Recent advances in the chemistry of two-carbon nitro-containing synthetic equivalents

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Abstract

To date, nitro-containing compounds form one of the most important classes of organic compounds. The chemistry of these molecules attracts attention primarily due to their use as high-energy reagents and drugs. Also, the introduction of a nitro group is a popular synthetic strategy for constructing new organic molecules. The present review summarizes the latest research findings of compounds bearing a nitro group on a two-carbon moiety such as aminonitroethylenes, α,α-bis(alkylsulfanyl)nitroalkenes and their amino derivatives, α-nitroketones, alkyl nitroacetates and nitroacetonitrile. The literature data are systematized according to the type of chemical reactions such as reactions between nucleophiles and electrophiles, various cyclization reactions, reactions at the C–H bond, etc. The reactivities of the said nitro compounds and the conditions of chemical transformations are compared to assess the prospects of their application. Bibliography — 314 references.

About the authors

Daniil Nikolaevich Lyapustin

Ural Federal University named after the First President of Russia B. N. Yeltsin

Victor Vladimirovich Fedotov

Ural Federal University named after the First President of Russia B. N. Yeltsin

Evgeny Nartsissovich Ulomsky

Ural Federal University named after the First President of Russia B. N. Yeltsin

Email: ulomsky@yandex.ru
Doctor of chemical sciences, Professor

Vladimir Leonidovich Rusinov

I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences; Ural Federal University named after the First President of Russia B. N. Yeltsin

Email: rusinov@htf.ustu.ru
Scopus Author ID: 7006493788
Doctor of chemical sciences, Head Scientist Researcher

Oleg Nikolaevich Chupakhin

I. Ya. Postovsky Institute of Organic Synthesis, Ural Branch of Russian Academy of Sciences; Ural Federal University named after the First President of Russia B. N. Yeltsin

Email: chupakhin@ios.uran.ru
Doctor of chemical sciences, Professor

References

  1. O.T.O'Sullivan, M.J.Zdilla. Chem. Rev., 120, 5682 (2020)
  2. Y.Qu, S.P.Babailov. J. Mater. Chem. A, 6, 1915 (2018)
  3. S.G.Zlotin, A.M.Churakov, I.L.Dalinger, O.A.Luk'yanov, N.N.Makhova, A.Y.Sukhorukov, V.A.Tartakovsky. Mendeleev Commun., 27, 535 (2017)
  4. H.Gao, Q.Zhang, J.M.Shreeve. J. Mater. Chem. A, 8, 4193 (2020)
  5. S.G.Zlotin, I.L.Dalinger, N.N.Makhova, V.A.Tartakovsky. Russ. Chem. Rev., 89, 1 (2020)
  6. M.Szala, J.J.Sabatini. Z. Anorg. Allg. Chem., 644, 262 (2018)
  7. J.H.Boyer. Nitroazoles: The C-Nitro Derivatives of Five- Membered N- and N,O-Heterocycles. (Weinheim: VCH Publishers, 1986)
  8. L.Larina, V.Lopyrev. Nitroazoles: Synthesis, Structure and Applications (Ser. Topics in Applied Chemistry). (Dordrecht, Heidelberg, London, New York: Springer, 2009)
  9. M.Kurpet, R.Jdrysiak, J.Suwinski. Chem. Heterocycl. Compd., 48, 1737 (2013)
  10. V.L.Rusinov, O.N.Chupakhin. Nitroaziny (Nitroazines). (Ed. V.M.Vlasov). (Novosibirsk: Izd. SO AN SSSR, 1991)
  11. A.M.Rice, Y.Long, S.B.King. Biomolecules, 11, 267 (2021)
  12. C.B.Scarim, C.M.Chin. Med. Chem. Res., 28, 2099 (2019)
  13. V.L.Rusinov, V.N.Charushin, O.N.Chupakhin. Russ. Chem. Bull., Int. Ed., 67, 573 (2018)
  14. V.L.Rusinov, E.N.Ulomskii, O.N.Chupakhin, V.N.Charushin. Russ. Chem. Bull., Int. Ed., 57, 985 (2008)
  15. K.Nepali, H.Y.Lee, J.P.Liou. J. Med. Chem., 62, 2851 (2019)
  16. N.Ono. The Nitro Group in Organic Chemistry. (New York: Wiley-VCH, 2001)
  17. S.Gabrielli, E.Chiurchi, A.Palmieri. Adv. Synth. Catal., 361, 630 (2019)
  18. A. apczuk-Krygier, A.Kcka-Zych, K.Kula. Curr. Chem. Lett., 8, 13 (2019)
  19. D.A.Alonso, A.Baeza, R.Chinchilla, C.Gomez, G.Guillena, I.M.Pastor, D.J.Ramcn. Molecules, 22, 895 (2017)
  20. B.Maji. Asian J. Org. Chem., 7, 70 (2018)
  21. A.Mondal, S.Bhowmick, A.Ghosh, T.Chanda, K.C.Bhowmick. Tetrahedron: Asymmetry, 28, 849 (2017)
  22. M.Marcekova, B.Ferko, K.R.Detkova, P.Jakubec. Molecules, 25, 3390 (2020)
  23. V.A.Motornov, S.L.Ioffe, A.A.Tabolin. Targ. Heterocycl. Syst., 23, 237 (2019)
  24. R.Ballini, N.Araujo, M.V.Gil, E.Roman, J.A.Serrano. Chem. Rev., 113, 3493 (2013)
  25. R.Ballini, A.Palmieri. Adv. Synth. Catal., 360, 2240 (2018)
  26. X.Li, L.Guo, C.Peng, B.Han. Chem. Rec., 19, 394 (2019)
  27. F.Hao, N.Nishiwaki. Heterocycles, 99, 54 (2019)
  28. G.K.Windler, P.F.Pagoria, K.P.C.Vollhardt. Synthesis, 46, 2383 (2014)
  29. Saigal, S.Khan, H.Rahman, Shafiullah, M.Khan. RSC Adv., 9, 14477 (2019)
  30. V.O.Hervin, E.P.Coutant, G.Gagnot, Y.L.Janin. Synthesis, 49, 4093 (2017)
  31. S.E.Creegan, D.G.Piercey. RSC Adv., 10, 39478 (2020)
  32. K.Iwai, N.Nishiwaki. J. Org. Chem., 86, 13177 (2021)
  33. V.L.Rusinov, R.A.Drokin, D.V.Tiufiakov, E.K.Voinkov, E.N.Ulomsky. Mendeleev Commun., 30, 177 (2020)
  34. J.Kuwabara, Y.Sawada, M.Yoshimatsu. Org. Lett., 20, 1130 (2018)
  35. E.Brenna, M.Crotti, F.G.Gatti, D.Monti, F.Parmeggiani, S.Santangelo. ChemCatChem., 9, 2480 (2017)
  36. M.V.Pilipecz, T.R.Varga, P.Krall, Z.Vincze, Z.Mucsi, R.Deme, P.T.Szabo, P.Nemes. Synth. Commun., 50, 1712 (2020)
  37. A.Alekszi-Kaszas, P.Nemes, G.Toth, J.Halasz, P.Scheiber. Synth. Commun., 48, 2099 (2018)
  38. D.N.Lyapustin, E.N.Ulomsky, T.O.Zanakhov, V.L.Rusinov. J. Org. Chem., 84, 15267 (2019)
  39. D.N.Lyapustin, E.N.Ulomsky, I.A.Balyakin, A.V.Shchepochkin, V.L.Rusinov, O.N.Chupakhin. Molecules, 26, 4719 (2021)
  40. D.N.Lyapustin, E.N.Ulomsky, V.L.Rusinov. Chem. Heterocycl. Compd., 56, 1465 (2020)
  41. C.H.Zhang, R.Huang, X.Qing, J.Lin, S.J.Yan. Chem. Commun., 56, 3488 (2020)
  42. Y.Siddaraju, K.R.Prabhu. J. Org. Chem., 82, 3084 (2017)
  43. S.Ogasawara, Y.Hayashi. Synthesis, 49, 424 (2017)
  44. Y.Luo, K.X.Xie, D.F.Yue, X.M.Zhang, X.Y.Xu, W.C.Yuan. Tetrahedron, 73, 6217 (2017)
  45. L.Rodriguez, R.Fisera, B.Gaalova, K.Koci, H.Bujdakova, M.Meciarova, R.Gorova, H.Jurdakova, R.Sebesta. Eur. J. Org. Chem., 2565 (2020)
  46. M.Micucci, M.Viale, A.Chiarini, D.Spinelli, M.Frosini, C.Tavani, M.Maccagno, L.Bianchi, R.Gangemi, R.Budriesi. Molecules, 25, 1056 (2020)
  47. J.Jose, C.D.J.Tavares, N.D.Ebelt, A.Lodi, R.Edupuganti, X.Xie, A.K.Devkota, T.S.Kaoud, C.L.van den Berg, E.V.Anslyn, S.Tiziani, C.Bartholomeusz, K.N.Dalby. ACS Med. Chem. Lett., 8, 1072 (2017)
  48. W.T.Barker, C.E.Chandler, R.J.Melander, R.K.Ernst, C.Melander. Bioorg. Med. Chem., 27, 1776 (2019)
  49. J.H.Son, P.W.Phuan, J.S.Zhu, E.Lipman, A.Cheung, K.Y.Tsui, D.J.Tantillo, A.S.Verkman, P.M.Haggie, M.J.Kurth. Eur. J. Med. Chem., 209, 112888 (2021)
  50. C.Dockendorff, D.M.Gandhi, I.H.Kimball, K.S.Eum, R.Rusinova, H.I.Ingclfsson, R.Kapoor, T.Peyear, M.W.Dodge, S.F.Martin, R.W.Aldrich, O.S.Andersen, J.T.Sack. Biochemistry, 57, 2733 (2018)
  51. W.Gao, H.Lv, T.Zhang, Y.Yang, L.W.Chung, Y.D.Wu, X.Zhang. Chem. Sci., 8, 6419 (2017)
  52. M.Pirola, M.E.Compostella, L.Raimondi, A.Puglisi, M.Benaglia. Synthesis, 50, 1430 (2018)
  53. B.Zhang, L.Shi. Catal. Lett., 149, 2836 (2019)
  54. B.A.Chalyk, K.V.Hrebeniuk, K.S.Gavrilenko, I.B.Kulik, A.B.Rozhenko, D.M.Volochnyuk, O.S.Liashuk, O.O.Grygorenko. Eur. J. Org. Chem., 5585 (2018)
  55. B.M.Trost, Y.Wang. Angew. Chem., Int. Ed., 57, 11025 (2018)
  56. B.M.Trost, Z.Jiao, C.I.Hung. Angew. Chem., Int. Ed., 58, 15154 (2019)
  57. B.M.Trost, C.Zhu, C.C.Ence. Org. Lett., 23, 2460 (2021)
  58. B.M.Trost, L.Zhang, T.M.Lam. Org. Lett., 20, 3938 (2018)
  59. B.M.Trost, D.Zell, C.Hohn, G.Mata, A.Maruniak. Angew. Chem., Int. Ed., 57, 12916 (2018)
  60. B.M.Trost, Z.Jiao, Y.Liu, C.Min, C.I.J.Hung. J. Am. Chem. Soc., 142, 18628 (2020)
  61. Y.Du, J.Li, K.Chen, C.Wu, Y.Zhou, H.Liu. BJOC, 13, 1342 (2017)
  62. V.Y.Shuvalov, A.S.Rupp, A.S.Fisyuk, A.K.Kuratova, A.A.Nefedov, G.P.Sagitullina. ChemistrySelect, 4, 1696 (2019)
  63. V.Y.Shuvalov, A.S.Rupp, A.K.Kuratova, A.S.Fisyuk, A.A.Nefedov, G.P.Sagitullina. Synlett, 30, 919 (2019)
  64. A.V.Lukashenko, D.V.Osipov, V.A.Osyanin, Y.N.Klimochkin. Chem. Heterocycl. Compd., 53, 1369 (2017)
  65. A.C.Lindsay, P.A.Kilmartin, J.Sperry. Org. Biomol. Chem., 19, 7903 (2021)
  66. D.Cheng, L.Wu, Z.Deng, X.Xu, J.Yan. Adv. Synth. Catal., 359, 4317 (2017)
  67. K.Aradi, A.Meszaros, B.L.Toth, Z.Vincze, Z.Novak. J. Org. Chem., 82, 11752 (2017)
  68. S.Verma, M.Kumar, A.K.Verma. Org. Lett., 22, 130 (2020)
  69. R.R.Zalte, A.A.Festa, N.E.Golantsov, K.Subramani, V.B.Rybakov, A.V.Varlamov, R.Luque, L.G.Voskressensky. Chem. Commun., 56, 6527 (2020)
  70. Patent EP 0104423 (1983)
  71. R.Gompper, H.Schaefer. Chem. Ber., 100, 591 (1967)
  72. H.Hosseini, M.Bayat. RSC Adv., 9, 7218 (2019)
  73. M.Bayat, F.S.Hosseini. Tetrahedron Lett., 58, 1616 (2017)
  74. M.Bayat, F.S.Hosseini. J. Sulfur Chem., 39, 279 (2018)
  75. Z.S.Razavi, M.Bayat, H.Hosseini. RSC Adv., 10, 31039 (2020)
  76. H.Hosseini, M.Bayat. RSC Adv., 8, 41218 (2018)
  77. A.A.Mohammadi, S.Taheri, A.Amouzegar, R.Ahdenov, M.R.Halvagar, A.S.Sadr. J. Mol. Struct., 1139, 166 (2017)
  78. S.Nasri, F.S.Hosseini, M.Bayat. Tetrahedron, 74, 4409 (2018)
  79. M.Bayat, F.S.Hosseini, B.Notash. Tetrahedron, 73, 1196 (2017)
  80. M.Bayat, M.Rezaei. Monatsh. Chem., 148, 2097 (2017)
  81. M.Bayat, M.Rezaei. J. Iran. Chem. Soc., 15, 769 (2018)
  82. M.Saeedi, M.Khoshdoun, S.Taheri, A.Z.Halimehjani, A.Mohammadi, M.R.Halvagar, V.Amani. SynOpen, 5, 108 (2021)
  83. A.A.Mohammadi, S.Taheri, A.Amouzegar. J. Heterocycl. Chem., 54, 2085 (2017)
  84. M.Bayat, M.Rezaee, L.-G.Zhu. J. Heterocycl. Chem., 54, 2748 (2017)
  85. Z.Zhang, A.Yuan, C.Zheng. Synth. Commun., 48, 2973 (2018)
  86. M.Bayat, F.Safari, S.Nasri, F.S.Hosseini. Monatsh. Chem., 150, 703 (2019)
  87. A.Alizadeh, F.Bayat, L.G.Zhu. J. Iran. Chem. Soc., 15, 337 (2018)
  88. M.M.Vala, M.Bayat, Y.Bayat. J. Sulfur Chem., 41, 542 (2020)
  89. X.Wu, Z.Zhao, Y.Song, C.Guo. Heterocycles, 94, 1736 (2017)
  90. M.Esmaielzade Rostami, B.Gorji, R.Zadmard. J. Heterocycl. Chem., 55, 2532 (2018)
  91. A.Alizadeh, A.Roosta, M.R.Halvagar. J. Iran. Chem. Soc., 14, 2157 (2017)
  92. A.Alizadeh, A.Roosta, R.Rezaiyehraad. J. Iran. Chem. Soc., 17, 1123 (2020)
  93. A.Rezvanian, F.Noorakhtar, G.M.Ziarani, F.Mahajer. Monatsh. Chem., 151, 1581 (2020)
  94. M.R.Asghariganjeh, A.A.Mohammadi, E.Tahanpesar, A.Rayatzadeh, S.Makarem. Mol. Divers., 25, 509 (2021)
  95. A.Rezvanian, F.Amoozadkhalili, A.Roosta. Chem. Pap., 75, 2417 (2021)
  96. F.Rahimi, M.Bayat, H.Hosseini. RSC Adv., 9, 16384 (2019)
  97. F.S.Hosseini, S.Nasri, M.Bayat. J. Sulfur Chem., 39, 622 (2018)
  98. F.S.Hosseini, M.Bayat. Curr. Org. Synth., 15, 982 (2018)
  99. N.Poomathi, P.T.Perumal, S.Ramakrishna. Green Chem., 19, 2524 (2017)
  100. Y.Ji, L.Li, G.Zhu, Y.Zhou, X.Lu, W.He, L.Gao, L.Rong. J. Heterocycl. Chem., 57, 1781 (2020)
  101. M.M.Khan, Saigal, S.Khan, S.Shareef, S.C.Sahoo. RSC Adv., 8, 41892 (2018)
  102. P.Anaikutti, P.Makam. Bioorg. Chem., 105, 104379 (2020)
  103. K.Hajiyeva, A.Ismiev, M.Franz, M.Schmidtmann, J.Martens, A.Maharramov. Synth. Commun., 47, 2031 (2017)
  104. X.X.Du, R.Huang, C.L.Yang, J.Lin, S.J.Yan. RSC Adv., 7, 40067 (2017)
  105. C.H.Zhang, R.Huang, X.M.Hu, J.Lin, S.J.Yan. J. Org. Chem., 83, 4981 (2018)
  106. B.Q.Wang, C.H.Zhang, X.X.Tian, J.Lin, S.J.Yan. Org. Lett., 20, 660 (2018)
  107. L.Chen, B.Wang, Y.Zhao, S.Yan, J.Lin. Chin. J. Org. Chem., 37, 1433 (2017)
  108. E.Safari, A.Maryamabadi, A.Hasaninejad. RSC Adv., 7, 39502 (2017)
  109. A.Maryamabadi, A.Hasaninejad, N.Nowrouzi, G.Mohebbi. Bioorg. Med. Chem., 25, 2057 (2017)
  110. C.H.Zhang, R.Huang, Z.W.Zhang, J.Lin, S.J.Yan. J. Org. Chem., 86, 5744 (2021)
  111. Q.Luo, R.Huang, Q.Xiao, Y.Yao, J.Lin, S.J.Yan. J. Org. Chem., 84, 1999 (2019)
  112. G.Z.Yang, X.F.Shang, P.le Cheng, X.D.Yin, J.K.Zhu, Y.Q.Liu, J.Zhang, Z.J.Zhang. Molecules, 23, 2422 (2018)
  113. R.Sayyar, S.Makarem, B.Mirza. J. Heterocycl. Chem., 56, 1839 (2019)
  114. X.X.Du, Q.X.Zi, Y.M.Wu, Y.Jin, J.Lin, S.J.Yan. Green Chem., 21, 1505 (2019)
  115. H.P.Zhu, K.Xie, X.H.He, W.Huang, R.Zeng, Y.Fan, C.Peng, G.He, B.Han. Chem. Commun., 55, 11374 (2019)
  116. M.Bayat, Z.Amiri. Tetrahedron Lett., 58, 4260 (2017)
  117. M.Afsharnezhad, M.Bayat, F.S.Hosseini. Mol. Divers., 24, 379 (2020)
  118. F.S.Hosseini, M.Bayat, M.Afsharnezhad. RSC Adv., 9, 39466 (2019)
  119. A.Mohammadi, M.Bayat, S.Nasri. RSC Adv., 9, 16525 (2019)
  120. S.Ghadiri, M.Bayat, F.S.Hosseini. Monatsh. Chem., 150, 1079 (2019)
  121. S.Ghadiri, M.Bayat, F.S.Hosseini. J. Heterocycl. Chem., 55, 2693 (2018)
  122. K.Sathish, S.Nagaraju, D.Kashinath. Synth. Commun., 51, 1242 (2021)
  123. M.M.Khan, B.Saigal, S.Shareef, S.Khan, S.C.Sahoo. Synth. Commun., 48, 2683 (2018)
  124. M.Khan, S.Shareef, Saigal, S.C.Sahoo. RSC Adv., 9, 26393 (2019)
  125. P.Padmaja, J.S.Anireddy, P.N.Reddy. Chem. Heterocycl. Compd., 54, 812 (2018)
  126. B.R.Reddy, P.N.Reddy. Asian J. Chem., 31, 785 (2019)
  127. P.Nagaraju, P.Padmaja, P.N.Reddy. Lett. Org. Chem., 16, 468 (2018)
  128. M.M.Khan, Saigal, S.Khan. J. Heterocycl. Chem., 56, 1020 (2019)
  129. Z.Pan, H.Xu, K.Mao, L.Dai, L.Zhao, L.Rong. J. Heterocycl. Chem., 56, 1393 (2019)
  130. J.Wang, Z.Zhao, Z.Li, J.Mao, W.Zhang, C.Guo. Chem. Heterocycl. Compd., 54, 25 (2018)
  131. S.D.Hadiyal, N.D.Parmar, P.L.Kalavadiya, J.N.Lalpara, H.S.Joshi. Russ. J. Org. Chem., 56, 671 (2020)
  132. A.V.Lukashenko, D.V.Osipov, V.A.Osyanin, Y.N.Klimochkin. Chem. Heterocycl. Compd., 56, 521 (2020)
  133. S.K.Krishnammagari, K.T.Lim, B.G.Cho, Y.T.Jeong. Phosphorus, Sulfur, Silicon Relat. Elem., 193, 574, (2018)
  134. V.V.Fedotov, E.N.Ulomsky, K.V.Savateev, E.M.Mukhin, D.A.Gazizov, E.B.Gorbunov, V.L.Rusinov. Synthesis, 52, 3622 (2020)
  135. M.V.Reddy, K.R.Byeon, S.H.Park, D.W.Kim. Tetrahedron, 73, 5289 (2017)
  136. A.M.Jadhav, Y.I.Kim, K.T.Lim, Y.T.Jeong. Tetrahedron Lett., 59, 554 (2018)
  137. A.B.Atar, E.Han, J.Kang. Mol. Divers.. 24. 443 (2020)
  138. F.Safari, M.Bayat, S.Nasri, S.Karami. Bioorg. Med. Chem. Lett., 30, 127111 (2020)
  139. M.Rezaei, M.Bayat, B.Notash. J. Heterocycl. Chem., 57, 880 (2020)
  140. M.Bayat, S.Nasri. Tetrahedron Lett., 58, 3107 (2017)
  141. B.Balachandra, S.Shanmugam. ChemistrySelect, 3, 2037 (2018)
  142. M.M.Khan, S.Khan, Saigal, A.Singh. Tetrahedron Lett., 60, 150996 (2019)
  143. A.Chaudhary, J.M.Khurana, G.Khanna, M.Saroha. ChemistrySelect, 3, 6334 (2018)
  144. F.Rahimi, H.Hosseini, M.Bayat. Tetrahedron Lett., 59, 818 (2018)
  145. S.Siddiqui, R.A.Rather, Z.N.Siddiqui. Appl. Organomet. Chem., 35, e6232 (2021)
  146. Q.X. Zi, C.L.Yang, K.Li, Q.Luo, J.Lin, S.J.Yan. J. Org. Chem., 85, 327 (2020)
  147. J.Liu, Q.Li, Z.M.Cao, Y.Jin, J.Lin, S.J.Yan. J. Org. Chem., 84, 1797 (2019)
  148. A.Alizadeh, H.Ghasemzadeh, H.P.Xiao. ChemistrySelect, 4, 7446 (2019)
  149. D.Y.Luo, X.M.Hu, R.Huang, S.S.Cui, S.J.Yan. Tetrahedron, 92, 132275 (2021)
  150. S.Mojikhalifeh, A.Hasaninejad. Tetrahedron Lett., 58, 2574 (2017)
  151. A.Hasaninejad, S.Mojikhalifeh, M.Beyrati. Appl. Organomet. Chem., 32, e4380 (2018)
  152. Y.Chen, X.Cao, X.Chen, Z.Li, X.Xu. J. Chem. Res., 45, 835 (2021)
  153. X.Zhang, Y.Wang, Z.Xu, X.Shao, Z.Liu, X.Xu, P.Maienfisch, Z.Li. J. Agric. Food Chem., 69, 3005 (2021)
  154. X.Zhang, W.Yu, X.Xu, X.Shao, Z.Li. Bioorg. Med. Chem. Lett., 43, 127960 (2021)
  155. Y.L.Ma, K.M.Wang, R.Huang, J.Lin, S.J.Yan. Green Chem., 19, 3574 (2017)
  156. Z.Pan, K.Mao, G.Zhu, C.Wang, J.Zhang, L.Rong. J. Org. Chem., 85, 3364 (2020)
  157. C.Lei, Z.Gao, X.Shao, X.Xu, Z.Li. Chin. J. Chem., 35, 1517 (2017)
  158. C.Lei, L.Geng, X.Xu, X.Shao, Z.Li. Bioorg. Med. Chem. Lett., 28, 831 (2018)
  159. A.Sagirli. Synth. Commun., 50, 3298 (2020)
  160. B.-Q.Wang, Q.Luo, Q.Xiao, J.Lin, S.-J.Yan. ACS Sustain. Chem. Eng., 5, 8382 (2017)
  161. F.Peytam, M.Adib, S.Mahernia, M.Rahmanian-Jazi, M.Jahani, B.Masoudi, M.Mahdavi, M.Amanlou. Bioorg. Chem., 87, 1 (2019)
  162. Y.Li, H.Liu, Z.Huang, H.Wang, Z.Yu. Tetrahedron Lett., 82, 153396 (2021)
  163. M.K.Rogacki, E.Pitta, O.Balabon, S.Huss, E.M.Lopez-Roman, A.Argyrou, D.Blanco-Ruano, M.Cacho, C.M.L.vande Velde, K.Augustyns, L.Ballell, D.Barros, R.H.Bates, F.Cunningham, P.van der Veken. J. Med. Chem., 61, 11221 (2018)
  164. S.Fuse, T.Oishi, K.Matsumura, Y.Hayashi, S.Kawauchi, H.Nakamura. Org. Biomol. Chem., 18, 93 (2019)
  165. P.Li, S.Wu, T.Xiao, Y.Li, Z.Su, W.Wei, F.Hao, G.Hu, F.Lin, X.Chen, Z.Gu, T.Lin, H.He, J.Li, S.Chen. Bioorg. Med. Chem., 28, 115551 (2020)
  166. A.V.Sadovoy, V.V.Kattsyna, P.S.Protopopova, Y.V.Nelyubina, A.A.Pavlov, K.A.Kochetkov, L.A.Sviridova. Heteroat. Chem., 29, e21451 (2018)
  167. S.Yellappa. J. Heterocycl. Chem., 57, 1083 (2020)
  168. R.I.Baichurin, A.A.Fedorushchenko, N.I.Aboskalova, L.V.Baichurina, A.V.Felgendler, S.V.Makarenko. Russ. J. Gen. Chem., 89, 870 (2019)
  169. H.Asahara, S.Kawakami, K.Yoshioka, S.Tani, K.Umezu, N.Nishiwaki. Bull. Chem. Soc. Jpn., 91, 1715 (2018)
  170. R.I.Baichurin, L.M.Alizada, N.I.Aboskalova, S.V.Makarenko. Russ. J. Gen. Chem., 88, 36 (2018)
  171. R.I.Baichurin, A.A.Reshetnikov, V.D.Sergeev, N.I.Aboskalova, S.V.Makarenko. Russ. J. Gen. Chem., 89, 865 (2019)
  172. S.Trichili, K.Khemakhem, L.Maktouf, H.Ammar, S.Abid. Lett. Org. Chem., 14, 2 (2017)
  173. L.Zhu, P.Yan, L.Zhang, Z.Chen, X.Zeng, G.Zhong. RSC Adv., 7, 51352 (2017)
  174. O.Y.Fedorovskii, A.Y.Volkonskii, A.S.Golubev, Y.Y.Spiridonov, N.D.Chkanikov. Russ. Chem. Bull., Int. Ed., 66, 1116 (2017)
  175. Y.S.Chen, Y.Zheng, Z.J.Chen, Z.Z.Xie, X.C.He, J.A.Xiao, K.Chen, H.Y.Xiang, H.Yang. Org. Biomol. Chem., 19, 7074 (2021)
  176. S.Peraka, A.Hussain, D.B.Ramachary. J. Org. Chem., 83, 9795 (2018)
  177. D.Pechalrieu, D.Dauzonne, P.B.Arimondo, M.Lopez. Eur. J. Med. Chem., 186, 111829 (2020)
  178. B.S.Gore, C.C.Lee, J.Lee, J.J.Wang. Adv. Synth. Catal., 361, 3373 (2019)
  179. A.Boguszewska-Czubara, A.Lapczuk-Krygier, K.Rykala, A.Biernasiuk, A.Wnorowski, L.Popiolek, A.Maziarka, A.Hordyjewska, R.Jasinski. J. Enzyme Inhib. Med. Chem., 31, 900 (2015)
  180. E.K.Voinkov, E.N.Ulomskiy, V.L.Rusinov, K.V.Savateev, V.V.Fedotov, E.B.Gorbunov, M.L.Isenov, O.S.Eltsov. Mendeleev Commun., 26, 172 (2016)
  181. T.Ling, V.Hadi, J.Bollinger, F.Rivas. Bioorg. Chem., 99, 103846 (2020)
  182. C.L.Hugelshofer, J.Bao, J.Du, E.Ashley, W.Yu, T.Ji, B.Hu, D.Liu, R.Rondla, S.Karampuri, V.Sharma, K.Ethiraj, Y.-H.Lim. Org. Lett., 23, 943 (2021)
  183. R.Mato, E.Reyes, L.Carrillo, U.Uria, L.Prieto, R.Manzano, J.L.Vicario. Chem. Commun., 56, 13149 (2020)
  184. X.M.Hu, H.Dong, Y.D.Li, P.Huang, Z.Tian, P.A.Wang. RSC Adv., 9, 27883 (2019)
  185. Y.J.Bai, X.M.Hu, Y.J.Bai, X.H.Zheng, S.Y.Zhang, P.-A.Wang. Tetrahedron, 101, 132511 (2021)
  186. Y.Liu, L.Ye, Z.Shi, X.Yang, Z.Zhao, X.Li. Chirality, 30, 1287 (2018)
  187. G.Bosica, K.Polidano. J. Chem., Art. ID 6267036 (2017)
  188. Y.Zhang, R.Li, Y.H.He, Z.Guan. Catal. Lett., 147, 633 (2017)
  189. G.Gagnot, V.Hervin, E.P.Coutant, S.Desmons, R.Baatallah, V.Monnot, Y.L.Janin. BJOC, 14, 2846 (2018)
  190. A.Cristofol, E.C.Escudero-Adan, A.W.Kleij. J. Org. Chem., 83, 9978 (2018)
  191. J.Wang, T.A.Young, F.Duarte, P.J.Lusby. J. Am. Chem. Soc., 142, 17743 (2020)
  192. J.Sun, Y.Li, Y.Gui, Y.Xu, Z.Zha, Z.Wang. Chin. Chem. Lett., 30, 569 (2019)
  193. M.Fofana, Y.Dudognon, L.Bertrand, T.Constantieux, J.Rodriguez, I.Ndiaye, D.Bonne, X.Bugaut. Eur. J. Org. Chem., 3486 (2020)
  194. K.Mondal, S.C.Pan. J. Org. Chem., 83, 5301 (2018)
  195. L.K.Faizullina, Y.S.Galimova, S.M.Salikhov, F.A.Valeev. Chem. Heterocycl. Compd., 56, 1434 (2020)
  196. H.Chen, J.Xie, D.Xing, J.Wang, J.Tang, Z.Yi, F.Xia, W.W.Qiu, F.Yang. Org. Biomol. Chem., 17, 1062 (2019)
  197. D.Song, F.Bi, N.Zhang, Y.Qin, X.Liu, Y.Teng, S.Ma. Bioorg. Med. Chem., 28, 115729 (2020)
  198. M.Vadivelu, S.Sampath, K.Muthu, K.Karthikeyan, C.Praveen. J. Org. Chem., 84, 13636 (2019)
  199. X.Pan, X.Xin, Y.Mao, X.Li, Y.Zhao, Y.Liu, K.Zhang, X.Yang, J.Wang. Molecules, 26, 3491 (2021)
  200. A.Rouf, E.ahin, C.Tanyeli. Tetrahedron, 73, 331 (2017)
  201. P.Das, M.H.Hasan, D.Mitra, R.Bollavarapu, E.J.Valente, R.Tandon, D.Raucher, A.T.Hamme. J. Org. Chem., 84, 6992 (2019)
  202. M.Vadivelu, S.Sampath, K.Muthu, K.Karthikeyan, C.Praveen. Adv. Synth. Catal., 363, 4941 (2021)
  203. K.I.Itoh, M.Hayakawa, R.Abe, S.Takahashi, K.Hasegawa, T.Aoyama. Synthesis, 53, 4636 (2021)
  204. A.L.Sigan, A.S.Golubev, E.V.Belyaeva, S.M.Gorfinkel, N.D.Kagramanov, Y.Y.Spiridonov, N.D.Chkanikov. Russ. Chem. Bull., Int. Ed., 68, 99 (2019)
  205. H.Yang, X.Q.Zhu, W.Wang, Y.Chen, Z.Hu, Y.Zhang, D.X.Hu, L.M.Yu, K.Agama, Y.Pommier, L.K.An. Bioorg. Chem., 111, 104881 (2021)
  206. S.C.Sahoo, S.C.Pan. Eur. J. Org. Chem., 1385 (2019)
  207. Y.Mukaijo, S.Yokoyama, N.Nishiwaki. Molecules, 25, 2048 (2020)
  208. H.J.Shen, Y.N.Duan, K.Zheng, C.Zhang. J. Org. Chem., 84, 14381 (2019)
  209. J.Svetlik, F.Turecek, K.Hartwich, K.Kozie, P.Pakulski, A.Paasz, J.Kalinowska-Tuscik, D.Ciez. Tetrahedron, 75, 2652 (2019)
  210. C.Y.Wang, F.Teng, Y.Li, J.H.Li. Org. Lett., 22, 4250 (2020)
  211. A.V.Aksenov, N.A.Aksenov, N.K.Kirilov, A.A.Skomorokhov, D.A.Aksenov, I.A.Kurenkov, E.A.Sorokina, M.A.Nobi, M.Rubin. RSC Adv., 11, 35937 (2021)
  212. T.Aoyama, K.-i.Itoh, T.Hanzawa, N.Meguro, M.Osanai, M.Hayakawa, A.Ouchi. Eur. J. Org. Chem., 6363 (2018)
  213. A.Y.Smirnov, E.R.Zaitseva, O.A.Belozerova, R.S.Alekseyev, N.S.Baleeva, M.B.Zagudaylova, A.A.Mikhaylov, M.S.Baranov. J. Org. Chem., 84, 15417 (2019)
  214. D.I.Weisblat, D.A.Lyttle. J. Am. Chem. Soc., 71, 3079 (1949)
  215. S.Sifniades. J. Org. Chem., 40, 3562 (1975)
  216. T.Zhu, C.Chen, S.Wang, Y.Zhang, D.Zhu, L.Li, J.Luo, L.Kong. Chem. Commun., 55, 8231 (2019)
  217. X.B.Wang, X.Hao, D.Zhang, Y.Jiang. Dyes Pigm., 142, 167 (2017)
  218. T.Kowada, T.Watanabe, Y.Amagai, R.Liu, M.Yamada, H.Takahashi, T.Matsui, K.Inaba, S.Mizukami. Cell. Chem. Biol., 27, 1521.e8 (2020)
  219. K.B.Manjappa, J.M.Lin, D.Y.Yang. J. Org. Chem., 82, 7648 (2017)
  220. R.K.Sharma, V.Singh, N.Tiwari, R.J.Butcher, D.Katiyar. Bioorg. Chem., 98, 103700 (2020)
  221. P.Seubert, M.Freund, R.Rudolf, Y.Lin, L.Altevogt, U.Bilitewski, A.Baro, S.Laschat. Synlett, 31, 1177 (2020)
  222. X.-f.Chen, C.Ren, X.y.Xu, X.-s.Shao, Z.Li. Tetrahedron Lett., 58, 1433 (2017)
  223. K.V.Savateev, A.A.Spasov, V.L.Rusinov. Russ. Chem. Rev., 91, RCR5041 (2022)
  224. G.A.Artem'ev, V.L.Rusinov, D.S.Kopchuk, M.I.Savchuk, S.Santra, E.N.Ulomsky, G.V.Zyryanov, A.Majee, W.Du, V.N.Charushin, O.N.Chupakhin. Org. Biomol. Chem., 20, 1828 (2022)
  225. V.L.Rusinov, I.M.Sapozhnikova, A.M.Bliznik, O.N.Chupakhin, V.N.Charushin, A.A.Spasov, P.M.Vassiliev, V.A.Kuznetsova, A.I.Rashchenko, D.A.Babkov. Arch. Pharm., 350, 1600361 (2017)
  226. E.K.Voinkov, R.A.Drokin, E.N.Ulomsky, O.N.Chupakhin, V.N.Charushin, V.L.Rusinov. Chem. Heterocycl. Compd., 56, 1254 (2020)
  227. E.K.Voinkov, R.A.Drokin, E.N.Ulomskiy, P.A.Slepukhin, V.L.Rusinov, O.N.Chupakhin. J. Chem. Crystallogr., 49, 213 (2019)
  228. I.Malik, J.Cizmarik, G.Kovac, M.Pechacova, L.Hudecova. Ceska Slov. Farm., 70, 18 (2021)
  229. O.N.Chupakhin, V.L.Rusinov, M.V.Varaksin, E.N.Ulomskiy, K.V.Savateev, I.I.Butorin, W.Du, Z.Sun, V.N.Charushin. Int. J. Mol. Sci., 23, 14537 (2022)
  230. T.S.Shestakova, S.L.Deev, I.Khalymbadzha, V.L.Rusinov, A.S.Paramonov, A.S.Arseniev, Z.O.Shenkarev, V.N.Charushin, O.N.Chupakhin. Chem. Heterocycl. Compd., 57, 479 (2021)
  231. T.Gupta, J.B.Singh, K.Mishra, R.M.Singh. RSC Adv., 7, 54581 (2017)
  232. X.b.Zhao, Y.m.Wang, H.f.Yu, Y.c.Lv, S.a.Jiang, N.Wang. Tetrahedron, 97, 132427 (2021)
  233. R.Khajuria, S.Mahajan, Ambica, K.K.Kapoor. J. Chem. Sci., 129, 1549 (2017)
  234. R.Vroemans, M.T.D.Tran, M.G.Sayed, S.Boodts, W.Dehaen. Dyes Pigm., 156, 61 (2018)
  235. A.V.Aksenov, V.Khamraev, N.A.Aksenov, N.K.Kirilov, D.A.Domenyuk, V.A.Zelensky, M.Rubin. RSC Adv., 9, 6636 (2019)
  236. N.A.Aksenov, N.A.Arutiunov, N.K.Kirillov, D.A.Aksenov, A.V.Aksenov, M.Rubin. Chem. Heterocycl. Compd., 56, 1067 (2020)
  237. D.A.Aksenov, N.A.Arutiunov, V.V.Maliuga, A.V.Aksenov, M.Rubin. BJOC, 16, 2903 (2020)
  238. A.V.Aksenov, N.K.Kirilov, N.A.Aksenov, D.A.Aksenov, E.A.Sorokina, C.Lower, M.Rubin. Molecules, 26, 5692 (2021)
  239. N.A.Aksenov, A.V.Aksenov, N.K.Kirilov, N.A.Arutiunov, D.A.Aksenov, V.Maslivetc, Z.Zhao, L.Du, M.Rubin, A.Kornienko. Org. Biomol. Chem., 18, 6651 (2020)
  240. Z.Zhang, J.Yang, R.Yu, K.Wu, J.Bu, S.Li, P.Qian, L.Sheng. Eur. J. Org. Chem., 5209 (2021)
  241. P.Yang, C.Zheng, Y.H.Nie, S.L.You. Chem. Sci., 11, 6830 (2020)
  242. J.A.C.Oliveira, G.Kiala, F.Siopa, A.Bernard, G.Gontard, J.Oble, C.A.M.Afonso, G.Poli. Tetrahedron, 76, 131182 (2020)
  243. L.F.Fan, P.S.Wang, L.Z.Gong. Org. Lett., 21, 6720 (2019)
  244. D.J.Sprague, A.Singh, J.N.Johnston. Chem. Sci., 9, 2336 (2018)
  245. D.J.Sprague, J.N.Johnston. Org. Lett., 22, 8496 (2020)
  246. T.J.Struble, I.Smajlagic, H.Foy, T.Dudding, J.N.Johnston. J. Org. Chem., 86, 15606 (2021)
  247. S.Gao, H.Liu, Z.Wu, H.Yao, A.Lin. Green Chem., 19, 1861 (2017)
  248. R.T.Davison, P.D.Parker, X.Hou, C.P.Chung, S.A.Augustine, V.M.Dong. Angew. Chem., Int. Ed., 60, 4599 (2021)
  249. K.Tran, R.van den Hauwe, X.Sainsily, P.Couvineau, J.Cote, L.Simard, M.Echevarria, A.Murza, A.Serre, L.Theroux, S.Saibi, L.Haroune, J.M.Longpre, O.Lesur, M.Auger- Messier, C.Spino, M.Bouvier, P.Sarret, S.Ballet, E.Marsault. J. Med. Chem., 64, 5345 (2021)
  250. X.Li, K.Zhou, H.He, Q.Zhou, Y.Sun, L.Hou, L.Shen, X.Wang, Y.Zhou, Z.Gong, S.He, H.Jin, Z.Gu, S.Zhao, L.Zhang, C.Sun, S.Zheng, Z.Cheng, Y.Zhu, M.Zhang, J.Li, S.Chen. ACS Med. Chem. Lett., 8, 969 (2017)
  251. R.Krasikova, M.Kondrashov, C.Avagliano, M.Petukhov, A.Vazquez-Romero, E.Revunov, P.Johnstrom, L.Tari, M.Toth, J.Hoggkvist, S.Erhardt, S.Cervenka, M.Schou. ACS Chem. Neurosci., 11, 1756 (2020)
  252. C.Hu, G.Hong, X.Qian, K.R.Kim, X.Zhu, L.Wang. Org. Biomol. Chem., 15, 4984 (2017)
  253. Q.Zhu, B.Meng, C.Gu, Y.Xu, J.Chen, C.Lei, X.Wu. Org. Lett., 21, 9985 (2019)
  254. C.Y.Meng, X.Liang, K.Wei, Y.R.Yang. Org. Lett., 21, 840 (2019)
  255. R.L.Liu, X.Z.Tang, X.J.Zhang, M.Yan, A.S.C.Chan. RSC Adv., 7, 6660 (2017)
  256. S.Singh, R.Samineni, S.Pabbaraja, G.Mehta. Angew. Chem., Int. Ed., 57, 16847 (2018)
  257. M.Beesu, G.Mehta. Adv. Synth. Catal., 363, 2877 (2021)
  258. S.Singh, R.Samineni, S.Pabbaraja, G.Mehta. Org. Lett., 21, 3372 (2019)
  259. S.Roscales, A.G.Csaky. Adv. Synth. Catal., 362, 111 (2020)
  260. E.Qu, S.Li, J.Bai, Y.Zheng, W.Li. Org. Lett., 24, 58 (2021)
  261. B.M.Trost, J.E.Schultz, Y.Bai. Angew. Chem., Int. Ed., 58, 11820 (2019)
  262. Y.A.Zobenko, S.A.Pozhidaeva, A.K.Kuratova, L.V.Glyzdinskaya, M.A.Vorontsova, G.P.Sagitullina. Chem. Heterocycl. Compd., 53, 1014 (2017)
  263. V.A.Koveza, I.V.Kulakov, Z.T.Shulgau, T.M.Seilkhanov. Chem. Heterocycl. Compd., 54, 1127 (2018)
  264. I.V.Kulakov, A.L.Oleshchuk, V.A.Koveza, I.V.Palamarchuk. Synth. Commun., 50, 2432 (2020)
  265. E.K.Voinkov, E.N.Ulomskiy, V.L.Rusinov, R.A.Drokin, V.V.Fedotov, E.B.Gorbunov. Mendeleev Commun., 27, 285 (2017)
  266. E.N.Ulomskiy, A.V.Ivanova, E.B.Gorbunov, I.L.Esaulkova, A.V.Slita, E.O.Sinegubova, E.K.Voinkov, R.A.Drokin, I.I.Butorin, E.R.Gazizullina, E.L.Gerasimova, V.V.Zarubaev, V.L.Rusinov. Bioorg. Med. Chem. Lett., 30, 127216 (2020)
  267. R.A.Drokin, D.V.Tiufiakov, E.K.Voinkov, P.A.Slepukhin, E.N.Ulomsky, Y.L.Esaulkova, A.S.Volobueva, K.S.Lantseva, M.A.Misyurina, V.V.Zarubaev, V.L.Rusinov. Chem. Heterocycl. Compd., 57, 473 (2021)
  268. C.Parida, S.C.Pan. BJOC, 17, 1447 (2021)
  269. R.Ding, P.R.Bakhshi, C.Wolf. J. Org. Chem., 82, 1273 (2017)
  270. Y.X.Song, D.M.Du. Adv. Synth. Catal., 361, 5042 (2019)
  271. R.Maity, C.Gharui, A.K.Sil, S.C.Pan. Org. Lett., 19, 662 (2017)
  272. Y.Liu, Y.Mo, X.Dong, L.Chen, L.Ye, X.Li, Z.Zhao, X.Li. Tetrahedron, 75, 2466 (2019)
  273. R.Maity, S.C.Sahoo, S.C.Pan. Eur. J. Org. Chem., 2297 (2019)
  274. R.Maity, S.C.Pan. Org. Biomol. Chem., 16, 1598 (2018)
  275. J.Zhou, L.J.Bai, G.J.Liang, Q.G.Xu, L.P.Zhou, H.Zhou. Org. Biomol. Chem., 18, 2641 (2020)
  276. C.Gharui, D.Behera, S.C.Pan. Adv. Synth. Catal., 360, 4502 (2018)
  277. P.Li, W.Yong, R.Sheng, W.Rao, X.Zhu, X.Zhang. Adv. Synth. Catal., 361, 201 (2019)
  278. J.H.Hu, H.J.Zheng. Synth. Commun., 49, 558 (2019)
  279. L.Greifenstein, T.Grus, J.Nagel, J.P.Sinnes, F.Rosch. Appl. Radiat. Isot., 156, 108867 (2020)
  280. E.S.Moon, Y.van Rymenant, S.Battan, J.de Loose, A.Bracke, P.van der Veken, I.de Meester, F.Rosch. Molecules, 26, 3482 (2021)
  281. H.Lahnif, T.Grus, S.Pektor, L.Greifenstein, M.Schreckenberger, F.Rosch. Molecules, 26, 6332 (2021)
  282. J.-P.Sinnes, J.Nagel, F.Rosch. EJNMMI Radiopharm. Chem., 4, 18 (2019)
  283. E.Chiurchi, S.Gabrielli, R.Ballini, A.Palmieri. Green Chem., 19, 4956 (2017)
  284. T.Nishimaru, K.Eto, K.Komine, J.Ishihara, S.Hatakeyama. Chem.-Eur. J., 25, 7927 (2019)
  285. N.Ezzat, K.Bobek, Y.Yuan. Synlett, 32, 689 (2021)
  286. B.Vigante, A.Plotniece, M.Rucins, M.Petrova, R.Muhamadejev, K.Pajuste, S.Belyakov, Y.G.Shermolovich, A.Sobolev. Tetrahedron, 74, 2596 (2018)
  287. W.Liu, S.Z.Ali, S.E.Ammann, M.C.White. J. Am. Chem. Soc., 140, 10658 (2018)
  288. X.Tang, C.X.A.Tan, W.L.Chan, F.Zhang, W.Zheng, Y.Lu. ACS Catal., 11, 1361 (2021)
  289. Y.An, X.M.Zhang, Z.Y.Li, W.H.Xiong, R.D.Yu, F.M.Zhang. Chem. Commun., 55, 119 (2018)
  290. M.K.Reddy, S.Mallik, I.Ramakrishna, M.Baidya. Org. Lett., 19, 1694 (2017)
  291. S.Bera, A.Studer. Synthesis, 49, 121 (2017)
  292. C.R.Reddy, A.D.Patil, S.Z.Mohammed. Chem. Commun., 56, 7191 (2020)
  293. B.Aegurla, N.Jarwal, R.K.Peddinti. Org. Biomol. Chem., 18, 6100 (2020)
  294. A.V.Aksenov, I.Y.Grishin, N.A.Aksenov, V.V.Malyuga, D.A.Aksenov, M.A.Nobi, M.Rubin. Molecules, 26, 4274 (2021)
  295. A.V.Aksenov, N.A.Aksenov, N.A.Arutiunov, V.V.Malyuga, S.N.Ovcharov, M.Rubin. RSC Adv., 9, 39458 (2019)
  296. M.J.Sarma, P.Phukan. Indian J. Chem., Sect. B, 57, 523 (2018)
  297. M.Subaramanian, P.M.Ramar, J.Rana, V.K.Gupta, E.Balaraman. Chem. Commun., 56, 8143 (2020)
  298. Z.Wang, X.Wu, Z.Li, Z.Huang, F.Chen. Org. Biomol. Chem., 17, 3575 (2019)
  299. A.Pelagalli, L.Pellacani, S.Fioravanti. Eur. J. Org. Chem., 3373 (2017)
  300. J.Tang, S.A.Jones, J.L.Jeffrey, S.R.Miranda, C.M.Galardi, D.M.Irlbeck, K.W.Brown, C.B.McDanal, B.A.Johns. Bioorg. Med. Chem. Lett., 27, 2689 (2017)
  301. T.Aoyama, K.I.Itoh, Y.Furukawa, M.Hayakawa, S.Shimada, A.Ouchi. Synlett, 28, 489 (2017)
  302. V.P.Kislyi, A.L.Laikhter, B.I.Ugrak, V.V.Semenov. Russ. Chem. Bull., Int. Ed., 43, 70 (1994)
  303. M.I.Kanishchev, N.V.Korneeva, S.A.Shevelev. Bull. Acad. Sci. USSR. Div. Chem. Sci., 35, 2145 (1986)
  304. Y.Tang, C.He, G.H.Imler, D.A.Parrish, J.M.Shreeve. Chem. Commun., 54, 10566 (2018)
  305. C.J.Snyder, T.W.Myers, G.H.Imler, D.E.Chavez, D.A.Parrish, J.M.Veauthier, R.J.Scharff. Propellants Explos. Pyrotech., 42, 238 (2017)
  306. D.G.Piercey, D.E.Chavez, B.L.Scott, G.H.Imler, D.A.Parrish. Angew. Chem., Int. Ed., 55, 15315 (2016)
  307. Y.Tang, C.He, G.H.Imler, D.A.Parrish, J.M.Shreeve. ACS Appl. Energy Mater., 2, 2263 (2019)
  308. J.-c.Zhang, Z.-y.Wang, B.-s.Wang, Y.-h.Liang, G.-x.Pan, J.-h.Zhang. Chin. J. Energ. Mater., 26, 983 (2018)
  309. D.Kumar, G.H.Imler, D.A.Parrish, J.M.Shreeve. Chem.-Eur. J., 23, 1743 (2017)
  310. S.E.Creegan, M.Zeller, E.F.C.Byrd, D.G.Piercey. Propellants Explos. Pyrotech., 46, 214 (2021)
  311. S.Feng, P.Yin, C.He, S.Pang, J.M.Shreeve. J. Mater. Chem. A, 9, 12291 (2021)
  312. E.K.Voinkov, R.A.Drokin, V.V.Fedotov, I.I.Butorin, K.V.Savateev, D.N.Lyapustin, D.A.Gazizov, E.B.Gorbunov, P.A.Slepukhin, N.A.Gerasimova, N.P.Evstigneeva, N.V.Zilberberg, N.V.Kungurov, E.N.Ulomsky, V.L.Rusinov. ChemistrySelect, 7, e202104253 (2022)
  313. N.Nishiwaki, Y.Kumegawa, K.Iwai, S.Yokoyama. Chem. Commun., 55, 7903 (2019)
  314. K.Iwai, H.Asahara, N.Nishiwaki. J. Org. Chem., 82, 5409 (2017)

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Используя сайт https://journals.rcsi.science, я (далее – «Пользователь» или «Субъект персональных данных») даю согласие на обработку персональных данных на этом сайте (текст Согласия) и на обработку персональных данных с помощью сервиса «Яндекс.Метрика» (текст Согласия).