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Synthesis of some 5-aryl(hetaryl)tetrazoles by ultrasonication

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The influence of ultrasound on the 1,3-dipolar cycloadditio of azides to organic nitriles to form of 1H-5-aryl(hetary)tetrazoles was studied. It was shown that ultrasound decreases the reaction time, and increases the yield of the desired compounds.

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References

  1. M. Haiza, J. Lee, and J. K. Snuder, J. Org. Chem.,55, 5008 (1990).

    Google Scholar 

  2. C. Einhorn, J. Einhorn, and L. Luche, Synthesis, No. 11, 793 (1989).

  3. W. J. Finnegan, R. H. Henry, and A. Lofgyst, J. Am. chem. Soc.,80, 3908 (1958).

    Google Scholar 

  4. V. A. Ostrovskii, V. S. Poplavskii, G. I. Koldobskii, and G. B. Erusalimskii, Khim. Geterotsikl. Soedin., No. 9, 1214 (1912).

  5. I. E. Tutova, V. S. Poplavskii, G. I. Koldobskii, V. A. Ostrovskii, V. D. Nikolaev, and G. B. Erusalimskii, Khim. Geterotsikl. Soedin., No. 8, 1086 (1986).

  6. G. I. Koldobskii, V. A. Ostrovskii, and V. S. Poplavskii, Khim. Geterotsikl. Soedin., No. 10, 1308 (1981).

  7. A. M. Goluba, Kh. Kelera, and V. V. Skopenko (eds.), The Chemistry of Pseudohalogenides [in Russian], High School, Kiev (1981), p. 23.

    Google Scholar 

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Institute of Organic Synthesis, Ural Region Russian Academy of Sciences, Ekaterinburg, 620219. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1375–1377. Original article submitted November 1, 1994.

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Pusinov, G.L., Ishmetova, R.I., Kitaeva, V.G. et al. Synthesis of some 5-aryl(hetaryl)tetrazoles by ultrasonication. Chem Heterocycl Compd 30, 1192–1194 (1994). https://doi.org/10.1007/BF01184883

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  • DOI: https://doi.org/10.1007/BF01184883

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