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A facile synthesis of 1,2-azidoalcohols by (TBA) 4PFeW11O39·3H2O-catalyzed azidolysis of epoxides with NaN3

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The catalytic efficiency of transition metal substituted polyoxometalates in the azidolysis of 1,2-epoxides has been studied in acetonitrile/water, using NaN3 as the source of the azido group. The reaction is regioselective and afforded the corresponding products in high to excellent yields under mild reaction conditions. Fe (III) substituted polyoxometalate was identified as the optimal catalyst.

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Acknowledgments

We are grateful to Institute for Advanced Studies in Basic Sciences (IASBS) for financial support of this work.

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Yadollahi, B., Danafar, H. A facile synthesis of 1,2-azidoalcohols by (TBA) 4PFeW11O39·3H2O-catalyzed azidolysis of epoxides with NaN3 . Catal Lett 113, 120–123 (2007). https://doi.org/10.1007/s10562-007-9021-0

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