[1] Zhu Z W, Schuster D I, Tuckerman M E. Molecular dynamics study of the connection between flap closing and binding of fullerene-based inhibitors of the HIV-1 protease[J]. Biochemistry, 2003, 42(5): 1326-1333.
[2] Marcheesan S, Da Ros T, Spalluto G, et al. Anti-HIV properties of cationic fullerene derivatives[J]. Bioorg Med Chem Lett, 2005, 15(15): 3615-3618.
[3] Mashino T, Shimotohno K, Ikegami N, et al. Human immunodeficiency virus-reverse transcriptase inhibition and hepatitis C virus RNA-dependent RNA polymerase inhibition activities of fullerene derivatives[J]. Bioorg Med Chem Lett, 2005, 15(4):1107-1109.
[4] Lee V S, Nimmanpipug P, Aruksakunwong O, et al. Structural analysis of lead fullerene-based inhibitor bound to human immunodeficiency virus type 1 protease in solution from molecular dynamics simulations[J]. J Mol Graphics Modell, 2007,26(2): 558-570.
[5] Yang X L, Fan C H, Zhu H S. Photo-induced cytotoxicity of malonic acid [C₆₀]fullerene derivatives and its mechanism[J]. Toxicol In Vitro, 2002, 16(1): 41-46.
[6] 熊垚,林中祥,范旭,邓慧敏,等.C₆₀与N-羧甲基脱氢枞胺的1,3-偶极环加成反应研究[J].化学通报, 2009, 72(5):474-477.
[7] 高健,林中祥,邓慧敏,等. 微波辐射下
[60]富勒烯与脱氢枞胺的加成反应[J]. 现代化工, 2007, 27(Z1): 266-268.
[8] Vileno B, Marcoux P R, Lekka M, et al. Spectroscopic and photophysical properties of a highly deivatized C₆₀ fullerol[J]. Adv Funct Mater, 2006, 16(1): 120-128.
[9] Arrais A, Diana E. Highly Water Soluble C₆₀ derivatives: A new synthesis[J]. Fuller Nanotub Carbon Nanostruct, 2003, 11(1): 35-46.
[10] Xing G, Zhang J, Zhao Y, et al. Influences of structural properties on stavility of fullerenols[J]. J Phys Chem B, 2004,108(31): 11473-11479.
[11] Wang S, He P, Zhang J M, et al. Noveland efficient synthesis of water-soluble
[60]Fullerenol by solvent-free reaction[J]. Synth Commun, 2005, 36(44): 1803-1807.
[12] 张云怀,黄宗卿,欧忠文.在相转移剂TABH存在下水溶性C₆₀(OH)_n的合成[J].化学研究与应用, 1998, 10(5): 507-509.
[13] 官文超, 许铭飞, 廖立琼. 多羟基富勒烯衍生物的合成与表征[J].华中科技大学学报:自然科学版, 2004, 32(11): 111-113.
[14] Chiang L Y, Upasani R B, Swirczewski J W, et al. Evidence of hemiketals incorporated in the structure of fullerols derived from aqueous acid chemistry[J]. J Am Chem Soc, 1993, 24(13): 5453-5457.
[15] 刘绪峰,官文超,程珍贤.6-氨基己酸及2-氨基乙磺酸C₆₀加成物的合成及溶解性[J].有机化学,2005,25(6):741-744.
[16] 江贵长,郑启新.富勒烯-甘氨酸衍生物的制备[J].化工新型材料,2005,33(8):24-26.
[17] 江贵长,郑启新.富勒烯-赖氨酸衍生物的合成及其体外抗癌活性研究[J].材料导报,2005,19(8):135-138.
[18] Sun T, Xu Z. Radical scavenging activites of α-alanine C₆₀ adduct[J]. Bioorg Med Chem Lett, 2006, 16(14): 3731-3734.
[19] Wang F, Xiao Z, Yao Z, et al. Lewis acid promoted preparation of isomerically pure fullerenols from fullerene peroxides C₆₀(OOt-Bu)₆ and C₆₀(O)(OOt-Bu)₆[J]. J Org Chem, 2006, 71(12): 4374-4382.
[20] 孙大勇,刘子阳,郭兴华,等.C₆₀(OH)_x的简便合成及性质[J].高等学校化学学报,1996,17(1):19-20.
[21] Irngartinger H, Weber A. Ring opening of the heterocycle in
[60] fullereno
[1,2-d]isoxazole[J].Tetrahedron Lett, 1997, 38(12): 2075-2076.
[22] Huang S, Xiao Z, Wang F, et al. Preparation of
[5,6]-and
[6,6]-oxahomofullerene derivatives and their interconversion by lewis acid assisted reactions of fullerene mixed peroxides[J]. Chemistry, 2005, 11(18): 5449-5456.
[23] Al-Matar H, Abdul-Sada A K, Avent A G, et al. Isolation and characterization of symmetrical C₆₀Me₆, C₆₀Me₅Cl and C₆₀Me₅O₂OH, together with unsymmetrical C₆₀Me₅O₃H, C₆₀Me₅OOH, C₆₀Me₄PhO₂OH, and C₆₀Me₁₂[J]. Chem Soc, Perkin Trans, 2002, 2(1): 53-58.
[24] Gan L, Zhou D, Luo C, et al. Synthesis of fullerene amino acid derivatives by direct interaction of amino acid ester with C₆₀[J]. J Org Chem, 1996, 61(6): 1954-1961.
[25] Gan L B, Luo C P, Xu L B, et al. Water-soluble fullerene derivatives synthesis and characterization of β-alanine C₆₀ addult [J]. Chin Chem Lett, 1994, 5(4):275-279.
[26] Miller G P, Millar J M, Liang B, et al. The absence of “globetrotting” hydrogen on the surfaces of aminated fullerenes: 3-D hydrogen bonding between aminated fullerenes and water revealed[J].J Chem Soc, Chem Commun, 1993(11):897-899.
[27] Maggini M, Scorrano G, Prato M. Chemlnforin abstiact:Addition of azomethine ylides to C₆₀: synthesis, characterization, and functionalization of fullerene pyrrolidines[J]. J Am Chem Soc, 1994,25(5): 9798-9799.
[28] Nishimura T, Maeda K, Chsawa S, et al. Helical arrays of aendant fullerenes on optically active poly(phenylacetylene)s[J]. Chem Eur J, 2005, 11(4): 1181-1190.
[29] Zhang X J, Willems M, Foote C S. 1,3-Dipolar cycloaddition of N-benzyl azomethine ylide to C₆₀:formation of a C₆₀-fused N-benzylpyrrolidine[J]. Tetrahedron Letters, 1993, 34(51): 8187-8188.
[30] Maria D L, Marcorin G L, Pirri G, et al. Synthesis of novel 60 ullerene-flavonoid dyads[J]. Tetrahedron Letters, 2002, 43(9): 1689-1691.