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A facile, efficient and substrate-selective oxidation of aldehydes to carboxylic acids with NaClO catalyzed by β-cyclodextrin in water has been developed. A series of aldehydes which could form inclusion complex with β-cyclodextrin (β-CD) were oxidized selectively with excellent yields.

A facile, efficient and substrate-selective oxidation of the primary amines with NaClO as oxidant catalyzed by β-cyclodextrin (β-CD) has been developed in water for the first time, and the behavior of β-cyclodextrin that catalyzed the primary amines to nitriles in water was investigated. It was found that the primary amines which could form host-guest complexes with β-cyclodextrin were oxidized to nitriles with excellent yields at ambient temperature. The results show that β-cyclodextrin worked not only as a solubilizing agent but also as a catalyst in these reactions.

A facile, substrate-selective and transition metal-free oxidation of benzylic and allylic alcohols catalyzed by β-cyclodextrin with NaOCl oxidant using water as an only solvent was developed.

A facile, efficient and substrate-selective oxidation of aldehydes to carboxylic acids with NaClO catalyzed by β-cyclodextrin in water has been developed. A series of aldehydes which could form inclusion complex with β-cyclodextrin (β-CD) were oxidized selectively with excellent yields.

A facile, substrate-selective and transition metal-free oxidation of benzylic and allylic alcohols catalyzed by β-cyclodextrin with NaOCl oxidant using water as an only solvent was developed.