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A mild and green chemistry approach for the synthesis of symmetrical spirooxindole derivatives

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Abstract

A simple and eco-friendly synthesis of the biologically important spirooxindole scaffold was done by the reaction of isatin with activated pyrazolones in the presence of a catalytic amount of p-toluenesulfonic acid in water at room temperature. A variety of symmetrical spirooxindole derivatives were obtained with excellent yields within short reaction time. This method is of great value because of its environmentally benign character, high yield, and easy handling.

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Acknowledgments

We gratefully acknowledge the financial support from the Research Council of the University of Isfahan.

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Correspondence to Abbas Rahmati.

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Rahmati, A., Rezayan, A.H., Alizadeh, M. et al. A mild and green chemistry approach for the synthesis of symmetrical spirooxindole derivatives. J IRAN CHEM SOC 10, 521–525 (2013). https://doi.org/10.1007/s13738-012-0187-z

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  • DOI: https://doi.org/10.1007/s13738-012-0187-z

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