Collect. Czech. Chem. Commun.
2000, 65, 58-76
https://doi.org/10.1135/cccc20000058
Reactivity Studies of [1]Benzothieno[3,2-b][1]benzofuran
Pavel Pihera and Jiří Svoboda*
Department of Organic Chemistry, Prague Institute of Chemical Technology, 166 28 Prague 6, Czech Republic
References
1. Collect. Czech. Chem. Commun. 1993, 58, 2983.
< J., Nič M., Paleček J.: https://doi.org/10.1135/cccc19932983>
2. Collect. Czech. Chem. Commun. 1996, 61, 888.
< J., Pihera P., Sedmera P., Paleček J.: https://doi.org/10.1135/cccc19960888>
3. Collect. Czech. Chem. Commun. 1997, 62, 1468.
< P., Pihera P., Svoboda J.: https://doi.org/10.1135/cccc19971468>
4. Collect. Czech. Chem. Commun. 1998, 63, 681.
< P., Paleček J., Svoboda J.: https://doi.org/10.1135/cccc19980681>
5. Collect. Czech. Chem. Commun. 1999, 64, 389.
< P., Dvořáková H., Svoboda J.: https://doi.org/10.1135/cccc19990389>
6. Chem. Listy 1997, 91, 936.
P., Svoboda J.:
7. Zh. Org. Khim. 1980, 16, 438.
A., Kubryavtsev A. B., Zheltov A. Ya., Stepanov B. I.:
8. Bair K. W.: Eur. Pat. Appl. EP 447,703 (1990); Chem. Abstr. 1992, 116, 6540.
9. Adv. Heterocycl. Chem. 1990, 47, 1.
A. R., Taylor R.:
10. Nič M., Svoboda J.: Unpublished results.
11. J. Org. Chem. 1979, 44, 4733.
< R. H., Lai Y.-H., Williams R. V.: https://doi.org/10.1021/jo00393a066>
12. Chem. Ber. 1960, 93, 88.
< A., Gross H., Höft E.: https://doi.org/10.1002/cber.19600930115>
13. Adv. Heterocycl. Chem. 1970, 11, 177.
< B., Scrowston R. M.: https://doi.org/10.1016/S0065-2725(08)60776-X>
14. Dokl. Akad. Nauk Tadzh. SSR 1979, 22, 667.
A. C., Numanov I. U.:
15. J. Chem. Soc. 1948, 1615.
< F., Clapham P. H.: https://doi.org/10.1039/jr9480001615>
16. Adv. Heterocycl. Chem. 1974, 16, 181.
< J., Cook C. C.: https://doi.org/10.1016/S0065-2725(08)60462-6>
17. J. Am. Chem. Soc. 1952, 74, 1165.
< R. K., Nelson N. A., Wood J. C.: https://doi.org/10.1021/ja01125a009>
18. J. Org. Chem. 1939, 3, 120.
< H., Jacoby A. L., Pacevitz H. A.: https://doi.org/10.1021/jo01219a004>
19. Phosphorus, Sulfur Silicon Relat. Elem. 1992, 74, 13.
< F., Bruns W., Musshoff D.: https://doi.org/10.1080/10426509208031536>
20. Anal. Chem. 1982, 54, 575.
D. F., Shabanowitz J.:
21. J. Prakt. Chem. 1993, 335, 209.
< R., Kaczmarek L., Nantka-Namirski P.: https://doi.org/10.1002/prac.19933350218>
22. J. Am. Chem. Soc. 1962, 84, 3684.
< G. A., Kuhn S. J.: https://doi.org/10.1021/ja00878a018>
23. Bull. Soc. Chim. Fr. 1968, 4575.
J., Suquet M., Comoy P., Clim T., Callet G.:
24. J. Am. Chem. Soc. 1951, 73, 2251.
< F. G., McKellin W. H.: https://doi.org/10.1021/ja01149a096>
25. J. Prakt. Chem. 1990, 332, 1099.
< F., Jordis U., Martinek P., Burkart M.: https://doi.org/10.1002/prac.19903320631>
26. Tetrahedron Lett. 1993, 34, 2107.
< M. W., Fieseler H., Jakubik D., Gabor B., Goddard R., Krüger C.: https://doi.org/10.1016/S0040-4039(00)60357-X>
27. Org. Magn. Reson. 1982, 20, 105.
< S. S., Al-Najjar I. M., Amin H. B.: https://doi.org/10.1002/mrc.1270200208>
28. J. Org. Chem. 1979, 44, 2887.
< P., Olivé J.-L., Ung S. N., El Fagdi M. A., Easton J. W., Beierbeck H., Saunders J. K.: https://doi.org/10.1021/jo01330a013>
29. J. Chem. Soc., Perkin Trans. 2 1990, 2071.
< A. R., Brinón M. C., de Bertorello M. M., Sierra M. G., Joseph-Nathan P.: https://doi.org/10.1039/p29900002071>
30. Magn. Reson. Chem. 1988, 26, 252.
< R. J., Haworth I. S.: https://doi.org/10.1002/mrc.1260260314>
31. Aust. J. Chem. 1967, 20, 103.
< Q. N.: https://doi.org/10.1071/CH9670103>
32. J. Am. Chem. Soc. 1966, 88, 2836.
< E. K., Meyerson S.: https://doi.org/10.1021/ja00964a038>
33. Tetrahedron 1966, 22, 3515.
< J. H., Williams D. H., Lawesson S.-O., Madsen J. O., Nolde C., Schroll G.: https://doi.org/10.1016/S0040-4020(01)92539-6>