Synthesis and structure elucidation of 3,4-dihydroxy-2-quinolin-2- ylpyrido[3,2,1-jk]carbazol-6-ones

Journal of Heterocyclic Chemistry

Volumn 44, Issue 1, 2007, Pages 161-165

  Dang, Hoai V ^a   Habib, Nargues S ^a   Kappe, Thomas ^a   Zangger, Klaus ^a   Stadlbauer, Wolfgang ^a  

^a UNIVERSITY OF GRAZ   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

CARBAZOLE DERIVATIVE; PYRIDONE DERIVATIVE; QUINOLINE DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 36749007651     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570440125     Document Type: Article

References (28)

1. The Merck Index (S. Budavari, ed.) 12, 9020 and 1476 (1996); Merck & Co Inc., Rahway, N.J., USA, Nr.;
2. [b] G. F. Smith in The Alkaloids (R. H. F. Manske, ed.), vol. VIII, 591 (1965);
3. [c] V. Prelog, S. Szpilfogel, J. Battegay, Helv. Chim. Acta, 30, 366 (1947).
4. T. R. Kasturi, L. Mathew and J. A. Sattigeri, Ind. J. Chem., 29B, 1004 (1990).
5. T. Ohmoto and K. Koike, Chem. Pharm. Bull., 33, 4901 (1985).
6. E. Ziegler, U. Rossmann, F. Litvan and H. Meier, Monatsh. Chem., 93, 26 (1962);
7. [b] Geigy Chemical Corp. (by E. Ziegler and F. Litvan), US Patent, 3 052 678 (1959); Chem. Abstr., 58, 3437e (1963);
8. [c] Geigy Chemical Corp., Brit. Patent, 912 289 (1960); Chem. Abstr., 59, 645 (1963);
9. [d] M. Harfenist and E. Magnien, J. Org. Chem., 28, 538 (1963).
10. O. S. Wolfbeis, E. Ziegler, A. Knierzinger, H. Wipfler and I. Trummer, Monatsh. Chem., 111, 93 (1980);
11. [b] Sandoz Ltd. (by U. Zirngibl), Ger. Offen. DE 2 142 334, 19 720 302 (1972); DE 71-2 142 334 - 19710824 (1971); Chem. Abstr., 77, 36383 (1972).
12. H. V. Dang, B. Knobloch, N. S. Habib, Th. Kappe and W. Stadibauer, J. Heterocyclic Chem., 42, 85 (2005).
13. H. V. Dang and W. Stadibauer, J. Heterocycl. Chem., 43, 65 (2006).
14. T. Kappe and W. Stadibauer, Molecules, 1, 255 (1996);
15. [b] Th. Kappe, Tetrahedron Lett., 5327 (1968).
16. J. Mehnert and J. Schnekenburger, Arch. Pharm. (Weinheim), 321, 897 (1988);
17. [b] C. Alonso, M. M. Olmstead, M. H. Nantz and M. J. Kurth, J. Chem. Soc., Chem. Commun., 639 (2001);
18. [c] Merck Sharp and Dohme Ltd., UK (by R. Baker, G. I. Stevenson, P. D. Leeson and M. Rowley), Eur. Pat. Appl., EP 459561, A2 19911204 (1991); Chem. Abstr., 116, 151591 (1992);
19. [d] D. H. Hey and J. M. Williams, J. Chem. Soc., 1678 (1950);
20. [e] T. Sheradsky and N. Itzhak, J. Chem. Soc., Perkin Trans. 1, 13 (1986);
21. [f] Y. Liu and M. J. Kurth, J. Org. Chem., 67, 2082 (2002);
22. [g] Fujisawa Pharmaceutical Co., Ltd., Japan (by M. Matsuo, K. Tsuji, K. Nakamura and G. W. Spears), PCT Int. Appl., IXXD2, WO 9218483, A1 19921029 (1992); Chem. Abstr., 118, 212903 (1993);
23. [h] M. Trkovnik, B. Bobarevic and T. Kappe, Z. Naturforsch., 27B, 476 (1972).
24. V. K. Ahluwalia, D. Kumar and S. Mehta, Heterocycles, 12, 259 (1979).
25. V. V. Mulwad and D. S. Satwe, Indian J. Chem., 43B, 2727 (2004).
26. G. Bodenhausen and D. J. Ruben, Chem. Phys. Lett., 69, 185 (1980);
27. [b] A. Bax and M. F. Summers, J. Am. Chem. Soc., 108, 2093 (1986);
28. [c] B. Reif, M. Köck, R. Kerssebaum, H. Kang, W. Fenical and C. Griessinger, J. Magn. Reson, 118A, 282 (1996).