sym-triazines. 8. Synthesis and some reactions of 4,6-disubstituted 2-(1H-pyrrolyl)-1,3,5-triazines

Chemistry of Heterocyclic Compounds

Volumn 44, Issue 3, 2008, Pages 339-348

  Chesnyuk, A A ^a   Mikhailichenko, S N ^b   Zaplishnyi, V N ^b   Konyushkin, L D ^c   Firgang, S I ^c  

^a KUBAN STATE AGRARIAN UNIVERSITY   (Russian Federation)

^b UNIVERSITY OF TORONTO   (Canada)

^c N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

Author keywords

2,5 dimethoxytetrahydrofuran; 4,6 disubstituted 2 amino 1,3,5 triazines; 4 substituted 2 (1H 1 pyrrolyl) 6 (1,2,3 triazol 1 yl) 1,3,5 triazines; 4 substituted 2 amino (1,3,5 triazinyl) 6 iminotriphenylphosphoranes

Indexed keywords

EID: 49849089940     PISSN: 00093122     EISSN: 15738353     Source Type: Journal    
DOI: 10.1007/s10593-008-0050-4     Document Type: Article

References (18)

1. S. N. Mikhailichenko, A. A. Chesnyuk, L. D. Konyushkin, S. I. Firgang, and V. N. Zaplishnyi, Khim. Geterotsikl. Soedin., 731 (2006).
2. [Chem. Heterocycl. Comp., 42, 642 (2006)].
3. S. N. Mikhailichenko, A. A. Chesnyuk, S. I. Firgang, L. D. Konyushkin, and V. N. Zaplishnyi, Khim. Geterotsikl. Soedin., 1343 (2004).
4. [Chem. Heterocycl. Comp., 40, 1162 (2004)].
5. S. N. Mikhailichenko, A. A. Chesnyuk, L. D. Konyushkin, and V. N. Zaplishnyi, Khim. Geterotsikl. Soedin., 1351 (2004).
6. [Chem. Heterocycl. Comp., 40, 1169 (2004)].
7. J. K. Chakrabarti D. E. Tupper 1974 J. Heterocycl. Chem. 11 417
8. Y. Fang D. Leysen H. C. J. Ouenheijm 1995 Synth. Commun. 25 1857
9. Z. Brzozowski F. Saczewski 2002 Eur. J. Med. Chem. Chim. Ther. 37 709
10. G. M. Pogosyan, V. A. Ponkratov, and V. N. Zaplishnyi, Polytriazines [in Russian], Armenian SSR Academy of Sciences Publishing House, Yerevan (1987).
11. E. A. Kaigorodova, A. A. Osipova, V. K. Vasilin, L. D. Konyuskhin, and G. D. Krapivin, Khim. Geterotsikl. Soedin., 444 (2003).
12. [Chem. Heterocycl. Comp., 39, 400 (2003)].
13. M. Yasutumo, K. Satoshi, and H. Yoji, J. Chem. Soc. Jpn. Chem. Ind. Chem., 396 (1990).
14. A. Gordon and R. Ford, The Chemist's Companion, Wiley-Interscience Publishers, John Wiley and Sons, New York, London, Sydney, Toronto (1972).
15. S. N. Mikhailichenko A. A. Chesnyuk A. I. Suslov A. I. Shkrebets M. M. Yukhomenko V. N. Zaplishnyi 2002 Izv. Vuzov. Khimiya, Khim. Tekhnologiya 45 4 136
16. S. N. Mikhailichenko, A. A. Chesnyuk, I. G. Dmitrieva, A. I. Suslov, N. S. Kotlyarov, and V. N. Zaplishnyi, Russian Fed. Pat. 2230066; Byul. Izobr., No. 16 (2004).
17. S. N. Mikhailichenko, A. A. Chesnyuk, I. G. Dmitrieva, N. S. Kotlyarov, and V. N. Zaplishnyi, Russian Fed. Pat. 2230065; Byul. Izobr., No. 16 (2004).
18. A. Weissberger, E. S. Proskauer, J. A. Riddick, and E. E. Toops, Organic Solvents, Interscience, New York (1955).