Email this article 
Hide
Show all
1,2,4-Triazine Chemistry Part II: Synthetic approaches for phosphorus containing 1,2,4-triazine derivatives
Reda Mohammady Abdel-Rahman (1)
, Magdy Ahmed Ibrahim (2) , Tarik El-Sayed Ali (3,*) (1) Department of Chemistry, Faculty of Education, Ain Shams University, Roxy, Cairo, EG-11711, Egypt
(2) Department of Chemistry, Faculty of Education, Ain Shams University, Roxy, Cairo, EG-11711, Egypt
(3) Department of Chemistry, Faculty of Education, Ain Shams University, Roxy, Cairo, EG-11711, Egypt
(*) Corresponding Author
Received: 06 Jun 2010, Accepted: 14 Aug 2010, Published: 22 Dec 2010
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.
Keywords
DOI: 10.5155/eurjchem.1.4.388-396.154
Article Metrics
This Abstract was viewed 938 times |
PDF Article downloaded 265 times
Citations
[1]. Mounir A. I. Salem, Wafaa M. Abdou, Tarik E. Ali, Azza A. Kamal, Reham F. Barghash
Electron Ionization Mass Spectra of Organophosphorus Compounds. Part III: Mass Spectrometric Fragmentation of Diethyl Spiro[Pyrimidino[5,3′][1,2]Oxazole] Phosphonate, Diethyl (Oxazolo[5,4-D]Pyrimidine-4,6-Dione)Phosphonate, and Diethyl (Pyrimidino[4,5-B][1,4]Oxazine)Phosphonate Derivatives
Phosphorus, Sulfur, and Silicon and the Related Elements 188(8), 1007, 2013
DOI: 10.1080/10426507.2012.723654
[2]. Suhailah S. Aljameel, Houda M. Fataftah, Soheir N. Abd El-Rahman, Asma, M. Elsharif, A. Hafiane, Madiha Kamoun
Ultrasound Synthesis of Benzimidazolo-1,3,5-Triazine Derivatives and Their Anti-Histamine and Anti-Diabetic Activities
Oriental Journal Of Chemistry 35(4), 1368, 2019
DOI: 10.13005/ojc/350417
[3]. Wen-Bin Chen, Zhi-Xin Li, Xin-Wei Yu, Meng Yang, Yan-Xuan Qiu, Wen Dong
M2+ and Ln3+-catalyzed synthesis of a [1,2,4]triazine core via intramolecular C–H/N–H functionalization and C–N bond formation (M = Mn, Zn, Cd; Ln = Dy, Tb)
New Journal of Chemistry 39(2), 1222, 2015
DOI: 10.1039/C4NJ01027B
[4]. Reda M. Abdel-Rahman, Mohamed S. T. Makki, Tarik E. Ali, Magdy A. Ibrahim
1,2,4-Triazine Chemistry Part IV: Synthesis and Chemical Behavior of 3-Functionalized 5,6-Diphenyl-1,2,4-triazines towards Some Nucleophilic and Electrophilic Reagents
Journal of Heterocyclic Chemistry 52(6), 1595, 2015
DOI: 10.1002/jhet.2014
[5]. Abeer N. Al-Romaizan, Mohammed S. T. Makki, Reda M. Abdel-Rahman
Synthesis of New Fluorine/Phosphorus Substituted 6-(2’-Amino Phenyl)-3-Thioxo-1,2,4-Triazin-5(2H, 4H)One and Their Related Alkylated Systems as Molluscicidal Agent as against the Snails Responsible for Bilharziasis Diseases
International Journal of Organic Chemistry 04(02), 154, 2014
DOI: 10.4236/ijoc.2014.42017
[6]. Mounir A. I. Salem, Magda I. Marzouk, Tarik E. Ali, Rizk E. Khidre
Electron ionization mass spectra of organophosphorus compounds, Part II: Mass spectrometric fragmentation of spiro(indene-2,3′-pyrazole)phosphonates, spiro(indene-2,3′-pyrazole)phosphanylidene, spiro(1,2,4-diazaphosphole-3,2′-indenes), and (1,3-dioxo-2H-i
Heteroatom Chemistry 23(3), 254, 2012
DOI: 10.1002/hc.21011
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.
How to cite
DOI Link: https://doi.org/10.5155/eurjchem.1.4.388-396.154
Refbacks
- There are currently no refbacks.
Copyright (c)
© Copyright 2019 • Atlanta Publishing House LLC • All Right Reserved.
The opinions expressed in all articles published in European Journal of Chemistry are those of the specific author(s), and do not necessarily reflect the views of Atlanta Publishing House LLC, or European Journal of Chemistry, or any of its employees.
Copyright 2019 Atlanta Publishing House LLC. All rights reserved. This site is owned and operated by Atlanta Publishing House LLC whose registered office is 4614 Lavista road, Tucker, GA, 30084, USA. Registered in USA.