| Literature DB >> 30729784 |
Yun-Fei Li1, Duo Zhang1, Hui-Juan Wang2, Fa-Bao Li1, Liang Sun1, Li Liu1, Chao-Yang Liu2, Abdullah M Asiri3, Khalid A Alamry3.
Abstract
A series of scarce N-alkyl-2,5-unsubstituted/monosubstituted fulleropyrrolidines were synthesized in moderate to excellent yields by the simple one-step thermal reaction of [60]fullerene with primary/secondary amines in the presence of paraformaldehyde without the addition of valuable metal salts. Intriguingly, the reaction with primary amines unexpectedly afforded N-alkyl-2,5-unsubstituted fulleropyrrolidines instead of the anticipated 2,5-monosubstituted fulleropyrrolidines. A plausible reaction pathway is proposed to elucidate the above-mentioned reaction process based on the experimental results.Entities:
Year: 2019 PMID: 30729784 DOI: 10.1021/acs.joc.9b00083
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354