Collect. Czech. Chem. Commun. 2002, 67, 645-664
https://doi.org/10.1135/cccc20020645

Reactivity of [1]Benzothieno[3,2-b][1]benzothiophene - Electrophilic and Metallation Reactions

Bedřich Košata, Václav Kozmík and Jiří Svoboda*

Department of Organic Chemistry, Institute of Chemical Technology, Prague, 166 28 Prague 6, Czech Republic

References

1. Goodby J. W., Blinc R., Clark N. A., Lagerwall T., Osipov M. A., Pikin S. A., Sakurai T., Yoshino K., Žekš B.: Ferroelectric Liquid Crystals. Gordon and Breach Science Pubs., Philadelphia 1991.
2. Demus D., Goodby J., Gray G. W., Spiess H.-W., Vill V. (Eds): Handbook of Liquid Crystals. Wiley–VCH Verlag GmbH, Weinheim 1998.
3. Bartlulin J., Zuniga C., Ramirez A., Muller H., Taylor T. R.: Mol. Cryst. Liq. Cryst. 1990, 185, 131.
4. Karamysheva L. A., Kovshlev E. J., Pavluchenko A. J., Roitman K. V., Titov V. T., Torgova S. I., Grebenkin M. F.: Mol. Cryst. Liq. Cryst. 1981, 67, 241. <https://doi.org/10.1080/00268948108070894>
5. Loos-Wildenauer M., Kunz S., Voigt-Martin I. G., Yakimanshi A., Wisherhoff E., Zentel R., Tschierke C., Muller M.: Adv. Mater. (Weinheim, Ger.) 1995, 7, 170. <https://doi.org/10.1002/adma.19950070215>
6. Haramoto Y., Kamogowa H.: Bull. Chem. Soc. Jpn. 1991, 63, 156. <https://doi.org/10.1246/bcsj.63.156>
7. Svoboda J., Váchal P., Glogarová M., Stibor I.: Mol. Cryst. Liq. Cryst. 1999, 328, 367.
8. Černovská K., Svoboda J., Stibor I., Glogarová M., Vaněk P., Novotná V.: Ferroelectrics 2000, 241, 231. <https://doi.org/10.1080/00150190008224996>
9. Černovská K., Nič M., Pihera P., Svoboda J.: Collect. Czech. Chem. Commun. 2000, 65, 1939. <https://doi.org/10.1135/cccc20001939>
10. Kaszynski P., Dougherty D. A.: J. Org. Chem. 1993, 58, 5209. <https://doi.org/10.1021/jo00071a034>
11. Haristoy D., Mery S., Heinrich B., Mager L., Nicoud J. F., Guillon D.: Liq. Cryst. 2000, 27, 321. <https://doi.org/10.1080/026782900202769>
12. Zheltov S. Yu., Barudi A., Zheltov A. Ya., Stepanov B. I.: Zh. Org. Khim. 1980, 16, 430.
13. Sashida H., Yasuike S.: J. Heterocycl. Chem. 1998, 35, 725. <https://doi.org/10.1002/jhet.5570350337>
14. Voronkov M. G., Udre E.: Khim. Geterotsikl. Soedin. 1965, 683.
15. Choi K. S., Sawada K., Dong H., Hoshino M., Nakayama Y.: Heterocycles 1998, 38, 143.
16. Schmidt M. W., Baldridge K. K., Boatz J. A., Elbert S. T., Gordon M. S., Jensen J. J., Koseki S., Matsunaga N., Nguyen K. A., Su S., Windus T. L., Dupuis M., Montgomery J. A.: J. Comput. Chem. 1993, 14, 1347. <https://doi.org/10.1002/jcc.540141112>
17. Barudi A., Kudryavtsev A. B., Zheltov A. Ya., Stepanov B. I.: Zh. Org. Khim. 1980, 16, 438.
18. Rieche A., Gross H., Höft E.: Chem. Ber. 1960, 93, 88. <https://doi.org/10.1002/cber.19600930115>
19. Eicher T., Hauptman S.: The Chemistry of Heterocycles, p. 80. G. Thieme Verlag, New York 1995.
20. Katritzky A. R., Perumal S.: J. Heterocycl. Chem. 1990, 27, 1737. <https://doi.org/10.1002/jhet.5570270642>
21. Smith M. B., March J.: Advanced Organic Chemistry, 5th ed., p. 850. J. Wiley, New York 2001.
22. Ricci A., Balucani D., Berardo B.: C. R. Acad. Sci., Ser. C 1972, 275, 139.