Collect. Czech. Chem. Commun. 2004, 69, 966-983
https://doi.org/10.1135/cccc20040966

Recent Advances in the Functionalizations of the Upper Rims of Thiacalix[4]arenes. A Review

Stephane Parola* and Cedric Desroches

Laboratoire des Multimatériaux et Interfaces UMR CNRS 5615, Université Claude Bernard Lyon 1, 43 Bd du 11 novembre 1918, 69622 Villeurbanne, France

References

1a. Gutsche C. D.: Calixarenes Revisited (J. F. Stoddart, Ed.). The Royal Society of Chemistry, Cambridge 1998.
1b. Mandolini L., Ungaro R.: Calixarenes in Action. Imperial College Press, London 2000.
1c. Asfari Z., Böhmer V., Harrowfield J., Vicens J. (Eds): Calixarenes 2001. Kluwer Academic Publishers, Dordrecht 2001.
2. Kumagai H., Hasegawa M., Miyanari S., Sugawa Y., Sato Y., Hori T., Ueda S., Kamiyama H., Miyano S.: Tetrahedron Lett. 1997, 38, 3971. <https://doi.org/10.1016/S0040-4039(97)00792-2>
3a. Kajiwara T., Kon N., Yokozawa S., Ito T., Iki N., Miyano S.: J. Am. Chem. Soc. 2002, 124, 11274. <https://doi.org/10.1021/ja0273391>
3b. Kon N., Iki N., Miyano S.: Tetrahedron Lett. 2002, 43, 2231. <https://doi.org/10.1016/S0040-4039(02)00214-9>
4. Lhoták P., Himl M., Pakhomova S., Stibor I.: Tetrahedron Lett. 1998, 39, 8915. <https://doi.org/10.1016/S0040-4039(98)01950-9>
5. Lang J., Dvořáková H., Bartošová I., Lhoták P.: Tetrahedron Lett. 1999, 40, 373. <https://doi.org/10.1016/S0040-4039(98)02315-6>
6. Lang J., Vlach J., Dvořáková H., Lhoták P.: J. Chem. Soc., Perkin Trans. 2 2001, 576. <https://doi.org/10.1039/b007887p>
7. Iki N., Narumi F., Fijimoto T., Morohashi N.: J. Chem. Soc., Perkin Trans. 2 1998, 2745. <https://doi.org/10.1039/a803734e>
8. Akdas H., Mislin G., Graf E., Hosseini M. W.: Tetrahedron Lett. 1999, 2113. <https://doi.org/10.1016/S0040-4039(99)00143-4>
9. Iki N., Narumi F., Suzuki T., Sugawara A., Miyano S.: Chem. Lett. 1998, 1065. <https://doi.org/10.1246/cl.1998.1065>
10. Katagiri H., Iki N., Hattori T., Kabuto C., Miyano S.: J. Am. Chem. Soc. 2001, 123, 779. <https://doi.org/10.1021/ja005573q>
11. Akdas H., Graf E., Hosseini M. W., De Cian A.: Chem. Commun. 2002, 1042. <https://doi.org/10.1039/b201379g>
12. Mislin G., Graf E., Hosseini M. W., De Cian A., Fischer J.: Chem. Commun. 1998, 1345. <https://doi.org/10.1039/a801860j>
13. Iki N., Kumagai H., Morohashi N., Ejima K.: Tetrahedron Lett. 1998, 39, 7559. <https://doi.org/10.1016/S0040-4039(98)01645-1>
14. Mislin G., Graf E., Hosseini M. W.: Tetrahedron Lett. 1999, 40, 1129. <https://doi.org/10.1016/S0040-4039(98)02586-6>
15. Morohashi N., Iki N., Kabuto C., Miyano S.: Tetrahedron Lett. 2000, 41, 2933. <https://doi.org/10.1016/S0040-4039(00)00313-0>
16. Iki N., Morohashi N., Narumi F., Miyano S.: Bull. Chem. Soc. Jpn. 1998, 71, 1597. <https://doi.org/10.1246/bcsj.71.1597>
17. Morohashi N., Iki N., Sugawara A., Miyano S.: Tetrahedron 2001, 57, 5557. <https://doi.org/10.1016/S0040-4020(01)00482-3>
18a. Iki N., Miyano S.: J. Inclusion Phenom. Macrocycl. Chem. 2001, 41, 99. <https://doi.org/10.1023/A:1014406709512>
18b. Shokova E. A., Kovalev V. V.: Russ. J. Org. Chem. 2003, 39, 1. <https://doi.org/10.1023/A:1023416409935>
19. Akdas H., Bringel L., Graf E., Hosseini M. W., Mislin G., Pansanel J., De Cian A., Fisher J.: Tetrahedron Lett. 1998, 39, 2311. <https://doi.org/10.1016/S0040-4039(98)00067-7>
20. Iki N., Fujimoto T., Miyano S.: Chem. Lett. 1998, 625. <https://doi.org/10.1246/cl.1998.625>
21. Desroches C., Parola S., Vocanson F., Ehlinger N., Miele P., Lamartine R., Bouix J., Eriksson A., Lindgren M., Lopes C.: J. Mater. Chem. 2001, 11, 3014. <https://doi.org/10.1039/b105034f>
22. Adams J. P., Paterson J. R.: J. Chem. Soc., Perkin Trans. 1 2000, 3695. <https://doi.org/10.1039/a901139k>
23. Shinkai S., Araki K., Tsubaki T., Arimura T., Manabe O.: J. Chem. Soc., Perkin Trans. 1 1987, 2297. <https://doi.org/10.1039/p19870002297>
24. Verboom W., Durie A., Egberink R., Asfari Z., Reinhoudt D.: J. Org. Chem. 1992, 57, 1313. <https://doi.org/10.1021/jo00030a050>
25. Kumar S., Kurur N. D., Chawla H. M., Varadarajan R.: Synth. Commun. 2001, 31, 775. <https://doi.org/10.1081/SCC-100103269>
26. Zhang W., Zheng Y., Huang Z.: Synth. Commun. 1997, 27, 3763. <https://doi.org/10.1080/00397919708007300>
27. Desroches C., Parola S., Vocanson F., Perrin M., Lamartine R., Létoffé J. M., Bouix J.: New J. Chem. 2002, 26, 651. <https://doi.org/10.1039/b110609k>
28. Lhoták P., Svoboda J., Jr. , Stibor I., Sýkora J.: Tetrahedron Lett. 2002, 43, 7413. <https://doi.org/10.1016/S0040-4039(02)01667-2>
29. Lhoták P., Morávek J., Stibor I.: Tetrahedron Lett. 2002, 43, 3665. <https://doi.org/10.1016/S0040-4039(02)00627-5>
30. Desroches C., Lopes C., Kessler V., Parola S.: Dalton Trans. 2003, 10, 2085. <https://doi.org/10.1039/b210252h>
31. Lhoták P., Himl M., Stibor I., Sýkora J., Císařová I.: Tetrahedron Lett. 2001, 42, 7107. <https://doi.org/10.1016/S0040-4039(01)01461-7>
32. Desroches C., Parola S.: Unpublished results.
33. Desroches C.: Ph.D. Thesis. Université Claude Bernard Lyon 1, Lyon 2002.
34. Desroches C., Parola S., Cornu D., Miele P., Baldeck P. L., Lopes C.: Mater. Res. Soc. Symp. Proc. 2003, 771, 237.
35. Arduini A., Manfredi G., Pochini A., Sicuri A. R., Ungaro R.: Chem. Commun. 1991, 936. <https://doi.org/10.1039/c39910000936>
36. Arora V., Chawla H. M., Santra A.: Tetrahedron 2002, 58, 5591. <https://doi.org/10.1016/S0040-4020(02)00551-3>
37. Gross H., Rieche A., Mattey G.: Chem. Ber. 1963, 96, 308. <https://doi.org/10.1002/cber.19630960138>
38. Desroches C., Kessler V. G., Parola S.: Tetrahedron Lett., in press.
39. Kasyan O., Swierczynski D., Drapailo A., Suwinska K., Lipkowski J., Kalchenko V.: Tetrahedron Lett. 2003, 44, 7167. <https://doi.org/10.1016/S0040-4039(03)01809-4>
40. Lhoták P., Šmejkal T., Stibor I., Havlíček J., Tkadlecová M., Petříčková H.: Tetrahedron Lett. 2003, 44, 8093. <https://doi.org/10.1016/j.tetlet.2003.09.048>