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Synthesis of a new heterocyclic system, 1-halomethyl-2-oxa-5-azoniaspiro[4.5]decane halides

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Abstract

1-Halomethyl-2-oxa-5-azoniaspiro[4.5]decane halides were synthesized by reaction of 1-(2-vinyloxy) ethylpiperidine with bromine and iodine. The product structure was confirmed by 1H NMR and IR spectroscopy, and their steric configuration was optimized in terms of the density functional theory.

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References

  1. Amosova, S.V., Nikol’skaya, A.N., Belogorlova, N.A., Gendin, D.V., Kashik, T.V., and Larin, M.F., Khim. Geterotsikl. Soedin., 1988, p. 982.

  2. Mikhant’ev, B.I., Mikhant’ev, V.B., Lapenko, V.L., and Voinov, V.K., Nekotorye vinil’nye monomery (Some Vinyl Monomers), Voronezh: Voronezh. Gos. Univ., 1970, p. 48.

    Google Scholar 

  3. Pokonova, Yu.V., Galoidefiry (Halo Ethers), Moscow: Khimiya, 1966, p. 227.

    Google Scholar 

  4. Shostakovskii, M.F., Skvortsova, G.G., and Tyrina, S.M., Khimiya atsetilena (Chemistry of Acetylene), Moscow: Nauka, 1972, p. 90.

    Google Scholar 

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Correspondence to D. G. Kim.

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Original Russian Text © D.G. Kim, A.L. Frolov, 2011, published in Zhurnal Organicheskoi Khimii, 2011, Vol. 47, No. 3, pp. 457–458.

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Kim, D.G., Frolov, A.L. Synthesis of a new heterocyclic system, 1-halomethyl-2-oxa-5-azoniaspiro[4.5]decane halides. Russ J Org Chem 47, 454–455 (2011). https://doi.org/10.1134/S1070428011030237

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  • DOI: https://doi.org/10.1134/S1070428011030237

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