Issue 39, 2015
From the journal:

RSC Advances

TsOH-mediated reaction of aziridinofullerene with diols for the preparation of fullerene-fused dioxygenated ring compounds†

Jun Wu,a   Fa-Bao Li,*a   Xiao-Feng Zhang,a   Ji-Long Shia  and  Li Liu*a  

* Corresponding authors

a Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, School of Chemistry and Chemical Engineering, Hubei University, Wuhan 430062, P. R. China
E-mail: lfb0615@hubu.edu.cn, liulihubei@hubu.edu.cn

Abstract

The double nucleophilic substitution reaction of aziridinofullerene with diols in the presence of p-toluenesulfonic acid affords a series of rare fullerene-fused dioxygenated ring compounds with six- to ten-membered heterocycles. A possible reaction mechanism for product formation is proposed.

Graphical abstract: TsOH-mediated reaction of aziridinofullerene with diols for the preparation of fullerene-fused dioxygenated ring compounds

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Article information

DOI
https://doi.org/10.1039/C5RA03751D
Article type
Paper
Submitted
03 Mar 2015
Accepted
24 Mar 2015
First published
24 Mar 2015

RSC Adv., 2015,5, 30549-30554

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TsOH-mediated reaction of aziridinofullerene with diols for the preparation of fullerene-fused dioxygenated ring compounds

J. Wu, F. Li, X. Zhang, J. Shi and L. Liu, RSC Adv., 2015, 5, 30549 DOI: 10.1039/C5RA03751D

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