Collect. Czech. Chem. Commun. 2007, 72, 1069-1093
https://doi.org/10.1135/cccc20071069

Synthesis and Study of Novel Benzothiazole Derivatives with Potential Nonlinear Optical Properties

Ivica Sigmundová, Pavol Zahradník* and Dušan Loos

Department of Organic Chemistry, Faculty of Natural Sciences, Comenius University, 84104 Bratislava, Slovakia

References

1. Nalwa H. S., Miyata S. (Eds): Nonlinear Optics of Organic Molecules and Polymers. CRC Press, New York 1997.
2. Dalton L. R.: Pure Appl. Chem. 2004, 76, 1421. <https://doi.org/10.1351/pac200476071421>
3. Marder S. R., Gorman S. B., Tiemann B. G., Cheng. L. T.: J. Am. Chem. Soc. 1993, 115, 3006. <https://doi.org/10.1021/ja00060a071>
4. Abotto A., Bradamante S., Facchetti A., Pagani G. A.: J. Org. Chem. 1997, 62, 5755. <https://doi.org/10.1021/jo970059x>
5. Dirk C. W., Katz H. E., Schilling M. L., King L. A.: Chem. Mater. 1990, 2, 700. <https://doi.org/10.1021/cm00012a020>
6. Hrobárik P., Zahradnik P., Fabian W. M. F.: Phys. Chem. Chem. Phys. 2004, 6, 495. <https://doi.org/10.1039/b314150k>
7. Moylan C. R., Twieg R. J., Lee V. Y., Swanson S. A., Betterton K. M., Miller R. D.: J. Am. Chem. Soc. 1993, 115, 12599. <https://doi.org/10.1021/ja00079a055>
8. Ćaleta I., Grdiša M., Mrvoš-Sermek D, Cetina M., Tralić-Kulenović V., Pavelić K., Karminski-Zamola G.: Farmaco 2004, 59, 297. <https://doi.org/10.1016/j.farmac.2004.01.008>
9. Sych E. D., Tolmachev A.: Ukr. Khim. Zh. 1961, 24, 80.
10. Veltman R. P.: Zh. Obshch. Khim. 1956, 26, 3388.
11. Mizuno Y., Adachi K.: J. Pharm. Soc. Jpn. 1952, 72, 745; Chem. Abstr. 1954, 48, 2689. <https://doi.org/10.1248/yakushi1947.72.6_745>
12. Mizuno Y., Adachi K.: J. Pharm. Soc. Jpn. 1952, 72, 1271; Chem. Abstr. 1953, 47, 12357. <https://doi.org/10.1248/yakushi1947.72.10_1271>
13. Kauffman J. M., Moyna G.: J. Org. Chem. 2003, 68, 839. <https://doi.org/10.1021/jo020333+>
14. Magdolen P., Mečiarová M., Toma Š.: Tetrahedron 2001, 57, 4781. <https://doi.org/10.1016/S0040-4020(01)00403-3>
15. Buffa R., Zahradník P., Foltínová P.: Heterocycl. Commun. 2001, 7, 331. <https://doi.org/10.1515/HC.2001.7.4.331>
16. Kanazawa R., Tokoroyama T.: Synthesis 1976, 526. <https://doi.org/10.1055/s-1976-24106>
17. Rodríguez J. G., Lafuente A., Martin-Vilamil R., Martínez-Alcazar M. P.: J. Phys. Org. Chem. 2001, 14, 859. <https://doi.org/10.1002/poc.422>
18. Dryanska V., Ivanov Ch.: Synthesis 1976, 37. <https://doi.org/10.1055/s-1976-23949>
19. Vompe A. F., Meshki L. M.: Zh. Org. Khim. 1981, 17, 1735.
20. Coe B. J., Harris J. A., Hall J. J., Brunschwig B. S., Hung S. T., Libaers W., Clays K., Coles S. J., Horton P. N., Light M. E., Hursthouse M. B., Garin J., Orduna J.: Chem. Mater. 2006, 18, 5907. <https://doi.org/10.1021/cm061594t>
21. AMPAC 5.0. Semichem, 7128 Summit, Shawnee 1994.
22. Cuadro A., Perez-Butragueno J., Pastor-Maeso M., Alvarez-Builla J., Martinez-Grueiro M. M., Martinez-Fernandez A. R.: Farmaco 1992, 47, 477.
23. Eastman Kodak Co.: U.S. 2345094, 1941; Chem. Abstr. 1944, 38, 3558.
24. Hrobárik P., Sigmundová I., Zahradnik P.: Synthesis 2005, 600. <https://doi.org/10.1055/s-2004-837309>
25. Miller R. D., Lee V. Y., Moylan Ch. R.: Chem. Mater. 1994, 6, 1023. <https://doi.org/10.1021/cm00043a026>
26. Garmaise D. L., Chambers C. H., Komlossy J., McCare R. C.: J. Med. Chem. 1967, 10, 897. <https://doi.org/10.1021/jm00317a031>
27. Kiprianov A. I., Ilchenko Ya.: Zh. Obshch. Khim. 1965 35, 498.
28. Solčániová E., Čulák I.: Magn. Reson. Chem. 1989, 27, 663. <https://doi.org/10.1002/mrc.1260270711>
29. Zenno H.: J. Pharm. Soc. Jpn. 1954, 74, 1236; Chem. Abstr. 1955, 49, 14736. <https://doi.org/10.1248/yakushi1947.74.11_1236>
30. Zeena S., Thomas K. G.: J. Am. Chem. Soc. 2001, 123, 7859. <https://doi.org/10.1021/ja010199v>