Эта публикация цитируется в 19 научных статьях (всего в 19 статьях)
Synthesis and electrochemical properties of N-isocyanurate-substituted aziridino[1,6][60]fullerene, an unusual product of cycloaddition to the 5,6-junction of fullerene
Аннотация:
The main product of the cycloaddition of 1,3-diallyl-5-(5’-azidopentyl)-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione to C60 at 100 °C is an N-isocyanurate-substituted aziridino[1,6][60]fullerene.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
O. G. Sinyashin, I. P. Romanova, G. G. Yusupova, V. I. Kovalenko, V. V. Yanilkin, N. M. Azancheev, “Synthesis and electrochemical properties of N-isocyanurate-substituted aziridino[1,6][60]fullerene, an unusual product of cycloaddition to the 5,6-junction of fullerene”, Mendeleev Commun., 10:3 (2000), 96–98
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4402
https://www.mathnet.ru/rus/mendc/v10/i3/p96
Эта публикация цитируется в следующих 19 статьяx:
Tong‐Xin Liu, Xin Wang, Shilu Xia, Muqing Chen, Mingjie Li, Panting Yang, Nana Ma, Ziqi Hu, Shangfeng Yang, Guisheng Zhang, Guan‐Wu Wang, “Dearomative Ring‐Fused Azafulleroids and Carbazole‐Derived Metallofullerenes: Reactivity Dictated by Encapsulation in a Fullerene Cage”, Angew Chem Int Ed, 62:46 (2023)
Tong‐Xin Liu, Xin Wang, Shilu Xia, Muqing Chen, Mingjie Li, Panting Yang, Nana Ma, Ziqi Hu, Shangfeng Yang, Guisheng Zhang, Guan‐Wu Wang, “Dearomative Ring‐Fused Azafulleroids and Carbazole‐Derived Metallofullerenes: Reactivity Dictated by Encapsulation in a Fullerene Cage”, Angewandte Chemie, 135:46 (2023)
Airat R. Tuktarov, Nuri M. Chobanov, Yulia H. Budnikova, Yulia B. Dudkina, Usein M. Dzhemilev, “Synthesis and Electrochemical Properties of Fullerenylstyrenes”, J. Org. Chem., 84:24 (2019), 16333
Ryo Mizunuma, Teruhiko Tanaka, Yoshihiro Nakamura, Yuki Kamijima, Yoshio Kabe, “Direct benzyne-C60 addition does not generate a [5,6] open fulleroid”, Tetrahedron, 74:5 (2018), 544
A. R. Akhmetov, A. R. Tuktarov, U. M. Dzhemilev, “Selective cycloaddition of aryl azides to fullerene C60 in the presence of Cu(OTf)2”, Russ J Org Chem, 52:1 (2016), 118
A. R. Akhmetov, A. R. Tuktarov, N. R. Porod'ko, U. M. Dzhemilev, “Cycloaddition of alkyl azides to fullerene C60 in the presence of Cu(OTf)2”, Mendeleev Commun., 25:5 (2015), 346–347
U. M. Dzhemilev, A. R. Tuktarov, I. R. Yarullin, A. R. Akhmetov, “The reaction of fullerene C60 with halogen azides”, Mendeleev Commun., 23:6 (2013), 326–328
Tong-Xin Liu, Tao Wei, San-E Zhu, Guan-Wu Wang, Mingzhi Jiao, Shangfeng Yang, Faye L. Bowles, Marilyn M. Olmstead, Alan L. Balch, “Azide Addition to an Endohedral Metallofullerene: Formation of Azafulleroids of Sc3N@Ih-C80”, J. Am. Chem. Soc., 134:29 (2012), 11956
A. R. Akhmetov, A. R. Tuktarov, U. M. Dzhemilev, I. R. Yarullin, L. A. Gabidullina, “First example of the interaction of fullerene C60 with hydrazoic acid”, Russ Chem Bull, 60:9 (2011), 1885
Irina P. Romanova, Andrey V. Bogdanov, Vladimir F. Mironov, Gulnara R. Shaikhutdinova, Olga A. Larionova, Shamil K. Latypov, Alsu A. Balandina, Dmitry G. Yakhvarov, Aidar T. Gubaidullin, Alina F. Saifina, Oleg G. Sinyashin, “Deoxygenation of Some α-Dicarbonyl Compounds by Tris(diethylamino)phosphine in the Presence of Fullerene C60”, J. Org. Chem., 76:8 (2011), 2548
Shinsook Yoon, Sung Ho Hwang, Weon Bae Ko, “Ultrasound‐assisted Cycloadditions of [70]Fullerene with Various 2‐Azidoethyl per‐O‐acetyl Glycosides”, Fullerenes, Nanotubes and Carbon Nanostructures, 17:5 (2009), 496
Vladislav V. Zverev, Valeriy I. Kovalenko, Irina P. Romanova, Oleg G. Sinyashin, “Structure and relative energies of regioisomers and valence isomers of C60 adducts. HF and DFT study”, Int J of Quantum Chemistry, 107:13 (2007), 2442
Yong Chen, Yali Wang, André Rassat, Pierre Sinaÿ, Yu Zhao, Yongmin Zhang, “Synthesis of water-soluble 2-alkylcyclodextrin–C60 conjugates and their inclusion complexation in aqueous solution”, Tetrahedron, 62:9 (2006), 2045
I. P. Romanova, G. G. Yusupova, O. A. Larionova, A. A. Balandina, Sh. K. Latypov, V. V. Zverev, D. G. Yakhvarov, G. L. Rusinov, O. G. Sinyashin, “Synthesis, electrochemical properties, and thermal transformations of 1-(5-nitropyrimidin-2-yl)[60]fullereno[1,2-b]aziridine”, Russ Chem Bull, 55:3 (2006), 502
I. P. Romanova, G. G. Yusupova, O. A. Larionova, A. A. Balandina, Sh. K. Latypov, D. G. Yakhvarov, V. V. Zverev, O. G. Sinyashin, “Synthesis and electrochemical properties of individual isomers of isocyanurate-substituted bis-organodiazadihomofullerenes”, Russ Chem Bull, 55:4 (2006), 697
I. P. Romanova, G. G. Yusupova, O. A. Larionova, A. A. Nafikova, D. G. Yakhvarov, V. V. Zverev, Yu. Ya. Efremov, O. G. Sinyashin, “Synthesis and unusual electrochemical properties of nitropyrimidine-substituted diazadihomo(C60-Ih)[6,6]fullerene”, Mendeleev Commun., 16:6 (2006), 309–311
Sumanta Bhattacharya, Sandip K. Nayak, Subrata Chattopadhyay, Manas Banerjee, Asok K. Mukherjee, “Study of Novel Interactions of Calixarene π-Systems with [60]- and [70]Fullerenes by the NMR Spectrometric Method”, J. Phys. Chem. B, 107:43 (2003), 11830
V. N. Ivanova, V. A. Nadolinnyi, I. A. Grigor'ev, E. Rejerse, “Synthesis and EPR spectroscopy of nitroxyl derivatives of the C60 fullerene”, Phys. Solid State, 44:3 (2002), 560
Oleg G. Sinyashin, Irina P. Romanova, Gulshat G. Yusupova, Valery I. Kovalenko, Vitaly V. Yanilkin, Nail M. Azancheev, “ChemInform Abstract: Synthesis and Electrochemical Properties of N‐Isocyanurate‐Substituted Aziridino[1,6][60]fullerene, an Unusual Product of Cycloaddition to the 5,6‐Junction of Fullerene.”, ChemInform, 31:43 (2000)
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