Collect. Czech. Chem. Commun.
2006, 71, 871-888
https://doi.org/10.1135/cccc20060871
Synthesis of Novel Conformationally Locked Carbocyclic Nucleosides Derived from 3-(Hydroxymethyl)bicyclo[2.2.1]heptane-2,5-diol
Hubert Hřebabecký*, Milena Masojídková, Martin Dračínský and Antonín Holý
Centre for New Antivirals and Antineoplastics, Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, CZ-166 10 Prague 6, Czech Republic
References
1. J. Antibiot. 1968, 21, 255.
< T., Yamamoto H., Shibata M., Muroi M., Kishi T., Mizuno K.: https://doi.org/10.7164/antibiotics.21.255>
2. J. Antibiot. 1981, 34, 359.
< S., Muto N., Tsujino M., Sudate Y., Hayashi M., Otani M.: https://doi.org/10.7164/antibiotics.34.359>
3a. J. Med. Chem. 1990, 33, 17.
< R., Hua M.: https://doi.org/10.1021/jm00163a004>
3b. Antimicrob. Agents Chemother. 1993, 37, 1004.
< W. B., Shaddix S. C., Bowdon B. J., Rose L. M., Vince R., Shannon W. N., Bennett L. L.: https://doi.org/10.1128/AAC.37.5.1004>
4a. J. Org. Chem. 1996, 61, 4192.
< M. T., King B. W.: https://doi.org/10.1021/jo960708p>
4b. Antimicrob. Agents Chemother. 1997, 41, 1082.
< S. M., Good S. S., Faletto M. B., Miller W. H., StClair M. H., Boone L. R., Tisdale M., Parry N. R., Reardon J. E., Dornsife R. E., Averett D. R., Krenitski T. A.: https://doi.org/10.1128/AAC.41.5.1082>
4c. Drugs 2000, 60, 447.
< P. S., Perry C. M.: https://doi.org/10.2165/00003495-200060020-00015>
5. Org. Lett. 2003, 5, 1665.
< H. S., Jacobson K. A.: https://doi.org/10.1021/ol034326z>
6. Bioorg. Med. Chem. 2004, 12, 5619.
< M., Costanzi S., Kim H. S., Kempeneers V., Vastmans K., Herdewijn P., Maddileti S., Gao Z.-G., Harden T. K., Jacobson K. A.: https://doi.org/10.1016/j.bmc.2004.07.067>
7. Collect. Czech. Chem. Commun. 2005, 70, 103.
< H., Masojídková M., Holý A.: https://doi.org/10.1135/cccc20050103>
8. Collect. Czech. Chem. Commun. 2005, 70, 519.
< H., Masojídková M., Holý A.: https://doi.org/10.1135/cccc20050519>
9. Collect. Czech. Chem. Commun. 2006, 71, 635.
< M., Hřebabecký H., Masojídková M., Holý A.: https://doi.org/10.1135/cccc20060635>
10. Chem. Ber. 1987, 120, 531.
< W., DeLucchi O., Pasquato L., Will B.: https://doi.org/10.1002/cber.19871200412>
11. J. Org. Chem. 1974, 39, 2382.
< S. W., Tomesch J. C.: https://doi.org/10.1021/jo00930a011>
12. Tetrahedron Lett. 1989, 30, 5599.
< G., Weetman J., Hady A. F. A., Helmchen G.: https://doi.org/10.1016/S0040-4039(01)93809-2>
13. Tetrahedron Lett. 1976, 1973.
< V., Kelly R. C., Cha D. Y.: https://doi.org/10.1016/S0040-4039(00)78093-2>
14. J. Am. Chem. Soc. 1988, 110, 7538.
< Y., Sharpless K. B.: https://doi.org/10.1021/ja00230a045>
15a. Nucleosides Nucleotides 1984, 3, 525.
< M. A., Martin J. C., Smee D. F., Mathews T. R., Verheyden J. P. H.: https://doi.org/10.1080/07328318408081287>
15b. Collect. Czech. Chem. Commun. 2004, 69, 435.
< H., Masojídková M., Holý A.: https://doi.org/10.1135/cccc20040435>
15c. Collect. Czech. Chem. Commun. 2004, 69, 918.
< M., Hřebabecký H., Masojídková M., Holý A.: https://doi.org/10.1135/cccc20040918>
16a. J. Org. Chem. 1959, 24, 1314.
< S. M., Ross L. O., Robins R. K.: https://doi.org/10.1021/jo01091a039>
16b. Bioorg. Med. Chem. 2002, 10, 2325.
< R. S., Vince R.: https://doi.org/10.1016/S0968-0896(02)00063-9>
16c. Synthesis 1990, 587.
< M., Boumchita H., Bisagni E: https://doi.org/10.1055/s-1990-26949>
17. Votruba I.: Unpublished results.
18. Balzarini J.: Unpublished resuts.