C59N+: A key intermediate in azaheterofullerene chemistry
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Isolation of the Heterofullerene C 59 N as Its Dimer (C 59 N) 2
2. A new route to nitrogen heterofullerenes and the first synthesis of (C69N)2
3. Fullerene Carbon Resonance Assignments through 15N−13C Coupling Constants and Location of the sp3 Carbon Atoms of (C59N)2
4. Synthesis of C59(CHPh2)N from (C59N)2 and C59HN. The First Derivatization of C59N
5. Synthesis of hydroazafullerene C59HN, the parent hydroheterofullerene
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1. First Synthesis of the Inherently Chiral Trans ‐4′ Bisadduct of C 59 N Azafullerene by Using Cyclo‐ [2]‐dodecylmalonate as a Tether;Chemistry – A European Journal;2021-08-31
2. Solution-phase molecular recognition of an azafullerene-quinoline dyad by a face-to-face porphyrin-dimer tweezer;RSC Advances;2020
3. A Long‐Lived Azafullerenyl Radical Stabilized by Supramolecular Shielding with a [10]Cycloparaphenylene;Angewandte Chemie International Edition;2019-12-02
4. A Long‐Lived Azafullerenyl Radical Stabilized by Supramolecular Shielding with a [10]Cycloparaphenylene;Angewandte Chemie;2019-10-21
5. Tether‐Directed Regioselective Synthesis of an Equatorial face Bisadduct of Azafullerene Using Cyclo ‐[2]‐octylmalonate;Chemistry – A European Journal;2019-03-26
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