Issue 11, 2018

Stereoselective synthesis of cyclopentafullerenes: the reaction of [60]fullerene with aldehydes and triethylamine promoted by magnesium perchlorate

Abstract

The magnesium perchlorate-mediated reaction of [60]fullerene with aldehydes and triethylamine under air conditions afforded a series of rare cyclopentafullerenes in moderate to good yields with high stereoselectivity. A plausible reaction mechanism was suggested to elucidate the formation of cyclopentafullerenes.

Graphical abstract: Stereoselective synthesis of cyclopentafullerenes: the reaction of [60]fullerene with aldehydes and triethylamine promoted by magnesium perchlorate

Supplementary files

Article information

Article type
Paper
Submitted
31 Mar 2018
Accepted
26 Apr 2018
First published
30 Apr 2018

New J. Chem., 2018,42, 9291-9299

Stereoselective synthesis of cyclopentafullerenes: the reaction of [60]fullerene with aldehydes and triethylamine promoted by magnesium perchlorate

M. Zhang, H. Zhang, H. Wang, F. Li, Y. Huang, L. Liu, C. Liu, A. M. Asiri and K. A. Alamry, New J. Chem., 2018, 42, 9291 DOI: 10.1039/C8NJ01578C

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