Библиография

1. 1. Prokhorov A.M., Kozhevnikov D.N. // Chem. Heterocycl. Compd. 2012. V. 48. № 8. P. 1153–1176. https://doi.org/10.1007/s10593-012-1117-9
2. 2. Wang S.-W., Guo W.-S., Wen Li-R., Li M. // RSC Adv. 2014. V. 4. P. 59218–59220. https://doi.org/10.1039/c4ra11294f
3. 3. Catozzi N., Bromley W.J., Wasnaire P., Gibson M., Taylor R.J.K. // Synlett. 2007. V. 14. P. 2217–2221. https://doi.org/10.1055/s-2007-984918
4. 4. Pfüller O.C., Sauer J. // Tetrahedron Lett. 1998. V. 39. № 48. P. 8821–8824. https://doi.org/10.1016/S0040-4039 (98)02043-7
5. 5. Shi B., Lewis W., Campbell I.B., Moody C.J. // Org. Lett. 2009. V. 11. № 16. P. 3686–3688. https://doi.org/10.1021/ol901502u
6. 6. Savchuk M.I., Shtaitz Y.K., Kopchuk D.S., Zyryanov G.V., Eltsov O.S., Pospelova T.A., Rusinov V.L., Chupa-khin  O.N. // Chem. Heterocycl. Comp. 2019. V. 55. P. 985–988. https://doi.org/10.1007/s10593-019-02566-7
7. 7. Kozhevnikov D.N., Kozhevnikov V.N., Prokhorov A.M., Ustinova M.M., Rusinov V.L., Chupakhin O.N., Aleksandrov G.G., König B. // Tetrahedron Lett. 2006. V. 47. P. 869–872. https://doi.org/10.1016/j.tetlet.2005.12.006
8. 8. Savchuk M.I., Kopchuk D.S., Taniya O.S., Nikonov I.L., Egorov I.N., Santra S., Zyryanov G.V., Chupakhin O.N., Charushin V.N. // J. Fluoresc. 2021. V. 31. P. 1099–1111. https://doi.org/10.1007/s10895-021-02714-3
9. 9. Chepchugov N.V., Kopchuk D.S., Kovalev I.S., Zyrya-nov G.V., Rusinov V.L., Chupakhin O.N. // Mendeleev Commun. 2016. V. 26. № 3. P. 220–222. https://doi.org/10.1016/j.mencom.2016.04.014
10. 10. Kopchuk D.S., Krinochkin A.P., Kovalev I.S., Taniya O.S., Zyryanov G.V., Rusinov V.L., Chupakhin O.N., Petrov A.Yu., Suvorova A.I. // AIP Conf. Proc. 2020. V. 2280. № 1. Article 040024. https://doi.org/10.1063/5.0018034
11. 11. Kopchuk D.S., Khasanov A.F., Chepchugov N.V., Kovalev I.S., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // Russ. J. Org. Chem. 2017. V. 53. P. 99–102. https://doi.org/10.1134/S1070428017010183
12. 12. Kopchuk D.S., Khasanov A.F., Kovalev I.S., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // Mendeleev Commun. 2013. V. 23. № 4. P. 209–211. https://doi.org/10.1016/j.mencom.2013.07.010
13. 13. Lorion M., Guillaumet G., Brière J.-F., Suzenet F. // Org. Lett. 2015. V. 17. № 12. P. 3154–3157. https://doi.org/10.1021/acs.orglett.5b01487
14. 14. Fershtat L.L., Larin A.A., Epishina M.A., Ovchinnikov I.V., Kulikov A.S., Ananyev I.V., Makhova N.N. // RSC Adv. 2016. V. 6. P. 31526–31539. https://doi.org/10.1039/C6RA05110C
15. 15. Kopchuk D.S., Nikonov I.L., Zyryanov G.V., Kovalev I.S., Rusinov V.L., Chupakhin O.N. // Chem. Heterocycl. Compd. 2014. V. 50. № 6. P. 907–910. https://doi.org/10.1007/s10593-014-1545-9
16. 16. Kopchuk D.S., Nikonov I.L., Khasanov A.F., Giri K., San-tra S., Kovalev I.S., Nosova E.V., Gundala S., Verkatapu-ram P., Zyryanov G.V., Majee A., Chupakhin O.N. // Org. Biomol. Chem. 2018. V. 16. № 28. P. 5119–5135. https://doi.org/10.1039/c8ob00847g
17. 17. Bhatt A., Singh R.K., Kant R. // Heterocyclic Chem. 2019. V. 56. P. 696–701. https://doi.org/10.1002/jhet.3451
18. 18. Nakka M., Tadikonda R., Rayavarapu S., Sarakula P., Vidavalur S. // Synthesis. 2015. V. 47. P. 517–525. https://doi.org/10.1055/s-0034-1378909
19. 19. Schmidt M.A., Qian X. // Tetrahedron Lett. 2013. V. 54. P. 5721–5726. https://doi.org/10.1016/j.tetlet.2013.08.024
20. 20. Alekseyev R.S., Amirova S.R., Kabanova E.V., Tere-nin V.I. // Chem. Heterocycl. Compd. 2014. V. 50. № 9. P. 1305–1315. https://doi.org/10.1007/s10593-014-1593-1
21. 21. Chupakhin O.N., Rusinov V.L., Ulomsky E.N., Kozhevnikov D.N., Neunhoeffer H. // Mendeleev Commun. 1997. V. 7. № 2. P. 66–67. https://doi.org/10.1070/MC1997v007n02ABEH000700
22. 22. Shabunina O.V., Shtaitz Y.K., Kopchuk D.S., Krinoch-kin A.P., Santra S., Zyryanov G.V., Wang Z., Rusinov V.L., Chupakhin O.N. // Chem. Heterocycl. Compd. 2021. V. 57. № 4. P. 462–466. https://doi.org/10.1007/s10593-021-02924-4
23. 23. Kozhevnikov V. Preparation of metal-pyridine derivative complexes for use in medical imaging. Patent WO 116037 (A1). 2019.
24. 24. Shtaitz Ya.K., Savchuk M.I., Starnovskaya E.S., Krinochkin A.P., Kopchuk D.S., Santra S., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // AIP Conf. Proc. 2019. V. 2063. Article 040050. https://doi.org/10.1063/1.5087382
25. 25. Savchuk M.I., Starnovskaya E.S., Shtaitz Y.K., Kop-chuk D.S., Nosova E.V., Zyryanov G.V., Rusinov V.L., Chupakhin O.N. // Russ. J. Gen. Chem. 2018. V. 88. P. 2213–2215. https://doi.org/10.1134/S1070363218100316
26. 26. Kumar N.S., Shafikov M.Z., Whitwood A.C., Donnio B., Karadakov P.B., Kozhevnikov V.N., Bruce D.W. // Chem. Eur. J. 2016. V. 22. P. 8215–8233. https://doi.org/10.1002/chem.201505072
27. 27. Shafikov M.Z., Kozhevnikov D.N., Bodensteiner M., Brandl F., Czerwieniec R. // Inorg. Chem. 2016. V. 55. P. 7457–7476. https://doi.org/10.1021/acs.inorgchem.6b00704
28. 28. Krayushkin M.M., Sedishev I.P., Yarovenko V.N., Zavarzin I.V., Kotovskaya S.K., Kozhevnikov D.N., Charu-shin V.N. // Russ. J. Org. Chem. 2008. V. 44. № 3. P. 407–411. https://doi.org/10.1134/S1070428008030160
29. 29. Wang S.-W., Guo W.-S., Wen L.-R., Li M. // RSC Adv. 2014. V. 4. P. 59218–59220. https://doi.org/10.1039/C4RA11294F
30. 30. Taylor E.C., McDaniel K.F., Warner J.C. // Tetrahedron Lett. 1987. V. 28. № 18. P. 1977–1980. https://doi.org/10.1016/S0040-4039 (00)96024-6
31. 31. Zhang Y., Tang Q., Luo M. // Org. Biomol. Chem. 2011. V. 9. P. 4977–4982. https://doi.org/10.1039/c1ob05328k
32. 32. Ren F., Zhang Y., Hu L., Luo M. // Arkivoc. 2013. V. 3. P. 165–173. https://doi.org/10.3998/ark.5550190.0014.313