Publication | Closed Access
An Efficient Biomimetic Cleavage of Aziridines with Nucleophiles Catalyzed by β-Cyclodextrin in Water
23
Citations
14
References
2001
Year
Combinatorial ChemistryRoom TemperatureEngineeringHeterocyclicCyclodextrin ProductionEfficient Biomimetic CleavageAromatic AminesOrganic ChemistryNucleophiles CatalyzedChemistrySynthetic ChemistryBiomolecular EngineeringGood Yields
Abstract β-Cyclodextrin catalyzed for the first time a facile ring opening of aziridines with nucleophiles such as aromatic amines and azides in water at room temperature to afford diamines and azidoamines respectively in good yields.
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