Collect. Czech. Chem. Commun.
2000, 65, 280-296
https://doi.org/10.1135/cccc20000280
Synthesis and Analgesic Activity of Some 1-Benzofurans, 1-Benzothiophenes and Indoles
Stanislav Rádla,*, Petr Hezkýa, Jitka Urbánkováb, Petr Váchalb and Ivan Krejčía
a Research Institute of Pharmacy and Biochemistry, Kouřimská 17, 130 60 Prague 3, Czech Republic
b Department of Organic Chemistry, Prague Institute of Chemical Technology, 166 28 Prague 6, Czech Republic
References
1. J. Pharmacol. Exp. Ther. 1996, 278, 304.
Z. R., Cechinel-Filho V., Yunes R. A., Calixto J. B.:
2. Eur. J. Med. Chem. 1996, 31, 833.
< V., Vaz Z. R., Zunino L., Calixto J. B., Yunes R. A.: https://doi.org/10.1016/0223-5234(96)83978-X>
3. Livingstone R. in: Rodd’s Chemistry of Carbon Compounds (S. Coffey, Ed.), Vol. IV, Part A, p. 83. Elsevier, Amsterdam 1973.
4. J. Chem. Soc. 1949, 2057.
< J. B. D., Robertson A., Bushra A., Towcis R.: https://doi.org/10.1039/jr9490002057>
5. Heterocycles 1986, 24, 771.
< T., Fujita H., Sasaki K., Namba T., Hayakawa S.: https://doi.org/10.3987/R-1986-03-0771>
6. J. Chem. Soc. 1955, 3693.
< M., Buu-Hoi N. P., Royer R.: https://doi.org/10.1039/jr9550003693>
7. Chem. Ber. 1925, 58, 1691.
< A., Bülow W.: https://doi.org/10.1002/cber.19250580849>
8. J. Chem. Soc. 1953, 1241.
< F. M., Robertson A.: https://doi.org/10.1039/jr9530001241>
9. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1987, 26, 57.
S. D., Srivastava S. K.:
10. Tetrahedron Lett. 1985, 26, 4807.
< K. E., Undheim J., Erdal J. E.: https://doi.org/10.1016/S0040-4039(00)94957-8>
11. Synth. Commun. 1988, 18, 191.
< I., Loft M.: https://doi.org/10.1080/00397918808077344>
12. J. Prakt. Chem. 1973, 315, 779.
< K., Jansch H.-J.: https://doi.org/10.1002/prac.19733150423>
13. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1981, 20, 391.
V. P., Mahajan S. B., Agasimundin Y. S. :
14. J. Chem. Soc., Perkin Trans. 1 1983, 2973.
< L. K. A., Scrowton R. M.: https://doi.org/10.1039/p19830002973>
15. J. Chem. Soc. C 1971, 3903.
< D. E. L., Clarke K., Scrowston R. M.: https://doi.org/10.1039/j39710003903>
16. J. Heterocycl. Chem. 1978, 15, 513.
< J. R.: https://doi.org/10.1002/jhet.5570150332>
17. Tetrahedron 1983, 39, 4153.
< R., Bois-Choussy M., Boudet B.: https://doi.org/10.1016/S0040-4020(01)88635-X>
18. J. Heterocycl. Chem. 1973, 10, 51.
< E. E., Benjamin L. E., Fryer R. I.: https://doi.org/10.1002/jhet.5570100112>
19. J. Org. Chem. 1983, 48, 2520.
< W. H., Simmons K. A.: https://doi.org/10.1021/jo00163a019>
20. Collect. Czech. Chem. Commun. 1991, 56, 2373.
< L., Brůnová B., Kocfeldová Z., Tíkalová J., Matunová E., Grimová J.: https://doi.org/10.1135/cccc19912373>
21. J. Org. Chem. 1974, 39, 1101.
< R. A., Knaus G. N., Uma V.: https://doi.org/10.1021/jo00922a019>
22. Chem. Ber. 1925, 58, 2081.
< K.: https://doi.org/10.1002/cber.19250580924>
23. J. Am. Chem. Soc. 1949, 71, 2205.
< H. E., Rigby G. W.: https://doi.org/10.1021/ja01174a077>
24. Justus Liebigs Ann. Chem. 1926, 450, 273.
< K., Frese E.: https://doi.org/10.1002/jlac.19264500121>
25. J. Chem. Soc., Perkin Trans. 1 1981, 514.
< E. V., Ferreira D., Roux D. G.: https://doi.org/10.1039/p19810000514>
26. Justus Liebigs Ann. Chem. 1950, 570.
W., Hahn-Weinheimer P.:
27. J. Org. Chem. 1977, 42, 3452.
< D. K.: https://doi.org/10.1021/jo00441a034>
28. J. Pharmacol. Exp. Ther. 1953, 80, 385.
N. B., Leimbach D.:
29. Fed. Proc. 1959, 18, 412.
R., Anderson M., De Beer J.:
30. Pharmacol. Exp. Ther. 1941, 72, 74.
F. E., Smith D. L. J.: