Publication | Closed Access
Regioselective Formation of Diazafulleroids Bridged by Glycol Diacetate and Glycol Chains
10
Citations
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References
1998
Year
Chemical EngineeringRegioselective FormationDouble 5EngineeringBiochemistryHeterocyclicNatural SciencesGlycol ChainsTriethylene Glycol DiazidesOrganic ChemistryGlycol DiacetateChemistryHeterocycle ChemistryAbstract Five DiazafulleroidsNatural Product SynthesisSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
Abstract Five diazafulleroids with neighbouring double 5, 6-insertion were regioselectively synthesized by the reactions of C60 with ethylene, diethylene, triethylene glycol di(2-azideacetates) and diethylene, triethylene glycol diazides in refluxing chlorobenzene.
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