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Prato

Prato M and Maggini M 1998 Fulleropyrrolidines a family of full-fledged fullerene derivatives Accounts. Chem. Res. 31 519-26... [Pg.2427]

Maggini M, Karlsson A, Pasimeni L, Scorrano G, Prato M and Valli L 1994 Synthesis of N-acylated... [Pg.2430]

Prato M 1997 [60]fullerene chemistry for materials science applications J. Mater. Chem. 7 1097-109... [Pg.2435]

Guldi D M, Maggini M, Scorrano G and Prato M 1997 Intramolecular electron transfer in fullerene/ferrocene based donor-bridge-acceptor dyads J. Am. Chem. See. 119 974-80... [Pg.2435]

Maggini M, Done A, Scorrano G and Prato M 1995 Synthesis of a [60]fullerene derivative covalently linked to a ruthenium (II) tris(bipyridine) complex J. Chem. Soc., Chem. Commun. 845-6... [Pg.2436]

Jensen A W, Wilson S R and Schuster D I 1996 Biological applications of fuiierenes—a review Bioorg. Med. Chem. 4 767-79 Martii n N, Sanchez L, lllescas B and Perez I 1998 Cgg-based electroactive organofullerenes Chem. Rev. 98 2527 Prato M 1997 [60]fullerene chemistry for materials science applications J. Mater. Chem. 7 1097-109... [Pg.2438]

M Maggini, A Karlsson, L Pasimeni, G Scorrano, M Prato, L Valli. Tet Lett 35 2985-2988,... [Pg.137]

Guldi, D. M., Rahman, G. M. A., Jux, N., Tagmatarchis, N. and Prato, M. (2004) Integrating single-wall carbon nanotubes into donor-acceptor nanohybrids. Angew. Chem. Int. Ed., 43, 5526-5530. [Pg.277]

Tasis D, Tagmatarchis N, Bianco A, Prato M. 2006. Chemistry of carbon nanotubes. Chem Rev 106 1105-1136. [Pg.634]

Tagmatarchis N, Prato M (2004) Organofullerene Materials 109 1-39 Takata M, Nishibori E, Sakata M, Shinohara M (2004) Charge Density Level Structures of Endohedral Metallofullerenes by MEM/Rietveld Method 109 59-84 Takenobu T, see Margadonna S (2004) 109 127-164 Talarico G, see BudzelaarPHM (2003) 105 141-165 Taniguchi H, see Itoh M (2007) 124 89-118... [Pg.226]

A. Andreotti, M.P. Colomhini, G. Gautier, Proceedings of the Organic Materials in Wall Paintings Project Workshop, Prato/Florence (Italy), 17 June (2003). [Pg.254]

T. Da Ros and M. Prato, Medicinal chemistry with fullerenes and fullerene derivatives, Chem. Commun. (1999) 663-669. [Pg.374]

S. Marchesan, T. Da Ros, G. Spalluto, J. Balzarini, and M. Prato, Anti-HIV properties of cationic fullerene derivatives, Bioorg. Med. Chem. Lett., 15 (2005)... [Pg.374]

A. Bianco, K. Kostarelos, and M. Prato, Applications of carbon nanotubes in drug delivery, Curr. Opin. Chem. Biol., 9 (2005) 674—679. [Pg.376]

M. Prato, K. Kostarelos, and A. Bianco, Functionalized carbon nanotubes in drug design and discovery, Acc. Chem. Res., 41 (2008) 60-68. [Pg.376]

L. Lacerda, A. Bianco, M. Prato, and K. Kostarelos, Carbon nanotubes as nanomedicines From toxicology to pharmacology, Adv. Drug Deliv. Rev., 58 (2006) 1460-1470. [Pg.376]

Bianco A, Kostarelos K, Prato M (2005) Curr Opin Chem Biol 9(6) 674... [Pg.274]

The following procedure adapted from Prato et al. (1996) is an example of how glycine and formaldehyde derivatives may be used to create fullerene modifications for subsequent bioconjugation purposes. [Pg.629]

The following procedure for creating the N-H fulleropyrrolidine is adapted from Maggini et al. (1994), Prato and Maggini (1998), and Prato et al. (1996). Extreme care should be taken when using TFMSA, as this acid is 30 times stronger than concentrated sulfuric acid. [Pg.631]


See other pages where Prato is mentioned: [Pg.253]    [Pg.207]    [Pg.592]    [Pg.293]    [Pg.320]    [Pg.1217]    [Pg.343]    [Pg.291]    [Pg.307]    [Pg.207]    [Pg.107]    [Pg.291]    [Pg.484]    [Pg.93]    [Pg.1864]    [Pg.109]    [Pg.276]    [Pg.276]    [Pg.276]    [Pg.278]    [Pg.225]    [Pg.300]    [Pg.374]    [Pg.376]    [Pg.414]    [Pg.629]    [Pg.1049]   
See also in sourсe #XX -- [ Pg.629 , Pg.631 ]

See also in sourсe #XX -- [ Pg.141 ]




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Prato cycloaddition reaction

Prato reaction

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