BF3·Et2O- or DMAP-Catalyzed Double Nucleophilic Substitution Reaction of Aziridinofullerenes with Sulfamides or Amidines
Author:
Affiliation:
1. School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China
2. Key Laboratory of Novel Thin Film Solar Cells, Institute of Plasma Physics, Chinese Academy of Sciences, P.O. Box 1126, Hefei 230031, China
Funder
National Natural Science Foundation of China
Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University
National Natural Science Foundation of Jiangsu Province
Priority Academic Program Development of Jiangsu Higher Education Institutions
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo5020596
Reference50 articles.
1. Visible-Light-Mediated Addition of α-Aminoalkyl Radicals to [60]Fullerene by Using Photoredox Catalysts
2. Ferric Chloride-Catalyzed Reaction of [60]Fullerene with tert-Butyl N-Substituted Carbamates: Synthesis of Oxazolidino[4,5:1,2][60]fullerenes
3. Synthesis of [60]Fullerene-Fused Tetrahydrobenzooxepine and Isochroman Derivatives via Hydroxyl-Directed C–H Activation/C–O Cyclization
4. Synthesis of [60]Fullerene-Fused Tetrahydroazepinones and Azepinonimines via Cu(OAc)2-Promoted N-Heteroannulation Reaction
5. Cu-Catalyzed C–H Amination of Hydrofullerenes Leading to 1,4-Difunctionalized Fullerenes
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