Pure and Applied Chemistry

Pure Appl. Chem., 2011, Vol. 83, No. 8, pp. 1543-1554

http://dx.doi.org/10.1351/PAC-CON-10-11-11

Published online 2011-06-24

Benzopyrrole derivatives as effective anion receptors in highly competitive solvents

References

• 1. J. Sessler, P. Gale, C. Won-Seob. Anion Receptor Chemistry, Royal Society of Chemistry, Cambridge (2006).
• 2. F. G. Bordwell, J. A. Harrelson, T. Y. Lynch. J. Org. Chem. 55, 3337 (1990). (http://dx.doi.org/10.1021/jo00297a064)
• 3. F. G. Bordwell, G. E. Drucker, H. E. Fried. J. Org. Chem. 46, 632 (1981). (http://dx.doi.org/10.1021/jo00316a032)
• 4. M. H. Abraham. Chem. Soc. Rev. 22, 73 (1993). (http://dx.doi.org/10.1039/cs9932200073)
• 5. P. Guardado, M. Balon, C. Carmona, M. A. Muñoz, C. Domene. J. Pharm. Sci. 86, 106 (1997). (http://dx.doi.org/10.1021/js960111p)
• 6. P. Gale, S. Camiolo, G. J. Tizzard, C. P. Chapman, M. E. Light, S. J. Coles, M. B. Hursthouse. J. Org. Chem. 66, 7849 (2001). (http://dx.doi.org/10.1021/jo016020g)
• 7. T. Zieliński, J. Jurczak. Tetrahedron 61, 4081 (2005). (http://dx.doi.org/10.1016/j.tet.2005.02.029)
• 8. S. J. Coles, P. A. Gale, M. B. Hursthouse, M. E. Light, C. N. Warriner. Supramol. Chem. 16, 469 (2004). (http://dx.doi.org/10.1080/10610270410001713303)
• 9. M. J. Chmielewski, M. Charon, J. Jurczak. Org. Lett. 6, 3501 (2004). (http://dx.doi.org/10.1021/ol048661e)
• 10. T. D. Thangadurai, N. J. Singh, I. Hwang, J. W. Lee, R. P. Chandran, K. S. Kim. J. Org. Chem. 72, 5461 (2007). (http://dx.doi.org/10.1021/jo070791o)
• 11. D. Gross, V. Mikkilineni, V. Lynch, J. Sessler. Supramol. Chem. 22, 135 (2010). (http://dx.doi.org/10.1080/10610270903304434)
• 12. M. Chmielewski. Synthesis 3067 (2010). (http://dx.doi.org/10.1055/s-0030-1258191)
• 13. T. Zieliński. Ph.D Thesis, Institute of Organic Chemistry, Polish Academy of Sciences, Warsaw (2006).
• 14. S. A. Samsoniya, M. V. Trapaidze, N. A. Kuprashvili, A. M. Kolecnikow, N. N. Suvorov. Khim. Geterotsikl Soedin. 1222 (1985).
• 15. D. Curiel, A. Espinosa, M. Más-Montoya, G. Sánchez, A. Tárraga, P. Molina. Chem. Commun. 7539 (2009). (http://dx.doi.org/10.1039/b913345c)
• 16. “Neutral pyrrole systems”, in: Anion Receptor Chemistry, J. Sessler, P. Gale, C. Won-Seob (Eds.), Royal Society of Chemistry, Cambridge (2006).
• 17. K. Xu, Y. He, H. Qin, G. Qing, S. Liu. Tetrahedron: Asymmetry 16, 1342 (2005).
• 18. G.-y. Qing, Y.-B. He, F. Wang, H.-J. Qin, C.-G. Hu, X. Yang. Eur. J. Org. Chem. 1768 (2007). (http://dx.doi.org/10.1002/ejoc.200600917)
• 19. T. Zieliński, P. Dydio, J. Jurczak. Tetrahedron 64, 568 (2008). (http://dx.doi.org/10.1016/j.tet.2007.11.012)
• 20. T. Zieliński, M. Kedziorek, J. Jurczak. Chem.—Eur. J. 14, 838 (2008).
• 21. C. Caltagirone, P. A. Gale, J. R. Hiscock, S. J. Brooks, M. B. Hursthouse, M. E. Light. Chem. Commun. 3007 (2008). (http://dx.doi.org/10.1039/b806238b)
• 22. G. W. Bates, P. A. Gale, M. E. Light. Chem. Commun. 2121 (2007). (http://dx.doi.org/10.1039/b703905k)
• 23. C. Caltagirone, A. Mulas, F. Isaia, V. Lippolis, P. Gale, M. E. Light. Chem. Commun. 6279 (2009). (http://dx.doi.org/10.1039/b912942a)
• 24. G. W. Bates, Triyanti, M. E. Light, M. Albrecht, P. Gale. J. Org Chem. 72, 8921 (2007). (http://dx.doi.org/10.1021/jo701702p)
• 25. P. Dydio, T. Zieliński, J. Jurczak. Chem. Commun. 4560 (2009). (http://dx.doi.org/10.1039/b907164d)
• 26. H. Bauer, E. Strauss. Ber. Dtsch. Chem. Ges. 65, 308 (1932).
• 27. G. Bartoli, G. Palmieri, M. Bosco, R. Dalpozzo. Tetrahedron Lett. 30, 2129 (1989). (http://dx.doi.org/10.1016/S0040-4039(01)93730-X)
• 28. P. Dydio, W. I. Dzik, M. Lutz, B. de Bruin, J. N. H. Reek. Angew. Chem., Int. Ed. 50, 396 (2011). (http://dx.doi.org/10.1002/anie.201005173)
• 29. P. Dydio, T. Zieliński, J. Jurczak. Org. Lett. 12, 1076 (2010). (http://dx.doi.org/10.1021/ol1000395)