BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

335 related articles for article (PubMed ID: 23311689)

  • 1. Synthesis of C60(O)3: an open-cage fullerene with a ketolactone moiety on the orifice.
    Xin N; Yang X; Zhou Z; Zhang J; Zhang S; Gan L
    J Org Chem; 2013 Feb; 78(3):1157-62. PubMed ID: 23311689
    [TBL] [Abstract][Full Text] [Related]  

  • 2. From fullerene-mixed peroxide to open-cage oxafulleroid C(59)(O)(3)(OH)(2)(OO(t)()Bu)(2) embedded with furan and lactone motifs.
    Wang F; Xiao Z; Gan L; Jia Z; Jiang Z; Zhang S; Zheng B; Gu Y
    Org Lett; 2007 Apr; 9(9):1741-3. PubMed ID: 17397174
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of [59]fullerenones through peroxide-mediated stepwise cleavage of fullerene skeleton bonds and X-ray structures of their water-encapsulated open-cage complexes.
    Xiao Z; Yao J; Yang D; Wang F; Huang S; Gan L; Jia Z; Jiang Z; Yang X; Zheng B; Yuan G; Zhang S; Wang Z
    J Am Chem Soc; 2007 Dec; 129(51):16149-62. PubMed ID: 18052066
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthesis and reactivity of 2H-pyran moiety in [60]fullerene cage skeleton.
    Yang D; Shi L; Huang H; Zhang J; Gan L
    J Org Chem; 2010 Jul; 75(13):4567-73. PubMed ID: 20521834
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Towards the rational synthesis of norfullerenes. controlled deletion of one carbon atom from C60 and preparation of 2,5,9-trioxo-1-nor(C60-Ih)[5,6]fullerene C59(O)3 derivatives.
    Yao J; Xiao Z; Gan L; Yang D; Wang Z
    Org Lett; 2008 May; 10(10):2003-6. PubMed ID: 18402464
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Reactivity of fullerene epoxide: preparation of fullerene-fused thiirane, tetrahydrothiazolidin-2-one, and 1,3-dioxolane.
    Yang X; Huang S; Jia Z; Xiao Z; Jiang Z; Zhang Q; Gan L; Zheng B; Yuan G; Zhang S
    J Org Chem; 2008 Apr; 73(7):2518-26. PubMed ID: 18336040
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthesis of 18-membered open-cage fullerenes through controlled stepwise fullerene skeleton bond cleavage processes and substituent-mediated tuning of the redox potential of open-cage fullerenes.
    Yu Y; Xie X; Zhang T; Liu S; Shao Y; Gan L; Li Y
    J Org Chem; 2011 Dec; 76(24):10148-53. PubMed ID: 22074545
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Synthesis, structure, and properties of novel open-cage fullerenes having heteroatom(s) on the rim of the orifice.
    Murata Y; Murata M; Komatsu K
    Chemistry; 2003 Apr; 9(7):1600-9. PubMed ID: 12658659
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Synthesis of fullerene oxides containing both 6,6-closed epoxide and 5,6-open ether moieties through thermolysis of fullerene peroxides.
    Yao J; Yang D; Xiao Z; Gan L; Wang Z
    J Org Chem; 2009 May; 74(9):3528-31. PubMed ID: 19334693
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Peroxide-mediated selective cleavage of [60]fullerene skeleton bonds: towards the synthesis of open-cage fulleroid C55O5.
    Gan L
    Chem Rec; 2015 Feb; 15(1):189-98. PubMed ID: 25345399
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Approaches to open fullerenes: synthesis and thermal stability of cis-1 bis(isobenzofuran) Diels-Alder adducts of C60.
    Sander M; Jarrosson T; Chuang SC; Khan SI; Rubin Y
    J Org Chem; 2007 Apr; 72(8):2724-31. PubMed ID: 17367187
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Concise Synthesis of Open-Cage Fullerenes for Oxygen Delivery.
    Zhou Z; Han H; Chen Z; Gao R; Liu Z; Su J; Xin N; Yang X; Gan L
    Angew Chem Int Ed Engl; 2019 Dec; 58(49):17690-17694. PubMed ID: 31591793
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structure of 7,9,12,15,18,20,39,24,45,57-C60(CF3)10(1,2:3,4-O)2. The first regiospecific diepoxidation of a fullerene derivative.
    Whitaker JB; Shustova NB; Strauss SH; V B
    Acta Chim Slov; 2013; 60(3):577-82. PubMed ID: 24169712
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Controlled regio- and chemoselective addition of isothiocyanate to the dione moiety of a cage-opened fullerene-mixed peroxide derivative.
    Yang X; Gan L; Wang Z
    Chem Commun (Camb); 2008 May; (17):1980-2. PubMed ID: 18536794
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Tethered bisadducts of C60 and C70 with addends on a common hexagonal face and a 12-membered hole in the fullerene cage.
    CerĂ³n MR; Izquierdo M; Aghabali A; Valdez JA; Ghiassi KB; Olmstead MM; Balch AL; Wudl F; Echegoyen L
    J Am Chem Soc; 2015 Jun; 137(23):7502-8. PubMed ID: 25980445
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A bowl-shaped fullerene encapsulates a water into the cage.
    Iwamatsu S; Uozaki T; Kobayashi K; Re S; Nagase S; Murata S
    J Am Chem Soc; 2004 Mar; 126(9):2668-9. PubMed ID: 14995161
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [6,6]-Open and [6,6]-closed isomers of C70(CF2): synthesis, electrochemical and quantum chemical investigation.
    Samoylova NA; Belov NM; Brotsman VA; Ioffe IN; Lukonina NS; Markov VY; Ruff A; Rybalchenko AV; Schuler P; Semivrazhskaya OO; Speiser B; Troyanov SI; Magdesieva TV; Goryunkov AA
    Chemistry; 2013 Dec; 19(52):17969-79. PubMed ID: 24248883
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular Containers Derived from [60]Fullerene through Peroxide Chemistry.
    Gan L
    Acc Chem Res; 2019 Jul; 52(7):1793-1801. PubMed ID: 31243971
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Isolation and structural characterization of a family of endohedral fullerenes including the large, chiral cage fullerenes Tb(3)N@C(88) and Tb(3)N@C(86) as well as the I(h) and D(5)(h) isomers of Tb(3)N@C(80).
    Zuo T; Beavers CM; Duchamp JC; Campbell A; Dorn HC; Olmstead MM; Balch AL
    J Am Chem Soc; 2007 Feb; 129(7):2035-43. PubMed ID: 17256857
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Selective synthesis of fullerenol derivatives with terminal alkyne and crown ether addends.
    Huang H; Zhang G; Liang S; Xin N; Gan L
    J Org Chem; 2012 Mar; 77(5):2456-62. PubMed ID: 22324338
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.