Collect. Czech. Chem. Commun. 2006, 71, 1161-1168
https://doi.org/10.1135/cccc20061161

A Carbocyclic 7-Deazapurine-Pyrimidine Hybrid Nucleoside

Naresh K. Sunkara, Sylvester L. Mosley and Katherine L. Seley-Radtke*

Department of Chemistry and Biochemistry, University of Maryland, Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250, U.S.A.

References

1. Leonard N. J., Laursen R. A.: J. Am. Chem. Soc. 1963, 85, 2026. <https://doi.org/10.1021/ja00896a036>
2. Leonard N. J., Laursen R. A.: Biochemistry 1965, 4, 354. <https://doi.org/10.1021/bi00878a027>
3. Schmidt C. L., Rusho W. J., Townsend L. B.: J. Chem. Soc., Chem. Commun. 1971, 1515. <https://doi.org/10.1039/c29710001515>
4. Schmidt C. L., Townsend L. B.: J. Org. Chem. 1975, 40, 2476. <https://doi.org/10.1021/jo00905a013>
5. De Clercq E.: Nucleosides Nucleotides 1998, 17, 625. <https://doi.org/10.1080/07328319808005205>
6. De Clercq E.: Biochem. Pharmacol. 1987, 36, 2567. <https://doi.org/10.1016/0006-2952(87)90533-8>
7. De Clercq E., Bernaerts R., Shealy Y. F., Montgomery J. A.: Biochem. Pharmacol. 1990, 39, 319. <https://doi.org/10.1016/0006-2952(90)90031-F>
8. De Clercq E.: Clin. Microbiol. Rev. 2001, 14, 382. <https://doi.org/10.1128/CMR.14.2.382-397.2001>
9. De Clercq E., Murase J., Marquez V. E.: Biochem. Pharmacol. 1991, 41, 1821. <https://doi.org/10.1016/0006-2952(91)90120-T>
10. Pan B.-C., Chen Z.-H., Chu E., Wang Chu M.-Y., Chu S.-H.: Nucleosides Nucleotides 1998, 17, 2367. <https://doi.org/10.1080/07328319808004324>
11. De Clercq E., Balzarini J., Torrence P. F., Mertes M. P., Schmidt C. L., Shugar D., Barr P. J., Jones A. S., Verhelst G., Walker R. T.: Mol. Pharmacol. 1981, 19, 321.
12. Seley K. L., Mosley S. L., Zeng F.: Org. Lett. 2003, 5, 4401. <https://doi.org/10.1021/ol035696q>
13. Seley K. L., Schneller S. W., Rattendi D., Bacchi C. J.: J. Med. Chem. 1997, 40, 622. <https://doi.org/10.1021/jm9605039>
14. Seley K. L., Schneller S. W., Rattendi D., Lane S., Bacchi C. J.: Antimicrob. Agents Chemother. 1997, 41, 1658. <https://doi.org/10.1128/AAC.41.8.1658>
15. Seley K. L., Schneller S. W., Rattendi D., Lane S., Bacchi C.: J. Med. Chem. 1997, 40, 625. <https://doi.org/10.1021/jm9606148>
16. Siddiqi S. M., Chen X., Rao J., Schneller S. W., Ikeda S., Snoeck R., Andrei G., Balzarini J., De Clercq E.: J. Med. Chem. 1995, 38, 1035. <https://doi.org/10.1021/jm00006a023>
17. Mitsunobu O.: Synthesis 1981, 1. <https://doi.org/10.1055/s-1981-29317>
18. Ludek O. R., Meier C.: Synthesis 2003, 13, 2101.
19. Cruickshank K. A., Jiricny J., Reese C. B.: Tetrahedron Lett. 1984, 25, 681. <https://doi.org/10.1016/S0040-4039(00)99971-4>
20. Yang M., Ye W., Schneller S. W.: J. Org. Chem. 2004, 69, 3993. <https://doi.org/10.1021/jo040119g>
21. Tanaka H., Hayakawa H., Lijima S., Haraguchi K., Miyasaka T.: Tetrahedron 1985, 41, 861. <https://doi.org/10.1016/S0040-4020(01)96402-6>
22. Esteban-Gamboa A., Balzarini J., Esnouf R., De Clercq E., Camarasa M. J., Perez-Perez M. J.: J. Med. Chem. 2000, 43, 971. <https://doi.org/10.1021/jm9911377>
23. Seley K. L., Schneller S. W.: J. Heterocycl. Chem. 1999, 36, 287. <https://doi.org/10.1002/jhet.5570360144>
24. Tolman R. L., Robins R. K., Townsend L. B.: J. Am. Chem. Soc. 1969, 91, 2102. <https://doi.org/10.1021/ja01036a040>
25. Bhattacharya B. K., Rao T. S., Revenkar G. R.: J. Chem. Soc., Perkin Trans. 1 1995, 1543. <https://doi.org/10.1039/p19950001543>