Collect. Czech. Chem. Commun.
2001, 66, 1638-1658
https://doi.org/10.1135/cccc20011638
Construction of Interconnected Acidity Functions Based on ortho Substituted Anilines and N-Methylanilines as Indicators
Oldřich Pytelaa,*, Jiří Kulháneka, Eva Jiráskováb and Taťjana Nevěčnáb
a Department of Organic Chemistry, University of Pardubice, 532 10 Pardubice, Czech Republic
b Department of Inorganic and Physical Chemistry, Palacký University Olomouc, 771 46 Olomouc, Czech Republic
References
1. L. P., Deyrup A. J.: J. Am. Chem. Soc. 1932, 54, 2721.
<https://doi.org/10.1021/ja01346a015>
2. Rochester C. H.: Acidity Functions. Academic Press, London 1970.
3. E. B., DunFord H. B.: J. Am. Chem. Soc. 1964, 86, 5080.
<https://doi.org/10.1021/ja01077a007>
4. M. A., Long F. A.: Chem. Rev. (Washington, D. C.) 1957, 57, 1.
<https://doi.org/10.1021/cr50013a001>
5. R. A, Yates K.: Can. J. Chem. 1983, 61, 2225.
<https://doi.org/10.1139/v83-388>
6. R. A.: Adv. Phys. Org. Chem. 2000, 35, 1.
<https://doi.org/10.1016/S0065-3160(00)35011-0>
7. J. F., Olsen F. P.: Can. J. Chem. 1966, 44, 1899.
<https://doi.org/10.1139/v66-286>
8. N. C., Cimino G. M., Passerini R. C.: J. Chem. Soc., Perkin Trans. 2 1973, 1915.
<https://doi.org/10.1039/p29730001915>
9. N. C., Traverso P. G., Passerini R. C.: J. Chem. Soc., Perkin Trans. 2 1977, 306.
<https://doi.org/10.1039/p29770000306>
10. N. C., Traverso P. G., Tomasin A., Passerini R. C.: J. Chem. Soc., Perkin Trans. 2 1977, 309.
<https://doi.org/10.1039/p29770000309>
11. N. C., Passerini R. C.: J. Chem. Soc., Perkin Trans. 2 1977, 845.
12. N. C., Tomasin A., Tortato C.: Org. React. 1996, 30, 29.
13. N. C., Tomasin A., Tortato C.: Org. React. 1996, 30, 39.
14. N. C., Tortato C., Sheikh-Osman A. A., Riego J. M., Zaldivar J. M.: Org. React. 1997, 31, 87.
15. N. C., Tomasin A., Tortato C., Isandelli P.: J. Chem. Soc., Perkin Trans. 2 1998, 2535.
<https://doi.org/10.1039/a803473g>
16. N. C., Tortato C., Ronchin L., Bianchi C.: Catal Lett. 1998, 56, 159.
<https://doi.org/10.1023/A:1019096726458>
17. R. A., Stewart R.: J. Am. Chem. Soc. 1976, 98, 488.
<https://doi.org/10.1021/ja00418a027>
18. R. A., Stewart R., Cook M. J., Katritzky A. R., Tack R. D.: Can. J. Chem. 1976, 54, 900.
<https://doi.org/10.1139/v76-130>
19. R. A., Yates K.: J. Am. Chem. Soc. 1978, 100, 3861.
<https://doi.org/10.1021/ja00480a033>
20. O.: Collect. Czech. Chem. Commun. 1997, 62, 645.
<https://doi.org/10.1135/cccc19970645>
21. P. G.: Can. J. Chem. 1984, 62, 153.
<https://doi.org/10.1139/v84-032>
22. C. D., Stratton B.: J. Org. Chem. 1986, 51, 4100.
<https://doi.org/10.1021/jo00372a003>
23. C. D., Stratton B.: J. Org. Chem. 1987, 52, 4798.
<https://doi.org/10.1021/jo00230a030>
24. K., Wai H.: J. Am. Chem. Soc. 1964, 86, 5408.
<https://doi.org/10.1021/ja01078a008>
25. P., Briggs A. G., Wilson J. M.: J. Chem. Soc. B 1970, 65.
<https://doi.org/10.1039/j29700000065>
26. K., Wai H., Welch G., McClelland R. A.: J. Am. Chem. Soc. 1973, 95, 418.
<https://doi.org/10.1021/ja00783a018>
27. E., Kulhánek J., Nevěčná T., Pytela O.: Collect. Czech. Chem. Commun. 1999, 64, 1253.
<https://doi.org/10.1135/cccc19991253>
28. J. J.: Rec. Trav. Chim. Pays-Bas 1902, 21, 261.
29. E., Kopp E.: Chem. Ber. 1905, 38, 3506.
<https://doi.org/10.1002/cber.190503803185>
30. H.: J. Prakt. Chem. 1930, 127, 20.
<https://doi.org/10.1002/prac.19301270103>
31. C. F.: Rec. Trav. Chim. Pays-Bas 1932, 51, 878.
<https://doi.org/10.1002/recl.19320510910>
32. B., Bendich A.: J. Am. Chem. Soc. 1939, 61, 2658.
<https://doi.org/10.1021/ja01265a022>
33. K., Frese E.: Chem. Ber. 1926, 59, 539.
<https://doi.org/10.1002/cber.19260590332>
34. C. D., Katritzky A. R., Shapiro S. A.: J. Am. Chem. Soc. 1969, 91, 6654.
<https://doi.org/10.1021/ja01052a021>
35. R., Dolman D.: Can. J. Chem. 1967, 45, 925.
<https://doi.org/10.1139/v67-156>
36. J. E. B., Tedder J. M.: J. Chem. Soc. 1955, 1218.
<https://doi.org/10.1039/jr9550001218>
37. K. N., Bell R. P.: J. Chem. Soc. 1959, 1096.
<https://doi.org/10.1039/jr9590001096>
38. R. S., Medvetskaya I. M., Vinnik M. I.: Zh. Fiz. Khim. 1966, 40, 339.
39. S. A., Rochester C. H.: J. Chem. Soc., Perkin Trans. 2 1974, 1624.
<https://doi.org/10.1039/p29740001624>
40. E. M., Mach G. W.: J. Am. Chem. Soc. 1966, 88, 1177.
<https://doi.org/10.1021/ja00958a019>
41. W. R., Kallen R. G.: J. Am. Chem. Soc. 1976, 98, 7777.
<https://doi.org/10.1021/ja00440a052>
42. L. D., Schowen R. L.: J. Am. Chem. Soc. 1971, 93, 2014.
43. L. L., Gidaspov B. V.: Zh. Org. Khim. 1982, 18, 685.

