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Title:	Triple Scission of a Six-Membered Ring on the Surface of C60 via Consecutive Pericyclic Reactions and Oxidative Cobalt Insertion
Source:	Journal of the American Chemical Society [0002-7863] Arce, María-José yr:1996

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description	1.	Murata, Y. "Solid-state [4+2] cycloaddition of fullerene C-60 with condensed aromatics using a high-speed vibration milling technique." Journal of organic chemistry 64.10 (1999): 3483-3488.
description	2.	Chuang, Shih-Ching C. "Fine tuning of the orifice size of an open-cage fullerene by placing selenium in the rim: insertion/release of molecular hydrogen." Chemical communications 2007.12 (2007): 1278-80.
description	3.	Zhang, Z. "Mechanochemical Diels-Alder Cycloaddition Reactions for Straightforward Synthesis of endo-Norbornene Derivatives." Synlett 19 (2010): 2895-2898.
description	4.	Saha, D. "Hydrogen adsorption on partially truncated and open cage C-60 fullerene." Carbon 48.12 (2010): 3471-3476.
description	5.	Levy, A. "Overcrowded 1,8-diazafluorenylidene-chalcoxanthenes. Introducing nitrogens at the fjord regions of bistricyclic aromatic enes." Organic & biomolecular chemistry 1.15 (2003): 2755-2763.
description	6.	Gareis, T. "Chromophore-appended C60 and C70 fullerenes. Anthracene and pyrene derivatives. Syntheses, cyclic voltammetry, and spectra." European journal of organic chemistry 8 (1998): 1549-1557.
description	7.	Yamamoto, Tatsuya a. "Selective synthesis, structure and oxidation properties of isomeric 1,4-dithiins fused to two benzo[b]thiophenes." Tetrahedron letters; 45.42 (2004): 7943-7946.
description	8.	Gelderman-Fuhrmann, Monique P. "Adverse effects of fullerenes on endothelial cells: Fullerenol C-60(OH)(24) induced tissue factor and ICAM-1 membrane expression and caused apoptosis in vitro." Blood 108.11 (2006): 511-511.
description	9.	Hawker, Craig J. "A Simple and Versatile Method for the Synthesis of C60 Copolymers." Macromolecules 27.17 (1994): 4836-4837.
description	10.	Iwamatsu, S. "Open-Cage Fullerene Derivatives Suitable for the Encapsulation of a Hydrogen Molecule." Journal of organic chemistry 70.12 (2005): 4820-4825.
description	11.	Xu, Daiwang W. "A one-pot regiospecific synthesis of highly functionalized 1,4-benzodioxin derivatives from an electrochemically induced Diels-Alder reaction." Organic letters 7.23 (2005): 5273-5276.
description	12.	Liu, S. "A new bioimaging carrier for fluorescent quantum dots: Phospholipid nanoemulsion mimicking natural lipoprotein core." Drug delivery 13.2 (2006): 159-164.
description	13.	Senna, M. "Consequences of molecular strain on the solid state addition reaction." Journal of materials science 39.16-17 (2004): 4995-5001.
description	14.	Hayashi, T. "Synthesis of (E)-1-Benzyloxy-3-fluoro-1,3-butadiene: A Novel Fluorinated Diene for Diels-Alder Reactions." Synlett 19 (2010): 2843-2846.
description	15.	Goksu, G. "Reductive Heck reactions of N-methyl-substituted tricyclic imides." Molecules 15.3 (2010): 1302-1308.
description	16.	Wakahara, T. "Preparation of endohedral metallofullerene nanowhiskers and nanosheets." Carbon 48.12 (2010): 3359-3363.
description	17.	Jeong, W. "Bio-Based Rubbers by Concurrent Cationic and Ring-Opening Metathesis Polymerization of a Modified Linseed Oil." Macromolecular materials and engineering 294.11 (2009): 756-761.
description	18.	Franc, G. ""Click'' methodologies: efficient, simple and greener routes to design dendrimers." Chemical Society reviews 39.5 (2010): 1536-1544.
description	19.	Weis, Christine e. "Fullerene-End-Capped Polystyrenes. Monosubstituted Polymeric C60 Derivatives." Macromolecules 28.1 (1995): 403-405.
description	20.	Maggini, M. "Addition of azomethine ylides to C60: synthesis, characterization, and functionalization of fullerene pyrrolidines." Journal of the American Chemical Society 115.21 (1993): 9798-9799.