European Journal of Chemistry

1,2,4-Triazine Chemistry Part II: Synthetic approaches for phosphorus containing 1,2,4-triazine derivatives



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Reda Mohammady Abdel-Rahman
Magdy Ahmed Ibrahim
Tarik El-Sayed Ali

Abstract

This review represents the methods developed for the synthesis of phosphorus containing 1,2,4-triazine moieties. These methods depends on the phosphorylation of side functional groups of 1,2,4-triazines and cyclization of side functional groups of 1,2,4-triazines with phosphorus reagents to give isolated and fused phosphorus heterocyclic systems.

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Abdel-Rahman, R. M.; Ibrahim, M. A.; Ali, T. E.-S. 1,2,4-Triazine Chemistry Part II: Synthetic Approaches for Phosphorus Containing 1,2,4-Triazine Derivatives. Eur. J. Chem. 2010, 1, 388-396.

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References

[1]. Holla, B. S.; Sarojini, B. K.; Gonsalves, R. Farmaco 1998, 53, 395-398.
doi:10.1016/S0014-827X(98)00036-6

[2]. Holla, B. S.; Sarojini, B. K.; Shridhara, K.; Antong, G. Farmaco 1999, 54, 149-151.
doi:10.1016/S0014-827X(99)00008-7

[3]. Deeb, A.; El-Mariah, F.; Hosny, M. Bioorg. Med. Chem. Lett. 2004, 14, 5013-5017.
doi:10.1016/j.bmcl.2004.06.102

[4]. El-Badawi, M. A.; El-Barbary, A. A.; Loksha, Y. M.; El-Daly, M. Phosphorus Sulfur Silicon Relat. Elem. 2002, 177, 587-596.
doi:10.1080/10426500210276

[5]. Ibrahim, M. A. Heterocycles 2010, 81, 1393-1418.
doi:10.3987/REV-10-668

[6]. Oganisyan, A. S.; Grigoryan, G. O.; Noravyan, A. S.; Dzhagatspanyan, I. A.; Melikyan, G. G. Pharm. Chem. J., 2001, 35, 124-126.
doi:10.1023/A:1010493426085

[7]. Boehner, B.; Ciba-Geigy, A. G. Eur. Pat. 1986; Chem. Abstr. 1986, 105, 6522e.

[8]. Timer, M.; Sauvard, S.; Georgescu, C. M. Biochem. Pharmacol. 1996, 15, 408-410.
doi:10.1016/0006-2952(66)90317-0

[9]. Singh, K.; Barwa, M. S.; Tyagi, P. Eur. J. Med. Chem. 2007, 42, 394-402.
doi:10.1016/j.ejmech.2006.10.016
PMid:17224205

[10]. Ali, T. E. Phosphorus Sulfur Silicon Relat. Elem. 2007, 182, 1717-1726.
doi:10.1080/10426500701313896

[11]. Ibrahim, M. A.; El-Mahdy, K. M. Phosphorus Sulfur Silicon Relat. Elem. 2009, 184, 2945-2958.
doi:10.1080/10426500802625594

[12]. El-Barbary, A. A.; Sakran, A. M.; El-Madani, A. M.; Claus, N. J. Heterocycl. Chem. 2005, 42, 935-941.
doi:10.1002/jhet.5570420528

[13]. El-Gendy, Z.; Morsy, J. M.; Allimony, H. A.; Abdel-Monem, W. R.; Abdel-Rahman, R. M. Pharmazie 2001, 56, 376-384.
PMid:11400552

[14]. Abdel-Rahman, R. M.; Morsy, J. M.; Hanafy, F.; Amene, H. A. Pharmazie 1999, 54, 347-355.
PMid:10368828

[15]. Dai, Q.; Chen, R. Phosphorus Sulfur Silicon Relat. Elem. 1997, 122, 261-267.
doi:10.1080/10426509708043515

[16]. He, L. N.; Cai, F.; Chen, R. Y., Zhou, J. Phosphorus Sulfur Silicon Relat. Elem. 1997, 130, 65-71
doi:10.1080/10426509708033698

[17]. Tang, J. S.; Verkade, J. G.; U S Patent No. 5 260 436 1993; Chem. Abstr. 1993, 120, 218836v.

[18]. Tiwari, A. K.; Dubey, B. K.; Shukla, I. C. J. Indian Chem. Soc. 2003, 80, 717-722.

[19]. Shukla, I. C.; Dwived, P. K. J. Indian Chem. Soc. 2005, 82, 670-675.

[20]. Caruso, F.; Rossi, M.; Tanski, J.; Pettinari, C.; Marchetti, F. J. Med. Chem. 2003, 46, 1737-1742.
doi:10.1021/jm0204690
PMid:12699391

[21].Ali, T. E.; Abdel-Rahman, R. M.; Makki, M. S. T.; Ibrahim, M. A. Eur. J. Chem. 2010, 1(3), 236-245.
doi:10.5155/eurjchem.1.3.236-245.54

[22]. El-Khoshnieh, Y. O. Phosphorus Sulfur Silicon Relat. Elem. 1998, 139, 163-172.
doi:10.1080/10426509808035685

[23]. Abdou, W. M.; Ganoub, N. A.; Fahmy, A. F.; Shaddy, A. A. Monatsch. fur Chem. 2006, 137, 105-116.
doi:10.1007/s00706-005-0403-y

[24]. El-Khoshnieh, Y. O.; Ibrahim, Y. A. Phosphorus Sulfur Silicon Relat. Elem. 1995, 101, 67-73.
doi:10.1080/10426509508042500

[25]. Ali, T. E.; Abdel-Rahman, R. M.; Hanafy, F. I.; El-Edfawy, S. M. Phosphorus, Sulfur Silicon Relat. Elem. 2008, 183, 2565-2577.
doi:10.1080/10426500801967864

[26]. Abdel-Rahman, R. M. Trends in Heterocycl. Chem. 2002, 8, 187-194.

[27]. Ibrahim, Y. A.; Kadry, A. M.; Ibrahim, M. R.; Lisgarten, J. N.; Potfer, B. S.; Palmer, R. A. Tetrahedron 1999, 55, 13457-13462.
doi:10.1016/S0040-4020(99)00830-3

[28]. Ali, T. E. Eur. J. Med. Chem. 2009, 44, 4539-4546.
doi:10.1016/j.ejmech.2009.06.022
PMid:19615792

[29]. Tandura, S. N.; Voronkov, M. G.; Alekseer, N. V. Top. Curr. Chem. 1986, 131, 99-189.

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