatitis C virus NS5B RNA-dependent RNA-polymerase. , 2012, Journal of medicinal chemistry.

[10]  J. Neyts,et al.  SAR studies of 9-norbornylpurines as Coxsackievirus B3 inhibitors. , 2011, Bioorganic & medicinal chemistry letters.

[11]  S. Dutta,et al.  Carba-LNA modified siRNAs targeting HIV-1 TAR region downregulate HIV-1 replication successfully with enhanced potency , 2011 .

[12]  J. Neyts,et al.  Design, synthesis, and biological evaluation of novel coxsackievirus B3 inhibitors. , 2010, Bioorganic & medicinal chemistry.

[13]  E. De Clercq,et al.  Antiviral Treatment of Chronic Hepatitis B Virus (HBV) Infections , 2010, Viruses.

[14]  D. Smee,et al.  (-)-Carbodine: enantiomeric synthesis and in vitro antiviral activity against various strains of influenza virus including H5N1 (avian influenza) and novel 2009 H1N1 (swine flu). , 2010, Bioorganic & medicinal chemistry letters.

[15]  J. Neyts,et al.  Norbornane as the novel pseudoglycone moiety in nucleosides , 2009 .

[16]  J. Neyts,et al.  Synthesis of novel racemic carbocyclic nucleoside analogues derived from 4,8-dioxatricyclo[4.2.1.03,7]nonane-9-methanol and 4-oxatricyclo[4.3.1.03,7]decane-10-methanol, compounds with activity against Coxsackie viruses , 2009 .

[17]  M. Erion,et al.  Prodrugs of phosphates and phosphonates. , 2008, Journal of medicinal chemistry.

[18]  T. Burnette,et al.  Application of phosphoramidate ProTide technology significantly improves antiviral potency of carbocyclic adenosine derivatives. , 2006, Journal of medicinal chemistry.

[19]  S. Hughes,et al.  The history of N-methanocarbathymidine: the investigation of a conformational concept leads to the discovery of a potent and selective nucleoside antiviral agent. , 2006, Antiviral research.

[20]  M. Dračínský,et al.  Synthesis of Novel Conformationally Locked Carbocyclic Nucleosides Derived from 3-(Hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol , 2006 .

[21]  Marc C Nicklaus,et al.  Experimental and structural evidence that herpes 1 kinase and cellular DNA polymerase(s) discriminate on the basis of sugar pucker. , 2004, Journal of the American Chemical Society.

[22]  K. Jacobson,et al.  Synthesis of a novel conformationally locked carbocyclic nucleoside ring system. , 2003, Organic letters.

[23]  K. Jacobson,et al.  Methanocarba analogues of purine nucleosides as potent and selective adenosine receptor agonists. , 2000, Journal of medicinal chemistry.

[24]  Victor E. Marquez,et al.  HIV-1 REVERSE TRANSCRIPTASE CAN DISCRIMINATE BETWEEN TWO CONFORMATIONALLY LOCKED CARBOCYCLIC AZT TRIPHOSPHATE ANALOGUES , 1998 .

[25]  R. Wagner,et al.  Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides , 1996 .

[26]  T. Cihlar,et al.  Nucleoside and nucleotide HIV reverse transcriptase inhibitors: 25 years after zidovudine. , 2010, Antiviral research.