Collect. Czech. Chem. Commun.
2003, 68, 837-848
https://doi.org/10.1135/cccc20030837
Cytostatic 6-Arylpurine Nucleosides V. Synthesis of 8-Substituted 6-Phenylpurine Ribonucleosides
Michal Hocek*, Dana Hocková and Jan Štambaský
Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, CZ-16610 Prague 6, Czech Republic
References
1. J. Med. Chem. 2000, 43, 1817.
< M., Holý A., Votruba I., Dvořáková H.: https://doi.org/10.1021/jm991167+>
2. Collect. Czech. Chem. Commun. 2001, 66, 483.
< M., Holý A., Votruba I., Dvořáková H.: https://doi.org/10.1135/cccc20010483>
3. Collect. Czech. Chem. Commun. 2000, 65, 1683.
< M., Holý A., Votruba I., Dvořáková H.: https://doi.org/10.1135/cccc20001683>
4. Collect. Czech. Chem. Commun. 1997, 62, 136.
< M., Masojídková M., Holý A.: https://doi.org/10.1135/cccc19970136>
5. Collect. Czech. Chem. Commun. 2000, 65, 1357.
< M., Hocek M., Holý A.: https://doi.org/10.1135/cccc20001357>
6. Collect. Czech. Chem. Commun. 2002, 67, 325.
< M., Holý A., Dvořáková H.: https://doi.org/10.1135/cccc20020325>
7. Synlett 1999, 1145.
< M., Hocek M., Česnek M., Dvořák D.: https://doi.org/10.1055/s-1999-2753>
8. Synthesis 2001, 1704.
< M., Dvořák D., Hocek M.: https://doi.org/10.1055/s-2001-16765>
9. J. Am. Chem. Soc. 2001, 123, 7779.
< M. K., Hilmer J. H., Martin J. Q., Keeler J. C., Dinh Y. Q. V., Ngassa F. N., Russon L. M.: https://doi.org/10.1021/ja0107172>
10. Eur. J. Org. Chem. 2003, 245.
< M.: https://doi.org/10.1002/ejoc.200390025>
11. Tetrahedron 2003, 59, 607.
< M., Votruba I., Dvořáková H.: https://doi.org/10.1016/S0040-4020(02)01586-7>
12. Acta Chem. Scand. 1999, 53, 366.
< J. M. J., Gundersen L.-L., Rise F.: https://doi.org/10.3891/acta.chem.scand.53-0366>
13. Tetrahedron 1993, 49, 4035.
< T. P., Kumar R. K., Ganesh K. N.: https://doi.org/10.1016/S0040-4020(01)89916-6>
14. Heterocycles 1993, 35, 325.
< Y., Makino T., Hirota K., Sato M.: https://doi.org/10.3987/COM-92-S20>
15. J. Am. Chem. Soc. 1964, 86, 1242.
< R. E., Robins R. K.: https://doi.org/10.1021/ja01060a057>
16a. Tetrahedron 1997, 53, 7237.
< A. S. B., Stevenson T. M., Citineni J. B., Nyzam V., Knochel P.: https://doi.org/10.1016/S0040-4020(97)00427-4>
16b. J. Org. Chem. 1980, 45, 3969.
< V., Richardson S. G.: https://doi.org/10.1021/jo01308a004>
17. J. Organomet. Chem. 2002, 653, 234.
< M. K.: https://doi.org/10.1016/S0022-328X(02)01267-6>
18a. J. Heterocycl. Chem. 1995, 32, 863.
< V., Persson T., Gronowicz S., Hörnfeldt A.-B.: https://doi.org/10.1002/jhet.5570320331>
18b. J. Org. Chem. 2000, 65, 7825.
< P., Magnin G., Mathis G., Burger A., Biellmann J.-F.: https://doi.org/10.1021/jo000841o>
18c. J. Am. Chem. Soc. 2001, 123, 3655.
< J. L., Sathiosatham M., Brown C. T., Rhodes T. A., Wiederrecht G.: https://doi.org/10.1021/ja005547s>
18d. Synlett 2002, 687.
< N., Wagenknecht H.-A.: https://doi.org/10.1055/s-2002-25349>
18e. Heterocycles 2002, 57, 871.
K., Müller C. E.:
19. J. Org. Chem. 1992, 57, 5268.
< K., Kitade Y., Kanbe Y., Maki Y.: https://doi.org/10.1021/jo00045a051>
20. Collect. Czech. Chem. Commun. 2000, 65, 1126.
< Z., Holý A., Masojídková M.: https://doi.org/10.1135/cccc20001126>
21. Collect. Czech. Chem. Commun. 2001, 66, 517.
< Z., Holý A., Masojídková M.: https://doi.org/10.1135/cccc20010517>
22a. Collect. Czech. Chem. Commun. 2000, 65, 1698.
< Z., Holý A., Masojídková M.: https://doi.org/10.1135/cccc20001698>
22b. Collect. Czech. Chem. Commun. 2001, 66, 1393.
< Z., Holý A., Masojídková M.: https://doi.org/10.1135/cccc20011393>
23. Votruba I.: Unpublished results.