Synthesis of derivatives of fullerenes C 60 and C 70 containing pharmacophore groups

Piotrovsky, 2006 Gubskaya, 2007, Org. Biomol. Chem., 5, 976, 10.1039/b617892h Kotelnikova, 2014, Med. Chem. Commun., 5, 1664, 10.1039/C4MD00194J Studentsov, 2009, Izv. SPbGTI (TU), 31, 3 Bakry, 2007, Int. J. Nanomed., 2, 639 Orlova, 2013, Onkogematologiya, 2, 83 Melnikova, 2015, Colloids Surf., B, 136, 314, 10.1016/j.colsurfb.2015.09.026 Buina, 1993, Pharm. Chem. J., 27, 754, 10.1007/BF00780402 Ungurenasu, 2005, Synthesis, 3, 361, 10.1055/s-2005-861794 Krayevsky, 1999, Molek. Biol., 3, 343 Pokrovsky, 2001, Nucleosides Nucleotides Nucleic Acids, 20, 767, 10.1081/NCN-100002426 Alvarez, 1994, J. Med. Chem., 37, 4185, 10.1021/jm00050a015 Kotelnikov, 2013, Org. Biomol. Chem., 11, 4397, 10.1039/c3ob40136g Partha, 2009, Int. J. Nanomed., 4, 261, 10.2217/nnm.09.11 Kalacheva, 2015, Bioorg. Med. Chem. Lett., 25, 5250, 10.1016/j.bmcl.2015.09.054 Lucafo, 2013, Toxicology, 314, 183, 10.1016/j.tox.2013.10.001 Ershova, 2016, Mutat. Res. Genet. Toxicol. Environ. Mutagen., 805, 45, 10.1016/j.mrgentox.2016.05.004 Kornev, 2013, Mendeleev Commun., 23, 323, 10.1016/j.mencom.2013.11.006 Lucafo, 2012, J. Nanopart. Res., 14, 830, 10.1007/s11051-012-0830-8 Huang, 2014, Nanomedicine, 9, 253, 10.2217/nnm.13.22 Perrone, 2013, New J. Chem., 37, 3559, 10.1039/c3nj00513e Ustinov, 2010, Russ. J. Bioorg. Chem., 36, 401, 10.1134/S1068162010040011 Severov, 2012, Efferent. Fiz.-Khim. Meditsina, 1, 10 Akhmetov, 2015, Mendeleev Commun., 25, 346, 10.1016/j.mencom.2015.09.009 Zhang, 2015, Mendeleev Commun., 25, 204, 10.1016/j.mencom.2015.05.015 Biglova, 2015, Mendeleev Commun., 25, 202, 10.1016/j.mencom.2015.05.014 Gubskaya, 2012, Russ. Chem. Bull., Int. Ed., 61, 1169, 10.1007/s11172-012-0159-6 Yin, 2006, J. Org. Chem., 71, 2267, 10.1021/jo052263n Wang, 2008, Green Chem., 10, 452, 10.1039/b718051a Derome, 1988 Atta-ur-Rahman, 1989