Synthesis of phosphorothioates using thiophosphate salts

Scholarly Works

• Zhang, Y.; Guo, Y.; Zhao, Y.; Cao, S. NaOAc-Assisted Aerobic Oxidation Protocol for the Synthesis of Pentacoordinate Chalcogenyl Spirophosphoranes with P-Se/P-S Bonds under Open Air. The Journal of organic chemistry 2024, 89, 3259–3270. doi:10.1021/acs.joc.3c02716
• Yang, B.; Zhang, X.; Yue, H.; Li, W.; Li, M.; Lu, L.; Wu, Z.; Li, J.; Sun, K.; Yang, S. A Promoter‐free Protocol for the Synthesis of Selenophosphates and Thiophosphates via a Spontaneous Process at Room Temperature. Advanced Synthesis & Catalysis 2022, 364, 3528–3538. doi:10.1002/adsc.202200625
• Chunqi, L.; Wang, L.; Zhang, X. Advances in the Synthesis of Phosphorothioate and Phosphinothioate. Chinese Journal of Organic Chemistry 2021, 41, 2964. doi:10.6023/cjoc202104002
• Ghoneim, A. A.; El-Farargy, A. F.; Elkanzi, N. A. A. Synthesis of some novel phenylfuro[3,2-d]pyrimidine glycosides derivatives with expected antimicrobial activity. Journal of the Iranian Chemical Society 2019, 17, 319–325. doi:10.1007/s13738-019-01768-2
• Mondal, M.; Saha, A. Benign synthesis of thiophosphates, thiophosphinates and selenophosphates in neat condition using N-chalcogenoimides as the source of electrophilic sulfur/selenium. Tetrahedron Letters 2019, 60, 150965. doi:10.1016/j.tetlet.2019.150965
• Chen, X.-Y.; Pu, M.; Cheng, H.-G.; Sperger, T.; Schoenebeck, F. Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear Pd I Catalysis. Angewandte Chemie (International ed. in English) 2019, 58, 11395–11399. doi:10.1002/anie.201906063
• Chen, X.; Pu, M.; Cheng, H.; Sperger, T.; Schoenebeck, F. Arylation of Axially Chiral Phosphorothioate Salts by Dinuclear PdI Catalysis. Angewandte Chemie 2019, 131, 11517–11521. doi:10.1002/ange.201906063
• Kovács, S.; Bayarmagnai, B.; Aillerie, A.; Gooßen, L. J. Practical Reagents and Methods for Nucleophilic and Electrophilic Phosphorothiolations. Advanced Synthesis & Catalysis 2018, 360, 1913–1918. doi:10.1002/adsc.201701549
• Sheikhhosseini, E. Design and effective synthesis of novel furo[2,3-d]pyrimidine derivatives containing ethylene ether spacers. Journal of Saudi Chemical Society 2018, 22, 337–342. doi:10.1016/j.jscs.2016.05.005
• Kaboudin, B.; Kazemi, F.; Habibi, F. Fe3O4@MgO nanoparticles as an efficient recyclable catalyst for the synthesis of phosphoroamidates via the Atherton–Todd reaction. Tetrahedron Letters 2015, 56, 6364–6367. doi:10.1016/j.tetlet.2015.09.129
• Wu, Y.; Liu, L. L.; Su, J.; Yan, K.; Wang, T.; Zhu, J.; Gao, X.; Gao, Y.; Zhao, Y. Reactivity of Germylene toward Phosphorus-Containing Compounds: Nucleophilic Addition and Tautomerism. Inorganic chemistry 2015, 54, 4423–4430. doi:10.1021/acs.inorgchem.5b00205
• Hossaini, Z.; Rostami-Charati, F. Synthesis of Functionalized Oxaphosphaphenanthrenes and Chromenes via Multicomponent Reactions of Trivalent Phosphorus Nucleophiles. International Journal of Chemical Engineering and Applications 2015, 6, 57–60. doi:10.7763/ijcea.2015.v6.451
• Timperley, C. M.; Renard, P.-Y.; Gomez, C. Chapter 4 – Phosphoryl Compounds. Best Synthetic Methods; Elsevier, 2015; pp 365–562. doi:10.1016/b978-0-08-098212-0.00004-2
• Alcaide, A.; Llebaria, A. Aziridine ring opening for the synthesis of sphingolipid analogues: Inhibitors of sphingolipid-metabolizing enzymes. The Journal of organic chemistry 2014, 79, 2993–3029. doi:10.1021/jo500061w
• Gupta, M. K.; Jadhav, S. K.; Bhoite, S. A.
• Weng, S.-S.; Lin, G.; Li, H.-C.; Yang, K.; Yang, T.-M.; Liu, H.; Sie, S. Nafion®‐supported oxovanadium‐catalyzed hydrophosphonylation of aldehydes under solventless conditions. Applied Organometallic Chemistry 2012, 26, 455–460. doi:10.1002/aoc.2879
• Kaboudin, B.; Haghighat, H. A novel method for the one-pot conversion of carboxylic acids to N,N-dimethylamides. Journal of the Iranian Chemical Society 2012, 9, 951–955. doi:10.1007/s13738-012-0112-5
• Kaboudin, B.; Mostafalu, R. Triethylphosphate/Phosphorus Pentoxide as an Efficient Reagent for the Phosphorylation of Phenols. Phosphorus, Sulfur, and Silicon and the Related Elements 2012, 187, 776–780. doi:10.1080/10426507.2011.639822
• Kaboudin, B.; Emadi, S.; Faghihi, M. R.; Fallahi, M.; Sheikh-Hasani, V. Synthesis of α-oxycarbanilinophosphonates and their anticholinesterase activities: the most potent derivative is bound to the peripheral site of acetylcholinesterase. Journal of enzyme inhibition and medicinal chemistry 2012, 28, 576–582. doi:10.3109/14756366.2012.663362
• Adelowo, F. E.

Explore citations to this article at