By using methyl(trifluoromethyl)dioxirane (TFDO), the direct mono- and bishydroxylation of cubane could be achieved in high yield under remarkably mild conditions. Comparison of the rates of dioxirane O-insertion with those of standard reference compounds, such as adamantine and cyclopropane, as well as ab initio computations provide useful hints concerning the mechanism of these transformations.

Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 6. On the Selective Hydroxylation of Cubane

Fusco C;
2009

Abstract

By using methyl(trifluoromethyl)dioxirane (TFDO), the direct mono- and bishydroxylation of cubane could be achieved in high yield under remarkably mild conditions. Comparison of the rates of dioxirane O-insertion with those of standard reference compounds, such as adamantine and cyclopropane, as well as ab initio computations provide useful hints concerning the mechanism of these transformations.
2009
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Inglese
11
3574
3577
4
Sì, ma tipo non specificato
6
info:eu-repo/semantics/article
262
Annese, C; D'Accolti, L; Fusco, C; Gandolfi, R; Eaton, P E; Curci, R
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/158522
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