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Języki publikacji
Abstrakty
The reaction of methyl- and methoxyaminobenzenethiols with acrylic acid resulted in formation of 8-methyl- and 8-methoxy-2,3-dihydro-1,5-benzothiazepin-4(5H)-ones, N-{2-[(2-carboxyethyl)sulfanyl]-4-methylphenyl}-b-alanine and 3-[(8-methoxy- 4- oxo-3,4-dihydro-1,5-benzothiazepin-5(2H)-yl]propanoic acid. Their cyclization to N-(5-methyl-4-oxo-3,4-dihydro-2H-thiochromen-8-yl)-b-alanine, 5-methyl- 9,10- dihydro-2Hthiopyrano[3,2-h]quinoline-4,7(3H,8H)-dione and 10-methyl- 2,3,6,7- tetrahydro-4H,8H-[1,4]thiazepino[2,3,4-ij]quinoline-4,8-dione is described.
Wydawca
Czasopismo
Rocznik
Tom
Strony
2341--2347
Opis fizyczny
Bibliogr. 22 poz., rys.
Twórcy
autor
autor
autor
- Faculty of Chemical Technology, Kaunas University of Technology, Radvil&enu st. 19, LT-50254 Kaunas, Lithuania Fax: +370 37 300 152; Ph: +370 37 300 151, zigmuntas.beresnevicius@ktu.lt
Bibliografia
- 1. Bradshaw T.D., Bibby M.C., Double J.A., Fichtner J., Cooper P.A., Alley M.C., Donohoue S.,Stinson S.R, Tomaszewski J.E., Sausville E.A. and Stevens M.F.G., Mol. Cancer Therapeutics, l, 239 (2002).
- 2. Racane L., Stojkovic R., Tralic-Kulenovic V. and Karminski-Zamola G., Molecules, 11, 325 (2006).
- 3. Racane L., Tralic-Kulenovic V., Fiser-Jakic L., Boykin D. W. and Karminski-Zamola G., Heterocycles,55,2085(2001).
- 4. Önkol T., Dogruer D.S., Ito S. and Sahin M.F., Arch. Pharm. Pharm. Med. Chem., 333, 337 (2000).
- 5. Dundar Y, Cakir B., Kupeli E., Sahin M.R and Noyanalpan N., Turk. J. Chem., 31, l (2007).
- 6. Cecchetti V., Tabarini O., Schaiaffella F. and Fravolini A., Bioorg. Med. Chem. Lett., 10, 465 (2000).
- 7. Hagemann J.P. and Kaye P.T., J. Chem. Soc., Perkin Trans. 7, 341 (1999).
- 8. Ghiasvand A.R., Shadabi S., Kakanejadifard A. and Khajehkoolaki A., Bull. Korean Chem. Soc., 26 (5), 781 (2005).
- 9. Nakazumi H., Uyeama T. and Kitao T., J. Heterocycl. Chem., 22, 1593 (1985).
- 10. Wang H.-K., Bastow K.F., Cosentino L.M. and Lee K.-H., J. Med. Chem., 39, 1975 (1996).
- 11. Bouchara E., Fr. Pat. 2354096, 1978; C. A., 89, 163409s (1978).
- 12. Kugita H., Inoue H., Ikezaki M., Konda M. and Takeok S., Chem. Pharm. Bull., 19, 595 (1971).
- 13. Schwartz M. and Tumelty D., J. Org. Chem., 64, 2219 (1999).
- 14. Micheli R, Degiorgis R, Feriani A., Paio A., Pozzan A., Zarantonello P. and Seneci R, J. Comb. Chem., 3, 224 (2001).
- 15. Beresneyittus Z.J., Viliunas V. and Kantminiene K., Chem. Heterocycl. Comp., 4, 394 (2000) (in Russian).
- 16. Beresnevičius Z J., Viliunas V.J., Raudeliunas V.J. and Baltrusis R.S., Chem. Heterocycl. Comp., l, 80 (l992) (in Russian).
- 17. Kantminiene K., Mikulskiene G., Hormi O. and Beresnevicius Z.J., Chem. Heterocycl. Comp., 38, 422 (2002).
- 18. Baltrusis R.S., Beresnevićius Z.J. and Mickevicius V.J., Chem. Heterocycl. Comp., 10, 1400 (1982) (in Russian).
- 19. Rutkauskas K. and Beresnevi£ius Z.J., Chem. HeterocycL Comp., 42, 227 (2006).
- 20. Fridman S.G., Russian J. Org. Chem., 20, 1195 (1950) (in Russian).
- 21. Rejean R, Lau C.K., Giudon V., Rokach J. and Yoakim C., US Pat. 4845083, Cl. 514/80, (1989).
- 22. Huppatz J.L. and Moore R.M.J., Aust. J. Chem., 24, 405 (1971).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ6-0025-0031