Issue 90, 2013

The first one-pot synthesis of a chiral pentakis-adduct of C60 utilising an opened-structure malonate tether

Abstract

A pentakis-adduct of C60 with an incomplete octahedral addition pattern was synthesised via a one-pot procedure using a tether equipped with five malonate moieties. The five-fold Bingel cyclopropanation of C60 was completely regioselective and afforded a chiral, C2-symmetric pentakis-adduct which was easily separated by column chromatography on SiO2.

Graphical abstract: The first one-pot synthesis of a chiral pentakis-adduct of C60 utilising an opened-structure malonate tether

Supplementary files

Article information

Article type
Communication
Submitted
04 Sep 2013
Accepted
25 Sep 2013
First published
26 Sep 2013

Chem. Commun., 2013,49, 10611-10613

The first one-pot synthesis of a chiral pentakis-adduct of C60 utilising an opened-structure malonate tether

C. P. Ioannou and N. Chronakis, Chem. Commun., 2013, 49, 10611 DOI: 10.1039/C3CC46755D

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