Issue 30, 2015

Copper(i)-catalyzed heteroannulation of [60]fullerene with ketoxime acetates: preparation of novel 1-fulleropyrrolines

Abstract

A cuprous bromide-catalyzed heteroannulation reaction of [60]fullerene with ketoxime acetates has been exploited to prepare novel 1-fulleropyrrolines through the cleavage of N–O and C–H bonds and formation of C–C and C–N bonds under thermal conditions. A plausible mechanism for the formation of 1-fulleropyrrolines is proposed on the basis of the experimental results. The electrochemistry of the obtained products has also been investigated.

Graphical abstract: Copper(i)-catalyzed heteroannulation of [60]fullerene with ketoxime acetates: preparation of novel 1-fulleropyrrolines

Supplementary files

Article information

Article type
Communication
Submitted
09 Feb 2015
Accepted
03 Mar 2015
First published
05 Mar 2015

Chem. Commun., 2015,51, 6548-6551

Author version available

Copper(I)-catalyzed heteroannulation of [60]fullerene with ketoxime acetates: preparation of novel 1-fulleropyrrolines

S. Jiang, Y. Su, K. Liu, Q. Wu and G. Wang, Chem. Commun., 2015, 51, 6548 DOI: 10.1039/C5CC01198A

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