Selective addition of H2O to fullerene C60 catalyzed by Ti, Zr, and Hf catalysts

Tetrahedron Letters

Volumn 49, Issue 5, 2008, Pages 808-810

  Tuktarov, Airat R ^a   Akhmetov, Arslan R ^a   Pudas, Marko ^b   Ibragimov, Askhat G ^a   Dzhemilev, Usein M ^a  

^a INSTITUTE OF PETROCHEMISTRY AND CATALYSIS   (Russian Federation)

^b UNIVERSITY OF OULU   (Finland)

Author keywords

1 Hydroxy 1,2 dihydrofullerene; Catalysis; Fullerene 60

Indexed keywords

1 HYDROXY 1,2 DIHYDROFULLERENE; CARBON; FULLERENE; FULLERENE DERIVATIVE; HYDROGEN PEROXIDE; TITANIUM; UNCLASSIFIED DRUG; ZIRCONIUM;

ADDITION REACTION; ARTICLE; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; REACTION TIME;

EID: 37648999850     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.11.191     Document Type: Article

References (15)

1. 60 into Water-Soluble Polyhydroxylated Fullerene Derivatives in The Chemistry of Fullerenes. In: Taylor R. (Ed). Advanced Series in Fullerenes Vol. 4 (1995), Word Scientific, London
2. Chiang L.Y., Swirczewski J.W., Hsu C.S., Chowdhury S.K., Cameron S., and Creegan K. J. Chem. Soc., Chem. Commun. (1992) 1791-1793
3. Li J., Takeuchi A., Ozawa M., Li X., Saigo K., and Kitazawa K. J. Chem. Soc., Chem. Commun. (1993) 1784-1785
4. Jin H., Chen W.Q., Tang X.W., Chiang L.Y., Yang C.Y., Schloss J.V., and Wu J.Y. J. Neurosci. Res. 62 (2000) 600-607
5. Ueng T.H., Kang J.J., Wang H.W., Cheng Y.W., and Chiang L.Y. Toxicol. Lett. 93 (1997) 29-37
6. Lee Y.T., Chiang L.Y., Chen W.J., and Hsu H.C. Proc. Soc. Exp. Biol. Med. 224 (2000) 69-75
7. Lu L.H., Lee Y.T., Chen H.W., Chiang L.Y., and Huang H.C. Br. J. Pharmacol. 123 (1998) 1097-1102
8. Chiang L.Y., Wang L.Y., Kuo C.S., Lin J.G., and Huang C.Y. Synth. Met. 84 (1997) 721-722
9. Dzhemilev U.M., Ibragimov A.G., Tuktarov A.R., D'yakonov V.A., Pudas M., and Bergmann U. Russ. J. Org. Chem. 43 (2007) 375-379
10. Dzhemilev U.M., Ibragimov A.G., Pudas M., D'yakonov V.A., and Tuktarov A.R. Russ. J. Org. Chem. 43 (2007) 370-374
11. 2) δ 56.19, 74.98, 137.00, 137.15, 137.23, 137.31, 137.59, 139.57, 139.79, 141.52, 141.63, 141.72, 141.77, 141.80, 142.31, 142.37, 144.15, 144.33, 145.04, 145.10, 145.16, 145.53, 145.74, 145.83, 145.97, 146.06, 146.85, 155.11, 156.96.
12. Inoue M., Machi L., Brown F., Inoue M.B., and Fernando Q. J. Mol. Struct. 345 (1995) 113-117
13. Seshadri R., Govindaraj A., Nagarajan R., Pradeep T., and Rao C.N.R. Tetrahedron Lett. 33 (1992) 2069-2070
14. 2) δ 59.36, 75.26, 128.14, 128.22, 128.94, 137.33, 137.37, 137.79, 139.78, 139.99, 141.73, 141.83, 141.93, 141.97, 142.01, 142.52, 142.57, 142.90, 142.96, 142.99, 144.36, 144.53, 144.86, 145.25, 145.30, 145.31, 145.36, 145.75, 145.95, 146.04, 146.17, 146.27, 147.06, 148.78, 155.34, 157.09, 178.72.
15. 2) δ 0.99, 57.07, 75.26, 128.67, 130.46, 137.39, 137.82, 137.95, 139.80, 140.02, 141.75, 141.86, 141.95, 142.03, 142.55, 142.60, 143.01, 144.38, 144.56, 145.27, 145.34, 145.38, 145.78, 145.97, 146.06, 146.20, 146.29, 147.09, 155.38, 157.12.