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Synlett 1997; 1997(10): 1196-1198
DOI: 10.1055/s-1997-980
DOI: 10.1055/s-1997-980
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© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
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or duplication of any kind, translating, preparation of microfilms, and electronic
data processing and storage.Dirhodium(II) Tetraacetate-Mediated Decomposition of Ethyldiazoacetate and Ethyldiazomalonate in the Presence of Fullerene. A New Procedure for the Selective Synthesis of [6-6]-Closed Methanofullerenes
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Publikationsverlauf
Publikationsdatum:
31. Dezember 2000 (online)

The reaction of C60 fullerene with carboalkoxycarbenoids generated by Rh2(OAc)4-catalyzed decomposition of α-diazoester precursors is reported. This reaction is the first example of a transition metal catalyzed carbenoid reaction with fullerene and represents a significative improvement in terms of reaction conditions, selectivity of the products obtained, and yields over previously reported methods.
fullerene - dirhodium(II)tetraacetate - carbenoidic reactions - carboalkoxymethanofullerene