Email this article 
Hide
Show all
OPEN ACCESS | 
PEER-REVIEWED |
REVIEW ARTICLE
|
DOWNLOAD PDF
|
VIEW FULL-TEXT PDF
| TOTAL VIEWS
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 | Revised: 11 Aug 2010 | Accepted: 14 Aug 2010 | Published: 22 Dec 2010 | Issue Date: December 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
Full Text:
PDF
DOI: 10.5155/eurjchem.1.4.388-396.154
Links for Article
| | | | | | |
| | | | | | |
| | |
Related Articles
Article Metrics
This Abstract was viewed 1392 times |
PDF Article downloaded 388 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]. S. M. Ivanov, L. M. Mironovich, N. G. Kolotyrkina, M. E. Minyaev
Synthesis of (3-tert-Butylpyrazolo[5,1-c][1,2,4]triazin-4-yl)phosphine Oxides
Russian Journal of Organic Chemistry 57(1), 47, 2021
DOI: 10.1134/S1070428021010073
[3]. 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
[4]. 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
[5]. Dina Abed Bakhotmah
A recent approach for the synthesis of 1,2,4-triazine systems bearing and/or containing phosphorus atoms as donor-acceptor interaction and their biocidal affects: An overview
Phosphorus, Sulfur, and Silicon and the Related Elements 195(6), 437, 2020
DOI: 10.1080/10426507.2020.1722668
[6]. Yang Wang, Wen-Xiong Zhang, Zhenfeng Xi
Carbodiimide-based synthesis of N-heterocycles: moving from two classical reactive sites to chemical bond breaking/forming reaction
Chemical Society Reviews 49(16), 5810, 2020
DOI: 10.1039/C9CS00478E
[7]. 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
[8]. 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
[9]. 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
The other citation formats (EndNote | Reference Manager | ProCite | BibTeX | RefWorks) for this article can be found online at: How to cite item
DOI Link: https://doi.org/10.5155/eurjchem.1.4.388-396.154
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
Save to Zotero
Save to Mendeley
European Journal of Chemistry 2010, 1(4), 388-396 | doi: https://doi.org/10.5155/eurjchem.1.4.388-396.154 | Get rights and content
Refbacks
- There are currently no refbacks.
Copyright (c)
© Copyright 2010 - 2021 • 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 2010-2021 Atlanta Publishing House LLC. All rights reserved. This site is owned and operated by Atlanta Publishing House LLC whose registered office is 2850 Smith Ridge Trce Peachtree Cor GA 30071-2636, USA. Registered in USA.