Synthesis and Biological Evaluation of 4'-C,3'-O-Propylene-Linked Bicyclic Nucleosides.

A set of pyrimidine nucleosides fused with a 4'-C,3'-O-propylene bridge was successfully synthesised in 12 steps from 1,2:5,6-di-O-isopropylidene-α-d-glucofuranose, an inexpensive starting material, based on a ring-closing metathesis (RCM) reaction followed by Vorbrüggen-type nucleobase coupling. Antiviral and cytotoxicity activities of the targeted modified nucleosides, as well as their phosphoramidate prodrugs, are described.

[1]  R. Schinazi,et al.  Efficient synthesis of nucleoside aryloxy phosphoramidate prodrugs utilizing benzyloxycarbonyl protection. , 2011, Tetrahedron.

[2]  M. Egli,et al.  An exocyclic methylene group acts as a bioisostere of the 2'-oxygen atom in LNA. , 2010, Journal of the American Chemical Society.

[3]  Vincent Roy,et al.  Preparation of cyclonucleosides. , 2010, Chemical reviews.

[4]  T. P. Prakash,et al.  Synthesis and biophysical evaluation of 2',4'-constrained 2'O-methoxyethyl and 2',4'-constrained 2'O-ethyl nucleic acid analogues. , 2010, The Journal of organic chemistry.

[5]  C. Len,et al.  Synthesis of bicyclonucleosides having a C-C bridge. , 2008, Chemical reviews.

[6]  D. Turner,et al.  Chemical synthesis of LNA-2-thiouridine and its influence on stability and selectivity of oligonucleotide binding to RNA. , 2009, Biochemistry.

[7]  Chuanzheng Zhou,et al.  The synthesis of therapeutic locked nucleos(t)ides. , 2009, Current opinion in drug discovery & development.

[8]  S. Harper,et al.  Phosphoramidate prodrugs of 2'-C-methylcytidine for therapy of hepatitis C virus infection. , 2009, Journal of medicinal chemistry.

[9]  R. Schinazi,et al.  Cu(I)-catalyzed Huisgen azide-alkyne 1,3-dipolar cycloaddition reaction in nucleoside, nucleotide, and oligonucleotide chemistry. , 2009, Chemical reviews.

[10]  J. Issa,et al.  Targeting DNA Methylation , 2009, Clinical Cancer Research.

[11]  P. Nielsen,et al.  Synthesis of bicyclic 2'-deoxynucleosides with alpha-L-ribo- and beta-D-xylo-configurations and restricted S- and N-type conformations. , 2009, The Journal of organic chemistry.

[12]  P. Sharma,et al.  Optimized synthesis of LNA uracil nucleosides , 2008 .

[13]  K. Miyashita,et al.  Design, synthesis, and properties of 2',4'-BNA(NC): a bridged nucleic acid analogue. , 2008, Journal of the American Chemical Society.

[14]  C. Périgaud,et al.  Recent Approaches in the Synthesis of Conformationally Restricted Nucleoside Analogues , 2008 .

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

[16]  Y. Kitade,et al.  Biologically Stable 2‐5A Analogues containing 3′‐O,4′‐C‐bridged Adenosine as Potent RNase L Agonists , 2007, ChemMedChem.

[17]  S. Maiti,et al.  Perspectives on chemistry and therapeutic applications of Locked Nucleic Acid (LNA). , 2007, Chemical reviews.

[18]  C. Len,et al.  Synthesis of 2′,3′‐Didehydro‐2′,3′‐dideoxynucleosides Having Variations at Either or Both of the 2′‐ and 3′‐Positions , 2006 .

[19]  C. Postel Synthesis of 2,3-Didehydro-2,3-dideoxynucleosides via Nucleoside Route. , 2006 .

[20]  R. Schinazi,et al.  Phosphoramidate and phosphate prodrugs of (-)-beta-D-(2R,4R)-dioxolane-thymine: synthesis, anti-HIV activity and stability studies. , 2006, Bioorganic & medicinal chemistry.

[21]  Y. Hari,et al.  Synthesis and properties of 2'-O,4'-C-methyleneoxymethylene bridged nucleic acid. , 2006, Bioorganic & medicinal chemistry.

[22]  S. Nolan,et al.  Metathesis Strategy in Nucleoside Chemistry , 2005 .

[23]  M. Mason,et al.  Anti-cancer ProTides: tuning the activity of BVDU phosphoramidates related to thymectacin. , 2005, Bioorganic & medicinal chemistry.

[24]  R. Schinazi,et al.  Efficient synthesis of various acycloalkenyl derivatives of pyrimidine using cross-metathesis and Pd(0) methodologies , 2005 .

[25]  T. Widlanski,et al.  Facile deprotection of O-Cbz-protected nucleosides by hydrogenolysis: an alternative to O-benzyl ether-protected nucleosides. , 2004, Organic letters.

[26]  J. Chattopadhyaya,et al.  Synthesis, physicochemical and biochemical studies of 1',2'-oxetane constrained adenosine and guanosine modified oligonucleotides, and their comparison with those of the corresponding cytidine and thymidine analogues. , 2004, Journal of the American Chemical Society.

[27]  Erik De Clercq,et al.  Antiviral drugs in current clinical use. , 2004 .

[28]  J. Balzarini,et al.  Aryloxy phosphoramidate triesters as pro-tides. , 2004, Mini reviews in medicinal chemistry.

[29]  A. Matsuda,et al.  Antitumor activity of sugar‐modified cytosine nucleosides , 2004, Cancer science.

[30]  M. Chun,et al.  Synthesis and biological evaluation of thymine nucleosides fused with 3',4'-tetrahydrofuran ring. , 2003, Bioorganic & medicinal chemistry letters.

[31]  M. Otto,et al.  Ribonucleoside Analogue That Blocks Replication of Bovine Viral Diarrhea and Hepatitis C Viruses in Culture , 2003, Antimicrobial Agents and Chemotherapy.

[32]  M. Otto,et al.  Antiviral Activities and Cellular Toxicities of Modified 2′,3′-Dideoxy-2′,3′-Didehydrocytidine Analogues , 2002, Antimicrobial Agents and Chemotherapy.

[33]  N. Bourgougnon,et al.  Synthesis of 4-C ,3 -O bicyclic thymidine analogues using ring closure metathesis † , 2002 .

[34]  P. Blumberg,et al.  Conformationally constrained analogues of diacylglycerol (DAG). Part 19: Asymmetric syntheses of (3R)- and (3S)-3-hydroxy-4,4-disubstituted heptono-1,4-lactones as protein kinase C (PK-C) ligands with increased hydrophilicity , 2002 .

[35]  Y. Hari,et al.  Synthesis and conformation of 3′,4′-BNA monomers, 3′-O,4′-C-methyleneribonucleosides , 2002 .

[36]  C. K. Chu,et al.  L-Nucleosides as chemotherapeutic agents. , 2001, FEMS microbiology letters.

[37]  S. Obika,et al.  2'-O,4'-C-Methylene bridged nucleic acid (2',4'-BNA): synthesis and triplex-forming properties. , 2001, Bioorganic & medicinal chemistry.

[38]  P. Savy,et al.  DNA triplex structures are stabilized by the incorporation of 3'-endo blocked pyrimidine nucleosides in the Hoogsteen strand. , 2000, Bioorganic & medicinal chemistry letters.

[39]  S. Shuto,et al.  Nucleosides and nucleotides. 183. Synthesis of 4'alpha-branched thymidines as a new type of antiviral agent. , 1999, Bioorganic & medicinal chemistry letters.

[40]  J. Arnold,et al.  Synthesis and duplex stability of oligodeoxyribonucleotides containing a 2′→5′-amide linkage , 1999 .

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

[42]  C. Olsen,et al.  SYNTHESIS OF 2'-O,3'-C-LINKED BICYCLIC NUCLEOSIDES AND BICYCLIC OLIGONUCLEOTIDES , 1997 .

[43]  H. Vorbrueggen Adventures in Silicon-Organic Chemistry , 1995 .

[44]  L. J. Kurz,et al.  4'-Substituted nucleosides as inhibitors of HIV : an unusual oxetane derivative , 1992 .

[45]  R. Schinazi,et al.  Activities of 3'-azido-3'-deoxythymidine nucleotide dimers in primary lymphocytes infected with human immunodeficiency virus type 1 , 1990, Antimicrobial Agents and Chemotherapy.

[46]  H. Mitsuya,et al.  1-(2,3-Anhydro-beta-D-lyxofuranosyl)cytosine derivatives as potential inhibitors of the human immunodeficiency virus. , 1988, Journal of medicinal chemistry.

[47]  J. Allard,et al.  A rapid and automated colorimetric assay for evaluating the sensitivity of herpes simplex strains to antiviral drugs. , 1986, Journal of biological standardization.

[48]  M. Sundaralingam,et al.  Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation. , 1972, Journal of the American Chemical Society.