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Cite the Following Article
1,2,3-Triazoles as leaving groups in SNAr–Arbuzov reactions: synthesis of C6-phosphonated purine derivatives
Kārlis-Ēriks Kriķis, Irina Novosjolova, Anatoly Mishnev and Māris Turks
Beilstein J. Org. Chem. 2021, 17, 193–202.
https://doi.org/10.3762/bjoc.17.19
How to Cite
Kriķis, K.-Ē.; Novosjolova, I.; Mishnev, A.; Turks, M. Beilstein J. Org. Chem. 2021, 17, 193–202. doi:10.3762/bjoc.17.19
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Scholarly Works
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- Burcevs, A.; Sebris, A.; Novosjolova, I.; Mishnev, A.; Turks, M. Synthesis of Indole Derivatives via Aryl Triazole Ring-Opening and Subsequent Cyclization. Molecules (Basel, Switzerland) 2025, 30, 337. doi:10.3390/molecules30020337
- Tulaite, K.; Jovaišaitė, J.; Jonusauskas, G.; Burcevs, A.; Kapilinskis, Z.; Novosjolova, I.; Turks, M.; Kreiza, G.; Hean, L.; Chu, H.-W.; Chang, H.-T.; Jursenas, S. Purine-Based Chemical Probe with Homo Switching for Intracellular Detection of Mercury Ions. Elsevier BV 2025. doi:10.2139/ssrn.5129922
- Ritere, A.; Jeminejs, A.; Bizde Na, E. R.; Turks, M. R.; Novosjolova, I. Synthesis of 6-Selanyl-2-triazolylpurine Derivatives Using 2,6-Bistriazolylpurines as Starting Materials. ACS omega 2024, 9, 6366–6380. doi:10.1021/acsomega.3c04994
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- Mele, L.; El Bekri Saudain, R.; Pirat, J.-L.; Virieux, D.; Ayad, T. Efficient microwave-assisted selective alkaline hydrolysis of diversely substituted phosphonate esters. Green Chemistry 2022, 24, 7900–7905. doi:10.1039/d2gc02288e
- Kostoudi, S.; Pampalakis, G. Improvements, Variations and Biomedical Applications of the Michaelis-Arbuzov Reaction. International journal of molecular sciences 2022, 23, 3395. doi:10.3390/ijms23063395
- Appy, L.; Peyrottes, S.; Roy, B. Supported Synthesis of Adenosine Nucleotides and Derivatives on a Benzene-Centered Tripodal Soluble Support. European Journal of Organic Chemistry 2021, 2022. doi:10.1002/ejoc.202100544
- Cīrule, D.; Novosjolova, I.; Bizdēna, Ē.; Turks, M. 1,2,3-Triazoles as leaving groups: SNAr reactions of 2,6-bistriazolylpurines with O- and C-nucleophiles. Beilstein journal of organic chemistry 2021, 17, 410–419. doi:10.3762/bjoc.17.37