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Volumn 34, Issue 11, 1999, Pages 1223-1230

Fullerene lipids: Synthesis of C60 fullerene derivatives bearing a long-chain saturated or unsaturated triester system

Author keywords

[No Author keywords available]

Indexed keywords

CHLORIDE; FULLERENE; FULLERENE DERIVATIVE; LONG CHAIN FATTY ACID; SODIUM AZIDE;

EID: 0032806370     PISSN: 00244201     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11745-999-0475-4     Document Type: Article
Times cited : (6)

References (20)
  • 3
  • 4
    • 0002930822 scopus 로고
    • 60 as a way to the understanding of the electronic and magnetic properties of fullerenes
    • (Prassides, K., ed.) Kluwer Academic Publishers, Dordrecht
    • 60 as a Way to the Understanding of the Electronic and Magnetic Properties of Fullerenes, in Physics and Chemistry of the Fullerenes, (Prassides, K., ed.) pp. 97-116, Kluwer Academic Publishers, Dordrecht.
    • (1994) Physics and Chemistry of the Fullerenes , pp. 97-116
    • Wudl, F.1    Prato, M.2    Maggini, M.3
  • 6
    • 0002856016 scopus 로고
    • Chemistry of fullerenes
    • (Billups, W.E., and Ciufolini, M.A., eds.) VCH Publishers, New York
    • Wudl, F. (1993) Chemistry of Fullerenes, in Buckminsterfullerenes, (Billups, W.E., and Ciufolini, M.A., eds.) pp. 317-333, VCH Publishers, New York.
    • (1993) Buckminsterfullerenes , pp. 317-333
    • Wudl, F.1
  • 7
    • 0009600865 scopus 로고
    • Regioselective additions of carbon nucleophiles and azides to [60]fullerene
    • (Kuzmany, H., Fink, J., Mehring, M., and Roth, S., eds.) World Scientific Publishing Co. Pte. Ltd., Singapore
    • Hirsch, A., Lamparth, I., Grosser, T., Prato, M., Lucchini, V., and Wudl, F. (1995) Regioselective Additions of Carbon Nucleophiles and Azides to [60]Fullerene, in Physics and Chemistry of Fullerenes and Derivatives, (Kuzmany, H., Fink, J., Mehring, M., and Roth, S., eds.) pp. 125-136, World Scientific Publishing Co. Pte. Ltd., Singapore.
    • (1995) Physics and Chemistry of Fullerenes and Derivatives , pp. 125-136
    • Hirsch, A.1    Lamparth, I.2    Grosser, T.3    Prato, M.4    Lucchini, V.5    Wudl, F.6
  • 8
    • 84881588462 scopus 로고    scopus 로고
    • Mimicking natural photosynthesis
    • October 26
    • Freemantle, M. (October 26, 1998) Mimicking Natural Photosynthesis, Chem. Eng. News, pp. 37-46.
    • (1998) Chem. Eng. News , pp. 37-46
    • Freemantle, M.1
  • 9
    • 0027244713 scopus 로고
    • Inhibition of the HIV-1 protease by fullerene derivatives: Model building studies and experimental verification
    • Friedman, S.H., DeCamp, D.L., Sijbesma, R.P., Srdanov, G., Wudl, F., and Kenyon, G.L. (1993) Inhibition of the HIV-1 Protease by Fullerene Derivatives: Model Building Studies and Experimental Verification, J. Am. Chem. Soc. 115, 6506-6509.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 6506-6509
    • Friedman, S.H.1    DeCamp, D.L.2    Sijbesma, R.P.3    Srdanov, G.W.F.4    Kenyon, G.L.5
  • 11
    • 0029809466 scopus 로고    scopus 로고
    • Biological activity of water-soluble fullerenes. Structural dependence of DNA cleavage, cytotoxicity, and enzyme inhibitory activities including HIV-protease inhibition
    • Nakamura, E., Tokuyama, H., Yamago, S., Shiraki, T., and Sugiura, Y. (1996) Biological Activity of Water-Soluble Fullerenes. Structural Dependence of DNA Cleavage, Cytotoxicity, and Enzyme Inhibitory Activities Including HIV-Protease Inhibition, Bull. Chem. Soc. Jpn. 69, 2143-2151.
    • (1996) Bull. Chem. Soc. Jpn. , vol.69 , pp. 2143-2151
    • Nakamura, E.1    Tokuyama, H.2    Yamago, S.3    Shiraki, T.4    Sugiura, Y.5
  • 12
    • 0031820631 scopus 로고    scopus 로고
    • Fullerene lipids: Synthesis of dialkyl 1,2 [6,6]-methano-[60]-fullerene dicarboxylate derivatives
    • Lie Ken Jie, M.S.F., and Cheung, S.W.H. (1998) Fullerene Lipids: Synthesis of Dialkyl 1,2 [6,6]-Methano-[60]-fullerene Dicarboxylate Derivatives, Lipids 33, 729-732.
    • (1998) Lipids , vol.33 , pp. 729-732
    • Lie Ken Jie, M.S.F.1    Cheung, S.W.H.2
  • 14
    • 0028587189 scopus 로고
    • Ultrasound in fatty acid chemistry: Synthesis of a 1-pyrroline fatty acid ester isomer from methyl ricinoleate
    • Lie Ken Jie, M.S.F., Syed-Rahmatullah, M.S.K., Lam, C.K., and Kalluri, P. (1994) Ultrasound in Fatty Acid Chemistry: Synthesis of a 1-Pyrroline Fatty Acid Ester Isomer from Methyl Ricinoleate, Lipids 29, 889-892.
    • (1994) Lipids , vol.29 , pp. 889-892
    • Lie Ken Jie, M.S.F.1    Syed-Rahmatullah, M.S.K.2    Lam, C.K.3    Kalluri, P.4
  • 16
    • 33748448195 scopus 로고
    • Direct room temperature esterification of carboxylic acids
    • Hassner, A., and Alexanian, V. (1978) Direct Room Temperature Esterification of Carboxylic Acids, Tetrahedron Lett. 46, 4475-4478.
    • (1978) Tetrahedron Lett. , vol.46 , pp. 4475-4478
    • Hassner, A.1    Alexanian, V.2
  • 17
    • 0009637465 scopus 로고
    • The N-(2-hydroxyarylidene) protecting group in peptide synthesis
    • (Greene, T.W., and Wuts, P.C.M., eds.) John Wiley & Sons, Inc., New York
    • Sheehan, J.C., and Grenda, V.J. (1962) The N-(2-hydroxyarylidene) Protecting Group in Peptide Synthesis, in Protective Groups in Organic Synthesis, (Greene, T.W., and Wuts, P.C.M., eds.) pp. 369-371, John Wiley & Sons, Inc., New York.
    • (1962) Protective Groups in Organic Synthesis , pp. 369-371
    • Sheehan, J.C.1    Grenda, V.J.2
  • 18
    • 0001126369 scopus 로고
    • The N-(2-hydroxyarylidene) protecting group in peptide synthesis
    • Sheehan, J.C., and Grenda, V.J. (1962) The N-(2-hydroxyarylidene) Protecting Group in Peptide Synthesis, J. Am. Chem. Soc. 84, 2417-2424.
    • (1962) J. Am. Chem. Soc. , vol.84 , pp. 2417-2424
    • Sheehan, J.C.1    Grenda, V.J.2
  • 19
    • 0016546643 scopus 로고
    • The PMR analysis of non-conjugated alkenoic and alkynoic acids and esters
    • Frost, D.J., and Gunstone, F.D. (1975) The PMR Analysis of Non-conjugated Alkenoic and Alkynoic Acids and Esters, Chem. Phys. Lipids 15, 53-85.
    • (1975) Chem. Phys. Lipids , vol.15 , pp. 53-85
    • Frost, D.J.1    Gunstone, F.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.