Gas-phase thermolysis of 1-acylnaphtho[1,8-de][1,2,3]triazines. Interesting direct routes towards condensed naphtho[1,8-de]heterocyclic ring systems

Tetrahedron

Volumn 61, Issue 44, 2005, Pages 10507-10513

  Al Awadi, Hanan ^a   Ibrahim, Maher R ^a   Dib, Hicham H ^a   Al Awadi, Nouria A ^a   Ibrahim, Yehia A ^a  

^a KUWAIT UNIVERSITY   (Kuwait)

Author keywords

FVP; Heterocycles; Naphtho 1,8 de 1,2,3 triazines; Naphtho 1,8 de 1,3 oxazines

Indexed keywords

AMIDE; HETEROCYCLIC COMPOUND; OXAZINE DERIVATIVE; TRIAZINE DERIVATIVE;

ARTICLE; CHEMICAL COMPOSITION; MOLECULAR INTERACTION; PRIORITY JOURNAL; PYROLYSIS; REACTION ANALYSIS; SYNTHESIS; TEMPERATURE SENSITIVITY;

EID: 25844505060     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.08.047     Document Type: Article

References (39)

1. Y.A. Ibrahim, N.A. Al-Awadi, and M.R. Ibrahim Tetrahedron 60 2004 9121 9130
2. H. Waldmann, and S. Back Ann. 545 1940 52 58
3. H. Sieper, and P. Tavs Ann. 704 1967 161 165
4. H.H. Dib, N.A. Al-Awadi, Y.A. Ibrahim, and O.M.E. El-Dusouqui Tetrahedron 59 2003 9455 9464
5. H.H. Dib, N.A. Al-Awadi, Y.A. Ibrahim, and O.M.E. El-Dusouqui J. Phys. Org. Chem. 17 2004 267 272
6. A.R. Katritzky, X. Lan, J.Z. Yang, and O.V. Denisko Chem. Rev. 98 1998 409 548
7. R. Lawrence, and E.S. Waight Org. Mass Spectrom. 3 1970 367 377
8. S.J. Barker, and R.C. Storr J. Chem. Soc., Perkin Trans. 1 1990 485 488
9. A. Maquestiau, D. Beugnies, R. Flammang, A.R. Katritzky, M. Soleiman, T. Davis, and J.N. Lam J. Chem. Soc., Perkin Trans. 2 1988 1071 1075
10. M. Cox, F. Heidarizadeh, and R.H. Prager Aust. J. Chem. 53 2000 665 671
11. C. Graebe, and F. Ullmann Justus Liebigs Ann. Chem. 291 1896 16 17
12. J. Kulagowski, C.J. Moody, and C.W. Rees J. Chem. Soc., Perkin Trans. 1 1985 2725 2732
13. J. Kulagowski, C.J. Moody, and C.W. Rees J. Chem. Soc., Perkin Trans. 1 1985 2733 2739
14. A. Maquestiau, M. Flammang-Barbieux, R. Flammang, and L.-Z. Chen Bull. Soc. Chim. Belg. 94 1988 245 254
15. P. Nantka-Nemirski, and J. Kalinowski Wydz. Mat. Fiz. Chem., Ser. Chem. 18 1975 259 271
16. A. Hubert J. Chem. Commun. 1969 328
17. P. Nantka-Nemirski, and J. Kalinowski Acta Pol. Pharm. 2 1974 137 145
18. A. Hurbert, and H. Reimlinger Chem. Ber. 103 1970 2828 2835
19. R.H. Prager, M.M. Baradarani, and J. Khalafy J. Heterocycl. Chem. 37 2000 631 637
20. D.C.K. Lin, and D.C. DeJongh J. Org. Chem. 39 1974 1780 1781
21. J. Khalafy, and R.H. Prager Aust. J. Chem. 51 1998 925 929
22. A. Maquestiau, D. Beugnies, R. Flammang, B. Freiermuth, and C. Wentrup Org. Mass Spectrom. 25 1990 197 203
23. J.D. Drulliner J. Am. Chem. Soc. 90 1968 6879 6880
24. M.M. Baradarani, J. Khalafy, and R.H. Prager Aust. J. Chem. 52 1999 773 780
25. M. Ohashi, K. Tsujimoto, A. Yoshino, and T. Yonezawa Org. Mass Spectrom. 4 1970 203 210
26. S.J. Barker, G.B. Jones, K.R. Randles, and R.C. Storr Tetrahedron Lett. 29 1988 953 954
27. P. Flowerday, and M.J. Perkins J. Chem. Soc. C 1970 298 303
28. I.A. Al-Juwaiser, N.A. Al-Awadi, and O.M.E. El-Dusouqui Can. J. Chem. 80 2002 499 503
29. N.A. Al-Awadi, B.J. George, H.H. Dib, M.R. Ibrahim, Y.A. Ibrahim, and O.M.E. El-Dusouqui Tetrahedron 61 2005 8257 8263
30. X. Zhang, C.-H. Liu, L.-H. Liu, F.-Y. Wu, L. Gua, X.-Y. Sun, C.-J. Wang, and Y.-B. Jiang Org. Biomol. Chem. 1 2003 728 732 and references cited therein
31. F. Muzik Collect. Czech. Chem. Commun. 30 1960 559 572
32. W.J. Dixon, and F. Hibbert J. Chem. Soc., Perkin Trans. 2 1994 795 798
33. F. Muzik Collect. Czech. Chem. Commun. 30 1965 559 572
34. M.A. Kerry, G.W. Boyd, S.P. Mackary, O. Meth-Cohn, and L. Platt J. Chem. Soc., Perkin Trans. 1 1999 2315 2321
35. F. Hibbert, and R.J. Sellens J. Chem. Soc., Perkin Trans. 2 1988 399 402
36. N.P. Lushina, A.I. Blesnova, V.I. Streikova, I.G. Stukalova, and A.G. Khomskaya J. Obschehei Khimii 47 1975 855 858
37. I. Mohammadpoor-Baltork, M.M. Sadeghi, and K. Esmayilpour J. Chem. Res. (S) 2003 348 350
38. N. Itoh, T. Sakamoto, E. Miyazawa, and Y. Kikugawa J. Org. Chem. 67 2002 7424 7428
39. M.J. Perkins J. Chem. Soc. 1964 3005 3008